Pierwotna postępująca afazja
Charakterystyka, pielęgnacja i opieka
Pierwotna postępująca afazja (PPA) to neurodegeneracyjne schorzenie z grupy zwyrodnień czołowo-skroniowych, charakteryzujące się stopniowym pogarszaniem funkcji językowych przy względnie zachowanych innych funkcjach poznawczych przez pierwsze 2 lata. Diagnoza i leczenie wymagają multidyscyplinarnego podejścia, angażującego neurologów, neuropsychologów, logopedów, psychiatrów oraz pracowników socjalnych. Terapia logopedyczna, choć nie zatrzymuje progresji choroby, jest kluczowa dla utrzymania zdolności komunikacyjnych i jakości życia pacjentów. Zaleca się spersonalizowane programy terapeutyczne, uwzględniające codzienne potrzeby pacjenta, z regularnymi kontrolami co około 6 miesięcy. W terapii stosuje się także strategie kompensacyjne i alternatywne metody komunikacji, w tym technologie AAC, takie jak tablety z oprogramowaniem komunikacyjnym czy urządzenia text-to-speech. Wsparcie rodzin i opiekunów, obejmujące edukację, doradztwo oraz planowanie opieki długoterminowej, jest integralną częścią kompleksowej opieki nad chorymi.
- Wprowadzenie do afazja/” title=”pierwotna postępująca afazja” class=”to-tag” data-termid=”63698″>pierwotnej postępującej afazji
- Zespół wielospecjalistyczny w opiece nad pacjentem z PPA
- Logopedia jako podstawowa forma terapii
- Cele i metody terapii logopedycznej
- Indywidualizacja terapii logopedycznej
- Grupowe interwencje logopedyczne
- Strategie kompensacyjne i alternatywne formy komunikacji
- Wsparcie dla opiekunów i rodzin
- Planowanie długoterminowej opieki
- Innowacyjne podejścia terapeutyczne
- Jakość życia i dobre samopoczucie
- Wyzwania związane z opieką nad pacjentami z PPA
- Podsumowanie podejścia do opieki nad pacjentem z PPA
Wprowadzenie do afazja/” title=”pierwotna postępująca afazja” class=”to-tag” data-termid=”63698″>pierwotnej postępującej afazji
Pierwotna postępująca afazja (PPA) jest rzadkim schorzeniem neurologicznym charakteryzującym się stopniowym pogarszaniem się zdolności językowych i komunikacyjnych. W przeciwieństwie do innych typów afazji, które są spowodowane nagłymi zdarzeniami jak udar czy uraz mózgu, PPA jest schorzeniem neurodegeneracyjnym, które prowadzi do powolnego, ale postępującego uszkodzenia obszarów mózgu odpowiedzialnych za mowę i język.12 PPA zaliczana jest do spektrum chorób związanych z zwyrodnieniem czołowo-skroniowym (FTD), choć może być również związana z innymi schorzeniami neurodegeneracyjnymi, takimi jak choroba Alzheimera.34
Pacjenci z PPA początkowo doświadczają trudności językowych, podczas gdy inne funkcje poznawcze, takie jak pamięć czy rozumowanie, pozostają względnie zachowane przez co najmniej pierwsze dwa lata choroby.5 Osoby dotknięte tym schorzeniem mogą przez wiele lat zachować zdolność do samodzielnej opieki i uczestnictwa w codziennych aktywnościach, jednak z biegiem czasu trudności komunikacyjne narastają, co ostatecznie prowadzi do utraty zdolności mówienia i pisania.67
Zespół wielospecjalistyczny w opiece nad pacjentem z PPA
Diagnoza i leczenie pierwotnej postępującej afazji wymaga zaangażowania wielodyscyplinarnego zespołu specjalistów. Ze względu na złożoność tego schorzenia, skuteczna opieka powinna obejmować współpracę różnych profesjonalistów medycznych, którzy wspólnie tworzą kompleksowy plan leczenia.89
Kluczowi członkowie zespołu terapeutycznego
W skład zespołu opieki nad pacjentem z PPA mogą wchodzić:1011
- Neurolog – specjalista w zakresie zaburzeń mózgu, który stawia diagnozę i monitoruje objawy choroby
- Neuropsycholog – ocenia zdolności poznawcze za pomocą specjalistycznych testów
- Logopeda – odgrywa kluczową rolę, zapewniając strategie maksymalizujące zdolności komunikacyjne
- Psychiatra – pomaga w zarządzaniu objawami behawioralnymi i nastrojowymi
- Pracownik socjalny – wspiera rodziny w podejmowaniu trudnych decyzji związanych z diagnozą
- Fizjoterapeuta i terapeuta zajęciowy – pomagają optymalizować ruch i czynności życia codziennego
- Specjaliści terapii kreatywnych – wspierają alternatywne formy ekspresji
Skład zespołu terapeutycznego może się różnić w zależności od indywidualnych potrzeb pacjenta i etapu choroby.12 W miarę postępu choroby mogą być włączani dodatkowi specjaliści, tacy jak specjaliści opieki paliatywnej czy hospicyjnej.13
Rola koordynacji opieki
Skuteczna koordynacja opieki jest kluczowa dla zapewnienia kompleksowego wsparcia pacjentom z PPA. Centra medyczne specjalizujące się w leczeniu PPA często oferują zintegrowane podejście, łączące neurologię, logopedię i opiekę wspierającą, aby pomóc pacjentom i ich rodzinom w radzeniu sobie z tą chorobą.14 Ważne jest, aby członkowie zespołu terapeutycznego komunikowali się ze sobą i koordynowali swoje działania w celu zapewnienia spójnej opieki.15
Pacjenci ze zdiagnozowaną PPA powinni zostać skierowani do ośrodków specjalistycznych posiadających doświadczenie w leczeniu tego rzadkiego schorzenia. Niestety, ze względu na rzadkość występowania PPA, wiele placówek opieki zdrowotnej ma ograniczone doświadczenie w leczeniu tego schorzenia.1617
Logopedia jako podstawowa forma terapii
Terapia logopedyczna jest uznawana za główną i najbardziej skuteczną formę interwencji dla pacjentów z pierwotną postępującą afazją.1819 Chociaż nie może ona zatrzymać postępu choroby, może znacząco poprawić jakość życia pacjentów poprzez utrzymanie zdolności komunikacyjnych tak długo, jak to możliwe.20
Cele i metody terapii logopedycznej
Główne cele terapii logopedycznej w PPA obejmują:2122
- Poprawę umiejętności komunikacyjnych, takich jak mówienie, pisanie i rozumienie języka
- Nauczanie alternatywnych metod komunikacji
- Wzmacnianie mięśni niezbędnych do mowy i pisania
- Poprawę pamięci i uwagi
- Maksymalizację niezależności funkcjonalnej
Logopedzi opracowują spersonalizowane plany terapeutyczne dostosowane do specyficznych potrzeb każdego pacjenta.23 W przeciwieństwie do terapii afazji poudarowej, w przypadku PPA nie należy oczekiwać takiego samego przeniesienia umiejętności, ponieważ choroba ma charakter postępujący.24
Indywidualizacja terapii logopedycznej
Skuteczna terapia logopedyczna dla pacjentów z PPA musi być spersonalizowana i skoncentrowana na słowach i zdaniach używanych w codziennym życiu pacjenta.25 Ogólne ćwiczenia nie są odpowiednie w terapii logopedycznej dla PPA.26 Bardzo ważne jest, aby rodzina została włączona w sesje terapii logopedycznej, aby mogła nauczyć się, jak wspierać komunikację w miarę upływu czasu.27
Po pierwszej rundzie terapii logopedycznej, pacjent i jego rodzina powinni odwiedzać logopedę co około sześć miesięcy. W miarę postępu PPA może być zalecana kolejna runda terapii, aby pacjent i jego rodzina mogli nauczyć się nowych strategii wspomagających komunikację.28
Grupowe interwencje logopedyczne
Oprócz indywidualnej terapii logopedycznej, osoby z PPA mogą również korzystać z terapii grupowej. Specjaliści w dziedzinie logopedii opracowali wytyczne dotyczące prowadzenia grup terapeutycznych dla osób z PPA.29 Takie grupy oferują nie tylko korzyści terapeutyczne, ale również wsparcie społeczne i emocjonalne poprzez kontakt z innymi osobami doświadczającymi podobnych trudności.3031
Przykładem takiego programu jest „Staying Connected” – 8-tygodniowy program edukacyjny dla osób z PPA i ich opiekunów, prowadzony przez logopedów. Program ten koncentruje się na edukacji na temat PPA oraz oferuje wsparcie zarówno dla pacjentów, jak i ich opiekunów.32
Strategie kompensacyjne i alternatywne formy komunikacji
Ponieważ PPA jest chorobą postępującą, opracowywanie i wdrażanie strategii kompensacyjnych oraz alternatywnych form komunikacji jest kluczowym elementem planu terapeutycznego.3334
Techniki wspierania komunikacji
Specjaliści mogą rekomendować różne strategie wspierające komunikację:3536
- Uproszczenie mowy – używanie prostych, konkretnych zdań bez infantylizowania przekazu
- Komunikacja niewerbalna – wykorzystanie gestów, wskazywania na obrazki czy przedmioty
- Karty identyfikacyjne – zawierające informację o trudnościach komunikacyjnych pacjenta
- Materiały wizualne – tablice z obrazkami, zdjęciami lub słowami
- Spowolnienie tempa komunikacji – dawanie pacjentowi czasu na odpowiedź
- Komunikacja twarzą w twarz – pozwalająca na obserwację mimiki i mowy ciała
- Minimalizacja rozpraszaczy – redukowanie hałasu tła i innych dystrakcji
W przypadku rozmowy z osobą z PPA, pomocne może być:37
- Cierpliwość, ciepło i zrozumienie
- Znajdowanie cichego miejsca do rozmowy
- Unikanie zadawania więcej niż jednego pytania naraz
- Uznawanie frustracji pacjenta, nie lekceważenie jej
- Pytanie pacjenta, jak można pomóc mu w komunikacji
- Mówienie wyraźnie i tak, aby pacjent mógł widzieć twarz mówiącego
- Sprawdzanie, czy przekaz został zrozumiany
Technologie wspomagające komunikację
Wraz z postępem choroby i pogarszaniem się zdolności werbalnych, coraz większą rolę odgrywają technologie wspomagające komunikację (AAC – Augmentative and Alternative Communication).3839
Do rozwiązań technologicznych wspierających komunikację należą:4041
- Tablety i aplikacje – specjalistyczne oprogramowanie do komunikacji
- Urządzenia typu „text-to-speech” – zamieniające tekst na mowę
- Banki głosu – nagrywanie głosu pacjenta przed znacznym pogorszeniem mowy, do wykorzystania w przyszłości
- Nieskomplikowane technologie – tablice komunikacyjne, albumy ze zdjęciami, karty z obrazkami
Badania prowadzone w obszarze alternatywnych i wspomagających metod komunikacji dostarczają obiecujących wyników dotyczących poprawy konwersacji w codziennych sytuacjach dla osób z PPA.42 Logopedzi powinni pomagać w doborze odpowiednich narzędzi technologicznych, uwzględniając indywidualne potrzeby i preferencje pacjenta.43
Wsparcie dla opiekunów i rodzin
Pierwotna postępująca afazja wpływa nie tylko na osobę chorą, ale również na jej rodzinę i bliskich. Utrata zdolności komunikacyjnych może być źródłem stresu i frustracji zarówno dla pacjenta, jak i dla jego opiekunów.44 Dlatego kompleksowa opieka nad pacjentem z PPA powinna obejmować również wsparcie dla rodziny i opiekunów.45
Edukacja i wsparcie rodzin
Rodziny i opiekunowie pacjentów z PPA powinni otrzymać odpowiednie szkolenie i wsparcie, aby skutecznie radzić sobie z wyzwaniami komunikacyjnymi.46 Kluczowe elementy wsparcia dla rodzin obejmują:4748
- Edukację na temat choroby – zrozumienie natury PPA i jej progresji
- Naukę strategii komunikacyjnych – dostosowanych do specyficznych potrzeb pacjenta
- Wsparcie emocjonalne – pomoc w radzeniu sobie ze stresem i frustracją
- Informacje o dostępnych zasobach – grupach wsparcia, usługach społecznych i opiece długoterminowej
- Planowanie przyszłej opieki – włączając kwestie finansowe i prawne
Pracownicy socjalni mogą odgrywać ważną rolę we wspieraniu rodzin, oferując:49
- Omówienie diagnozy i dostarczenie aktualnych informacji o chorobie
- Wskazówki dotyczące komunikacji w obliczu zmieniających się zdolności językowych
- Doradztwo w zakresie zmieniających się ról w rodzinie
- Pomoc w zapewnieniu opiekunom odpowiedniej samoopieki i wzmacnianiu sieci wsparcia
- Skierowania do indywidualnego, małżeńskiego lub rodzinnego poradnictwa
- Pomoc w kontakcie z prawnikami specjalizującymi się w prawie starszych osób
- Doradztwo w zakresie dyrektyw na przyszłość
Grupy wsparcia i zasoby społecznościowe
Grupy wsparcia mogą być niezwykle wartościowe dla osób z PPA i ich opiekunów, oferując możliwość wymiany doświadczeń i strategii radzenia sobie z chorobą.5051 Organizacje takie jak National Aphasia Association, Association for Frontotemporal Degeneration czy lokalne grupy wsparcia mogą dostarczyć cennych informacji i wsparcia emocjonalnego.52
Centra specjalistyczne często oferują programy poprawiające jakość życia, które mogą być pomocne dla osób z PPA i ich rodzin.53 Programy te mogą obejmować:54
- Grupy edukacyjne i wsparcia
- Zajęcia ruchowe
- Wydarzenia społeczne
- Programy zapewniające celowe i znaczące aktywności
Ważne jest również, aby opiekunowie pamiętali o własnych potrzebach i dbali o swoje zdrowie fizyczne i psychiczne.55 Odpoczynek, zachowanie czasu na aktywności społeczne i korzystanie z dostępnych zasobów wsparcia może pomóc opiekunom w radzeniu sobie z wyzwaniami związanymi z opieką nad osobą z PPA.56
Planowanie długoterminowej opieki
Ponieważ PPA jest chorobą postępującą, ważne jest wczesne planowanie przyszłej opieki. W miarę postępu choroby pacjenci będą wymagać coraz większego wsparcia w codziennym funkcjonowaniu.57
Kwestie prawne i finansowe
Rodziny osób z PPA powinny rozważyć następujące kwestie prawne i finansowe:5859
- Pełnomocnictwa – do podejmowania decyzji medycznych i finansowych
- Planowanie majątku – testament, trust i inne dokumenty prawne
- Ubezpieczenie długoterminowej opieki – możliwości finansowania przyszłej opieki
- Świadczenia dla osób niepełnosprawnych – programy rządowe i inne formy wsparcia
- Dyrektywy dotyczące opieki zdrowotnej – preferencje dotyczące przyszłego leczenia
Ważne jest, aby rozpocząć ten proces wcześnie, kiedy pacjent z PPA jest jeszcze w stanie uczestniczyć w podejmowaniu decyzji dotyczących swojej przyszłej opieki.6061 Jak podkreśla aktorka Kimberly Williams-Paisley, dzieląc się doświadczeniem swojej rodziny z PPA: „Przydałoby się wiedzieć, czego chciała moja matka w zakresie długoterminowej opieki. […] To jest rodzaj pytania, które chciałabym, żebyśmy zadali, zanim było za późno.”62
Przejście do opieki instytucjonalnej
W zaawansowanych stadiach PPA większość pacjentów będzie wymagać specjalistycznej opieki, która może obejmować opiekę domową lub instytucjonalną.63 Ważne jest, aby personel placówek opiekuńczych był świadomy specyficznych potrzeb osób z PPA, chociaż ze względu na rzadkość tego schorzenia może być trudno znaleźć placówkę lub personel zaznajomiony z PPA.64
Niektóre ośrodki opiekuńcze oferują specjalistyczne programy dla osób z zaburzeniami komunikacyjnymi, a personel może skorzystać z krótkich filmów edukacyjnych i innych materiałów informacyjnych na temat PPA.65 Opieka domowa może również oferować wiele korzyści dla pacjentów z afazją, umożliwiając im pozostanie w znajomym środowisku, co może zwiększyć stopień powrotu do zdrowia.66
Innowacyjne podejścia terapeutyczne
Chociaż pierwotna postępująca afazja jest chorobą nieuleczalną, naukowcy badają nowe podejścia terapeutyczne, które mogą pomóc w zarządzaniu objawami i poprawie jakości życia pacjentów.67
Przezczaszkowa stymulacja prądem stałym
Jednym z obiecujących podejść jest przezczaszkowa stymulacja prądem stałym (tDCS), która może być stosowana jako uzupełnienie terapii logopedycznej.68 Ta nieinwazyjna technika wykorzystuje słaby prąd elektryczny do stymulowania określonych obszarów mózgu i może potencjalnie zwiększyć skuteczność treningu językowego u pacjentów z PPA.69
Badanie kierowane przez dr Leigh Charvet wykazało, że pacjenci z PPA, którzy przeszli 20 codziennych sesji 45-minutowego spersonalizowanego treningu odzyskiwania słów z jednoczesną stymulacją tDCS lewego dolnego zakrętu czołowego przez pierwsze 30 minut, wykazali poprawę w nazywaniu ćwiczonych elementów w porównaniu z niećwiczonymi.70
Telemedycyna i zdalne usługi terapeutyczne
Pandemia COVID-19 przyspieszyła rozwój usług telemedycznych, które mogą być szczególnie korzystne dla pacjentów z PPA, zwłaszcza tych mieszkających z dala od specjalistycznych ośrodków medycznych.71 Zdalne świadczenie usług logopedycznych i innych form terapii może zwiększyć dostęp do specjalistycznej opieki i poprawić wyniki leczenia.72
Jak wyjaśnia dr Rogalski: „Znaleźliśmy sposób na świadczenie opieki, który tworzy nieco bardziej równe pole gry. Osoby z PPA nie muszą mieszkać obok dużego akademickiego centrum medycznego lub ośrodka specjalistycznego, aby skontaktować się z ekspertem i otrzymać leczenie.”73
Jakość życia i dobre samopoczucie
Mimo że pierwotna postępująca afazja jest schorzeniem postępującym, istnieje wiele strategii, które mogą pomóc w utrzymaniu dobrej jakości życia pacjentów.74
Utrzymanie aktywności fizycznej i społecznej
Badania wykazały, że aktywność fizyczna sprzyja zdrowiu mózgu i poprawia nastrój oraz ogólną sprawność.75 Zrównoważona dieta, odpowiednia ilość snu i ograniczone spożycie alkoholu to inne ważne sposoby promowania dobrego zdrowia.76
Utrzymanie kontaktów społecznych i uczestnictwo w znaczących aktywnościach jest również kluczowe dla dobrego samopoczucia psychicznego.77 Osoby z PPA powinny być zachęcane do kontynuowania hobby i aktywności, które sprawiają im przyjemność, tak długo, jak to możliwe.78
Zarządzanie zdrowiem psychicznym
Osoby z PPA mogą doświadczać depresji lub lęku ze względu na problemy z mową i językiem.79 Te problemy są uleczalne, dlatego ważne jest, aby były wykrywane i skutecznie zarządzane, w tym poprzez skierowanie do specjalisty zdrowia psychicznego, gdy jest to potrzebne.80
Niektóre leki, takie jak selektywne inhibitory wychwytu zwrotnego serotoniny, mogą być pomocne w leczeniu objawów depresji i lęku związanych z PPA.8182
Wyzwania związane z opieką nad pacjentami z PPA
Opieka nad pacjentami z pierwotną postępującą afazją wiąże się z wieloma wyzwaniami, zarówno dla systemów opieki zdrowotnej, jak i dla samych pacjentów i ich rodzin.83
Bariery w dostępie do specjalistycznej opieki
Jednym z głównych wyzwań jest ograniczony dostęp do specjalistycznej opieki dla osób z PPA. Ze względu na rzadkość tego schorzenia, wielu pacjentów może doświadczać:8485
- Opóźnionej lub nieprawidłowej diagnozy – prowadzącej do opóźnień w dostępie do ograniczonych opcji leczenia
- Ograniczonego dostępu do logopedów – mimo że jest to kluczowa forma interwencji
- Nierówności geograficznych – różnice w dostępie do specjalistycznej opieki w zależności od lokalizacji
- Ograniczonej wiedzy na temat PPA wśród pracowników służby zdrowia – co może wpływać na jakość opieki
Istnieje pilna potrzeba poprawy dostępu do specjalistycznej opieki dla osób z PPA, w tym do usług logopedycznych na poziomie krajowym.8687
Potrzeby edukacyjne profesjonalistów
Badania wykazały znaczne braki w przygotowaniu i wsparciu zawodowym, które otrzymują logopedzi na całym świecie, charakteryzujące się niewystarczającym czasem poświęconym na PPA podczas kursów uniwersyteckich, rzadkim kontaktem z PPA podczas praktyk klinicznych, ograniczonym dostępem do mentorów będących ekspertami w tym schorzeniu oraz wyrażoną potrzebą bardziej funkcjonalnych i specjalistycznych zasobów dla tego schorzenia.88
Respondenci wskazali kursy online (92,5%), przykładowe narzędzia i aktywności do interwencji (64,8%) oraz konkretne szkolenia dotyczące opieki w zaawansowanych stadiach i końcu życia (58,3%) jako kluczowe obszary potrzeb w ich obecnej pracy.89
Na podstawie wyników badań istnieje pilna potrzeba wzmocnienia obecnych możliwości edukacyjnych i ciągłego szkolenia w celu lepszego promowania dobrostanu pacjentów z PPA i ich rodzin oraz zapewnienia odpowiedniego przygotowania obecnej i przyszłej kadry logopedycznej.90
Podsumowanie podejścia do opieki nad pacjentem z PPA
Opieka nad pacjentem z pierwotną postępującą afazją wymaga kompleksowego, wielodyscyplinarnego podejścia, które adresuje nie tylko objawy językowe, ale również wszystkie aspekty życia pacjenta i jego rodziny.9192
Kluczowe elementy skutecznej opieki nad pacjentem z PPA obejmują:9394
- Wczesną i dokładną diagnozę – umożliwiającą odpowiednie planowanie opieki
- Multidyscyplinarny zespół specjalistów – pracujących razem, aby zapewnić kompleksową opiekę
- Terapię logopedyczną – jako główną formę interwencji, dostosowaną do indywidualnych potrzeb
- Strategie kompensacyjne – umożliwiające komunikację pomimo postępujących trudności językowych
- Wsparcie dla rodzin i opiekunów – obejmujące edukację, doradztwo i zasoby społecznościowe
- Planowanie przyszłej opieki – włączając kwestie prawne, finansowe i długoterminową opiekę
- Skupienie na jakości życia – promowanie aktywności fizycznej, społecznej i dobrego samopoczucia psychicznego
Choć pierwotna postępująca afazja jest schorzeniem postępującym, dla którego nie ma obecnie leku, odpowiednie interwencje mogą znacząco poprawić jakość życia pacjentów i ich rodzin.95 Jak podkreśla dr Rogalski: „Znalezienie lekarstwa nie jest jedynym sposobem, w jaki możemy pomóc ludziom. Maksymalizacja niezależności, dobrego samopoczucia emocjonalnego, pewności siebie – wszystkie te rzeczy mogą mieć wiele praktycznych aspektów w codziennym życiu.”96
Strategia opieki powinna być regularnie aktualizowana w miarę postępu choroby, z naciskiem na zachowanie godności, niezależności i dobrego samopoczucia pacjenta przez cały czas trwania choroby.97 Jak podsumowuje jeden z opiekunów: „Terapia logopedyczna była dla nas ratunkiem, gdy żyjemy z pierwotną postępującą afazją mojej żony. Pomaga nam zachować zdolność komunikacji, utrzymując naszą więź silną i maksymalizując jakość życia. Pomaga nam pozostać blisko i nadal dzielić znaczące chwile razem.”98
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Materiały źródłowe
- #1 Primary Progressive Aphasia (PPA): Symptoms & Treatmenthttps://my.clevelandclinic.org/health/diseases/17387-primary-progressive-aphasia-ppa
Primary progressive aphasia (PPA) is a neurological condition that causes you to lose language skills. […] Primary progressive aphasia (PPA) is a neurological disorder that affects a persons ability to speak and communicate. […] The condition worsens over time, as people lose their ability to write, speak or understand language. […] Primary progressive aphasia symptoms may include: Difficulty finding the correct word for an object consistently. […] There isnt a cure for primary progressive aphasia and no way to stop its progression. But some treatments may slow the diseases progression or increase your quality of life. […] People may benefit from: Participating in speech therapy and cognitive therapy can help to maintain language and thinking skills for as long as possible. […] There isnt a way to reverse primary progressive aphasia, but treatment may help you maintain communication skills for as long as possible.
- #2 Primary Progressive Aphasia (PPA) | Conditions & Treatments | UR Medicinehttps://www.urmc.rochester.edu/conditions-and-treatments/primary-progressive-aphasia
PPA is diagnosed through a comprehensive evaluation that includes: […] Treatment focuses on maximizing communication abilities and improving quality of life. UR Medicine offers a multidisciplinary approach, combining neurology, speech-language pathology, and supportive care to help individuals and families navigate this condition. […] Families and caregivers receive training and resources to help manage communication challenges and support their loved ones effectively. […] Integrated neuropsychology services to address changes in memory, behavior, and emotional well-being. […] Education, counseling, and support groups to help families and caregivers navigate the challenges of PPA.
- #3 Care Partner Training: Resources and Guidance for Managing Primary Progressive Aphasiahttps://states.aarp.org/virginia/care-partner-training-resources-and-guidance-for-managing-primary-progressive-aphasia
Dementia is not only a disease that affects older people. […] Primary Progressive Aphasia (PPA) is part of the spectrum associated with Frontal Temporal Degeneration. […] A diagnosis of PPA helps create a plan of care, said Reiter. […] Reiter strongly recommends the use of a speech language pathologist (SLP) to develop a personalized plan of care and address issues between the patient and others. […] In the early stages of PPA, the focus is on creating an environment where there is better communication and understanding. […] Care partners can help by reducing background noise and distractions, using face-to-face communication as much as possible, speaking slowly and allowing time for a response, and asking for clarification. […] During the middle stage of PPA, a speech language pathologist can help develop scripts to help conversations on items of interest or favorite activities.
- #4 Aphasia or Primary Progressive Aphasia?https://blog.chsc.org/blog/aphasia-or-primary-progressive-aphasia
Primary Progressive Aphasia (PPA) is a neurological syndrome impacting language. PPA differs from aphasia resulting from a stroke or brain injury as it is caused by neurodegenerative diseases (Alzheimers Disease, Frontotemporal Dementia, Amyotrophic Lateral Sclerosis). PPA is caused by deterioration of the brain tissue used for speech production and language. The symptoms of PPA differ from person to person as the symptoms are dependent on which parts of the left hemisphere of the brain are damaged. […] Individuals with PPA may benefit from using new communication skills provided by a speech-language pathologist, or by augmenting their communication with a speech-generating device. […] We offer individual therapy services to address a variety of difficulties experienced after a stroke or diagnosis of PPA. We focus on building a treatment plan together with the client, their family, and caregivers to enhance their quality of life.
- #5 Primary Progressive Aphasia – Northwestern University Center for Audiology, Speech, Language, and Learninghttps://nucasll.northwestern.edu/speech-language-pathology/aphasia/primary-progressive-aphasia/
Primary Progressive Aphasia (PPA) is a condition that involves a progressive deterioration of language functioning. […] PPA results from degeneration in areas of the brain responsible for speech and language. […] According to Mesulam and colleagues, PPA is defined as a progressive disorder of language, with cognitive functions and activities of daily living remaining relatively preserved for at least two years. […] Most people with primary progressive aphasia maintain ability to take care of themselves, pursue hobbies, and, in some instances, remain employed. […] Speech-language therapy can help improve communication and assist individuals to compensate for the loss of language, resulting in improved quality of life. […] The Northwestern University Center for Audiology, Speech, Language, and Learning provides comprehensive evaluation and therapy services on the Evanston campus. […] Diagnostic evaluations determine the course of treatment, including frequency and appropriateness of individual and/or group therapy.
- #6 Primary progressive aphasia – Symptoms and causes – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/symptoms-causes/syc-20350499
Primary progressive aphasia care at Mayo Clinic […] People with primary progressive aphasia eventually lose the ability to speak and write. This may take anywhere from 3 to 15 years. People with the condition also have trouble understanding written and spoken language. […] As the disease progresses, other mental skills such as memory, planning and organizing can be affected. Some people develop other symptoms such as problems with movement, balance and swallowing. With these complications, people with the disease eventually need help with day-to-day care. […] People with primary progressive aphasia also can develop depression as the disease progresses. Other complications might include blunted emotions such as not showing concern, poor judgment or social behavior that’s not appropriate.
- #7 Primary progressive aphasiahttps://johnsonmemorial.org/jmh-health/disease-conditions/con-20155110
Primary progressive aphasia is a rare nervous system syndrome that affects the ability to communicate. […] People with primary progressive aphasia may continue caring for themselves and participating in daily activities for several years. […] People with primary progressive aphasia eventually lose the ability to speak and write. […] With these complications, people with the disease eventually will need help with day-to-day care. […] If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. […] Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. […] Support groups may be offered for caregivers and people with primary progressive aphasia or related conditions.
- #8https://www.brain.northwestern.edu/dementia/primary-progressive-aphasia/treatment.html
Many clinicians are involved in the diagnosis and care of individuals living with primary progressive aphasia (PPA) and their families. […] The members of one’s care team will vary by individual and over time. […] Examples of individuals who may be a part of the care team include: Neurologist (specialists in brain disorders who make the diagnosis and monitors its symptoms), Neuropsychologist (evaluate cognitive abilities through specialized paper and pencil tests), Psychiatrist (assist with behavioral and mood symptoms), Social worker (help families navigate the difficult decisions related to their diagnosis), Speech and language pathologist (provide strategies to maximize communication abilities), Physical and occupational therapists (help optimize movement and activities of daily living).
- #9 Primary Progressive Aphasia – The National Aphasia Associationhttps://aphasia.org/aphasia-resources/primary-progressive-aphasia/
There is no cure for PPA, but some services and medications can help manage some of the symptoms of PPA. […] It is important that a team of professionals with a lot of PPA knowledge work together to help the person with PPA and their family members. […] Speech-language pathologists (aka speech therapists) work with people with PPA and PPAOS and their families to understand the disease, how it impacts communication, and develop strategies to maximize communication in daily life. […] Speech therapy is for the person with PPA or PPAOS and their families. It is important to include family in speech therapy sessions so that they can learn how to support communication over time. […] Speech therapy should always be personalized to target words and sentences used in the persons daily life. Generic exercises do not have a place in speech therapy for PPA.
- #10https://www.brain.northwestern.edu/dementia/primary-progressive-aphasia/treatment.html
Many clinicians are involved in the diagnosis and care of individuals living with primary progressive aphasia (PPA) and their families. […] The members of one’s care team will vary by individual and over time. […] Examples of individuals who may be a part of the care team include: Neurologist (specialists in brain disorders who make the diagnosis and monitors its symptoms), Neuropsychologist (evaluate cognitive abilities through specialized paper and pencil tests), Psychiatrist (assist with behavioral and mood symptoms), Social worker (help families navigate the difficult decisions related to their diagnosis), Speech and language pathologist (provide strategies to maximize communication abilities), Physical and occupational therapists (help optimize movement and activities of daily living).
- #11 Living with PPA – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/living-with-ppa/
This page is designed to provide guidance to help manage some of the day-to-day experiences and symptoms of primary progressive aphasia (PPA) […] It is important to note that, as PPA is rare, many healthcare services do not have much experience supporting people with PPA. However, you may still find it helpful to seek support from a variety of health and social care professionals such as GPs and nurses, community mental health teams and social workers. […] Speech and language therapy can help people living with PPA and their families to better manage their communication difficulties. Speech and language therapy can help people use electronic devices and other strategies to help bypass their speech difficulty. […] Assessment of swallowing and diet is another important role for speech and language therapists swallowing can become affected in the later stages of PPA.
- #12https://www.brain.northwestern.edu/dementia/primary-progressive-aphasia/treatment.html
Many clinicians are involved in the diagnosis and care of individuals living with primary progressive aphasia (PPA) and their families. […] The members of one’s care team will vary by individual and over time. […] Examples of individuals who may be a part of the care team include: Neurologist (specialists in brain disorders who make the diagnosis and monitors its symptoms), Neuropsychologist (evaluate cognitive abilities through specialized paper and pencil tests), Psychiatrist (assist with behavioral and mood symptoms), Social worker (help families navigate the difficult decisions related to their diagnosis), Speech and language pathologist (provide strategies to maximize communication abilities), Physical and occupational therapists (help optimize movement and activities of daily living).
- #13https://www.brain.northwestern.edu/dementia/primary-progressive-aphasia/treatment.html
Other professionals may include creative arts therapists, individual/family therapists, elder law and estate planning attorneys, palliative care/hospice, mediation services, companion care, adult day services and nursing services. […] Our center offers quality-of-life programs that may be helpful for individuals with PPA and their families. […] Speech and language therapy is an important intervention for all individuals with PPA. […] Speech-language therapists can help identify strategies to maximize communication abilities and quality of life throughout the course of the illness. […] Because every individual living with PPA is different, strategies may vary from individual to individual. […] Social workers are available in the Neurobehavior and Memory Clinic to meet with patients and families to develop a personal and customized approach to care.
- #14 Primary Progressive Aphasia (PPA) | Conditions & Treatments | UR Medicinehttps://www.urmc.rochester.edu/conditions-and-treatments/primary-progressive-aphasia
PPA is diagnosed through a comprehensive evaluation that includes: […] Treatment focuses on maximizing communication abilities and improving quality of life. UR Medicine offers a multidisciplinary approach, combining neurology, speech-language pathology, and supportive care to help individuals and families navigate this condition. […] Families and caregivers receive training and resources to help manage communication challenges and support their loved ones effectively. […] Integrated neuropsychology services to address changes in memory, behavior, and emotional well-being. […] Education, counseling, and support groups to help families and caregivers navigate the challenges of PPA.
- #15 UT Health Austin | Primary Progressive Aphasiahttps://uthealthaustin.org/conditions/primary-progressive-aphasia
Primary progressive aphasia (PPA) is a neurodegenerative disorder that predominantly affects speech and language abilities during the initial stages. […] Currently, there are no medications to cure PPA and its underlying disease. However, behavioral treatment with a speech-language pathologist can often help individuals maintain current communication abilities as well as explore alternative forms of communication (e.g., nonverbal communication using gestures, pointing, low-tech or high-tech devices, etc.) to help meet communication needs as the disorder progresses. […] At UT Health Austin, we take a multidisciplinary approach to your care. This means you will benefit from the expertise of multiple specialists across a variety of disciplines caring for you in one place to avoid having to schedule multiple appointments with providers at locations all over the city. The Comprehensive Memory Center care team includes neurologists, a geriatric psychiatrist, neuropsychologists, nurses, a speech-language pathologist, social workers, and more who work together to help you get back to the things in your life that matter most to you. […] We are committed to communicating and coordinating your care with referring physicians and other partners in the community to ensure that we are providing you with comprehensive, whole-person care.
- #16 Support in later stages – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/support-in-later-stages-ppa/
This page aims to guide all those affected by a diagnosis of primary progressive aphasia (PPA) through the later stages of the condition. This includes carers, family and friends. […] It is important that care home staff are aware of the specific needs of someone living with PPA. However, because it is so rare it is difficult to find a care home or care staff who are familiar with PPA. […] Care home staff may also find our short film useful, which features people living with different forms of PPA discussing their everyday experiences and challenges, as well as clinical explanations and insights. […] When a person with dementia is approaching the advanced stages of their condition, it can be a very difficult time for them and their loved ones. […] The duration of PPA differs from person to person. Although PPA itself is a life-shortening condition, people with PPA will often be affected by another illness, such as pneumonia.
- #17 Living with PPA – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/living-with-ppa/
This page is designed to provide guidance to help manage some of the day-to-day experiences and symptoms of primary progressive aphasia (PPA) […] It is important to note that, as PPA is rare, many healthcare services do not have much experience supporting people with PPA. However, you may still find it helpful to seek support from a variety of health and social care professionals such as GPs and nurses, community mental health teams and social workers. […] Speech and language therapy can help people living with PPA and their families to better manage their communication difficulties. Speech and language therapy can help people use electronic devices and other strategies to help bypass their speech difficulty. […] Assessment of swallowing and diet is another important role for speech and language therapists swallowing can become affected in the later stages of PPA.
- #18 Group interventions for people with primary progressive aphasia and their care partners: Considerations for clinical practice – PubMedhttps://pubmed.ncbi.nlm.nih.gov/39213021/
Primary progressive aphasia (PPA) describes a group of language-led dementias. […] Speech and language therapy is the main available intervention for people with PPA. […] The aim of this study was to gather the collective intelligence of expert speech and language therapists/pathologists delivering group therapy for people with PPA to synthesize guidance for clinicians. […] This initial synthesis of the current state of the art in PPA therapy groups highlights several important considerations around candidacy, content and ecological validity of delivering group intervention for people with PPA.
- #19 4 Approaches to Primary Progressive Aphasia Treatmenthttps://www.healthline.com/health/primary-progressive-aphasia-treatment
Treatments for primary progressive aphasia are aimed at managing symptoms, enhancing communication, and improving quality of life. […] While no cure exists, treatments are available to effectively manage symptoms and enhance communication strategies. […] While research has increased our understanding of primary progressive aphasia (PPA)s underlying mechanisms, the primary treatment emphasis remains on alleviating symptoms, enhancing communication strategies, and enhancing the overall quality of life for affected individuals. […] Speech and language therapy: Studies show that training programs that emphasize language skills (e.g., sentence production, naming tests, verbal fluency) can be helpful for people with PPA. […] Communication strategies: Learning alternative methods of communication, such as using gestures, writing, or trying augmentative and alternative communication (AAC) devices, can help improve communication as language abilities begin to decline.
- #20 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Our caring team of Mayo Clinic experts can help you with your primary progressive aphasia-related health concerns […] Primary progressive aphasia can’t be cured, and there are no medicines to treat it. However, some therapies might help improve or maintain your ability to communicate and manage your condition. […] Working with a speech-language pathologist, focusing primarily on ways to make up for lost language skills, can be helpful. Although speech and language therapy can’t stop the progression of the condition, it can help you manage your condition. The therapy also may slow the progression of some symptoms. Your therapist may recommend that your caregivers also attend the appointments. […] If your symptoms affect movement and balance, working with a physical therapist and an occupational therapist can help manage the symptoms.
- #21 Primary progressive aphasia (PPA): Symptoms, treatment, morehttps://www.medicalnewstoday.com/articles/primary-progressive-aphasia
Primary progressive aphasia (PPA) is a neurological condition that affects a persons ability to communicate. […] There is currently no cure for PPA, but speech therapy and other communication strategies can help manage the symptoms and improve a persons quality of life. […] Speech and language therapy is the primary form of treatment for PPA. This therapy aims to: improve communication skills such as speaking, writing, and understanding language; teach alternative communication methods such as using gestures and writing notes; teach exercises to strengthen the muscles necessary for speech and writing; help improve memory and attention. […] Currently, there is no cure for PPA, but treatments are available to help manage symptoms. For example, speech and language therapy can help a person communicate, and medications can manage mental health symptoms. […] Individuals with PPA and their caregivers should seek support from healthcare professionals, support groups, and other resources. With proper care and management, people with PPA can maintain their connections with others.
- #22 Primary Progressive Aphasia – Symptoms and Therapieshttps://speechpathologysolutions.com/primary-progressive-aphasia-symptoms-and-therapies/
Primary Progressive Aphasia (PPA) is a neurological condition that increasingly impairs language abilities, affecting many aspects of communication. […] Effective management of Primary Progressive Aphasia requires a multidisciplinary approach that addresses both communication and cognitive aspects of the condition. […] Speech and Language Therapy: This therapy is crucial in PPA management. It includes tailored exercises focused on maintaining existing language abilities. […] Cognitive Rehabilitation: PPA can indirectly affect cognitive functions like memory, problem-solving, and attention. […] Family Education and Support: Involving family members in the therapy process is essential. Educating them about PPA helps them understand the condition and how to communicate effectively. […] The integration of technology into the therapy for Primary Progressive Aphasia has significantly enhanced treatment approaches and outcomes. […] Communication Strategies: Individuals with PPA often learn new ways to communicate as their condition progresses. […] Support Systems: Having support from healthcare professionals, such as speech-language pathologists, guides in managing the condition.
- #23 Primary Progressive Aphasia – Northwestern University Center for Audiology, Speech, Language, and Learninghttps://nucasll.northwestern.edu/speech-language-pathology/aphasia/primary-progressive-aphasia/
Primary Progressive Aphasia (PPA) is a condition that involves a progressive deterioration of language functioning. […] PPA results from degeneration in areas of the brain responsible for speech and language. […] According to Mesulam and colleagues, PPA is defined as a progressive disorder of language, with cognitive functions and activities of daily living remaining relatively preserved for at least two years. […] Most people with primary progressive aphasia maintain ability to take care of themselves, pursue hobbies, and, in some instances, remain employed. […] Speech-language therapy can help improve communication and assist individuals to compensate for the loss of language, resulting in improved quality of life. […] The Northwestern University Center for Audiology, Speech, Language, and Learning provides comprehensive evaluation and therapy services on the Evanston campus. […] Diagnostic evaluations determine the course of treatment, including frequency and appropriateness of individual and/or group therapy.
- #24 Primary Progressive Aphasia: Therapy Tips for the Speech-Language Pathologisthttps://tactustherapy.com/ppa-treatment-slp-primary-progressive-aphasia/
With PPA, dont expect the same carryover of skills as you would when treating a stroke survivor with aphasia. […] Create opportunities for your client to practice important words and phrases. […] If its early in the progression of primary progressive aphasia, have the family and the client pay attention to routines and phrases used in everyday life. […] As you do with aphasia or dementia, identifying and using communication strengths can help you determine effective compensatory strategies, as well as build confidence. […] Clients who are still independent in the community may benefit from carrying an individualized information card. […] As PPA progresses and communication skills (especially verbal skills) decline, nonverbal skills become that much more important. […] Many people choose to preserve their loved ones voice by voice banking.
- #25 Primary Progressive Aphasia – The National Aphasia Associationhttps://aphasia.org/aphasia-resources/primary-progressive-aphasia/
There is no cure for PPA, but some services and medications can help manage some of the symptoms of PPA. […] It is important that a team of professionals with a lot of PPA knowledge work together to help the person with PPA and their family members. […] Speech-language pathologists (aka speech therapists) work with people with PPA and PPAOS and their families to understand the disease, how it impacts communication, and develop strategies to maximize communication in daily life. […] Speech therapy is for the person with PPA or PPAOS and their families. It is important to include family in speech therapy sessions so that they can learn how to support communication over time. […] Speech therapy should always be personalized to target words and sentences used in the persons daily life. Generic exercises do not have a place in speech therapy for PPA.
- #26 Primary Progressive Aphasia – The National Aphasia Associationhttps://aphasia.org/aphasia-resources/primary-progressive-aphasia/
There is no cure for PPA, but some services and medications can help manage some of the symptoms of PPA. […] It is important that a team of professionals with a lot of PPA knowledge work together to help the person with PPA and their family members. […] Speech-language pathologists (aka speech therapists) work with people with PPA and PPAOS and their families to understand the disease, how it impacts communication, and develop strategies to maximize communication in daily life. […] Speech therapy is for the person with PPA or PPAOS and their families. It is important to include family in speech therapy sessions so that they can learn how to support communication over time. […] Speech therapy should always be personalized to target words and sentences used in the persons daily life. Generic exercises do not have a place in speech therapy for PPA.
- #27 Primary Progressive Aphasia – The National Aphasia Associationhttps://aphasia.org/aphasia-resources/primary-progressive-aphasia/
There is no cure for PPA, but some services and medications can help manage some of the symptoms of PPA. […] It is important that a team of professionals with a lot of PPA knowledge work together to help the person with PPA and their family members. […] Speech-language pathologists (aka speech therapists) work with people with PPA and PPAOS and their families to understand the disease, how it impacts communication, and develop strategies to maximize communication in daily life. […] Speech therapy is for the person with PPA or PPAOS and their families. It is important to include family in speech therapy sessions so that they can learn how to support communication over time. […] Speech therapy should always be personalized to target words and sentences used in the persons daily life. Generic exercises do not have a place in speech therapy for PPA.
- #28 Primary Progressive Aphasia – The National Aphasia Associationhttps://aphasia.org/aphasia-resources/primary-progressive-aphasia/
After your first round of speech therapy, it is important for you and your family to visit your speech therapist every six months or so. Another round of therapy may be recommended as PPA progresses so that you and your family can learn new strategies to help communication. […] Occupational therapists and physical therapists may help with home safety, mobility, and activities of daily living.
- #29 Group interventions for people with primary progressive aphasia and their care partners: Considerations for clinical practice – PubMedhttps://pubmed.ncbi.nlm.nih.gov/39213021/
Primary progressive aphasia (PPA) describes a group of language-led dementias. […] Speech and language therapy is the main available intervention for people with PPA. […] The aim of this study was to gather the collective intelligence of expert speech and language therapists/pathologists delivering group therapy for people with PPA to synthesize guidance for clinicians. […] This initial synthesis of the current state of the art in PPA therapy groups highlights several important considerations around candidacy, content and ecological validity of delivering group intervention for people with PPA.
- #30 Primary Progressive Aphasia (PPA) Programs – Minnesota Connect Aphasia Nowhttps://mncan.org/primary-progressive-aphasia-ppa-program/
Primary Progressive Aphasia (PPA) is language disorder that gradually impairs a persons ability to speak or comprehend language over time. […] Staying Connected is an introductory 8-week session for persons with PPA and their care partners offered by MnCAN two times per year. […] MnCAN strongly encourages a care partner (friend or family member) to also participate in the full class. […] The Staying Connected program is designed for people diagnosed with PPA in the first 1-2 years. Following completion of the Staying Connected program, a monthly PPA support group is offered. […] The overall program goals are to offer support to both the care partner AND person with PPA. […] Over the course of 8 weekly 2-hour sessions, a speech-language pathologist with the support of graduate student(s), provides education about Primary Progressive Aphasia.
- #31 Primary Progressive Aphasia (PPA) Programs – Minnesota Connect Aphasia Nowhttps://mncan.org/primary-progressive-aphasia-ppa-program/
This small group of 6-7 people with PPA meets weekly to engage in conversation on topics of interest. […] This group is for people who have completed the MnCAN Staying Connected Education Class. […] The PPA Support Group is an ongoing support group for persons with PPA and their care partners who have completed the Staying Connected Class. […] The purpose of this group is to provide ongoing support during the journey with PPA. Both care partners and persons with PPA are invited to attend. […] The support group has an in-person option OR virtual option. The group is facilitated by a speech-language pathologist. No tuition or registration is required.
- #32 Primary Progressive Aphasia (PPA) Programs – Minnesota Connect Aphasia Nowhttps://mncan.org/primary-progressive-aphasia-ppa-program/
Primary Progressive Aphasia (PPA) is language disorder that gradually impairs a persons ability to speak or comprehend language over time. […] Staying Connected is an introductory 8-week session for persons with PPA and their care partners offered by MnCAN two times per year. […] MnCAN strongly encourages a care partner (friend or family member) to also participate in the full class. […] The Staying Connected program is designed for people diagnosed with PPA in the first 1-2 years. Following completion of the Staying Connected program, a monthly PPA support group is offered. […] The overall program goals are to offer support to both the care partner AND person with PPA. […] Over the course of 8 weekly 2-hour sessions, a speech-language pathologist with the support of graduate student(s), provides education about Primary Progressive Aphasia.
- #33 4 Approaches to Primary Progressive Aphasia Treatmenthttps://www.healthline.com/health/primary-progressive-aphasia-treatment
Treatments for primary progressive aphasia are aimed at managing symptoms, enhancing communication, and improving quality of life. […] While no cure exists, treatments are available to effectively manage symptoms and enhance communication strategies. […] While research has increased our understanding of primary progressive aphasia (PPA)s underlying mechanisms, the primary treatment emphasis remains on alleviating symptoms, enhancing communication strategies, and enhancing the overall quality of life for affected individuals. […] Speech and language therapy: Studies show that training programs that emphasize language skills (e.g., sentence production, naming tests, verbal fluency) can be helpful for people with PPA. […] Communication strategies: Learning alternative methods of communication, such as using gestures, writing, or trying augmentative and alternative communication (AAC) devices, can help improve communication as language abilities begin to decline.
- #34 Primary Progressive Aphasia | Memory and Aging Centerhttps://memory.ucsf.edu/dementia/primary-progressive-aphasia
Primary progressive aphasia (PPA) is a condition that slowly damages the parts of the brain that control speech and language. People with PPA usually have difficulty speaking, naming objects, or understanding conversations. […] People with language difficulties may benefit from speech therapy to help them learn alternative ways to supplement and compensate for their lost skills. Maintaining adequate communication and social connections are critical. […] Unlike many people who develop aphasia from head injury or stroke, people with PPA do not typically improve with time, but a therapist may be helpful in maximizing abilities and exploring other ways to communicate. Non-verbal techniques for communicating, such as gesturing or pointing to pictures may help people express themselves. […] Aphasia identification cards explaining that the person has a language problem may be helpful. Many speech pathologists and occupational therapists have their own practices, while others are available through local hospitals and medical centers.
- #35 Help & Support: Communicating with Persons Living with PPA – Tips and Strategies | AFTDhttps://www.theaftd.org/posts/help-and-hope/communicating-with-persons-living-with-ppa-tips-and-strategies/
Primary progressive aphasia (PPA) is characterized by a gradual loss of oneâs ability to speak, read, write, and understand speech. The inability to communicate is troublesome for the person living with FTD, as well for those caring for and supporting them. […] Adapting how one communicates with persons living with FTD can increase their understanding. Below are some tips and tools that may help you do just that. […] Simplify your speech without dumbing it down. […] Use communication aids that the person living with PPA is enthusiastic about using, such as: […] Ask a speech language therapist for help identifying other tools that will meet your specific needs and abilities. […] When using written language (for example, emails) to communicate to someone living with PPA, consider the following: […] When in a conversation with a person living with PPA: […] Other tips: […] Some reminders: […] All communication strategies and aids should build on the strengths of the person with living PPA. If they werenât technologically savvy before their diagnosis, that probably wonât change.
- #36 Primary progressive aphasia support – Alzheimer’s Research UKhttps://www.alzheimersresearchuk.org/dementia-information/types-of-dementia/primary-progressive-aphasia/support/
A diagnosis of PPA will affect people in different ways and can come as a shock. People and their families may need time to come to terms with a diagnosis. With the right information and support, people can carry on with their day to day lives for some time. Some people find that talking to others in the same situation can help. […] You can also talk to your doctor or nurse for advice on caring for someone with PPA. […] For people with any type of PPA, their speech and language is affected first. […] When talking to someone with PPA, there are things you can do to help them: Be patient, warm and understanding. Find a quiet place to talk. Donât ask more than one question at a time. Acknowledge their frustration when they show it, donât dismiss it. Ask the person how you can help them communicate. Speak clearly and so that the person can see you speaking. Check that you have understood what they mean. One-to-one conversations can work better than talking in groups.
- #37 Primary progressive aphasia support – Alzheimer’s Research UKhttps://www.alzheimersresearchuk.org/dementia-information/types-of-dementia/primary-progressive-aphasia/support/
A diagnosis of PPA will affect people in different ways and can come as a shock. People and their families may need time to come to terms with a diagnosis. With the right information and support, people can carry on with their day to day lives for some time. Some people find that talking to others in the same situation can help. […] You can also talk to your doctor or nurse for advice on caring for someone with PPA. […] For people with any type of PPA, their speech and language is affected first. […] When talking to someone with PPA, there are things you can do to help them: Be patient, warm and understanding. Find a quiet place to talk. Donât ask more than one question at a time. Acknowledge their frustration when they show it, donât dismiss it. Ask the person how you can help them communicate. Speak clearly and so that the person can see you speaking. Check that you have understood what they mean. One-to-one conversations can work better than talking in groups.
- #38 Primary Progressive Aphasia: Therapy Tips for the Speech-Language Pathologisthttps://tactustherapy.com/ppa-treatment-slp-primary-progressive-aphasia/
With PPA, dont expect the same carryover of skills as you would when treating a stroke survivor with aphasia. […] Create opportunities for your client to practice important words and phrases. […] If its early in the progression of primary progressive aphasia, have the family and the client pay attention to routines and phrases used in everyday life. […] As you do with aphasia or dementia, identifying and using communication strengths can help you determine effective compensatory strategies, as well as build confidence. […] Clients who are still independent in the community may benefit from carrying an individualized information card. […] As PPA progresses and communication skills (especially verbal skills) decline, nonverbal skills become that much more important. […] Many people choose to preserve their loved ones voice by voice banking.
- #39 Primary Progressive Aphasia: Symptoms, Diagnosis, Treatment, and Morehttps://www.healthline.com/health/primary-progressive-aphasia
Primary progressive aphasia is a rare type of aphasia that is caused by brain atrophy. Its associated with dementia. While theres no cure, treatment can help with its progression. […] Most types of aphasia can be treated, and recovery is often possible. However, there is currently no cure for a rare type of aphasia called primary progressive aphasia. […] Treatments such as speech therapy can help maintain communication skills and slow down the progression of symptoms, but they cannot cure this type of aphasia entirely. […] Therapy can help you manage primary progressive aphasia and slow the progression of your symptoms. Speech and language therapy is the primary form of treatment. […] During speech and language therapy, a speech therapist will guide you through communication exercises and will give you the tools you need for daily life with primary progressive aphasia. […] Sometimes, communication devices and other aids are helpful for people with primary progressive aphasia. Your speech therapist will help you find what works best for you. […] There is no cure for primary progressive aphasia, but speech therapy can help slow down the progression of symptoms.
- #40 Nonfluent Variant Primary Progressive Aphasia | Memory and Aging Centerhttps://memory.ucsf.edu/dementia/primary-progressive-aphasia/nonfluent-variant-primary-progressive-aphasia
People with nfvPPA gradually have more trouble expressing themselves, even though they still understand the meaning of words. […] Speech therapy may help improve communication between people with nfvPPA and others. Communication devices, like tablets and type-to-talk instruments, or picture books, can help the person with nfvPPA express what they want to say with less anxiety. […] If symptoms of weakness or difficulty using the arm or leg develop, physical and occupational therapy may help manage them and provide coping skills and strategies. A swallowing evaluation and a modification of diet and consistency of liquids may be necessary for people with nfvPPA who develop swallowing difficulties. […] Research has shown that physical exercise helps to enhance brain health and improves mood and general fitness. A balanced diet, enough sleep, and limited alcohol intake are other important ways to promote good health. Other illnesses that affect the brain, such as diabetes, high blood pressure, and high cholesterol, should also be treated if present.
- #41 Primary Progressive Aphasia – Symptoms and Therapieshttps://speechpathologysolutions.com/primary-progressive-aphasia-symptoms-and-therapies/
Primary Progressive Aphasia (PPA) is a neurological condition that increasingly impairs language abilities, affecting many aspects of communication. […] Effective management of Primary Progressive Aphasia requires a multidisciplinary approach that addresses both communication and cognitive aspects of the condition. […] Speech and Language Therapy: This therapy is crucial in PPA management. It includes tailored exercises focused on maintaining existing language abilities. […] Cognitive Rehabilitation: PPA can indirectly affect cognitive functions like memory, problem-solving, and attention. […] Family Education and Support: Involving family members in the therapy process is essential. Educating them about PPA helps them understand the condition and how to communicate effectively. […] The integration of technology into the therapy for Primary Progressive Aphasia has significantly enhanced treatment approaches and outcomes. […] Communication Strategies: Individuals with PPA often learn new ways to communicate as their condition progresses. […] Support Systems: Having support from healthcare professionals, such as speech-language pathologists, guides in managing the condition.
- #42 [Primary Progressive Aphasia] | OHSUhttps://www.ohsu.edu/reknew/primary-progressive-aphasia
The goal of our research was to determine whether using Augmentative and Alternative Communication technology improves conversation in everyday settings for individuals with primary progressive aphasia. We have developed several applications that are accessed through personal tablets at home. […] For more information about primary progressive aphasia, please contact Aimee Mooney, M.S., CCC-SLP/L. […] Here you will find short descriptions of the grants that we have completed on primary progressive aphasia. […] Writing papers about our work is an important part of the research process. […] Every year our diverse team attends conferences around the country and presents the important work we are doing: […] We hope you will find these handouts helpful for those with primary progressive aphasia: […] We encourage research participants and their families to take a look:
- #43 Help & Support: Communicating with Persons Living with PPA – Tips and Strategies | AFTDhttps://www.theaftd.org/posts/help-and-hope/communicating-with-persons-living-with-ppa-tips-and-strategies/
Primary progressive aphasia (PPA) is characterized by a gradual loss of oneâs ability to speak, read, write, and understand speech. The inability to communicate is troublesome for the person living with FTD, as well for those caring for and supporting them. […] Adapting how one communicates with persons living with FTD can increase their understanding. Below are some tips and tools that may help you do just that. […] Simplify your speech without dumbing it down. […] Use communication aids that the person living with PPA is enthusiastic about using, such as: […] Ask a speech language therapist for help identifying other tools that will meet your specific needs and abilities. […] When using written language (for example, emails) to communicate to someone living with PPA, consider the following: […] When in a conversation with a person living with PPA: […] Other tips: […] Some reminders: […] All communication strategies and aids should build on the strengths of the person with living PPA. If they werenât technologically savvy before their diagnosis, that probably wonât change.
- #44 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Losing the ability to communicate can be stressful and frustrating. This is true for both the person with primary progressive aphasia and for friends and family. If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. Have the person with the condition carry an identification card and other materials that can help explain the condition to others. Give the person time to talk. Speak slowly in simple, adult sentences and listen carefully. Talk with the person with the condition about how you can help. Take care of your personal needs. Get enough rest and make time for social activities. […] Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved.
- #45
- #46 Primary Progressive Aphasia (PPA) | Conditions & Treatments | UR Medicinehttps://www.urmc.rochester.edu/conditions-and-treatments/primary-progressive-aphasia
PPA is diagnosed through a comprehensive evaluation that includes: […] Treatment focuses on maximizing communication abilities and improving quality of life. UR Medicine offers a multidisciplinary approach, combining neurology, speech-language pathology, and supportive care to help individuals and families navigate this condition. […] Families and caregivers receive training and resources to help manage communication challenges and support their loved ones effectively. […] Integrated neuropsychology services to address changes in memory, behavior, and emotional well-being. […] Education, counseling, and support groups to help families and caregivers navigate the challenges of PPA.
- #47 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Losing the ability to communicate can be stressful and frustrating. This is true for both the person with primary progressive aphasia and for friends and family. If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. Have the person with the condition carry an identification card and other materials that can help explain the condition to others. Give the person time to talk. Speak slowly in simple, adult sentences and listen carefully. Talk with the person with the condition about how you can help. Take care of your personal needs. Get enough rest and make time for social activities. […] Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved.
- #48 Primary Progressive Aphasia – Symptoms and Therapieshttps://speechpathologysolutions.com/primary-progressive-aphasia-symptoms-and-therapies/
Primary Progressive Aphasia (PPA) is a neurological condition that increasingly impairs language abilities, affecting many aspects of communication. […] Effective management of Primary Progressive Aphasia requires a multidisciplinary approach that addresses both communication and cognitive aspects of the condition. […] Speech and Language Therapy: This therapy is crucial in PPA management. It includes tailored exercises focused on maintaining existing language abilities. […] Cognitive Rehabilitation: PPA can indirectly affect cognitive functions like memory, problem-solving, and attention. […] Family Education and Support: Involving family members in the therapy process is essential. Educating them about PPA helps them understand the condition and how to communicate effectively. […] The integration of technology into the therapy for Primary Progressive Aphasia has significantly enhanced treatment approaches and outcomes. […] Communication Strategies: Individuals with PPA often learn new ways to communicate as their condition progresses. […] Support Systems: Having support from healthcare professionals, such as speech-language pathologists, guides in managing the condition.
- #49https://www.brain.northwestern.edu/dementia/primary-progressive-aphasia/treatment.html
Social workers will: Review the diagnosis and provide the opportunity to ask questions and obtain up to date disease information, Discuss changing language, behaviors and other diagnosis-related symptoms and offer helpful communication strategies, Provide counseling regarding changing roles as the disease progresses, Help you to assure your own self-care and to strengthen your support network, Provide referrals for individual, couples and/or family counseling, Connect you to elder law attorneys for estate planning to and to establish powers of attorney for healthcare and finances, Provide counseling regarding advance directives, Guide you to specialized support and education groups for newly diagnosed individuals and families, quality-of-life programs for meaningful and purposeful activity and other community programs.
- #50 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Support groups may be offered for caregivers and people with primary progressive aphasia or related conditions. Ask your social worker or other members of your healthcare team about community resources or support groups. Other sources of information include the National Aphasia Association and the Association for Frontotemporal Degeneration.
- #51 Primary progressive aphasia | UM Health-Sparrowhttps://www.uofmhealthsparrow.org/departments-conditions/conditions/primary-progressive-aphasia
Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved. […] Support groups may be offered for caregivers and people with primary progressive aphasia or related conditions. Ask your social worker or other members of your healthcare team about community resources or support groups. Other sources of information include the National Aphasia Association and the Association for Frontotemporal Degeneration.
- #52 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Support groups may be offered for caregivers and people with primary progressive aphasia or related conditions. Ask your social worker or other members of your healthcare team about community resources or support groups. Other sources of information include the National Aphasia Association and the Association for Frontotemporal Degeneration.
- #53https://www.brain.northwestern.edu/dementia/primary-progressive-aphasia/treatment.html
Other professionals may include creative arts therapists, individual/family therapists, elder law and estate planning attorneys, palliative care/hospice, mediation services, companion care, adult day services and nursing services. […] Our center offers quality-of-life programs that may be helpful for individuals with PPA and their families. […] Speech and language therapy is an important intervention for all individuals with PPA. […] Speech-language therapists can help identify strategies to maximize communication abilities and quality of life throughout the course of the illness. […] Because every individual living with PPA is different, strategies may vary from individual to individual. […] Social workers are available in the Neurobehavior and Memory Clinic to meet with patients and families to develop a personal and customized approach to care.
- #54 Primary Progressive Aphasia | Norton Healthcare Louisville, Ky.https://nortonhealthcare.com/services-and-conditions/neurosciences/services/primary-progressive-aphasia/
Itâs part of Norton Neuroscience Instituteâs goal to care for the whole person, not just the condition. […] Dedicated patient navigators can help schedule follow-up appointments, coordinate prescription assistance, create customized diet plans and provide guidance on disability benefits, housing, financial and employment concerns, and more. […] Patients can access support groups, exercise classes and other educational events to connect with others and learn how to make the most of life while managing a neurologic condition. […] Norton Neuroscience Institute Resource Center navigators help educate patients and their families about new diagnoses, available treatments and ways to manage their disease.
- #55 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Losing the ability to communicate can be stressful and frustrating. This is true for both the person with primary progressive aphasia and for friends and family. If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. Have the person with the condition carry an identification card and other materials that can help explain the condition to others. Give the person time to talk. Speak slowly in simple, adult sentences and listen carefully. Talk with the person with the condition about how you can help. Take care of your personal needs. Get enough rest and make time for social activities. […] Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved.
- #56 Primary progressive aphasia | UM Health-Sparrowhttps://www.uofmhealthsparrow.org/departments-conditions/conditions/primary-progressive-aphasia
Primary progressive aphasia can’t be cured, and there are no medicines to treat it. However, some therapies might help improve or maintain your ability to communicate and manage your condition. […] Working with a speech-language pathologist, focusing primarily on ways to make up for lost language skills, can be helpful. Although speech and language therapy can’t stop the progression of the condition, it can help you manage your condition. The therapy also may slow the progression of some symptoms. Your therapist may recommend that your caregivers also attend the appointments. […] If your symptoms affect movement and balance, working with a physical therapist and an occupational therapist can help manage the symptoms. […] Losing the ability to communicate can be stressful and frustrating. This is true for both the person with primary progressive aphasia and for friends and family. If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. Have the person with the condition carry an identification card and other materials that can help explain the condition to others. Give the person time to talk. Speak slowly in simple, adult sentences and listen carefully. Talk with the person with the condition about how you can help. Take care of your personal needs. Get enough rest and make time for social activities.
- #57 Primary progressive aphasia – Symptoms and causes – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/symptoms-causes/syc-20350499
Primary progressive aphasia care at Mayo Clinic […] People with primary progressive aphasia eventually lose the ability to speak and write. This may take anywhere from 3 to 15 years. People with the condition also have trouble understanding written and spoken language. […] As the disease progresses, other mental skills such as memory, planning and organizing can be affected. Some people develop other symptoms such as problems with movement, balance and swallowing. With these complications, people with the disease eventually need help with day-to-day care. […] People with primary progressive aphasia also can develop depression as the disease progresses. Other complications might include blunted emotions such as not showing concern, poor judgment or social behavior that’s not appropriate.
- #58 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Losing the ability to communicate can be stressful and frustrating. This is true for both the person with primary progressive aphasia and for friends and family. If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. Have the person with the condition carry an identification card and other materials that can help explain the condition to others. Give the person time to talk. Speak slowly in simple, adult sentences and listen carefully. Talk with the person with the condition about how you can help. Take care of your personal needs. Get enough rest and make time for social activities. […] Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved.
- #59 Primary progressive aphasia | UM Health-Sparrowhttps://www.uofmhealthsparrow.org/departments-conditions/conditions/primary-progressive-aphasia
Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved. […] Support groups may be offered for caregivers and people with primary progressive aphasia or related conditions. Ask your social worker or other members of your healthcare team about community resources or support groups. Other sources of information include the National Aphasia Association and the Association for Frontotemporal Degeneration.
- #60 Primary progressive aphasia – Diagnosis and treatment – Mayo Clinichttps://www.mayoclinic.org/diseases-conditions/primary-progressive-aphasia/diagnosis-treatment/drc-20350504
Losing the ability to communicate can be stressful and frustrating. This is true for both the person with primary progressive aphasia and for friends and family. If you’re a caregiver of someone with primary progressive aphasia, taking these steps can help everyone cope: Learn all you can about the condition. Have the person with the condition carry an identification card and other materials that can help explain the condition to others. Give the person time to talk. Speak slowly in simple, adult sentences and listen carefully. Talk with the person with the condition about how you can help. Take care of your personal needs. Get enough rest and make time for social activities. […] Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved.
- #61 Primary progressive aphasia | UM Health-Sparrowhttps://www.uofmhealthsparrow.org/departments-conditions/conditions/primary-progressive-aphasia
Family members eventually may need to make long-term care choices for the person with primary progressive aphasia. They also may need to plan the person’s finances and help make legal decisions to prepare for more-serious stages of the condition. Start this process early so the person with primary progressive aphasia can be involved. […] Support groups may be offered for caregivers and people with primary progressive aphasia or related conditions. Ask your social worker or other members of your healthcare team about community resources or support groups. Other sources of information include the National Aphasia Association and the Association for Frontotemporal Degeneration.
- #62 Primary Progressive Aphasia: A Rare Dementia Story | Alzheimers.nethttps://www.alzheimers.net/10-19-15-primary-progressive-aphasia-rare-dementia-story
Actress Kimberly Williams-Paisley shares her familys journey through her mothers primary progressive aphasia and gives advice to younger generations who may be facing the future with uncertainty. […] Learn more about this rare form of dementia and get her thoughts and advice for future dementia caregivers. […] Like all forms of dementia, there is no real treatment or cure for primary progressive aphasia. […] She admits that she wishes they would have asked her mother her wishes for long-term care before the disease took over, stating: It would have been helpful to know what my mother wanted in terms of long-term care. What do you want to do when you are no longer able to care for yourself? This is the kind of question I wished wed asked before it was too late. By the time we thought of it, her mind wasnt there.
- #63 Support in later stages – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/support-in-later-stages-ppa/
This page aims to guide all those affected by a diagnosis of primary progressive aphasia (PPA) through the later stages of the condition. This includes carers, family and friends. […] It is important that care home staff are aware of the specific needs of someone living with PPA. However, because it is so rare it is difficult to find a care home or care staff who are familiar with PPA. […] Care home staff may also find our short film useful, which features people living with different forms of PPA discussing their everyday experiences and challenges, as well as clinical explanations and insights. […] When a person with dementia is approaching the advanced stages of their condition, it can be a very difficult time for them and their loved ones. […] The duration of PPA differs from person to person. Although PPA itself is a life-shortening condition, people with PPA will often be affected by another illness, such as pneumonia.
- #64 Support in later stages – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/support-in-later-stages-ppa/
This page aims to guide all those affected by a diagnosis of primary progressive aphasia (PPA) through the later stages of the condition. This includes carers, family and friends. […] It is important that care home staff are aware of the specific needs of someone living with PPA. However, because it is so rare it is difficult to find a care home or care staff who are familiar with PPA. […] Care home staff may also find our short film useful, which features people living with different forms of PPA discussing their everyday experiences and challenges, as well as clinical explanations and insights. […] When a person with dementia is approaching the advanced stages of their condition, it can be a very difficult time for them and their loved ones. […] The duration of PPA differs from person to person. Although PPA itself is a life-shortening condition, people with PPA will often be affected by another illness, such as pneumonia.
- #65 Support in later stages – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/support-in-later-stages-ppa/
This page aims to guide all those affected by a diagnosis of primary progressive aphasia (PPA) through the later stages of the condition. This includes carers, family and friends. […] It is important that care home staff are aware of the specific needs of someone living with PPA. However, because it is so rare it is difficult to find a care home or care staff who are familiar with PPA. […] Care home staff may also find our short film useful, which features people living with different forms of PPA discussing their everyday experiences and challenges, as well as clinical explanations and insights. […] When a person with dementia is approaching the advanced stages of their condition, it can be a very difficult time for them and their loved ones. […] The duration of PPA differs from person to person. Although PPA itself is a life-shortening condition, people with PPA will often be affected by another illness, such as pneumonia.
- #66 Aphasia Patients Near Mission Hills Benefit From Home Carehttps://pegasushomecare.com/services/pegasus-skilled-care/aphasia-patients-near-mission-hills-benefit-home-care/
Home care professionals near Mission Hills have the training, skills, and experience to provide physical and mental benefits for aphasia patients and their families. […] Therapy combined with home care near Mission Hills helps aphasia patients recover some of their losses. […] Home care near Mission Hills helps aphasia patients learn and practice the best technique for them. […] Home care professionals recognize that each aphasia patient is unique. They customize their care to fit the individual. Their goal is to help each patient achieve as much independence as possible. […] Skilled home care offers many benefits to aphasia patients. Being able to live at home rather than going to a facility increases a patients degree of recovery. Patients and their families can learn new ways of effectively communicating with one another.
- #67 4 Approaches to Primary Progressive Aphasia Treatmenthttps://www.healthline.com/health/primary-progressive-aphasia-treatment
Medications: Current research indicates that medications that have been examined as possible treatments for PPA have limited effectiveness in improving cognitive deficits. However, certain medications, such as antidepressants, anti-anxiety medications, sleep aids, antipsychotics, cholinesterase inhibitors (ChEIs), and N-Methyl-D-aspartate receptor antagonists (NMDA antagonists), may be used for various symptoms related to PPA. […] While theres no cure, treatment focuses on managing symptoms and improving communication skills through interventions like speech therapy, cognitive training, and supportive strategies. […] These treatments can help you maintain your ability to communicate, engage in daily activities, and enhance your overall quality of life.
- #68 Primary Progressive Aphasia – MD Searchlighthttps://mdsearchlight.com/neurology/primary-progressive-aphasia/
Currently, no medicines have been found to be effective for Primary Progressive Aphasia (PPA), a neurological syndrome that affects language capabilities. The best way to manage this condition is by first meticulously examining the patients language and speech history. […] Hence, a referral to a speech and language specialist is crucial for correctly identifying language issues and working out the best treatment plan. Its proven that speech and language therapy is the most successful way to manage PPA, particularly for motor speech issues. […] In addition to this, transcranial direct current stimulation, a treatment that uses a simple electric current to stimulate specific areas of the brain, is viewed as a hopeful strategy to improve the results of language therapy in PPA patients. Its affordability, safety, and non-invasive nature make it worth researching its potential to boost behavioral solutions and slow down language deterioration in PPA. […] To manage these complications, we need a team of specialists. This team should include speech and language therapists, cognitive rehabilitation specialists, psychosocial support staff, and caregiver educators. These professionals will help improve the quality of life and care for the patient.
- #69 Therapeutic Potential of Transcranial Direct Current Stimulation in Primary Progressive Aphasia: Leigh Charvet, PhDhttps://www.neurologylive.com/view/therapeutic-potential-transcranial-direct-current-stimulation-primary-progressive-aphasia-leigh-charvet
Primary progressive aphasia (PPA), a type of dementia, is a neurological condition that affects a persons ability to speak and communicate. Aphasia is a language disorder that results from damage to key parts of the brain that are responsible for understanding or producing speech and/or writing. While there are no cures for PPA, patients have benefited from participating in speech and cognitive therapy, as well as taking certain medications, such as selective serotonin reuptake inhibitors or therapies that are approved for Alzheimer disease. […] Led by Leigh Charvet, PhD, the trial enrolled 10 patients with PPA notable word-finding difficulties who underwent 20 daily (5/week) sessions of 45-minutes of personalized word retrieval training with concurrent tDCS stimulation over the left inferior frontal gyrus for the first 30 minutes. Following treatment, patients showed improvement in naming for trained vs untrained items (25.1 [4.3] vs 20.2 [7.5]; P = .003). From baseline to intervention end, the group significantly improved in confrontation naming (6.2 [5.6] vs 7.8 [5.2]; P = .016). Charvet, a professor of neurology at the NYU Grossman School of Medicine, sat down with NeurologyLive during the meeting to discuss the study in detail, and some of the major clinical takeaways. She provided context on the feasibility of combining tDCS with individualized word retrieval and why this may be an effective approach for language issues in patients with PPA.
- #70 Therapeutic Potential of Transcranial Direct Current Stimulation in Primary Progressive Aphasia: Leigh Charvet, PhDhttps://www.neurologylive.com/view/therapeutic-potential-transcranial-direct-current-stimulation-primary-progressive-aphasia-leigh-charvet
Primary progressive aphasia (PPA), a type of dementia, is a neurological condition that affects a persons ability to speak and communicate. Aphasia is a language disorder that results from damage to key parts of the brain that are responsible for understanding or producing speech and/or writing. While there are no cures for PPA, patients have benefited from participating in speech and cognitive therapy, as well as taking certain medications, such as selective serotonin reuptake inhibitors or therapies that are approved for Alzheimer disease. […] Led by Leigh Charvet, PhD, the trial enrolled 10 patients with PPA notable word-finding difficulties who underwent 20 daily (5/week) sessions of 45-minutes of personalized word retrieval training with concurrent tDCS stimulation over the left inferior frontal gyrus for the first 30 minutes. Following treatment, patients showed improvement in naming for trained vs untrained items (25.1 [4.3] vs 20.2 [7.5]; P = .003). From baseline to intervention end, the group significantly improved in confrontation naming (6.2 [5.6] vs 7.8 [5.2]; P = .016). Charvet, a professor of neurology at the NYU Grossman School of Medicine, sat down with NeurologyLive during the meeting to discuss the study in detail, and some of the major clinical takeaways. She provided context on the feasibility of combining tDCS with individualized word retrieval and why this may be an effective approach for language issues in patients with PPA.
- #71 Primary progressive aphasia research updates – UChicago Medicinehttps://www.uchicagomedicine.org/forefront/neurosciences-articles/2024/november/primary-progressive-aphasia-papers-november-2024
We found a way to deliver care that creates a little bit more of an equal playing field, Rogalski explained. Persons with PPA don’t have to be living next to a major academic medical center or specialty center to get in touch with an expert and receive treatment. […] Providing hope and practical support for these families is really important, Rogalski said. Too many people have lived experiences in which, even when they find a specialist, that specialist may say, There’s nothing we can do. It’s a terminal diagnosis. But finding a cure isn’t the only way we can help people. Maximizing independence, emotional well-being, confidence all of those things can have a lot of practical aspects on one’s daily life. If we can ramp those up as much as possible while we’re simultaneously looking for pharmacological solutions, that’s a winning combination.
- #72 Primary progressive aphasia research updates – UChicago Medicinehttps://www.uchicagomedicine.org/forefront/neurosciences-articles/2024/november/primary-progressive-aphasia-papers-november-2024
We found a way to deliver care that creates a little bit more of an equal playing field, Rogalski explained. Persons with PPA don’t have to be living next to a major academic medical center or specialty center to get in touch with an expert and receive treatment. […] Providing hope and practical support for these families is really important, Rogalski said. Too many people have lived experiences in which, even when they find a specialist, that specialist may say, There’s nothing we can do. It’s a terminal diagnosis. But finding a cure isn’t the only way we can help people. Maximizing independence, emotional well-being, confidence all of those things can have a lot of practical aspects on one’s daily life. If we can ramp those up as much as possible while we’re simultaneously looking for pharmacological solutions, that’s a winning combination.
- #73 Primary progressive aphasia research updates – UChicago Medicinehttps://www.uchicagomedicine.org/forefront/neurosciences-articles/2024/november/primary-progressive-aphasia-papers-november-2024
We found a way to deliver care that creates a little bit more of an equal playing field, Rogalski explained. Persons with PPA don’t have to be living next to a major academic medical center or specialty center to get in touch with an expert and receive treatment. […] Providing hope and practical support for these families is really important, Rogalski said. Too many people have lived experiences in which, even when they find a specialist, that specialist may say, There’s nothing we can do. It’s a terminal diagnosis. But finding a cure isn’t the only way we can help people. Maximizing independence, emotional well-being, confidence all of those things can have a lot of practical aspects on one’s daily life. If we can ramp those up as much as possible while we’re simultaneously looking for pharmacological solutions, that’s a winning combination.
- #74 Primary progressive aphasia research updates – UChicago Medicinehttps://www.uchicagomedicine.org/forefront/neurosciences-articles/2024/november/primary-progressive-aphasia-papers-november-2024
We found a way to deliver care that creates a little bit more of an equal playing field, Rogalski explained. Persons with PPA don’t have to be living next to a major academic medical center or specialty center to get in touch with an expert and receive treatment. […] Providing hope and practical support for these families is really important, Rogalski said. Too many people have lived experiences in which, even when they find a specialist, that specialist may say, There’s nothing we can do. It’s a terminal diagnosis. But finding a cure isn’t the only way we can help people. Maximizing independence, emotional well-being, confidence all of those things can have a lot of practical aspects on one’s daily life. If we can ramp those up as much as possible while we’re simultaneously looking for pharmacological solutions, that’s a winning combination.
- #75 Nonfluent Variant Primary Progressive Aphasia | Memory and Aging Centerhttps://memory.ucsf.edu/dementia/primary-progressive-aphasia/nonfluent-variant-primary-progressive-aphasia
People with nfvPPA gradually have more trouble expressing themselves, even though they still understand the meaning of words. […] Speech therapy may help improve communication between people with nfvPPA and others. Communication devices, like tablets and type-to-talk instruments, or picture books, can help the person with nfvPPA express what they want to say with less anxiety. […] If symptoms of weakness or difficulty using the arm or leg develop, physical and occupational therapy may help manage them and provide coping skills and strategies. A swallowing evaluation and a modification of diet and consistency of liquids may be necessary for people with nfvPPA who develop swallowing difficulties. […] Research has shown that physical exercise helps to enhance brain health and improves mood and general fitness. A balanced diet, enough sleep, and limited alcohol intake are other important ways to promote good health. Other illnesses that affect the brain, such as diabetes, high blood pressure, and high cholesterol, should also be treated if present.
- #76 Nonfluent Variant Primary Progressive Aphasia | Memory and Aging Centerhttps://memory.ucsf.edu/dementia/primary-progressive-aphasia/nonfluent-variant-primary-progressive-aphasia
People with nfvPPA gradually have more trouble expressing themselves, even though they still understand the meaning of words. […] Speech therapy may help improve communication between people with nfvPPA and others. Communication devices, like tablets and type-to-talk instruments, or picture books, can help the person with nfvPPA express what they want to say with less anxiety. […] If symptoms of weakness or difficulty using the arm or leg develop, physical and occupational therapy may help manage them and provide coping skills and strategies. A swallowing evaluation and a modification of diet and consistency of liquids may be necessary for people with nfvPPA who develop swallowing difficulties. […] Research has shown that physical exercise helps to enhance brain health and improves mood and general fitness. A balanced diet, enough sleep, and limited alcohol intake are other important ways to promote good health. Other illnesses that affect the brain, such as diabetes, high blood pressure, and high cholesterol, should also be treated if present.
- #77 Primary Progressive Aphasia | Norton Healthcare Louisville, Ky.https://nortonhealthcare.com/services-and-conditions/neurosciences/services/primary-progressive-aphasia/
Itâs part of Norton Neuroscience Instituteâs goal to care for the whole person, not just the condition. […] Dedicated patient navigators can help schedule follow-up appointments, coordinate prescription assistance, create customized diet plans and provide guidance on disability benefits, housing, financial and employment concerns, and more. […] Patients can access support groups, exercise classes and other educational events to connect with others and learn how to make the most of life while managing a neurologic condition. […] Norton Neuroscience Institute Resource Center navigators help educate patients and their families about new diagnoses, available treatments and ways to manage their disease.
- #78 search-iconhttps://news.christianacare.org/2023/07/frontotemporal-dementia-and-aphasia-what-to-know/
As much as possible, continue with activities your loved one enjoys. Spend time together having simple conversations, reading magazines, newspapers or tablets, looking at photo albums, listening and singing along to music, playing board games or word games. […] Follow-up care is a key part of your loved ones treatment and safety. Keep all appointments, and call your loved ones health care provider if they are having problems. Its also a good idea to know test results and keep a list of the medicines they take.
- #79 Living with PPA – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/living-with-ppa/
Treatment therefore focuses on helping people to manage their symptoms and on supporting them and those around them. […] Understandably, people living with any form of PPA can become depressed or anxious due to the problems with speech and language. These are treatable problems, so it is important that they are detected and managed effectively, including referral to a mental health professional where needed.
- #80 Living with PPA – Rare Dementia Supporthttps://www.raredementiasupport.org/primary-progressive-aphasia/living-with-ppa/
Treatment therefore focuses on helping people to manage their symptoms and on supporting them and those around them. […] Understandably, people living with any form of PPA can become depressed or anxious due to the problems with speech and language. These are treatable problems, so it is important that they are detected and managed effectively, including referral to a mental health professional where needed.
- #81 4 Approaches to Primary Progressive Aphasia Treatmenthttps://www.healthline.com/health/primary-progressive-aphasia-treatment
Medications: Current research indicates that medications that have been examined as possible treatments for PPA have limited effectiveness in improving cognitive deficits. However, certain medications, such as antidepressants, anti-anxiety medications, sleep aids, antipsychotics, cholinesterase inhibitors (ChEIs), and N-Methyl-D-aspartate receptor antagonists (NMDA antagonists), may be used for various symptoms related to PPA. […] While theres no cure, treatment focuses on managing symptoms and improving communication skills through interventions like speech therapy, cognitive training, and supportive strategies. […] These treatments can help you maintain your ability to communicate, engage in daily activities, and enhance your overall quality of life.
- #82 Therapeutic Potential of Transcranial Direct Current Stimulation in Primary Progressive Aphasia: Leigh Charvet, PhDhttps://www.neurologylive.com/view/therapeutic-potential-transcranial-direct-current-stimulation-primary-progressive-aphasia-leigh-charvet
Primary progressive aphasia (PPA), a type of dementia, is a neurological condition that affects a persons ability to speak and communicate. Aphasia is a language disorder that results from damage to key parts of the brain that are responsible for understanding or producing speech and/or writing. While there are no cures for PPA, patients have benefited from participating in speech and cognitive therapy, as well as taking certain medications, such as selective serotonin reuptake inhibitors or therapies that are approved for Alzheimer disease. […] Led by Leigh Charvet, PhD, the trial enrolled 10 patients with PPA notable word-finding difficulties who underwent 20 daily (5/week) sessions of 45-minutes of personalized word retrieval training with concurrent tDCS stimulation over the left inferior frontal gyrus for the first 30 minutes. Following treatment, patients showed improvement in naming for trained vs untrained items (25.1 [4.3] vs 20.2 [7.5]; P = .003). From baseline to intervention end, the group significantly improved in confrontation naming (6.2 [5.6] vs 7.8 [5.2]; P = .016). Charvet, a professor of neurology at the NYU Grossman School of Medicine, sat down with NeurologyLive during the meeting to discuss the study in detail, and some of the major clinical takeaways. She provided context on the feasibility of combining tDCS with individualized word retrieval and why this may be an effective approach for language issues in patients with PPA.
- #83 Global perspectives on the management of primary progressive aphasia | Scientific Reportshttps://www.nature.com/articles/s41598-024-70156-5
Speech-language therapists/pathologists (SLT/Ps) are key professionals in the management and treatment of primary progressive aphasia (PPA), however, there are gaps in education and training within the discipline, with implications for skills, confidence, and clinical decision-making. […] Best practice principles for SLT/Ps working with PwPPA were used to frame the latter two sections of this survey. […] Respondents identified instructional online courses (92.5%), sample tools and activities for interventions (64.8%), and concrete training on providing care for advanced stages and end of life (58.3%) as central areas of need in their current work. […] Based on survey outcomes, there is a pressing need to enhance current educational and ongoing training opportunities to better promote the well-being of PwPPA and their families, and to ensure appropriate preparation of the current and future SLT/P workforce.
- #84 Campaign to improve care for people living with Primary Progressive Aphasia (PPA) launched | RCSLThttps://www.rcslt.org/news/campaign-to-improve-care-for-people-living-with-primary-progressive-aphasia-ppa-launched/
A national campaign has been launched to address the urgent need for specialised services for individuals living with Primary Progressive Aphasia. […] The campaign, led by the Royal College of Speech and Language Therapists (RCSLT) and the specialist charity Dyscover, calls on the Government to include Primary Progressive Aphasia (PPA) in its list of conditions requiring nationally commissioned services through NHS England. […] PPA is recognised as a rare form of dementia by NHS England, but services for individuals living with this condition are not commissioned at a national level. This has created significant barriers for those affected, limiting access to the specialised speech and language therapy that is crucial for diagnosis and ongoing support. […] Without nationally commissioned services, the consequences for those with PPA are serious: Misdiagnosis: A lack of specialist support means many people are misdiagnosed or diagnosed too late, leading to delays in accessing the limited treatment options available.
- #85 Global perspectives on the management of primary progressive aphasia | Scientific Reportshttps://www.nature.com/articles/s41598-024-70156-5
Evidence demonstrates that PwPPA must begin speech and language intervention as early as possible to avoid the risk of not benefitting from impairment-based or functional interventions. […] Furthermore, as highlighted by Swaffer (2019), people living with early-onset dementias, such as PPA, and their families seek support to optimize participation and quality of life outcomes, which is bolstered by appropriate and timely access to SLT/P intervention. […] In response to these concerns, a group of international expert clinician-academic SLT/Ps worked collaboratively to establish best-practice principles to guide SLT/P services for PwPPA and their families. […] The principles provide a framework for the essential components of SLT/P intervention and can be used to guide clinical decision-making, care coordination and service development in the SLT/P field.
- #86 Campaign to improve care for people living with Primary Progressive Aphasia (PPA) launched | RCSLThttps://www.rcslt.org/news/campaign-to-improve-care-for-people-living-with-primary-progressive-aphasia-ppa-launched/
A national campaign has been launched to address the urgent need for specialised services for individuals living with Primary Progressive Aphasia. […] The campaign, led by the Royal College of Speech and Language Therapists (RCSLT) and the specialist charity Dyscover, calls on the Government to include Primary Progressive Aphasia (PPA) in its list of conditions requiring nationally commissioned services through NHS England. […] PPA is recognised as a rare form of dementia by NHS England, but services for individuals living with this condition are not commissioned at a national level. This has created significant barriers for those affected, limiting access to the specialised speech and language therapy that is crucial for diagnosis and ongoing support. […] Without nationally commissioned services, the consequences for those with PPA are serious: Misdiagnosis: A lack of specialist support means many people are misdiagnosed or diagnosed too late, leading to delays in accessing the limited treatment options available.
- #87 Campaign to improve care for people living with Primary Progressive Aphasia (PPA) launched | RCSLThttps://www.rcslt.org/news/campaign-to-improve-care-for-people-living-with-primary-progressive-aphasia-ppa-launched/
The benefits of having nationally commissioned speech and language therapy services are also clear, leading to: more timely and accurate diagnosis. […] better and more equitable support for people with PPA and their families to enable them to maintain their quality of life and live better for longer. […] community services having access to the specialist speech and language therapy experience and expertise they require. […] âSpeech and language therapy has been a lifeline for us as we live with my wifeâs Primary Progressive Aphasia. It helps us preserve the ability to communicate, keeping our connection strong and maximising quality of life. It helps us stay close and continue to share meaningful moments together.â
- #88 Global perspectives on the management of primary progressive aphasia | Scientific Reportshttps://www.nature.com/articles/s41598-024-70156-5
Furthermore, the best practice principles can guide the development of educational modules and training tools for future and current SLT/Ps seeking to provide consistent and evidence-based care for PwPPA. […] To develop a relevant and viable resource, gaps in current educational opportunities and exposure to aspects of the PwPPA care continuum must be addressed. […] The majority of speech-language intervention research for PPA has been undertaken in English-speaking populations. […] Our findings demonstrate a shortfall in the preparedness and professional support capacity that SLT/Ps receive internationally, characterized by insufficient time spent on PPA in university courses, infrequent or rare exposure to PPA during clinical placements, limited access to mentors that are experts in the condition, and an expressed need for more functional and specialized resources for the condition. […] The findings support use of the best practice principles to guide the systematic development of education, training and professional support opportunities for the SLT/P profession.
- #89 Global perspectives on the management of primary progressive aphasia | Scientific Reportshttps://www.nature.com/articles/s41598-024-70156-5
Speech-language therapists/pathologists (SLT/Ps) are key professionals in the management and treatment of primary progressive aphasia (PPA), however, there are gaps in education and training within the discipline, with implications for skills, confidence, and clinical decision-making. […] Best practice principles for SLT/Ps working with PwPPA were used to frame the latter two sections of this survey. […] Respondents identified instructional online courses (92.5%), sample tools and activities for interventions (64.8%), and concrete training on providing care for advanced stages and end of life (58.3%) as central areas of need in their current work. […] Based on survey outcomes, there is a pressing need to enhance current educational and ongoing training opportunities to better promote the well-being of PwPPA and their families, and to ensure appropriate preparation of the current and future SLT/P workforce.
- #90 Global perspectives on the management of primary progressive aphasia | Scientific Reportshttps://www.nature.com/articles/s41598-024-70156-5
Speech-language therapists/pathologists (SLT/Ps) are key professionals in the management and treatment of primary progressive aphasia (PPA), however, there are gaps in education and training within the discipline, with implications for skills, confidence, and clinical decision-making. […] Best practice principles for SLT/Ps working with PwPPA were used to frame the latter two sections of this survey. […] Respondents identified instructional online courses (92.5%), sample tools and activities for interventions (64.8%), and concrete training on providing care for advanced stages and end of life (58.3%) as central areas of need in their current work. […] Based on survey outcomes, there is a pressing need to enhance current educational and ongoing training opportunities to better promote the well-being of PwPPA and their families, and to ensure appropriate preparation of the current and future SLT/P workforce.
- #91 Primary Progressive Aphasia – Symptoms and Therapieshttps://speechpathologysolutions.com/primary-progressive-aphasia-symptoms-and-therapies/
Primary Progressive Aphasia (PPA) is a neurological condition that increasingly impairs language abilities, affecting many aspects of communication. […] Effective management of Primary Progressive Aphasia requires a multidisciplinary approach that addresses both communication and cognitive aspects of the condition. […] Speech and Language Therapy: This therapy is crucial in PPA management. It includes tailored exercises focused on maintaining existing language abilities. […] Cognitive Rehabilitation: PPA can indirectly affect cognitive functions like memory, problem-solving, and attention. […] Family Education and Support: Involving family members in the therapy process is essential. Educating them about PPA helps them understand the condition and how to communicate effectively. […] The integration of technology into the therapy for Primary Progressive Aphasia has significantly enhanced treatment approaches and outcomes. […] Communication Strategies: Individuals with PPA often learn new ways to communicate as their condition progresses. […] Support Systems: Having support from healthcare professionals, such as speech-language pathologists, guides in managing the condition.
- #92 Primary Progressive Aphasia – Rare Dementias – Topic guides at Dementia Australia Library Servicehttps://dementia-org.libguides.com/Rare-dementia-support/primary-progressive-aphasia
My experience of person-centered and personalized care in early-stage primary progressive aphasia (2025)I received an early and accurate clinical diagnosis of the nonfluent/agrammatic variant of PPA, supported by imaging. I am fortunate to have benefited from exemplary individualized care from a multidisciplinary medical team from the onset of my difficulties with language. In this paper, I discuss my lived experience of all aspects of this personalized and person-centered care, describing how it was founded on shared decision-making and a holistic, dementia-inclusive approach encompassing the physical, mental, emotional, psychosocial and spiritual dimensions of living with an incurable neurodegenerative disease. Douglas JT. My experience of person-centered and personalized care in early-stage primary progressive aphasia. Dementia. 2025;24(3):353-367.
- #93 Primary Progressive Aphasia – Rare Dementias – Topic guides at Dementia Australia Library Servicehttps://dementia-org.libguides.com/Rare-dementia-support/primary-progressive-aphasia
Speech and language therapy approaches to managing primary progressive aphasia (2019)Speech and language therapists have developed several impairment-based interventions and compensatory strategies for use in the clinic. This review highlights the reasons why neurologists should refer people with PPA to speech and language therapists. Volkmer, A., Rogalski, E., Henry, M., Taylor-Rubin, C., Ruggero, L., Khayum, R., Kindell, J., Gorno-Tempini, M. L., Warren, J. D., Rohrer, J. D. (2020). Speech and language therapy approaches to managing primary progressive aphasia. Practical neurology, 2019,19. doi:10.1136/practneurol-2018-001921
- #94
- #95 Primary progressive aphasia research updates – UChicago Medicinehttps://www.uchicagomedicine.org/forefront/neurosciences-articles/2024/november/primary-progressive-aphasia-papers-november-2024
We found a way to deliver care that creates a little bit more of an equal playing field, Rogalski explained. Persons with PPA don’t have to be living next to a major academic medical center or specialty center to get in touch with an expert and receive treatment. […] Providing hope and practical support for these families is really important, Rogalski said. Too many people have lived experiences in which, even when they find a specialist, that specialist may say, There’s nothing we can do. It’s a terminal diagnosis. But finding a cure isn’t the only way we can help people. Maximizing independence, emotional well-being, confidence all of those things can have a lot of practical aspects on one’s daily life. If we can ramp those up as much as possible while we’re simultaneously looking for pharmacological solutions, that’s a winning combination.
- #96 Primary progressive aphasia research updates – UChicago Medicinehttps://www.uchicagomedicine.org/forefront/neurosciences-articles/2024/november/primary-progressive-aphasia-papers-november-2024
We found a way to deliver care that creates a little bit more of an equal playing field, Rogalski explained. Persons with PPA don’t have to be living next to a major academic medical center or specialty center to get in touch with an expert and receive treatment. […] Providing hope and practical support for these families is really important, Rogalski said. Too many people have lived experiences in which, even when they find a specialist, that specialist may say, There’s nothing we can do. It’s a terminal diagnosis. But finding a cure isn’t the only way we can help people. Maximizing independence, emotional well-being, confidence all of those things can have a lot of practical aspects on one’s daily life. If we can ramp those up as much as possible while we’re simultaneously looking for pharmacological solutions, that’s a winning combination.
- #97
- #98 Campaign to improve care for people living with Primary Progressive Aphasia (PPA) launched | RCSLThttps://www.rcslt.org/news/campaign-to-improve-care-for-people-living-with-primary-progressive-aphasia-ppa-launched/
The benefits of having nationally commissioned speech and language therapy services are also clear, leading to: more timely and accurate diagnosis. […] better and more equitable support for people with PPA and their families to enable them to maintain their quality of life and live better for longer. […] community services having access to the specialist speech and language therapy experience and expertise they require. […] âSpeech and language therapy has been a lifeline for us as we live with my wifeâs Primary Progressive Aphasia. It helps us preserve the ability to communicate, keeping our connection strong and maximising quality of life. It helps us stay close and continue to share meaningful moments together.â