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PPA is a condition caused by a neurological disease that gradually affects a person’s ability to use and understand language. Sometimes speaking is also difficult. PPA begins slowly and worsens over time. This is different from aphasia from stroke or injury. Many people with PPA say: “I can’t remember words” or “I can’t put sentences together well anymore” It’s helpful to think of PPA as a progressive “access” issue — it becomes harder to get to words, sentences, and sounds that were once easy to use.
There are different types (called “variants”) of PPA. Each PPA variant is associated with focal problems in different parts of the language network. The three main types of PPA are the semantic variant, nonfluent/agrammatic variant, and the logopenic variant (see What is Primary Progressive Apraxia of Speech? for information about this related problem).
PPA is caused by a gradual loss of function within brain cells in the areas of the brain that control language. These changes happen slowly and get worse over time. These changes happen because of disease inside brain cells. Eventually, those parts of the brain shrink away (or “atrophy”). Semantic variant PPA and nonfluent/agrammatic variant PPA are most commonly caused by Frontotemporal Degeneration (FTD). Logopenic variant is most commonly caused by Alzheimer’s-related plaques and tangles.
Diagnosing PPA usually takes a team. You may see several doctors, neuropsychologists, and speech-language pathologists. You may get brain scans to help figure out the problem.
Common steps include:
Accurate diagnosis is key. PPA is not well known by many medical providers. Many people have to go to specialty medical centers at universities before they get a correct diagnosis. Contact us for personalized guidance.
There is no cure for PPA, but speech-language treatment can help maintain skills and quality of life.
Speech-language treatment for PPA focuses on:
Learn more about speech-language treatments for PPA and communication strategies for PPA
PPA changes over time in different ways for different people. Talking and understanding get harder over time for everyone. The type of PPA that you have can help doctors guess what kind of problems might happen later on. But not everyone follows a typical pattern of decline. Some people have changes that do not follow the usual path.
Living with PPA can be lonely and frustrating. Both individuals with PPA and their care partners may experience grief, loss, and changes in roles.
You’re not alone. Support is available. The NAA offers:
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