The Amyloidosis Alliance wishes you a happy holiday season
Season’s greetings from the Amyloidosis Alliance to patients, families and supporters, with more actions around amyloidosis to come in the new year.
Newsroom
December 2022
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Amyloidoisis: access to care
Sara, who lives in Israel, shares her experience of amyloidosis and how access to care is improving in her country. Watch her story in this short…
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A hereditary form of Amyloidosis
Anne-Marie, a member of TTR Amyloidosis Canada, lives with a hereditary form of amyloidosis and urged her siblings to get tested. Watch her video testimony.