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.
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My Amylostory : amyloidosis testimonies
My Amylostory: a video series drawn from the testimonies of patients and families affected by amyloidosis, collected for the first World Amyloidosis Day.
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Back to World Amyloidosis day in video: thanks to all partners and sponsors
The Amyloidosis Alliance thanks the partners, sponsors, scientific committee and patient organizations who took part in World Amyloidosis Day 2022.
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World Amyloidosis experts interviewed about the disease
Amyloidosis experts from France, Italy and Brazil explain advances in the diagnosis and treatment of the disease, in videos for World Amyloidosis Day.
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The World Amyloidosis day 2022: experts round table
For World Amyloidosis Day 2022, patients, doctors and international experts discuss amyloidosis, its management and future treatments in a round table.
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The World Amyloidosis day 2022: the videos testimonies
Patients and relatives from around the world share their experience of amyloidosis in video testimonies recorded for World Amyloidosis Day 2022.
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Launch of the communication campaign for the World Amyloidosis Day 2022
The World Amyloidosis Day 2022 campaign launches with a video from the board, patient and expert testimonies, and street interviews about the disease.
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Summary of the presentations and highlights of the ISA Congress by Ben Woltering
Ben Woltering summarises the 18th International Symposium on Amyloidosis (ISA), held in Heidelberg in September 2022 with some 1,100 participants.