
Amyloidosis Progress
Diagnosis, treatment and research: how the care of cardiac amyloidosis has evolved over recent decades, based on a review of three parallel advances.

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Research advances, patient stories, policy work and news from the associations of the Alliance network.

Diagnosis, treatment and research: how the care of cardiac amyloidosis has evolved over recent decades, based on a review of three parallel advances.

Amyloidosis can affect the heart, kidneys and nerves. Why regular physical activity adapted to each person can play a useful role alongside treatment.

Cardiac amyloidosis often goes unrecognised, even by doctors. What it is, a case seen in an emergency department, and why earlier diagnosis matters.
At a World Heart Federation forum in Geneva in May 2023, patient representatives, including for ATTR cardiomyopathy, spoke about rare heart diseases.
Plain language summaries of key ATTR amyloidosis clinical trial publications are now available in seven languages, to make results accessible to patients.

Early results for an antibody designed to clear transthyretin amyloid deposits were presented at a heart failure congress, pointing to a possible new approach.

ATTRv amyloidosis is the hereditary form of ATTR. Its symptoms, its impact on daily life, how it is diagnosed and the treatment options, explained simply.
The 4th European ATTR amyloidosis meeting for patients and physicians takes place on 2 and 3 November 2023, on site and online, with two programmes.
First described in 1838, amyloidosis remains a young field of research. An overview of what is known about its causes, current treatments and research.
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