Newsroom
From diagnosis to long-term follow-up, healthcare professionals play a key role in amyloidosis care. How the Alliance works to support them with resources.
The Amyloidosis Alliance brings together patient organizations from around the world. Who we are, our mission, and how your organization can join us.
The Amyloidosis Alliance will attend the XIX International Symposium on Amyloidosis in Rochester, MN, from 26 to 30 May 2024, covering all systemic forms.
Caregivers play a vital role in the lives of people with amyloidosis. A tribute to their dedication, the challenges they face and the support they need.
The first International AL Amyloidosis Meeting, organized by the Amyloidosis Alliance, takes place in Belgium on 5 and 6 July 2024. Discover the programme.
Rare Disease Day takes place on 29 February 2024. How the Amyloidosis Alliance and its members are mobilizing to highlight amyloidosis among rare diseases.
For Rare Disease Day 2024, the Amyloidosis Alliance launches a video campaign on amyloidosis, opening with a tribute to the caregivers of patients.
An overview of recent developments in amyloidosis research, from new treatment approaches to biomarkers that could support earlier detection.
The International Society of Amyloidosis launches a fellowship programme offering grants for clinical training in all the types of amyloidosis.
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