Join Us at the XIX International Symposium on Amyloidosis in Rochester, MN
The Amyloidosis Alliance will attend the XIX International Symposium on Amyloidosis in Rochester, MN, from 26 to 30 May 2024, covering all systemic forms.
Newsroom
News
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Honoring the unsung Heroes: caregivers in the Fight Against Amyloidosis
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.
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Unveiling Breakthroughs: the 1st International AL Amyloidosis congress in Belgium
The first International AL Amyloidosis Meeting, organized by the Amyloidosis Alliance, takes place in Belgium on 5 and 6 July 2024. Discover the programme.
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Rare disease day 2024 is fast approaching!
Rare Disease Day takes place on 29 February 2024. How the Amyloidosis Alliance and its members are mobilizing to highlight amyloidosis among rare diseases.
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Shining Light on rare disease day: Amyloidosis Alliance’s Video Campaign
For Rare Disease Day 2024, the Amyloidosis Alliance launches a video campaign on amyloidosis, opening with a tribute to the caregivers of patients.
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Important Amyloidosis research updates worldwide
An overview of recent developments in amyloidosis research, from new treatment approaches to biomarkers that could support earlier detection.
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The ISA International Amyloidosis fellowship program
The International Society of Amyloidosis launches a fellowship programme offering grants for clinical training in all the types of amyloidosis.
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Amyloidosis breakthroughs in 2023: a year of Progress and Hope
A look back at 2023 in the amyloidosis community: research, awareness campaigns and events, and a video summarising the year of the Amyloidosis Alliance.
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Embracing Hope and Unity: a new year’s message from The Amyloidosis Alliance
The Amyloidosis Alliance looks back on 2023 and shares its wishes for 2024: more collaboration, more awareness and earlier diagnosis of amyloidosis.