In the realm of rare diseases like Amyloidosis, caregivers stand as pillars of strength, compassion, and support. Their unwavering dedication and selflessness often go unnoticed amidst the challenges faced by…
Read MoreIn the realm of medical advancements, every breakthrough holds promise, especially for those grappling with rare diseases. The 5th and 6th of July, Belgium becomes the epicenter of hope as…
Read MoreFebruary 29 marks world rare disease day, a special occasion to raise public awareness of the challenges faced by those living with rare diseases. The Amyloidosis Alliance is once again mobilizing worldwide to support the cause and highlight the impact of amyloidosis
Read MoreAs the world gears up to observe Rare Disease Day on February 29th, the Amyloidosis Alliance stands at the forefront, championing awareness and support for those affected by Amyloidosis.
Read MoreForefront of amyloidosis research! In the Amyloidosis Alliance, We’re committed to fostering collaboration among members associations worldwide to accelerate research progress
Read MoreThe ISA International Amyloidosis Fellowship Program The fight against amyloidosis, a rare but devastating disease, is taking on a new dimension thanks to the International Amyloidosis Society (ISA) Fellowship Programme….
Read More2023 has proven to be a remarkable year filled with significant actions, groundbreaking events, and notable advancements in the field of amyloidosis research and awareness.
Read MoreAs we usher in the promising dawn of 2024, The Amyloidosis Alliance stands united and extends heartfelt wishes for the upcoming year…
Read MoreIn the spirit of World Amyloidosis Day 2023, the Amyloidosis Alliance is thrilled to present an inspiring and heartfelt video featuring a remarkable couple who have been fittingly diagnosed with Amyloidosis h-ATTR
Read MoreThe Amyloidosis Alliance board members visit to the National Amyloidosis Reference Centre in Pavia, Italy.
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