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Join Us at the XIX International Symposium on Amyloidosis in Rochester, MN We are thrilled to announce that the Amyloidosis Alliance will be gathering at the XIX International Symposium on…

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…

In 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…

February 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

As 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.

Forefront of amyloidosis research! In the Amyloidosis Alliance, We’re committed to fostering collaboration among members associations worldwide to accelerate research progress

The 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….

2023 has proven to be a remarkable year filled with significant actions, groundbreaking events, and notable advancements in the field of amyloidosis research and awareness.

As we usher in the promising dawn of 2024, The Amyloidosis Alliance stands united and extends heartfelt wishes for the upcoming year…

In 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