Category 2

We wish you a wonderful holiday season. May they be filled with smiles and happy moments with your family.We will meet again in 2023 for even more actions around Amyloidosis.

Access to care – Sara tells us about her country, Israel, where she finds that accessibility to care is increasing. Find out more about her story by watching the video.

Amyloidosis and heredity Anne-Marie has a hereditary form of amyloidosis. She has warned her siblings to get tested as well. Find out more about her story by watching this video…

Amyloidosis testimonies from all around the world After this month of November, and the month of the second World Amyloidosis Day in October, we thought it would be interesting to…

A huge thank you to all the partners, laboratories and sponsors who supported us and the cause of amyloidosis during the Word Amyloidosis Day this year. We don’t forget to…

World Amyloidosis experts interviewed about the disease
As part of World Amyloidosis Day, the world’s leading experts on the disease were interviewed and tell you more about it.
It is interesting to hear from them, to learn about advances in treatment and diagnosis of the disease.

The World Amyloidosis Day 2022 experts round table Tomorrow is the World Amyloidosis Day 2022 . Sit back and expect 1.5 hours of viewing time for Amyloidosis, and interesting discussions…

World Amyloidosis Day on 26 October 2022: the videos testimonies In the framework of the International Amyloidosis Day on October 26, many testimonies and interviews were conducted around the world….

Launch of the communication campaign for World Amyloidosis Day This week saw the launch of the communication campaign for World Amyloidosis Day 2022 on 26 October. The Amyloidosis Alliance board…

The 18th International Symposium on Amyloidosis, “ISA” by Ben Woltering. From 4th – 8th September 2022 this symposium took place in Heidelberg, Germany. It is a worldwide congress on amyloidosis…