Category 2

Uniting Against Amyloidosis: Highlights from the European ATTR Congress Amyloidosis is a rare and complex group of diseases that involve the buildup of abnormal proteins in various organs, leading to…

We’re thrilled to announce that the countdown to the very first International World Amyloidosis Day has officially begun! This is an incredible opportunity for all of us to come together…

Dear members of our committed community, We need your testimonies for World Amyloidosis Day on 26 October! We are launching a major awareness campaign to highlight the impact of all…

Unraveling Amyloidosis: A Misunderstood Disorder Impacting Family Communication. there are still widespread misunderstandings surrounding this disorder, which can lead to communication problems within families dealing with its impact.

Amyloidosis is a rare disease that affects a small number of people worldwide. It is a complex condition that can cause a range of symptoms, from fatigue and weakness to…

Great news to share with the community. 

This press release announces that the BioBridge laboratory will now be able to submit an approval dossier to the health authorities.

Hereditary amyloidosis is a rare genetic disease. This disease is characterised by the unusual deposition of protein clusters in tissues, between cells, and often in the walls of small vessels….

Understanding amyloidosis: symptoms, diagnosis and outlook Amyloidosis is a rare disease affecting a limited number of people worldwide. Although little known, it can have a significant impact on patients’ quality…

For almost 150 years after its discovery, amyloidosis was considered incurable. Historically, the complexity of the disease delayed research. Why invest time and money in research on such a complex…

Amyloidosis is a rare disease that occurs when abnormal proteins build up in tissues and organs throughout the body. This build-up can lead to a variety of health problems and…