Fabry disease
Forum

/static/themes-v3/default/images/default/home/bg-generic.jpg?1516194360

Back

Fabry disease is a rare hereditary disease. How to fight against the pains it causes? How to support a loved one with this condition? What are the available treatments? Our forum includes several discussions that will allow you to exchange with other members on these topics.

Ongoing discussions - Fabry disease

Living with Fabry disease

Current topics:

- What was your age of diagnosis?
Hello everyone, With the rarity of Fabry disease, the condition can be underdiagnosed and misdiagnosed, leading to a delay in ultimate diagnosis. What about you? What was your age of diagnosis with

See all the discussions

Treatments for Fabry disease

Current topics:

- Share your experience with enzyme replacement therapy?
One of the main treatments for Fabry disease is enzyme replacement therapy with agalsidase-alpha (Replagal) or agalsidase beta (Fabrazyme) to help normalize kidney function, heart function, and blood

See all the discussions

Symptoms and complications of Fabry disease

Current topics:

- What were the initial signs / symptoms of Fabry disease experienced?
There are various signs and symptoms one may experience with Fabry disease. Some common signs and symptoms often experienced are: pain and burning sensations; small, dark red spots on the sking; cloud

See all the discussions

News and information

Fact sheet