The Marfan Foundation is dedicated to the education and support of our global community of people living with Marfan and related conditions.
The Foundation was a founding member of Marfan World (formerly known as the International Federation of Marfan Syndrome Organizations) and continues its commitment to:
- Share current, accurate information about Marfan syndrome and related conditions worldwide.
- Facilitate international communication among medical professionals who serve the Marfan, Loeys-Dietz, and VEDS community.
- Facilitate communication between international organizations representing individuals and families affected with Marfan, Loeys-Dietz, VEDS, and other genetic aortic and vascular conditions.
- Support and foster global research initiatives.
- Convene international meetings to facilitate research and bring the global patient community together.
Don’t Miss our
April 13, Austin, TX
(Check back soon for registration link)
Resources in Multiple Languages
We are happy to provide information about Marfan syndrome and how it affects the body in several languages. We offer resources that you can download that cover the following aspects of Marfan syndrome: diagnosis, basic facts, bones and joints, cardiac surgery, eyes, lungs, skin, teeth, family planning, and physical activity.
Aortic Disease Awareness Week
Aortic Disease Awareness Week is a focused effort by physicians, researchers, patients, family members, and many organizations to raise awareness about aortic disease around the world every September. It is dedicated to create community for people who care about aortic disease, celebrate survivors, and share information that can be life-saving for people who are at risk.
Marfan World, which was formally known as the International Federation of Marfan Syndrome Organizations was founded in 1992 at the Second International Symposium on Marfan Syndrome in San Francisco, California.