
WELCOME
Welcome to the Marfans Research Foundation Ireland. We are dedicated to raising awareness, supporting families, and funding research into Marfan Syndrome, a rare genetic condition affecting connective tissue. Together, we aim to improve understanding, diagnosis, and care for those living with Marfan Syndrome in Ireland.
UPCOMING EVENTS

Dublin Women’s Mini MarathonSun, 31 MayDublin
Marfans Research Golf ClassicDate and time is TBDLocation is TBD
Bag Pack(TBD)Location is TBD
WHAT PEOPLE SAY
Testimonials

Geraldine McGrath, Founder
“Marfans Research Foundation was born from our family’s journey through life-saving heart surgeries and the profound impact Marfan syndrome has had on our lives. Having experienced both loss and hope, I truly believe that research saves lives.
The unwavering support of our community has been extraordinary, with every cent raised going directly to research—bringing hope to families like ours and to future generations.”

Michael McGrath, Founder
“I know first-hand the importance of Marfan syndrome research. I have supported my wife Geraldine and our sons through their Marfan journey—from clinic visits to major open-heart surgeries—sharing in both the challenges and the relief that follows successful treatment.
I fully endorse Marfans Research Foundation and believe research is vital in improving outcomes and giving hope to families now and in the future.”

Marfan Patient
“I was diagnosed with Marfan syndrome at a young age and monitored through Crumlin Children’s Hospital and later the Mater Hospital. I had surgery at 17 in June 2005. Thanks to regular check-ups, I now live a full, active life without restrictions. Having a family of my own, I see how important research is for the future. Marfans Research Foundation is doing vital work funding research and raising awareness locally.”
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