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Fanconi Anemia stories
Unrelated donor 9/10 match September 2012
bone marrow transplant at St. Mary's hospital Paddington, London
Parents set up UK charity called Fanconi Hope
diagnosed in 2007 at Southampton general Hospital
IVIGs X1 every mont...
Views: 629 Feb 15, 2020, 9:47 PM by Louise Dalgleish
I have Fanconi Anemia, it doesn't have me.
Views: 583 Dec 31, 2015, 10:28 PM by Lisa
Raymond was born in April and weighed only 3 lbs. We knew before he was ever born that he was special. Missing both radius bones and both his thumbs we didn't know what was wrong. Then he had a double bubble in his tummy. So at 3 days old he h...
Views: 533 Dec 30, 2015, 2:57 PM by raymond
Born in 1998, dx at 2.5 yr old with Fanconi Anemia. Multiple deformaties, too high risk for bmt. Bone marrow failure at 9 yr old, tranfusion dependent for 3.5 years. Developed MDS and a year later developed Leukemia, markers for both ...
Views: 526 Dec 30, 2015, 12:38 PM by Nicholas
My name is Jacy Louise Box. I was born 11/08/1991. I was born with an extra thumb on my right hand (surgically removed) when I was an infant. My left hand had no ligament (had surgery). I was born with a cleft palate (I've had plenty of surgeries on ...
Views: 343 Mar 27, 2017, 9:53 PM by Jacy
Fanconi Anemia forum
Hello,
I am working on Famconi anemia in Pakistan. The MPhil project of our team identified four novel mutations in Pakistani patients. My aim is to work more here on Fanconi anemia so want to have a proper platform and international friends to guid...
Views: 414 Dec 21, 2015, 3:25 AM by saima
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