On 22 November, Europe will light up in red on 22q11 Day! November 22nd is the International 22q11 Day, a European movement to raise awareness about 22q11 microdeletion syndrome by…
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22q11.2 deletion syndrome (22q11DS) is a genetic condition associated with a markedly increased risk for psychosis. Psychotic experiences are classically evaluated by clinical interviews that give little information about these…
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My name is Aine, I am 33 years old and I live in Ireland. I was diagnosed with 22q11 at 21 years old. Growing up I had textbook symptoms, I…
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Every two years, 22q11 Europe organizes a conference in coordination with a local 22q11 association. The objective of this conference is to keep patients and relatives informed with recent researches,…
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Hello, My name is Audrey and my husband is Sebastien. We are the parents of a 5 year old little boy, named Jonas. We learned that he was a carrier…
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Hello, my name is Gwenaelle, I’m 29 years old and I’ve been lucky enough to have two children (and the best choice): a 7 year old boy, Enzo, and a…
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Charlotte was the 3rd born child, 1st girl and was the last piece of our family puzzle. She was born at 40 weeks no complications. Initially as a newborn i…
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You can still register for the 4th European 22q11 Congress! Registration link After a long time of only virtual encounters and lockdown, the 4th European 22q11 Congress will take place…
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My name is Nathalie and my companion Samuel and I have a three year old boy, Andrea, who has the 22q11 deletion syndrome. We found out about it on the…
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We are very happy to announce that Stichting Steun 22q11 has joined 22q11 Europe! Stichting Steun 22q11 raises awareness about 22q11 in the Netherlands, through information, events, projects and contributions to…