Chromosome 22 Central
supports
all
chromosome 22
disorders
22q11.2 Deletion (Velocardiofacial and DiGeorge Syndrome),
22q11 Microduplication Syndrome, Emanuel Syndrome and the 11/22
translocation,
Cat Eye Syndrome, Mosaic Trisomy 22,
Complete Trisomy 22, Phelan-McDermid Syndrome (22q13 deletion, Chromosome 22 Ring),
and many unique chromosome 22
conditions.
Raising the Goddess of Spring: A guide for parents raising children with rare chromosome disorders
New book for parents
All profits support C22C!
Compassion,
Connection, Community.
Stronger, together. Since
1996.
C22C is a global collection of parents and people
affected by chromosome 22 disorders who connect,
advocate and grow, together.
Our website is a hub for people to find immediate connections with others through our various social media platforms, and to find basic information and links to other resources. Started in 1996 with just 17 families of children with what is now known as Emanuel syndrome, C22C has grown over the past 25 years into a community for anyone needing support or information about any of the disorders of chromosome 22.
Our families come together to find connections around the world.