Connect


C22C Connect!

Connect with other families and caregivers of Chromosome 22 Disorders.

Our main group for all members worldwide. Join over 3000 families to share and learn. 

For our C22C members looking to connect in Canada

For C22C members looking to connect with other members in the USA.


For our C22C members looking to connect in Asia

For C22C members looking to connect down under!

For our C22C members looking to connect in Europe


For our C22C members looking to connect in Latin American countries.

Specific for C22C members living in South Africa.


Our group specific to support families and caregivers of people living with Emanuel syndrome, and for carriers of the t(11;22)

Our group for those families who support those who are living with chromosome 22 disorders that are unique or very rare.

Our group specific to support families and caregivers of people living with 22q12 an 22q13 duplications


For C22C members who carry any chromosome difference that impacts their ability to build a family. Admin is a balanced translocation carrier who has experienced miscarriage, has a child affected with a chromosome 22 disorder, and who has adopted. Share resources,  support, ask questions and help others going through these same challenges.

Are you a father of a child with a chromosome 22 disorder? This is the place for you.

Our group specific to support siblings who have a family member with a chromosome 22 disorder. 


Our group specific for grandparents of people with chromosome 22 disorders.

A pool of C22C members who may be interested in supporting and volunteering for C22C projects from time to time. Joining does not obligate you to participate. If requests are posted and you feel you can help out C22C when you can – this is the group for you!

This is a place for people living with any chromosome 22 disorder to connect with others on the same journey.


All proceeds of “Raising the Goddess of Spring: A Guide for Parents Raising Children with Rare Chromosomal Disorders” are donated directly to Chromosome 22 Central.

Contact C22C