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Support for Disorders of
Chromosome 22
 
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 CONTACT DISORDERSCONNECTSHOP C22CEVENTSRESEARCHABOUT C22CJOIN C22C

Chromosome 22 Central
 supports ALL chromosome 22 disorders, including:

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

Chromosome 22 Ring

22q13 Deletion (Phelan-McDermid Syndrome)

and many unique chromosome 22 conditions.



22q11.2 Parent Conference -ONLINE

Theme: Mental Health Matters

See full poster attached

Organized in partnership with the Sick Kids 22q11.2 Deletion clinic

Scheduled monthly, virtual events / presentations from
November 2020 to May 2021.
Registration for each session is a separate event in Eventbrite.
Below is a link to the program. You’ll find a registration link beside each session – use these links to access registration for each event.
Zoom links for each event will be sent out closer to each date.
We hope you are able to join us and connect with our 22q Community.

FOR MORE INFORMATION CONTACT COMMITTEE CO-CHAIRS

Christine MacDonald & Lorraine Sutherns at Connect22qFamilies@rogers.com