CHROMOSOME 22 CENTRAL 
SUPPORT FOR
ALL CHROMOSOME 22 RELATED DISORDERS 

We are all about connecting! 
Click here for an online membership form to JOIN US!
 
Registered members receive our newsletter and can choose to be listed in our parent registry.

C22C is a parent driven group with more than 1000 members in 45+ countries. 

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Chromosome 22 Central Inc. is a registered Canadian Non-Profit Organization 
and Registered Charity BN# 86009 3665 RR0001, and a Registered US Corporation with Non-Profit Status

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Please provide sufficient details when subscribing. A verification email from the moderator will be sent to you with request for further info before approval, for the security of our families.

 

C22C Friends - a discussion group for families and others who support people who have ALL chromosome 22 issues. This replaces our previous C22C list. 

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If you are a parent or caregiver of an adult with a 
chromosome 22 disorder, this group has been 
established specifically for you

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Not requiring peer support at this time but want to be notified of news from C22C? Join our NEWS ONLY list. You will receive occasional updates from our group about our activities, current research, or upcoming events with C22C news.

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C22C Loss - a unique grief support list for those who have suffered miscarriage(s) or infant loss due to chromosome 22 issues.

 

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Pour les membres francophones

 


HEAD OFFICE - for ALL inquiries: Chromosome 22 Central, c/o Stephanie St-Pierre, 338 Spruce Street North, Timmins, Ontario, Canada P4N 6N5 tel: (705) 268-3099, EMAIL:  steph.stpierre@gmail.com

  US Head Office - for US donations: Chromosome 22 Central, c/o Murney Rinholm, 7108 Partinwood Drive, Fuquay-Varina, North Carolina, 27526  USA, tel (919) 567-8167, EMAIL: bgr@nc.rr.com

  Latin America / Spanish inquiries - Laura Munoz, Robinson Crusoe 1209, Las Condes - Santiago, Chile tel: 02-3251262 EMAIL: lauramuno@hotmail.com