CHROMOSOME 22 CENTRAL 
SUPPORT FOR ALL CHROMOSOME 22 RELATED DISORDERS 

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

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MESSAGE BOARDS

• Trisomy 22 and Rare C22 Disorders

• Cat Eye Syndrome 

• 22q Deletions

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C22C INTERNATIONAL PARENT CONTACTS

LEARN ABOUT

• Chromosome 22 Central

• 22q11 Deletion Syndrome (DiGeorge Syndrome, Velocardiofacial Syndrome)

• Microduplication 22q11 Syndrome

• The 11/22 Translocation (Emanuel Syndrome, partial trisomy 11/22)

• 22q13 Deletion Syndrome (Phelan-McDermid Syndrome)

• Cat Eye Syndrome

• Complete or Full Trisomy 22

• Mosaic Trisomy 22

• Chromosome 22 Ring

• Monosomy 22 Mosaicism 

• Unique Chromosome 22 Disorders

• Books

 NEWSLETTERS

• NOVEMBER 2006
• FEBRUARY 2007 
• MAY 2007 
• SEPTEMBER 2007
• DECEMBER 2007 
• MAY 2008

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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

CHROMOSOME 22 CENTRAL
DISCLAIMER

Please read our Privacy Policy regarding how confidential information is handled.

Chromosome 22 Central is a volunteer based organization. Every effort has been made to ensure the accuracy of the information provided on this website.

Links to other resources are provided solely as a means of further information, and C22C Inc. does not endorse any such resources.

Any information provided to members or the general public is provided for educational purposes only, and is not intended to replace professional advice from doctors or therapists. C22C Inc. representatives, members or board members DO NOT under any circumstances offer medical advice. Our group's purpose is to strictly offer support and basic information. We are run by a group of caring parents and are not trained to offer advice. All information we provide is strictly on an information basis only, and should be shared with your own medical professionals.

It is important to understand that when reading facts about specific disorders, that not all people affected will be the same. As with any disorder, there are degrees of severity, and it is important for parents to understand these facts. It is recommended that information you receive from C22C Inc. be shared with professionals for comments or advice.

Any concerns regarding the content of our website can be directed to Stephanie St-Pierre. steph.stpierre@gmail.com  

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Effective date: July 9, 2003

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USA members for DONATIONS Please forward a cheque or money order to our US HEAD OFFICE so that you can obtain a tax receipt.

Head Office - for ALL inquiries: Chromosome 22 Central, c/o Stephanie St-Pierre, 237 Kent Avenue, Timmins, Ontario, Canada P4N 3C2 
tel/fax: (705) 268-3099, EMAIL:  steph.stpierre@gmail.com

US Head Office - donations only: 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