A support list for families and those interested who are affected by chromosome 22 disorders. For members of Chromosome 22 Central. www.c22c.org.

Please note that Chromosome 22 Central does not take responsibility for any of the views presented in this forum. Please be cautious and do not take peer to peer advice as medical advice. Always consult your health care provider for treatment of your child. Please refrain from flaming. Remember that this group is made up of people from different countries, cultures and religions and respect for each other is expected. You can direct questions to Stephanie St-Pierre at steph.stpierre@c22c.org.