Welcome to the World Arnold Chiari Malformation Association's kids' group! We are a group for kids and young adults who have been diagnosed with Chiari Malformations and who may or may not have other related disorders. We talk about anything and everything here. From diagnoses and symptoms, to surgery and going back to school. We hope that you'll find it a wonderful place to get accurate information and support from other young Chiarians. Be prepared to make lots of new friends. We look forward to getting to know you! For more information on ACM please check out our links page on your left or go to www.wacma.com

If you have any questions email:
Cody Parker at call_on_cody@yahoo.com
(Wacma Junior Staff)


Please note this group is 'NOT FOR PARENTS' of kids with Chiari.
The parents group is at:
http://health.groups.yahoo.com/group/wacmaparents/