Read Micheal’s story. When Micheal was diagnosed with Chiari, he sought out a local support group for his rare condition and found that there were no support groups near him. Micheal took action and began working with Conquer Chiari of America, where he has helped organize fundraisers and walks. Micheal is also working on creating a nonprofit foundation to help Mississipians with chiari, syringomyelia, and related conditions. 

Do you belong to a local support group? What kinds of resources has your group provided?

Hello, unfortuately there are no local support groups in MS! I'm is still working on my foundation; I been slowed down very much do to the pandemics! I have been destributing most of the info I receieve form Conquero Chiari!