Chiari Online Support Group

Mast Cell Activation-EDS

Hi All,
I went to the Charlotte area meet and greet and learned some very interesting information about Mast Cell Activation. Wow! These symptoms ALL fit many of Hope’s newest issues. I heard that it is common with EDS and I’m still doing research but I’m curious about a connection to Chiari as well. Do any of you know about this? I especially find it interesting that it has an effect on how the body metabolizes medications. I’d love to hear from anyone else that has experience with this particular genetic issue. Thank you in advance :purple_heart: