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@colleenyoung

Welcome @candace317, I can imagine that you are very concerned for your daughter. I'm tagging fellow EDS members who have also talked about having migraines or headaches with EDS and/or also having POTS - members like @deb914 @cutlertc @mhjs123 @briisessions @julianned @hedstrong @guderianj @spoeps @anniemaggie @nlamont @katemschultz @lisafl @jthigpen @lifetimepain @wittmack @breick and others

While we wait for others to post about their experiences, you might wish to read these blog posts written my Mayo Clinic EDS experts:
- Headaches and EDS – Common and Painful https://connect.mayoclinic.org/blog/ehlers-danlos-syndrome/newsfeed-post/headaches-and-eds-common-and-painful/
- POTS Part II: Treatment https://connect.mayoclinic.org/blog/ehlers-danlos-syndrome/newsfeed-post/pots-part-ii-treatment/

Candace, is your daughter seeing an EDS specialist?

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Replies to "Welcome @candace317, I can imagine that you are very concerned for your daughter. I'm tagging fellow..."

Thank you. She is seeing Dr. Mooney at the Pain Rehab Clinic at Childrens Healthcare Of Atlanta at the center for advanced pediatrics. I do not know if that person is an EDS specialist. I would love any Atlanta recommendations if you have them. Should I push insurance to get her to Mayo PRC in Rochester? I am pretty sure I can get it approved but don't know if treatment will vary?