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@slip275

Has anyone gone to Mayo Clinic to have EDS symptoms evaluated as a whole by a team of specialists? If so, how was your experience?

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Replies to "Has anyone gone to Mayo Clinic to have EDS symptoms evaluated as a whole by a..."

Hi @slip275, while we wait for fellow patients to share their experiences about Mayo Clinic, I thought you might appreciate these related blogs and discussions:

- EDS Clinic Updates, EDS Awareness
https://connect.mayoclinic.org/blog/ehlers-danlos-syndrome/newsfeed-post/eds-clinic-updates-eds-awareness/
- The EDS Clinic at Mayo Clinic Florida
https://connect.mayoclinic.org/blog/ehlers-danlos-syndrome/newsfeed-post/the-eds-clinic-at-mayo-clinic-florida/
@katemschultz posted this informative message when she was preparing for her first EDS visit to Mayo in Rochester
– What to expect at Mayo Clinic, Rochester https://connect.mayoclinic.org/discussion/what-to-expect-at-rochester

@jthigpen writes about their experience at the EDS Clinic at Mayo Clinic in Florida here: https://connect.mayoclinic.org/comment/320392/