hEDS and hypermobility

Hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders affect connective tissue throughout the body. They can contribute to joint pain, instability, fatigue, dysautonomia, GI symptoms, and a higher rate of co-occurring POTS and MCAS.

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How we approach it

hEDS and hypermobility is rarely a problem on its own.

At Vindara Health, hEDS and hypermobility is treated as part of the whole picture, not in isolation. Your clinician looks at how it interacts with the other systems involved in your health, orders advanced testing when it is clinically appropriate, and builds a plan that adapts as your symptoms change — with the same team alongside you between visits, not just on the day of an appointment.

  • A clinician who understands it. You should not have to explain hEDS and hypermobility from scratch.
  • A full review first. We start from your records, labs, timelines, and history — not a blank page.
  • Testing and treatment that fit your case. Advanced testing where appropriate, and evidence-informed treatment options.
  • Care between visits. Questions, results, and changes do not wait for the next appointment, and neither do we.

Often appears alongside

Complex illness rarely travels alone.

Many patients with hEDS and hypermobility also live with one or more of these. We care for them together.

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