Hypermobile EDS Treatment: Rule Out Low Tone First

Many people with hEDS are steered toward treatments aimed at the joint. Our team starts one step earlier, by checking whether the looseness is coming from the nervous system.

What does hEDS treatment involve?

As the video at the top of this page lays it out, hEDS care ranges from rehab and exercise to injections like PRP and prolotherapy, stem cells, and fusion. A 2021 systematic review found weak controlled-trial evidence that conservative care beats its comparators in syndromic hypermobility. Our team's view is that the first step is ruling out hypotonia, low muscle tone that can come from the nervous system, because it can look like hypermobility and bring dizziness and autonomic symptoms with it.

How Is Hypermobile EDS Usually Treated?

Many people with hypermobility and dysautonomia reason that if loose joints are behind the autonomic problems, fixing the joints should fix the rest. We think that's sound logic, and in our experience that road often leads to injections or surgery. The clinic sees those options as relatively invasive and wants a less invasive path tried first.

A systematic review of conservative care in syndromic hypermobility found that controlled trial evidence for conservative management beating its comparators is weak, and that there is some evidence people improve over time (Palmer, 2021). In a retrospective study of patients with hEDS and hypermobility spectrum disorders, physical activity or exercise was among the treatments patients self-reported as helping their pain, though few reported improvement from any single treatment listed (Wilson, 2025).

Could It Be Hypotonia Instead of Hypermobility?

A hypermobile EDS diagnosis is made clinically, and a flexibility check called the Beighton score is one part of it. Genetic testing can identify other types of EDS, but no gene has been found for the hypermobile type. Our team's view is that one check often gets skipped: muscle tone. Hypotonia means muscle tone sits lower than it should, which gives a floppy, slumped-forward look. Low tone can let joints go past their usual limits, and our team finds that some people who seem hypermobile have low muscle tone instead.

People with cerebellar problems, which can show up as ataxia or dysmetria, are one example. In our experience, they tend to have low tone and weaker reflexes, and when they move, they drift toward the end range of their joints much like someone with EDS.

The video describes the concern as not placing everyone in the EDS category while overlooking people whose joint looseness has a neurologic basis in hypotonia.

Why Would Low Muscle Tone Come With Dizziness or Autonomic Symptoms?

In our team's view, the reflexes that set muscle tone, which run largely through the cerebellum and brainstem, also control reflexes tied to the blood vessels, cardiac output and the body's anticipation of gravity when you're upright. That's why, as we see it, hypotonia generated by the cerebellum can come with autonomic problems, balance trouble, dizziness and problems with eye movements or tracking.

Studies point to autonomic involvement in some people with hEDS (Dell'Aversana, 2026). POTS and EDS: why they show up together covers the mechanisms researchers have proposed.

Low muscle tone: tone signal weak cerebellum tone signal heart and vessels balance and eyes end range ligament muscle tone Illustrative, not measured data
Illustrative, not measured data, showing our team's view. In both states the elbow reaches the same end range, so a flexibility check alone can't tell them apart. With low muscle tone, the tone signal from the cerebellum is weak, and in our team's view that same weak signal reaches the heart and vessels and the balance and eye systems. Some people have both. Tap "Loose tissue" or "Low muscle tone" to compare.

Where Do PRP, Prolotherapy, Stem Cells and Surgery Fit?

As the video at the top of this page describes them, PRP reinjects parts of your own blood into the injured area, prolotherapy injects a dextrose solution meant to set off a local immune response, and stem cell injections add cells that can turn into other tissue. Each one aims to start a healing response in the area, and fusion sits at the far end of the range. The video's view is that rehab stays the core and that these can be added to rehab. Our team's view, as with craniocervical instability, is that without outcome data in hEDS it's hard to make a definitive statement on what they do.

Where Do Exercise and Loading Fit?

The video at the top of this page names isometric loading as the main method. You contract the muscles and push against something without moving the joint, so the limb isn't taken through a range that could feel risky. The video also says many different joints can be involved and to start light. That's general education, so check with your own clinician first.

What If You Have hEDS and POTS?

A 2026 systematic review concluded that EDS and POTS frequently co-occur (Kwok, 2026), though co-occurrence alone doesn't show that one causes the other. Our team's part is testing the brain's regulation of heart rate, blood pressure and brain blood flow, and checking muscle tone along with it. POTS and EDS: why they show up together covers the overlap.

See how our team tests upright regulation in 3D

Watch brain blood flow and heart rate respond as you go from lying down to upright.

Take the 3D Tour

Hypermobile and dizzy when you stand? See how the clinic evaluates dysautonomia.

See dysautonomia care

Hypermobile EDS Treatment: FAQ

What are the treatment options for Ehlers-Danlos syndrome?

For hypermobile EDS, options range from rehab and exercise to PRP, prolotherapy and stem cell injections, with fusion at the far end. A systematic review found that controlled evidence for conservative care beating its comparators is weak (Palmer, 2021). Our team's view is to rule out hypotonia first, and the video at the top of this page treats rehab as the core.

What exercises help hypermobile EDS?

In one retrospective study, physical activity or exercise was among the treatments patients with hEDS and hypermobility spectrum disorders self-reported as helping their pain (Wilson, 2025). The video at the top of this page describes isometric holds, where muscles tighten without the joint moving, as one way to load a joint without taking it through a range that could feel risky. That's general education, so check with your own clinician first.

Can you have hEDS and POTS at the same time?

A 2026 systematic review found that EDS and POTS frequently co-occur, so having both is common (Kwok, 2026). Our team's part is testing the brain's regulation of heart rate, blood pressure and brain blood flow, and checking muscle tone along with it.

Sources

  1. Palmer S, Davey I, Oliver L, et al. The effectiveness of conservative interventions for the management of syndromic hypermobility: a systematic literature review. Clinical Rheumatology. 2021;40(3):1113-1129. doi:10.1007/s10067-020-05284-0
  2. Wilson FC, Bruno KA, Fairweather D, et al. Treatment Modalities, Pain Response, and Referrals for Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders: A Retrospective Study. Mayo Clinic Proceedings: Innovations, Quality & Outcomes. 2025;9(6):100672. doi:10.1016/j.mayocpiqo.2025.100672
  3. Dell’Aversana D, Provitera V, Trinchillo A, et al. Distinct sensory and autonomic involvement in hypermobile Ehlers-Danlos syndrome compared with idiopathic small fiber neuropathy: a multimodal study. Scientific Reports. 2026. doi:10.1038/s41598-026-60461-6
  4. Kwok CS, Hagger G, Gillespie D, et al. The co-existence of Ehlers-Danlos syndrome and postural orthostatic tachycardia syndrome: A systematic review of the literature. Autonomic Neuroscience. 2026;267:103453. doi:10.1016/j.autneu.2026.103453

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