Our virtual health platform provides accurate, accessible, and affordable online evaluation for the diagnosis of Hypermobile Ehlers Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD) so you can finally get the clarity you need to move forward.
If you're here, we know you've probably already been through a lot.
People with hEDS and HSD typically spend years - decades - navigating complex multi-systemic symptoms, seeing specialist after specialist while no one connects the dots.
EDS Connective was created by someone who lived this journey and knows how life-changing the right diagnosis can be.
We work with the world's leading experts in the Ehlers Danlos Syndromes and hypermobility to help you reach that turning point sooner.
Timely diagnosis provides validation, protection from harm, and healthcare empowerment.
You deserve a thorough, detail-oriented diagnostic evaluation — the kind most primary care providers don't have the time or training to complete. That's exactly what we're built for.
We don't replace your care team - we equip you and your providers with answers and clear path forward.
We provide a comprehensive virtual clinical evaluation for Hypermobile Ehlers Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD), which may include a recommendation for genetic testing for other subtypes of Ehlers Danlos Syndromes and Connective Tissue Disorders where indicated.
Your case is evaluated for diagnosis by a board-certified MD or DO, trained by the Ehlers-Danlos Society in their ECHO program, and following the official hEDS diagnostic criteria.
100% online and licensed in all 50 US states. No referrals or pre-authorizations needed. Asynchronous evaluation at your own pace - no appointments, no travel, no waiting rooms, no doctor's office anxiety.
$399 for a comprehensive diagnostic evaluation. HSA-eligible with flexible payment plans and financial assistance available.
Your support makes a difference. We're zebra-owned and we give back to the EDS/HSD community. As the exclusive Diamond Sponsor of the Ehlers-Danlos Society, 20% of our revenue is donated to support their critical EDS research and advocacy. Additionally, 5% of every EDS Connective purchase funds financial assistance for patients who need it most.

Once our platform launches in Summer 2026, you can get finally answers in as little as 3 days.
Complete your intake in about an hour, at your own pace, to help us understand your symptoms, medical history, and assess your hypermobility.
An ECHO-trained, board-certified MD or DO digs into your full history and follows up with you directly.
A detailed clinical report explains your diagnosis results, genetic testing recommendation, and personalized care plan for you and your primary care team. Finally, answers you can act on.
Complete your intake in about an hour, at your own pace, to help us understand your symptoms, medical history, and assess your hypermobility.
Your board-certified MD or DO, expertly trained by the Ehlers Danlos Society ECHO program, evaluates your individual case, communicating with you asynchronously via chat and/or video.
A detailed clinical report explains your diagnosis results, genetic testing recommendation, and personalized care plan for you and your primary care team. Finally, answers you can act on.
A diagnosis is just the beginning. We'll help set you up for success for everything that comes next.
A comprehensive clinical evalutation following the current official diagnostic criteria for hEDS and HSD.
Clear determination of hEDS, HSD, or neither, with a full, point=by-point explanation for you and your care team.
We screen for other EDS subtypes and connective tissue disorders, and recommend genetic testing as indicated.
Documentation for your healthcare team with clinical findings, next steps, and ongoing care considerations.
Condition-specific recommendations for you and your care team with short and long-term goals.
Educational information, research, partner resources, and treatment options to support your ongoing health journey.
Have unexplained, multi-systemic symptoms that no one can connect?
Been told you're "just flexible" or "there's no point in trying to get a diagnosis"?
Need documentation for referrals, insurance, accommodations, or disability?
Been waiting months or years to see a geneticist or other specialists?
Suspect hEDS or HSD but don't know where to start?
If any of this sounds familiar, we can help.
You deserve answers. Let's get started.
Our new virtual health platform for hEDS and HSD diagnosis is launching in summer of 2026. Sign up to get early access.
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You're in. We'll reach out as we get closer to summer 2026.
In the meantime, check out the Ehlers-Danlos Society's website and their Provider Directory.
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8,000+ people are ready. Are you?
A diagnosis means finally being seen, heard, and taken seriously."
It changed my life to finally be diagnosed and on a treatment plan. I'm so excited for others to feel the same relief and to watch their quality of life flourish."
My whole life makes sense now."