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Launching Summer 2026

Answers in Days, not Decades.

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.

 
We believe you. We believe in you.
Board certified physicians, EDS ECHO trained
100% online, all 50 states
Founded, owned & operated by a hEDS patient
who we are

Our Focus is Diagnosis.

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.

 

One answer can change everything.

We understand because we've been there.

Learn more about us →
What We Do

Expert Evaluation for hEDS and HSD

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. 

Accurate

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.

Accessible

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.

Affordable

$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.

EDS Society Logo
How It Works

3 Steps to Answers

Once our platform launches in Summer 2026, you can get finally answers in as little as 3 days.

1

Tell Us Your Story

Complete your intake in about an hour, at your own pace, to help us understand your symptoms, medical history, and assess your hypermobility.

2

Physician Reviews Your Case

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.

3

Get Your Results & Care Plan

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.

What You Get

What's Included?

A diagnosis is just the beginning. We'll help set you up for success for everything that comes next.

Virtual hEDS / HSD Evaluation

A comprehensive clinical evalutation following the current official diagnostic criteria for hEDS and HSD.

Official Diagnosis Documentation

Clear determination of hEDS, HSD, or neither, with a full, point=by-point explanation for you and your care team.

Genetic Testing 

We screen for other EDS subtypes and connective tissue disorders, and recommend genetic testing as indicated.

Provider Letter

Documentation for your healthcare team with clinical findings, next steps, and ongoing care considerations.

Care Plan

Condition-specific recommendations for you and your care team with short and long-term goals.

 Resources

Educational information, research, partner resources, and treatment options to support your ongoing health journey.

Is This For You?

You're In The Right Place

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Have unexplained, multi-systemic symptoms that no one can connect?

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Been told you're "just flexible" or "there's no point in trying to get a diagnosis"?

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Need documentation for referrals, insurance, accommodations, or disability?

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Been waiting months or years to see a geneticist or other specialists?

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Suspect hEDS or HSD but don't know where to start?

 

If any of this sounds familiar, we can help.

What you're saying

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."

You've Waited Long Enough.

 

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.