Launching Summer 2026

Answers in Days, Not Decades.

EDS Connective is a virtual health platform that facilitates access to specialized evaluation for the diagnosis of hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD).

Get Early Access

We believe you. We believe in you.

✦ Expert physicians, EDS ECHO trained

✦ 100% online, available across the US

✦ Founded 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 these complex, multi-systemic conditions often spend years or decades navigating dozens of symptoms before receiving a hEDS or HSD diagnosis.

We understand how much diagnosis matters, because our founder experienced the same journey herself.

Answers 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 timely, comprehensive diagnostic evaluation by a qualified physician. 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.

Our platform connects you with independent doctors who are are expertly trained to provide a telehealth clinical evaluation for Hypermobile Ehlers Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD), which may include a referral for genetic testing for other subtypes of Ehlers-Danlos Syndrome and Connective Tissue Disorders where indicated.

Expert

Your case is evaluated for diagnosis by a licensed MD or DO, trained by the Ehlers-Danlos Society, and following the official diagnostic criteria.

Accessible

100% online and available in all 50 US states. No referrals or pre-authorizations needed. Asynchronous evaluation at your own pace - no appointments, no travel, no waiting rooms.

Affordable

$399 for a comprehensive diagnostic evaluation. May be eligible for HSA or FSA reimbursement. Flexible payments and financial assistance may be available.

Your support makes a difference. We're zebra-owned, woman-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 research and advocacy. Additionally, 5% of every EDS Connective purchase funds financial assistance for our users in need.

Learn more about how we give back →

How It Works

3 Steps to Answers

Once our platform launches in Summer 2026, you can get answers in as little as 3-5 days.

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.

Physician Reviews Your Case

Your provider evaluates your individual case, communicating with you asynchronously via chat and/or video.

Get Your Results & Documentation

In as little as 3-5 days following your intake submission, you will receive your diagnostic evaluation results, including detailed documentation for your care team and a referral for genetic testing if indicated.

Learn more about how it works →

What You Get

What's Included?

Your evaluation includes the information and resources you and your care team need to move forward.

Telehealth hEDS / HSD Evaluation

A comprehensive online 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 Referral

Your provider will screen for other EDS subtypes and connective tissue disorders, and refer for medical-grade genetic testing as indicated.

Provider Letter

Information for your primary care team to help them understand our process, your diagnostic results, and how to approach ongoing care.

Letter of Medical Necessity

This document may be required if submitting for HSA/FSA reimbursement or other purposes.

Resources

Education, research, community, and partner content to support your journey- including our new ebook guide.

Is This For You?

You're In The Right Place

Have chronic, unexplained, multi-systemic symptoms?

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, you may be in the right place.