Three steps to a thorough, expert evaluation for hEDS and HSD diagnosis.
Complete your intake at your own pace — symptoms, history, and hypermobility assessment. Takes approximately 1 hour. No appointment needed, no waiting room, no travel required. Start and stop whenever you need to.
An independent board-certified MD or DO reviews your full intake and follows up with you directly — asynchronously, on your schedule. They dig into your history, ask clarifying questions, and apply the official diagnostic criteria. No rushing, no time limits.
A detailed Clinical Summary and Provider Letter for you and your primary care team. Genetic testing referral (where indicated). Clear documentation for specialists, employers, and insurance.
Everything is included in your $399 evaluation — no hidden fees, no surprises.
Telehealth hEDS/HSD Evaluation
A comprehensive online clinical evaluation following the current official diagnostic criteria for hEDS and HSD.
Official Diagnosis Documentation
Clear determination of hEDS, HSD, or neither — with a full explanation you can share with 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.
Clinical Summary
A thorough report covering your assessment, diagnostic criteria, and findings — useful for your care team, insurance, HSA/FSA reimbursement, or accommodation requests.
Educational Resources
Education, research, community, and partner content to support your journey, including our new ebook guide to life after diagnosis.
One clear price. No insurance mazes, no prior authorizations, no surprise bills.
Diagnostic Evaluation
$399
one-time, self-pay
May be HSA & FSA Eligible
You may be able to submit for reimbursement from your Health Savings Account or Flexible Spending Account.
Financial Assistance
A limited amount of financial asssistance is available for those who need it. Learn more →
You Help Us Give Back
Approximately 20% of revenue is donated to the Ehlers-Danlos Society. 5% of every evaluation funds our financial assistance program. Learn more →
EDS Connective is built for people who've been searching for answers.
You have hypermobility plus unexplained, multi-systemic symptoms that no one can connect.
You've been told you're "just flexible" or "too young to be in this much pain."
You need documentation for specialists, workplace accommodations, or disability.
You've been waiting months or years to see a geneticist.
You suspect hEDS or HSD but don't know where to start.
You've been told there's no point in a diagnosis when there's no cure — and you disagree.
Available in all 50 states and Washington D.C. No referral needed.
EDS Connective is fully online and available across the United States. Your primary care provider does not need to refer you — you can get started on your own, whenever you're ready.
Your primary care team knows your history, and they're best positioned to manage your ongoing care. We help give them the clarity they need to support you with confidence.
What We Are
What We're Not
Our goal is collaboration.
Once your diagnosis is established, you continue your long-term relationship with your primary care provider — equipped with clear documentation and a stronger foundation for ongoing care.
The Early Access Program is live now. Join the waitlist in order to claim your spot. Once you receive your invitation to get started, you can get results in as little as 3-5 days.
