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, ECHO-trained, 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 report 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.
Comprehensive Diagnostic Evaluation
Symptom review, family history, and hypermobility assessment — thorough enough to get it right.
Official Clinical Documentation
Clear determination of hEDS, HSD, or neither — with full explanation you can share with your care team.
Provider Letter
Documentation for your healthcare team with clinical findings and care recommendations — ready to share at your next appointment.
Genetic Testing Referral
Your provider will screen for other EDS subtypes and connective tissue disorders, and refer for medical-grade genetic testing as indicated.
Letter of Medical Necessity
May be used to submit cost of your evaluation for HSA/FSA reimbursement or work and school accomodations.
Educational Resources
Condition-specific materials, resources, and self-management information to help you understand and navigate your 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
20% of revenue is donated to the Ehlers-Danlos Society. 5% of every evaluation funds our internal financial assistance program.
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.
We value and respect the role of primary care. Most providers want to help — but the diagnosis of hEDS and HSD require a level of specialized evaluation that a standard appointment simply isn't built for. That's not your fault.
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.
100% online. Independent, board-certified, EDS ECHO-trained providers. No referral needed. All 50 states and Washington D.C. Launching summer 2026.
