Hypermobile Ehlers Danlos (hEDS) Evaluations
Evidence-based evaluations for hypermobility and connective tissue concerns'
Whether you’re exploring hypermobile Ehlers-Danlos syndrome (hEDS) or another connective tissue disorder, genetic counseling and testing can help clarify possible causes and guide next steps for care and management.
Services Include:
hEDS Evaluation – Clinical assessment using established diagnostic criteria
Connective Tissue Disorder Assessment – Review for other forms of EDS and related syndromes
Comprehensive History Review – Detailed personal and family history to identify inheritance patterns
Genetic Testing Coordination – Discussion and ordering of testing when indicated
Referrals & Resources – Guidance for follow-up care, management, and supportive services
What You Can Expect
Review of your medical, developmental, and family history
Clinical assessment for hypermobility and connective tissue features
Discussion and ordering of genetic testing when appropriate
Personalized summary with findings, recommendations, and next steps
How Testing Works
I’ll order the appropriate test through a CLIA-certified lab
A test kit is mailed to your home with all materials included
You’ll provide a saliva sample and return it to the lab using the prepaid mailer
We’ll review your results together by telehealth, typically within 4–6 weeks
Pricing & Billing
Session Fees
All sessions are conducted via secure telehealth.
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A 75-90 minute session with a detailed review of your history, clinical assessment, discussion of possible diagnoses, and genetic testing options when appropriate.
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A shorter session to go over genetic test results, update your care plan, or revisit specific concerns.
Access & Affordability
If cost is a concern, don’t hesitate to reach out. I believe financial barriers should never prevent someone from accessing supportive genetic counseling services.
FAQs
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I offer a thorough clinical assessment and can evaluate whether your symptoms meet the current diagnostic criteria for hEDS or a related condition. When appropriate, I also coordinate genetic testing to explore other connective tissue or hereditary conditions. While I do not issue formal diagnoses, I can help you understand where you fall within the diagnostic framework and provide referral recommendations if further evaluation is needed.
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The key difference is that most other types of connective tissue disorders, like classic EDS or vascular EDS, have a known genetic cause that can be identified through testing. hEDS does not yet have a specific genetic marker, which means it is currently diagnosed based on clinical criteria after other conditions have been ruled out.
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I currently work with adults only for hEDS evaluations. Children and teens should begin with their pediatrician, who can refer them to the appropriate specialists for evaluation and care.
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No referral is required. You can book an evaluation directly. If a provider or therapist has recommended an hEDS assessment, you’re welcome to include any notes or background when you reach out.
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Genetic testing is billed separately by the laboratory. Genetic testing panels typically start at $500 for out-of-pocket costs, though the final price can vary depending on the type of test and your insurance coverage. Many labs also offer financial assistance programs to help reduce costs if insurance does not cover testing.
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Unfortunately, I am unable to bill insurance directly. I can provide a superbill with the necessary codes upon request.
Curious if hEDS or another connective tissue disorder could explain your symptoms?
Let’s start your evaluation together.