WE’RE ON A MISSION TO DRASTICALLY REDUCE THE TIME TO
Receive your EDS diagnosis
You’ve waited long enough. It’s time to finally get the answers — and care — you deserve.
Currently licensed in: NH, MA, VT, ME, RI, FL and CA.
Currently licensed in: NH, MA, VT, ME, RI, FL and CA.
LET’S OFFICIALLY DIAGNOSE YOUR EDS SYMPTOMS
So you can start alleviating them ASAP
There’s a reason you haven’t been diagnosed with Ehlers–Danlos Syndrome yet. Many doctors don’t even know what it is, let alone how to determine if you have it. Some may be downright dismissive of your symptoms.
But if you’re here, you know something’s wrong — and you suspect EDS is the cause.
Chances are, you’re right.
If that’s the first time you’ve heard those words from a medical provider, welcome. You’re in the right place.
We’re here to help you get the quick, accurate, compassionate EDS diagnosis you deserve.
Why choose Connective Wellness for your EDS diagnosis?
SHORT TIMELINE
Receive your clinical EDS diagnosis in as little as 4-6 weeks from the time of booking (compared with the average time to diagnosis of 10–14 years!).
THOROUGH ASSESSMENT
Get the most comprehensive diagnosis possible, using your health history, traditional EDS diagnostic criteria, and our proprietary Prince–Cole Scale™.
TEAM APPROACH
Have your results reviewed by not just one provider, but a full team of specialists who truly care about helping you find (and address) the reason for your symptoms.
“I’ve been struggling for as long as I can remember…”
“I’m very new to even knowing this condition exists, but a few months ago, I connected the dots specifically and have been trying to get answers. Lo and behold, I found Connective Wellness. THERE IS HOPE. People are learning and want to help."
–Emily Holmes
What is the Prince–Cole Scale™?
the Prince–Cole Scale™ evaluates your full-body health to provide the most thorough, data-driven EDS diagnosis possible.
Until now, providers have used the basic Beighton Scale and 2017 Diagnostic Criteria to measure Hypermobile Ehlers-Danlos Syndrome (hEDS). While this scale is useful, it’s also incomplete. It doesn’t assess systemic involvement, comorbidities, or the severity of your symptoms beyond hypermobility. That means you could have debilitating hEDS symptoms, yet not get diagnosed for it simply because you score low on the Beighton Scale.
That’s why we developed the Prince–Cole Scale™.
Instead of looking only at hypermobility, the Prince–Cole Scale™ evaluates your full-body health to provide the most thorough, data-driven EDS diagnosis possible.
You’ll receive an objective score from 1–100 to determine your EDS likelihood and severity. The results will also flag whether your symptoms indicate if you should pursue genetic testing—a rare but important marker that most evaluations won’t catch.
The Prince–Cole Scale™ looks at ALL your symptoms to provide an accurate diagnosis…
⟣ Joint hypermobility
(beyond Beighton Score)
⟣ Neurological and autonomic symptoms
⟣ Autoimmune symptoms
⟣ Pain levels and chronic pain syndromes
⟣ Cardiovascular symptoms (including POTS)
⟣ Familial medical history
⟣ Gastrointestinal dysfunction
⟣ Mast cell activation disorder symptoms
⟣ Impact on daily life and disability severity
“Working with Christina has been the most fulfilling experience I have ever had in regard to my health.”
After years of seeking support for symptoms dismissed by my primary care provider, I sought out support through functional medicine. Christina truly took the time to hear me and honored my instincts.
–Sarah M.
What happens next?
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Call our clinic to book your diagnostics intake appointment. A $500 deposit is required to book your intake, and the remaining $1395 is due at the time of booking your diagnostic evaluation. HSA/FSA funds and CareCredit are accepted.
During this 30-minute virtual call with one of our Nurse Practitioners, you will learn more about the diagnostics process, share briefly about yourself, and ask any questions you may have.
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After your intake call, you will receive an email with instructions on submitting your pre-assessment questionnaires—our proprietary Prince-Cole Scale Diagnostic Tool™ (PCSDT) and Wellness Insight Index™ (WII)—prior labs, and medical records.
Need help during the process? We’ve allotted up to an hour of support by our Patient Advocate in this package.Once you’re finished, a Patient Coordinator will reach out to schedule your diagnostics evaluation within 2-4 weeks to give your care team enough time to go over your materials.
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Your materials will be personally reviewed by a team of specialists, who will hold a diagnostics meeting to provide you with an objective, multidisciplinary assessment.
You will then schedule a 90-minute meeting Integrative Diagnostic Evaluation (IDE) with one of our nurse practitioners to discuss our findings, clarify any questions, confirm your diagnosis, and discuss genetic testing, which we recommend for all patients.
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Once you’ve completed your diagnostics, we schedule for an hourlong meeting with our Chronic Illness Coach, Nicole, who will help you navigate your new diagnosis. She is available for ongoing support at an additional charge. Additionally, you’ll gain access to three free months inside our CW Collective membership for continued education and community.
Within 4 weeks of your final consultation, you will receive a detailed diagnostic letter, which serves as a medical summary you can share with other healthcare providers to guide your treatment going forward.
If you’d like ongoing care, we provide a full range of EDS services tailored to your specific needs. While many of our services are in-person at our Amherst, NH office, we offer many more through our virtual programming if your geography prevents you from visiting our clinic regularly. We’re here for you, from diagnosis to beyond!
investment
Diagnostic Pathway — $1895
FAQs about EDS diagnosis
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It depends on what you're looking for.
If you already have an hEDS or HSD diagnosis but feel lost, dismissed, or unsupported, our process can help by:
Validating your diagnosis with a deeper, more comprehensive assessment.
Identifying comorbidities that may have been overlooked (POTS, MCAS, GI dysfunction, etc.).
Providing a structured roadmap for treatment rather than just confirming a label.
For many patients, getting a diagnosis was only the first step. Our process is designed to help you move forward in care—not just stop at a diagnosis.
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If you don’t meet the diagnostic criteria, that doesn’t mean we stop helping you!
We will:
Thoroughly explain your results and why you may or may not fit the criteria.
Identify other possible explanations for your symptoms, such as:
Connective tissue disorders with a different genetic basis.
Neurological or autonomic dysfunction that needs targeted care.
Chronic pain conditions that need specialized treatment.
Provide next steps and referrals based on your specific concerns.
You won’t be left without answers—we will help you determine what to do next, even if your symptoms don’t fit hEDS/HSD.
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Yes! We offer virtual diagnostic evaluations for patients who can’t travel to our physical location. Currently licensed in New Hampshire, Florida, Maine, Massachusetts, Rhode Island, California and Vermont, with more states pending.
You can complete the entire intake and consultation remotely.
We may ask you to provide videos, images, or previous test results to assist in the assessment.
You’ll still receive the same in-depth report and recommendations as in-person patients.
If further in-person evaluations are required (such as physical therapy assessments), our patient advocates can help you find local providers or provide guidance on next steps.
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Because genetic research has significant emerging understanding of the complex nature of hEDS, in particular, as a condition that is not monogenic in nature, we highly recommend that everyone we see pursue genetic testing. Specifically, we recommend Ambry Genetics for their Patient for Life™ program. Your exome will be sequenced now, and will continue to be revisited as new data and research emerges for the duration of your life.
While you can elect not to pursue genetic testing, or to pursue testing through another laboratory, we strongly recommend completing this process as part of your full diagnostic picture. -
If you have been diagnosed with hEDS or another EDS subtype or connective tissue disorder (CTD), your child is at risk of inheriting it.
We can:
Evaluate your child’s symptoms to determine if early intervention is needed.
Provide preventative guidance to minimize complications.
Offer referrals for pediatric specialists if necessary.
Many children with hypermobility are dismissed until they have severe symptoms—we believe in early recognition and proactive care.
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Yes, but we guide you on exactly what specialists to see based on your specific symptoms and care needs.
Many patients diagnosed with hEDS or HSD are left without direction, but our process ensures you get:
A personalized care roadmap based on your symptom profile.
Recommendations for hypermobility-aware specialists (cardiology, neurology, gastroenterology, pain management, etc.).
In-house access to our hypermobility-specific physical therapy, functional nutrition, and autonomic support services.
Unlike other diagnostic experiences where patients are left to "figure it out," we make sure you know your next steps.
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Yes! If you need ongoing care near your home, we can:
Help you identify hypermobility-aware practitioners in your area.
Provide a comprehensive diagnostic report you can take to other doctors.
Offer virtual follow-ups when possible to help you navigate care remotely.
We understand that finding knowledgeable providers is difficult, and we don’t leave you to do it alone.
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If you’ve already been diagnosed with hEDS, HSD, or another connective tissue disorder, but you feel lost, we can help.
Our diagnostic process isn’t just about identifying the condition—it’s about:
Understanding how your symptoms interact (e.g., pain, GI issues, autonomic dysfunction).
Creating a structured care pathway so you know exactly where to start.
Identifying overlooked symptoms that may need specialized care.
Even if you already have a diagnosis, we help you turn that diagnosis into a plan of action.
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Absolutely! Many patients find it helpful to have a support person with them, especially if:
They need help remembering details.
They want someone to advocate for them.
They are overwhelmed with medical experiences.
We encourage bringing a trusted person to help you feel comfortable and supported.
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We are a hypermobility-friendly, disability-inclusive practice.
Let us know if you need:
Seating accommodations for pain management.
Low-stimulation environments (quiet rooms, dimmed lights).
Breaks during long discussions to manage fatigue.
Virtual options if in-person visits are too challenging.
We believe in making healthcare accessible and comfortable for all patients.
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Traditional specialists like rheumatologists and geneticists can diagnose EDS, but our process is far more comprehensive because we:
Look at the full-body impact of hEDS, not just hypermobility.
Evaluate all co-occurring conditions (POTS, MCAS, GI issues, pain syndromes).
Provide clear next steps instead of just confirming a diagnosis.
Many patients leave rheumatology or genetics offices with a diagnosis and no direction. We ensure you have both answers and a plan.
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While your underlying connective tissue disorder won’t change, symptoms can fluctuate with:
Aging
Hormonal shifts
Stress levels
Injury or illness
This is why ongoing support and symptom management are key. We help you adjust your care plan as your needs evolve.
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Yes! While hEDS and HSD are our primary focus, our diagnostic process can also flag:
Other types of EDS (vascular EDS, classical EDS, etc.)
Marfan syndrome
Loeys-Dietz syndrome
Stickler syndrome
Other hypermobility-related conditions
If we suspect a rarer disorder, we will refer you for genetic testing to confirm the diagnosis.
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We completely understand. Many of our patients have been gaslit or dismissed by doctors who don’t understand hEDS and its comorbidities. That’s exactly why Connective Wellness was created—by people who have been through this themselves.
Our team is hypermobility-literate and trauma-informed, meaning we:
Validate your lived experience.
Listen without judgment—we won’t dismiss your pain or symptoms.
Use data-driven tools like the Prince-Cole Scale™ to ensure your experience is quantified and recognized.
Approach care with collaboration, not skepticism.
Every person who walks through our doors deserves to be heard, believed, and given real answers—and that’s exactly what we do.
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You are not imagining your symptoms, and they are not “just anxiety.” Many of our patients have been told this before, and it is frustrating and harmful.
Our diagnostic process is different because:
We recognize that many hEDS symptoms overlap with autonomic dysfunction, nervous system dysregulation, and mast cell issues—which can present like anxiety but are physiological, not psychological.
We don’t brush off symptoms like fatigue, dizziness, pain, GI issues, or brain fog—we investigate them as real medical concerns.
We use objective measures, including clinical scoring tools and symptom mapping, to provide an evidence-based diagnosis.
You deserve to be taken seriously, and we treat every patient with respect and validation.
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This is one of the biggest myths in medicine! While some genetically confirmed EDS subtypes are rare, hEDS and HSD are NOT.
hEDS and HSD are far more common than previously believed—they’ve simply been underdiagnosed.
Many healthcare providers were never trained to recognize them, leading to years of misdiagnosis or dismissal.
You don’t have to “look” a certain way to have hEDS. We assess symptoms holistically and scientifically, not based on outdated assumptions.
If your symptoms fit, you deserve a thorough evaluation, no matter what you’ve been told in the past.
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Absolutely not. A diagnosis at Connective Wellness isn’t the end—it’s the beginning.
Unlike other providers who might say, “You have EDS, good luck,” we provide:
A clear diagnosis (if applicable)—based on a comprehensive evaluation.
A personalized care pathway—with real next steps for pain management, PT, nutrition, autonomic support, and more.
A roadmap to help you get the right care—instead of sending you in circles.
You won’t leave our office wondering what to do next. You’ll leave with real answers and an action plan.
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While some primary care doctors may diagnose hEDS, most aren’t trained to recognize it or evaluate all the necessary comorbidities.
At Connective Wellness, we go beyond a basic diagnosis and provide:
Multidisciplinary review by a nurse practitioner, functional nutritionist, and hypermobility-aware physical therapist.
Symptom mapping to determine what systems are most affected and what care should come next.
The Prince-Cole Scale™, which quantifies how hEDS/HSD impacts you for a clearer diagnostic picture.
A care pathway based on your individual symptoms—not a generic treatment plan.
Most PCPs do not have the time or expertise to do this level of assessment, which is why so many patients are misdiagnosed or ignored.
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Yes! The Beighton Score is outdated as a sole diagnostic tool, and we do not rely on it alone.
Many people with hEDS don’t meet the Beighton criteria but still have significant symptoms—which is why we use a much broader evaluation method.
Hypermobility decreases with age, meaning many adults don’t score as high as they would have in childhood.
We look at joint instability, pain, comorbidities, and functional impact—not just how far your joints bend.
If you don’t fit the Beighton Score but have other clear signs of hEDS or HSD, we will still take your case seriously.
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We completely understand—many of our patients have been let down before. That’s exactly why we built a diagnostic process that we would have wanted for ourselves.
At Connective Wellness, we:
Believe you. Your symptoms are real, and we will never dismiss them.
Are experts in hypermobility and complex care. This isn’t a side specialty—it’s our primary focus.
Offer more than just a diagnosis. We provide a clear path forward, so you don’t feel lost after your appointment.
Use cutting-edge tools (like the Prince-Cole Scale™) to ensure every detail is considered and validated.
We know how exhausting it is to fight to be heard. That’s why, at Connective Wellness, you don’t have to fight anymore.
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Once you receive your diagnosis, we provide:
A detailed diagnostic report to bring to other providers.
A personalized care roadmap showing what treatments to prioritize.
Access to specialized care including PT, pain management, nutrition, and more.
You won’t be left wondering what to do next. We help you navigate what comes after diagnosis so you can take action and start feeling better.
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A formal diagnosis can be a critical step in getting workplace, school, or disability accommodations, but every case is different.
We provide a comprehensive diagnostic report that outlines your condition and how it impacts daily functioning.
We can guide you on what documentation you may need for ADA accommodations, educational IEPs, or disability applications.
While we cannot guarantee approval for disability benefits, having a validated diagnosis strengthens your case significantly.
If accommodations are part of your goal, let us know—we can tailor our documentation to support your needs.
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At this time, we are an out-of-network provider, meaning insurance does not directly cover the diagnostic process.
However, you may be able to:
Submit a superbill for potential reimbursement from your insurance.
Use HSA or FSA funds to cover your appointment.
Apply for financing options through CareCredit
We are fully transparent about costs upfront and will work with you to ensure you get the care you need without surprises.
GET RESULTS IN AS LITTLE AS 4-6 WEEKS!
Ready to finally receive your EDS diagnosis?
Let’s put you on the path to healing. Reach out to book your diagnostic intake appointment, so we can start giving you the personal, attentive care you’ve been missing.