Stop Chronic Pain Now: Is Ehlers-Danlos the Cause? Next Steps | Ubie Doctor's Note

Published on: 4/13/2026

Always Hurting? Why Ehlers-Danlos Syndrome Is the Cause & Medically Approved Next Steps

Reviewed by Yoshinori Abe, MD

Internal Medicine

Persistent, widespread pain may indicate Ehlers-Danlos syndrome (EDS), a genetic connective tissue disorder that weakens collagen. Common EDS symptoms include joint hypermobility, frequent sprains, chronic pain, stretchy or fragile skin, fatigue, migraines, and POTS. Most EDS types are not life-threatening, but rare vascular EDS carries serious risks—seek urgent care for sudden severe chest or abdominal pain, unexplained bleeding, or repeated fainting.

Medically recommended next steps for suspected Ehlers-Danlos syndrome include:

Tracking your symptoms and pain patterns

Taking a symptom check to clarify possible causes

Getting evaluated by primary care, rheumatology, or genetics

Starting targeted physical therapy with joint protection

Using cautious pain management strategies

Treating related conditions like POTS or migraines

Because EDS overlaps with many other conditions, identifying the right path forward can feel overwhelming. A free, instant, online symptom check can help you understand what your symptoms may mean and guide your next steps—before your appointment, and without any cost or signup.

Reviewed for medical accuracy: 07/03/2026

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Explanation

Always Hurting? Why Ehlers-Danlos Syndrome May Be the Cause — and Medically Approved Next Steps

If you feel like you're always hurting — sore joints, frequent sprains, unexplained aches, constant fatigue — you may have been told it's "just stress" or that you're "overdoing it." But for some people, ongoing pain has a medical explanation.

One possible cause is Ehlers-Danlos syndrome (EDS), a group of inherited connective tissue disorders that can affect joints, skin, blood vessels, and other organs. While Ehlers-Danlos syndrome is not extremely common, it is often underdiagnosed — especially in people who appear otherwise healthy.

Here's what you need to know, based on established medical evidence and clinical guidelines.

What Is Ehlers-Danlos Syndrome?

Ehlers-Danlos syndrome (EDS) is a genetic condition that affects collagen — the protein that gives structure and strength to your:

Joints

Skin

Blood vessels

Ligaments

Internal organs

When collagen doesn't work properly, connective tissues become weaker and more flexible than normal.

There are 13 recognized types of Ehlers-Danlos syndrome. The most common is hypermobile Ehlers-Danlos syndrome (hEDS).

Why Does Ehlers-Danlos Syndrome Cause Chronic Pain?

Pain in Ehlers-Danlos syndrome happens for several reasons:

1. Joint Instability

Loose ligaments allow joints to move beyond their normal range. This is called hypermobility. Over time, unstable joints can cause:

Frequent sprains

Dislocations or partial dislocations

Muscle strain

Early joint wear

2. Muscle Overwork

When ligaments don't stabilize joints properly, muscles must work harder to compensate. This can lead to:

Chronic muscle tension

Fatigue

Trigger points

3. Nerve Irritation

Loose tissues may irritate nearby nerves, contributing to:

Burning or shooting pain

Tingling sensations

Increased sensitivity to pain

4. Secondary Conditions

People with Ehlers-Danlos syndrome are more likely to experience:

Migraines

Temporomandibular joint (TMJ) pain

Pelvic pain

Digestive issues

Autonomic dysfunction (such as POTS)

Pain may begin in childhood or adolescence but can worsen in adulthood if not managed properly.

Common Symptoms of Ehlers-Danlos Syndrome

Symptoms vary depending on the type, but common features include:

Joint-Related Symptoms

Very flexible or "double-jointed"

Frequent sprains or joint injuries

Joints that pop, click, or give way

Chronic joint or muscle pain

Skin Symptoms

Soft, velvety skin

Skin that stretches more than usual

Easy bruising

Slow wound healing

Wide or thin scars

Other Possible Signs

Chronic fatigue

Dizziness upon standing

Digestive issues (bloating, constipation, reflux)

Pelvic floor dysfunction

Family history of similar symptoms

Not everyone with hypermobility has Ehlers-Danlos syndrome. Many people are flexible without having a connective tissue disorder. Diagnosis depends on a detailed medical evaluation.

How Is Ehlers-Danlos Syndrome Diagnosed?

Diagnosis depends on the type of Ehlers-Danlos syndrome.

For most types, genetic testing can confirm the diagnosis. However, for hypermobile Ehlers-Danlos syndrome (hEDS), there is currently no known genetic marker. Doctors diagnose hEDS using:

A physical exam

A Beighton score (measures joint flexibility)

A detailed medical history

Family history

Exclusion of other connective tissue disorders

Because symptoms overlap with other conditions (like fibromyalgia or autoimmune disorders), evaluation by a knowledgeable healthcare professional is important.

Is Ehlers-Danlos Syndrome Dangerous?

For many people, especially those with hypermobile Ehlers-Danlos syndrome, the condition is not life-threatening, but it can significantly affect quality of life.

However, some rare types — such as vascular Ehlers-Danlos syndrome — can involve fragile blood vessels and organs and may carry serious risks. This is why an accurate diagnosis matters.

If you experience symptoms like:

Sudden severe chest, abdominal, or back pain

Unexplained internal bleeding

Frequent unexplained fainting

Seek immediate medical attention.

Medically Approved Next Steps If You Suspect Ehlers-Danlos Syndrome

If you are always hurting and suspect Ehlers-Danlos syndrome, here are practical, medically supported steps:

1. Start With a Medical Evaluation

Speak with:

A primary care doctor

A rheumatologist

A geneticist (if recommended)

Bring:

A symptom timeline

Family history information

Details about frequent injuries

2. Consider a Symptom Check

If you're experiencing persistent pain and want to better understand what might be causing your symptoms before your appointment, take a free symptom checker assessment to help organize what you're feeling and prepare meaningful questions for your doctor.

This does not replace medical care but can help you communicate more effectively about your pain patterns.

3. Begin Physical Therapy

Physical therapy is one of the most important treatments for Ehlers-Danlos syndrome.

A knowledgeable physical therapist can help you:

Strengthen stabilizing muscles

Improve joint control

Reduce injury risk

Build endurance safely

High-impact or aggressive stretching programs are usually not recommended.

4. Learn Joint Protection Strategies

These may include:

Avoiding locking joints

Using supportive braces when appropriate

Modifying exercise routines

Prioritizing low-impact activities like swimming or cycling

5. Pain Management

Pain treatment may include:

Physical therapy

Topical medications

Limited use of oral medications

Cognitive behavioral therapy for pain coping

Treatment of related conditions (like migraines or GI disorders)

Long-term opioid use is generally not recommended for chronic connective tissue pain due to limited benefit and risk.

6. Address Associated Conditions

If present, conditions like:

Postural Orthostatic Tachycardia Syndrome (POTS)

Mast cell activation symptoms

should be evaluated and treated individually.

Mental Health Matters

Chronic pain can affect mood, sleep, and daily functioning. Anxiety and depression are more common in people with persistent pain — not because symptoms are "in your head," but because living with pain is exhausting.

Evidence-based treatments such as:

Cognitive behavioral therapy (CBT)

Pain coping skills training

Sleep optimization

can improve overall quality of life.

What Ehlers-Danlos Syndrome Is Not

It's important to clarify:

It is not caused by lack of exercise.

It is not laziness.

It is not "just anxiety."

It is not something you caused.

It is a genetic connective tissue condition.

However, not all chronic pain is Ehlers-Danlos syndrome. Many other treatable causes exist, which is why professional evaluation is essential.

Living Well With Ehlers-Danlos Syndrome

There is currently no cure for Ehlers-Danlos syndrome, but many people live active, fulfilling lives with proper management.

Long-term success usually includes:

Ongoing muscle strengthening

Injury prevention

Realistic activity pacing

Coordinated medical care

Self-education

The earlier it is identified, the better the long-term joint protection.

When to Speak to a Doctor Urgently

If you have Ehlers-Danlos syndrome — or suspect it — seek immediate medical care if you experience:

Sudden severe chest or abdominal pain

Signs of stroke

Severe unexplained bleeding

Repeated fainting

A joint that will not relocate

These may signal serious complications that require urgent attention.

The Bottom Line

If you're always hurting and can't explain why, Ehlers-Danlos syndrome may be one possibility — especially if you're unusually flexible or have frequent joint injuries.

While not always dangerous, Ehlers-Danlos syndrome is real, medically recognized, and manageable with the right care plan.

Start by:

Tracking your symptoms

Using a free AI symptom checker to help identify patterns and potential causes of your discomfort

Scheduling a medical evaluation

Most importantly, speak to a doctor about persistent pain or any symptoms that could be serious or life-threatening. Getting answers may not happen overnight, but informed, structured care can significantly improve your quality of life.

You deserve to understand why you hurt — and to take clear, medically supported next steps forward.

(References)

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* Malfait F, Francomano R, Byers P, Belmont J, Berglund B, Bober M, Broadgate S, Castori F, Cohen H, Dormer J, East K, Elliott A, Fikowski J, Grahame R, Hakim A, Hamonet C, Henderson H, Houweling P, Juul-Kristensen B, Kono M, Lepper J, Levine B, Mendoza-Londono R, Miller L, Mortier G, Mulliken J, Narayanan R, Nishimura G, Opitz J, Peters G, Pope M, Pyeritz R, Ramirez H, Richer L, Rivard L, Roman C, Rutman C, Savarirayan R, Sillence D, Spranger J, Steinman B, Symoens S, Tsipouras P, Van Damme T, Van Mechelen M, Vroman R, Wechsler H, Weksberg R, Wilson R, Wordsworth P, Zabel B. The 2017 international classification of the Ehlers-Danlos syndromes. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. PMID: 28387229.

* Ali A, Farooq M, Arfeen S, Nayeem Z, Amlani B, Khan M, Hussain R, Khowaja M, Arfeen N. Management of Ehlers-Danlos Syndrome: A Comprehensive Review. Cureus. 2023 Dec 13;15(12):e49909. doi: 10.7759/cureus.49909. PMID: 38222047; PMCID: PMC10786961.

* Gillam E, Agaliotis M, Tynan M, Johnson S, Malcarne C, Hilder L, Spruell S, Al-Dahhan T, Naffah-Mazzacoratti MG, Sankar S, Ali N. Hypermobile Ehlers-Danlos Syndrome (hEDS): A Comprehensive Review of Clinical Presentation, Diagnosis, and Management. Curr Rheumatol Rep. 2023 Jul;25(7):221-236. doi: 10.1007/s11926-023-01103-y. Epub 2023 Jun 2. PMID: 37266946.

* Zoli A, Busa V, Spadaro A, Sanna D, Valerio N, Sgarlata M, Alaimo S, Calabrese V, Vitale S, Caccamo M, Iannuzzi R, Sposato G, Iacono A. Therapeutic Approaches for Ehlers-Danlos Syndromes: From Symptomatic Treatment to Targeted Therapies. Biomedicines. 2023 Oct 30;11(11):2898. doi: 10.3390/biomedicines11112898. PMID: 37946890; PMCID: PMC10669145.

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