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  • Ehlers-Danlos Syndrome (EDS) Treatment

Ehlers-Danlos Syndrome (EDS) Treatment and Osteopathic Support in Surrey

Ehlers-Danlos Syndrome (EDS) is a group of inherited connective tissue disorders that affect the way collagen is produced and functions in the body. Collagen is the most abundant structural protein, responsible for providing strength and elasticity to skin, ligaments, tendons, joints, blood vessels, and internal organs. When collagen is altered, tissues become more fragile and hyper-flexible, which explains why patients often present with joint hypermobility, musculoskeletal pain, recurrent dislocations, chronic fatigue, fragile skin, easy bruising, and even cardiovascular or gastrointestinal complications.

Although considered a rare genetic disorder, EDS is increasingly recognised as part of a spectrum that includes hypermobility spectrum disorder (HSD). Many people with severe hypermobility symptoms may not meet the strict diagnostic criteria for EDS but still experience significant instability, pain, and secondary health issues that require ongoing management.

At Key Osteopaths in Surrey, our focus is not on “curing” EDS, since it is a hereditary condition, but on helping patients manage symptoms, protect joints, improve functional stability, and reduce day-to-day pain. Osteopathic support is often integrated alongside care from GPs, rheumatologists, physiotherapists, and clinical geneticists, making treatment genuinely multi-disciplinary. Our approach combines gentle manual therapy, postural education, rehabilitation strategies, and lifestyle guidance to give patients tools that make a real difference in quality of life.
For people in Surrey living with EDS or related hypermobility conditions, the right support can improve both physical resilience and psychological confidence. Early assessment and tailored management are key to reducing injury risk and helping patients maintain an active, independent lifestyle.
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What Is Ehlers-Danlos Syndrome (EDS)?

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Ehlers-Danlos Syndrome refers to a collection of thirteen recognised subtypes of connective tissue disorders, classified internationally in 2017. These subtypes vary from the relatively common hypermobile EDS (hEDS) to rarer but more serious types such as vascular EDS. What unites them is a defect in collagen formation, structure, or processing, which leaves tissues unusually stretchy, weak, or fragile.

The condition is most often inherited in an autosomal dominant or recessive pattern, and genetic testing may confirm the diagnosis in some subtypes. In hypermobile EDS, where no single causative gene has yet been identified, diagnosis is based on clinical assessment, Beighton scoring for joint hypermobility, and detailed medical history
Because collagen is present throughout the body, EDS can have widespread systemic effects. Patients may experience:
  • Joint instability, frequent sprains, and early-onset osteoarthritis
  • Chronic pain and muscle fatigue from constant overuse of unstable joints
  • Skin that is fragile, hyper-extensible, or prone to poor wound healing
  • Autonomic dysfunction such as postural tachycardia syndrome (PoTS)
  • Digestive problems including reflux, irritable bowel-type symptoms, and poor motility
  • Cardiovascular concerns such as mitral valve prolapse or arterial fragility
EDS is not a single-presentation disorder. One patient may primarily struggle with shoulder dislocations and sports injuries, while another may face long-term fatigue, migraines, and gastrointestinal distress. This variability makes personalised care strategies essential, since what works for one patient may not be suitable for another.
For residents of Surrey and the surrounding areas, professional assessment of suspected EDS provides not just diagnosis but also a pathway into evidence-based management, whether through osteopathic care, physiotherapy, pain management, or referral to genetics and rheumatology.

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Understanding Connective Tissue Disorders and Hypermobility Spectrum

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Ehlers-Danlos Syndrome sits within the wider group of heritable connective tissue disorders, conditions that affect proteins such as collagen, elastin, and fibrillin. When these proteins are altered, tissues lose the normal balance of strength and elasticity, which explains the hallmark features of joint hypermobility, skin fragility, poor wound healing, and musculoskeletal pain.

Not every patient with symptomatic hypermobility will meet the diagnostic criteria for EDS. This is where the concept of Hypermobility Spectrum Disorder (HSD) is important. HSD describes patients with chronic musculoskeletal pain, instability, and fatigue caused by joint hypermobility, but without enough diagnostic markers to be formally classified as EDS. Clinically, however, the management of HSD often mirrors EDS: rehabilitation strategies, postural training, proprioceptive re-education, and long-term musculoskeletal support.

Recognising this overlap ensures that patients are not dismissed simply because they do not fit the exact genetic or clinical definition of EDS. Whether a diagnosis is EDS or HSD, the functional impact can be very real, and effective care should always be centred on the individual’s needs rather than the label alone.

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Different Types of Ehlers-Danlos Syndrome Recognised in Clinical Practice

Ehlers-Danlos Syndrome is not one single condition but a group of related disorders. Doctors currently recognise thirteen different subtypes, though some are very rare. The important point for patients to understand is that all types share the same underlying problem: fragile connective tissue caused by changes in collagen. What differs is which body systems are most affected.
Hypermobile EDS (hEDS)

This is the most common type. People with hEDS usually have very flexible joints that can move beyond the normal range. While this might sound like an advantage, it often leads to repeated sprains, dislocations, chronic pain, and muscle fatigue. It is also closely linked with hypermobility spectrum disorder (HSD), so many patients experience very similar symptoms even without a confirmed EDS diagnosis.

Classical EDS

In addition to joint hypermobility, people with this type tend to have soft, stretchy skin that bruises easily and may scar in a distinctive way.

Vascular EDS

This is one of the rarer but more serious types. It affects the blood vessels and internal organs, making them more fragile. Because of this, it requires careful medical supervision and sometimes urgent intervention.

Other rarer subtypes

There are several other forms of EDS that mostly appear in childhood and are much less common. They may involve severe muscle weakness, fragile eyes, scoliosis, or early dental problems. While important for specialists to recognise, they account for only a small proportion of EDS diagnoses.

For most people seeking help in clinics, the hypermobile type is the main one encountered. Knowing which subtype you have is important, but the day-to-day challenges such as joint instability, pain, fatigue, and the emotional impact of living with a chronic condition are often shared across the spectrum.
This is why management always focuses on supporting mobility, protecting joints, strengthening muscles, and improving confidence in movement, regardless of the specific subtype.

How EDS Affects Joints, Skin, Blood Vessels, and Overall Health

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Ehlers-Danlos Syndrome can affect many different parts of the body, not just the joints. Because collagen is present in almost every tissue, the condition can create challenges that go far beyond flexibility. Understanding how EDS affects the body helps patients and families make sense of the wide range of symptoms they may experience.
Joints and Muscles

The most obvious effects are in the joints. People with EDS often have hypermobile joints that move more than normal. This can lead to repeated sprains, partial dislocations (subluxations), or full dislocations. Over time, the extra movement puts strain on muscles, tendons, and ligaments, creating chronic pain and fatigue. Muscle weakness is common, not because the muscles are inherently defective, but because they are constantly working overtime to stabilise loose joints.

Skin and Soft Tissues

In some forms of EDS, the skin is unusually soft, velvety, or stretchy. It may bruise more easily, and wounds can take longer to heal. Scars may look wider or thinner than normal. Even when skin symptoms are mild, fragile connective tissue can contribute to hernias, gum problems, or pelvic floor weakness.

Blood Vessels and Internal Organs

In vascular EDS, one of the rarer types, blood vessels and hollow organs such as the bowel or uterus can be more fragile. This carries more serious health risks and requires ongoing medical supervision. Even outside vascular EDS, many patients experience circulation-related issues, such as dizziness on standing (known as postural tachycardia syndrome or PoTS).

Whole-Body Effects

Because collagen is found everywhere, EDS can also influence digestion, bladder control, cardiovascular function, and even the nervous system. This explains why many patients live with a wide collection of symptoms, from reflux and constipation to palpitations, headaches, and sleep disturbance.

Although the list of possible symptoms can seem overwhelming, no two patients are alike. One person might struggle most with joint instability, while another has few joint problems but significant digestive or cardiovascular issues. This is why a personalised management plan is essential, one that considers the whole person, not just the musculoskeletal system.
If you or a loved one are living with Ehlers-Danlos Syndrome or hypermobility spectrum disorder, contact Key Osteopaths in Surrey today to schedule a consultation and explore how tailored osteopathic care can support your long-term health.
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Common Symptoms and Challenges Faced by EDS Patients

Living with Ehlers-Danlos Syndrome is rarely about one single symptom. Because collagen is present throughout the body, patients often experience a wide variety of problems that affect movement, energy levels, and overall wellbeing. The symptoms can change over time, and two people with the same diagnosis may present in completely different ways. Recognising these shared patterns helps patients, families, and clinicians understand what is happening and why support is needed.

I have seen Anna twice with a slipped disc in my lower back. On both occasions she has turned me from Yoda (hunched over a walking stick) to an… read more

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Super helpfull, friendly and informative. Cant recommend highly enough.

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Chronic Joint Pain, Instability, and Frequent Dislocations

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For many people with EDS, the most noticeable challenge is joint instability. Joints may move too far or in directions they were never designed to, leading to repeated sprains or even full dislocations. Sometimes joints only partially slip out of place, known as subluxations, which can still cause severe pain and swelling.
Because the muscles are forced to work constantly to stabilise the joints, fatigue and muscle ache are common. This explains why some patients describe feeling as though their body is “working twice as hard” just to do everyday tasks. Over time, the extra strain can also contribute to early osteoarthritis and chronic musculoskeletal pain.
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Fatigue, Muscle Weakness, and Reduced Exercise Tolerance

Beyond the joints, fatigue is one of the most disabling symptoms of EDS. Even without major dislocations, many patients feel drained after short periods of activity. The reasons are often complex: weak connective tissues make muscles work harder, poor circulation can reduce oxygen supply, and pain itself takes a toll on energy.

This leads to reduced exercise tolerance. Activities like walking long distances, climbing stairs, or standing for extended periods can feel exhausting. Some patients also experience postural tachycardia syndrome (PoTS), a condition where the heart races upon standing, worsening tiredness and dizziness.
Practical strategies such as pacing, energy conservation, and structured rehabilitation can make a big difference in managing these symptoms day to day.

Gastrointestinal, Cardiovascular, and Neurological Symptoms Linked to EDS

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EDS is much more than a musculoskeletal condition. Because connective tissue is everywhere, patients often live with complex multi-system problems.

Gastrointestinal

Reflux, constipation, abdominal pain, irritable bowel-type symptoms, or poor gut motility.

Cardiovascular

Palpitations, mitral valve prolapse, and in rarer cases arterial fragility in vascular EDS.

Neurological

Migraines, dizziness, sensory sensitivities, and in some cases problems with coordination or balance.

The combination of pain, fatigue, and systemic issues can have a significant impact on work, education, social life, and mental health. Many patients feel misunderstood because their condition is not outwardly visible, yet the challenges are daily and very real.
Support therefore needs to go beyond symptom control, focusing also on reassurance, education, and building strategies for confidence in everyday living.
If you are experiencing joint instability, chronic pain, or fatigue linked to EDS, book a consultation with Key Osteopaths in Surrey to learn how our osteopathic approach can help you protect your joints and improve daily function.
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Causes, Genetics, and Risk Factors of Ehlers-Danlos Syndrome

Ehlers-Danlos Syndrome is considered a heritable connective tissue disorder, meaning the underlying cause is genetic. While the exact genes vary depending on the subtype, the common factor is that collagen, the structural protein that holds the body together, is either produced in the wrong form or not produced in sufficient quality. This explains the characteristic tissue fragility, joint hypermobility, and systemic complications seen across EDS patients.

Anna came highly recommended and I have not been disappointed. My back and hip problem have been resolved in a mere two very good sessions. Anna knows what she’s… read more

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Anna is a brilliant osteopath she has helped me with varioys limitations and helped improve my quality of life

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Collagen Abnormalities and Hereditary Factors

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Collagen is the most abundant protein in the human body, forming the framework for skin, tendons, ligaments, cartilage, and blood vessels. In EDS, specific gene changes alter how collagen is built or assembled. Depending on the type of EDS, these changes may be inherited in an autosomal dominant pattern (one faulty gene copy is enough) or an autosomal recessive pattern (two faulty copies are required).

This is why family history can be a key factor. If a close relative has EDS, there may be a higher chance of other family members developing the condition. Genetic testing is available for many, but not all, subtypes. For hypermobile EDS, diagnosis still relies on clinical criteria such as the Beighton score for hypermobility and detailed assessment by a clinician familiar with connective tissue disorders.
Although the genetic basis is complex, what matters most for patients is that EDS is not caused by lifestyle, injury, or weakness. It is a structural condition present from birth, and understanding this helps remove stigma and self-blame for symptoms that are beyond personal control.
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The Overlap Between EDS and Hypermobility Spectrum Disorders

Not everyone with significant hypermobility symptoms fits the strict criteria for EDS. Hypermobility Spectrum Disorder (HSD) is the term used for those who have pain, fatigue, instability, and systemic features linked to hypermobility, but without meeting the formal EDS classification.
For patients, this distinction can feel confusing. However, in practice the two groups often share similar management strategies:
  • Protecting joints through postural training and stability work
  • Managing pain and fatigue with pacing and rehabilitation exercises
  • Addressing systemic issues such as digestive or cardiovascular symptoms with supportive care
Whether labelled as EDS or HSD, the lived experience can be equally challenging. That is why management is focused on function and quality of life rather than the label alone.
If you have long-standing hypermobility, recurrent sprains, or unexplained fatigue, arranging a professional assessment can help determine whether you may fall within the EDS spectrum or have a related condition such as HSD. Having this clarity allows you to access the right support sooner. Contact our clinic today.

Why Early Recognition of Symptoms Can Prevent Long-Term Complications

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Ehlers-Danlos Syndrome is often described as an “invisible” condition because many symptoms, such as pain, fatigue, or dizziness are not outwardly obvious. This invisibility means diagnosis is frequently delayed, sometimes for years. Unfortunately, late recognition can lead to avoidable complications.
Joint health

Without support, repeated sprains, dislocations, and unstable joints can cause long-term damage, early osteoarthritis, and reduced mobility.

Skin and wound care

In classical EDS, fragile skin and abnormal scarring can be better managed when identified early, preventing infection and long-term discomfort.

Cardiovascular risk

In rarer forms such as vascular EDS, early monitoring of blood vessels and heart valves can be life-saving.

Mental health

Living with unexplained symptoms often leads to frustration, anxiety, and reduced confidence. Early diagnosis provides clarity and reassurance.

Recognising symptoms early allows healthcare professionals to design personalised management plans that focus on joint protection, rehabilitation strategies, and systemic monitoring. This proactive approach helps patients maintain independence, avoid unnecessary injuries, and reduce the risk of complications later in life.
If you or a family member are experiencing repeated joint instability, unexplained bruising, or chronic fatigue, seeking a professional opinion can provide both peace of mind and practical steps toward long-term management.
For a holistic approach to managing Ehlers-Danlos Syndrome and hypermobility spectrum disorders, contact Key Osteopaths in Surrey today. Our integrated treatment strategies focus on stability, pain management, and supporting your overall well-being.
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How EDS Is Diagnosed and Assessed

Diagnosis of Ehlers-Danlos Syndrome can be challenging because symptoms overlap with other musculoskeletal and systemic conditions. A thorough process is needed to distinguish EDS from more common causes of joint pain and hypermobility. This usually involves clinical evaluation, sometimes supported by genetic testing, and always guided by a multi-disciplinary approach when required.

Myself, my husband, my son and my daughter have all seen Anna over the past few years for either neck, back, knee, shoulder or elbow problems. She has always managed… read more

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I found the experience reassuring .Ana was very supportive and professional.I feel the care received was excellent

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Anna has been brilliant, not only helping me getting rid of my neck pain, but also teaching me how to keep my body strong and healthy. Very professional, yet friendly,… read more

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Clinical History, Beighton Score, and Physical Examination

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The first step in diagnosing EDS is a detailed clinical history. This includes information on joint instability, chronic pain, fatigue, skin changes, cardiovascular symptoms, and family history. A structured scoring system known as the Beighton score is often used to measure joint hypermobility.
Alongside this, clinicians assess musculoskeletal function, posture, flexibility, and signs such as bruising or unusual scars. Because EDS can affect multiple systems, examination may also include heart checks, skin assessment, and questions about digestive or neurological symptoms. The aim is to build a clear picture of how connective tissue fragility is impacting the body.
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Genetic Testing and When to Refer to a Specialist

For many subtypes of EDS, genetic testing can confirm the diagnosis by identifying changes in the collagen-related genes. This is particularly important for rarer subtypes such as vascular EDS, where early monitoring and specialist oversight can reduce serious health risks.
Not every type of EDS can currently be identified by genetic testing. For hypermobile EDS, no single causative gene has yet been found, so diagnosis remains clinical. In these cases, referral to a geneticist, rheumatologist, or specialist EDS clinic may be advised to confirm or exclude other connective tissue disorders.

The Importance of Multi-Disciplinary Care for EDS Patients

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EDS often affects more than just joints, which means diagnosis and management usually require input from different healthcare professionals. Osteopaths, GPs, rheumatologists, physiotherapists, and genetic specialists may all play a role in assessment and ongoing care.
This collaborative approach ensures that not only are symptoms explained, but potential complications such as cardiovascular or gastrointestinal issues are monitored. It also provides patients with a clearer understanding of the condition and more comprehensive support.
If you are experiencing unexplained joint instability, persistent fatigue, or other symptoms suggestive of Ehlers-Danlos Syndrome, contact our clinic today. You can book an appointment by using our online booking system or call our clinic directly to arrange a consultation.
Don’t let Ehlers-Danlos Syndrome hold you back from living fully. Book a consultation with Key Osteopaths today and take the first step toward greater resilience, reduced pain, and improved confidence in movement.
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Osteopathic Approaches to Managing Ehlers-Danlos Syndrome

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Gentle Manual Therapy for Hypermobile Joints and Soft Tissues

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When treating patients with Ehlers-Danlos Syndrome, traditional manual therapy techniques must be adapted to account for fragile connective tissue and unstable joints. Instead of high-force manipulation, treatment focuses on gentle, supportive methods designed to ease pain, reduce tension, and improve comfort without placing unnecessary stress on the body.
For many patients, surrounding muscles work overtime to stabilise joints that are prone to slipping or subluxing. This constant muscular effort can lead to fatigue, tightness, and pain. Osteopathic treatment may therefore include:
  • Soft tissue release to reduce overactivity in muscles that are compensating for joint laxity.
  • Gentle mobilisation to encourage movement in stiff areas that are overprotecting unstable joints.
  • Subtle cranial or functional osteopathic techniques to calm the nervous system and reduce pain sensitivity.
The aim is not to increase flexibility, as this is already excessive in hypermobile patients, but to restore balance between stability and mobility. Gentle manual therapy can improve circulation, reduce muscle guarding, and provide a sense of ease that helps patients move with greater confidence.
Combined with advice on posture and rehabilitation, these techniques form part of a long-term strategy to protect joints and reduce the risk of recurring injury.
If you are managing EDS and would like to explore safe, supportive treatment options, contact our clinic today. You can call us directly or book an appointment using our online booking system.
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Postural Re-Education and Musculoskeletal Stability Strategies

Posture plays a central role in how patients with Ehlers-Danlos Syndrome experience pain and fatigue. Because connective tissue provides less support than normal, joints often rest in positions that place them under strain without the patient realising it. Over time, this can worsen instability, increase muscle fatigue, and contribute to repetitive injuries.
Osteopathic care includes postural re-education, where patients are guided on how to align their bodies in ways that reduce joint stress and conserve energy. This may involve simple adjustments such as changing sitting positions, using ergonomic supports, or altering workstation set-ups.
Alongside postural guidance, exercises are introduced to build musculoskeletal stability. These focus on activating the deep stabiliser muscles, such as those in the core and shoulder girdle, which provide essential joint support. Proprioceptive training, exercises that improve awareness of where joints are in space, also helps reduce the risk of dislocations and improves coordination.
The combination of better posture and stronger stabiliser muscles creates a protective framework, allowing patients to move more confidently and with less pain in daily life.

Pain Management, Movement Modification, and Rehabilitation Exercises

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Chronic pain is one of the most common and distressing symptoms of EDS. Pain may arise from repeated micro-injuries, muscle overuse, or the strain of constantly stabilising hypermobile joints. Osteopathic treatment integrates several strategies to help manage this ongoing discomfort.
Pain management

Gentle hands-on treatment to ease tight muscles, improve circulation, and reduce nervous system sensitivity.

Movement modification

Practical advice on adapting daily tasks, such as lifting, walking, or sitting, in ways that protect vulnerable joints.

Rehabilitation exercises

Carefully structured routines to strengthen weak areas without overloading fragile tissues. These may include low-impact strengthening, balance work, and paced activity programs.

A key principle is pacing: doing enough to strengthen the body but not so much that it triggers a flare-up. Patients are encouraged to listen to their bodies and progress steadily, which over time reduces fatigue and improves confidence.
If you are living with joint hypermobility or Ehlers-Danlos Syndrome and would like support in managing pain and building long-term resilience, call our clinic today or book an appointment using our online booking system.

Myself, my husband, my son and my daughter have all seen Anna over the past few years for either neck, back, knee, shoulder or elbow problems. She has always managed… read more

Kerry Bartter Avatar Kerry Bartter

I found the experience reassuring .Ana was very supportive and professional.I feel the care received was excellent

Deborah Sawin Avatar Deborah Sawin

Anna has been brilliant, not only helping me getting rid of my neck pain, but also teaching me how to keep my body strong and healthy. Very professional, yet friendly,… read more

Lucia Mosko Avatar Lucia Mosko

Holistic Care for People Living With EDS

Supporting the Autonomic Nervous System and Reducing Stress

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For many people with Ehlers-Danlos Syndrome, symptoms extend beyond the joints and muscles. A common but often overlooked feature is dysautonomia, where the autonomic nervous system, the part that controls heart rate, blood pressure, digestion, and temperature regulation does not function smoothly. One of the most recognised forms is postural tachycardia syndrome (PoTS), where the heart rate rises excessively upon standing, leading to dizziness, palpitations, and fatigue.
Stress can make these symptoms worse. When the body is constantly in a “fight or flight” state, pain becomes harder to control, muscles tighten, and the nervous system is more reactive. This is why supporting autonomic balance is such an important part of holistic care for EDS. Osteopathic treatment may include gentle techniques that encourage parasympathetic activity, often referred to as the “rest and digest” response. Breathing exercises, relaxation strategies, and paced movement can also help calm the nervous system and reduce overall symptom sensitivity.
Beyond hands-on care, stress management may involve lifestyle adjustments such as mindfulness, graded activity, and regular routines that promote consistency for the body. By addressing both the physical and neurological aspects, patients often find they can manage dizziness, fatigue, and pain more effectively.
If you would like to explore holistic approaches that support both body and nervous system function, contact our clinic today.
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The Role of Nutrition, Hydration, and Sleep in Connective Tissue Health

Although Ehlers-Danlos Syndrome is genetic and cannot be corrected through diet alone, lifestyle factors such as nutrition, hydration, and sleep play a significant role in how symptoms are managed. Connective tissues depend on a steady supply of nutrients to repair micro-injuries, maintain collagen strength, and support the immune system.
Nutrition

A balanced diet rich in protein, vitamins C and D, zinc, and copper helps support tissue repair and collagen synthesis. Many patients also benefit from guidance on gut health, since gastrointestinal issues are common in EDS. Eating smaller, more frequent meals and focusing on easily digestible foods can reduce reflux and discomfort.

Hydration

Adequate hydration is essential, especially for those with PoTS or circulatory problems. Maintaining fluid and electrolyte balance can help reduce dizziness, improve energy levels, and support cardiovascular stability.

Sleep

Quality sleep allows the body to restore muscle function, regulate hormones, and manage inflammation. Poor sleep can amplify pain and fatigue, so establishing good routines around bedtime, limiting stimulants, and creating a calm environment is especially important.

Optimising these basic but essential areas provides a foundation for better long-term management of EDS symptoms.

Lifestyle Adjustments and Pacing Techniques for Chronic Fatigue

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Fatigue is one of the most disabling aspects of EDS and can feel overwhelming without a clear strategy. Unlike ordinary tiredness, chronic fatigue in EDS is often a combination of muscle overuse, poor joint stability, nervous system dysregulation, and systemic complications such as digestive or circulatory problems.

Pacing techniques help patients balance activity and rest, avoiding the “boom and bust” cycle where overexertion leads to days of recovery. This might involve planning tasks in smaller chunks, using adaptive equipment for support, and prioritising energy for the most important activities.
Lifestyle adjustments can also make a significant difference. Structured daily routines, ergonomic seating, supportive footwear, and adaptive aids all help reduce unnecessary strain on joints. Gentle, low-impact movement such as swimming or pilates can maintain strength without overloading fragile tissues.
By combining pacing with supportive habits, patients can achieve greater consistency in their energy levels and avoid frequent flare-ups. Over time, this leads to improved independence and a stronger sense of control over symptoms.
If fatigue, pain, or instability are affecting your daily life, call our clinic today or book an appointment online. A consultation can provide you with strategies tailored to your specific needs.

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Why Choose Key Osteopaths for EDS Care

Managing Ehlers-Danlos Syndrome requires more than general musculoskeletal treatment. It needs a practitioner who understands the complexity of connective tissue disorders, the overlap with hypermobility spectrum conditions, and the impact on every aspect of daily life. At Key Osteopaths, our focus is on personalised care that respects the unique challenges of each patient.

Experience in Treating Hypermobility and Complex Musculoskeletal Disorders

Our team has extensive experience in working with patients who live with joint hypermobility, chronic pain, and instability. We understand how fragile connective tissue can influence not only the joints, but also posture, circulation, and even energy levels. This depth of knowledge allows us to adapt treatment safely and effectively.
Beyond the clinic, we keep up to date with current research and national guidance on managing EDS and related conditions. This ensures our approach is aligned with best practice and provides the most reliable support possible.
If you are looking for experienced, professional care for EDS or hypermobility, get in touch with us today to find out how we can support your journey.

Book an Appointment With Key Osteopaths

Living with the daily challenges of EDS can feel overwhelming, but specialist support can make a real difference. A tailored consultation offers not only hands-on treatment but also education, reassurance, and a clear management plan to help you move forward with confidence.

Early Assessment Helps Prevent Worsening Symptoms

The earlier EDS-related issues are addressed, the easier it is to prevent them from becoming long-term complications. Identifying joint instability, cardiovascular concerns, or musculoskeletal strain at an early stage allows for protective strategies to be put in place before they escalate.
An initial consultation can provide clarity, reduce uncertainty, and set you on the right path to effective symptom management.

How to Arrange a Consultation With Our Osteopaths Today

We make the process of booking straightforward. You can arrange your consultation by calling the clinic, using our online booking system, or contacting us directly for more information. During your first appointment, we will listen carefully, assess your symptoms, and work with you to create a safe, personalised care plan.
Rather than letting EDS dictate what you can or cannot do, take the first step toward better support. Reach out today and let us help you find practical ways to manage your symptoms and improve your quality of life.
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Frequently Asked Questions About TMJ / Jaw Pain Treatment

Q: Can osteopathy help with TMJ and jaw pain?

A: Yes, osteopathy can be an effective treatment option for TMJ and jaw pain. Osteopathic treatment focuses on restoring proper alignment, function, and mobility of the temporomandibular joint and surrounding structures. Through manual therapy techniques, joint mobilisation, and soft tissue manipulation, osteopaths can help relieve pain, reduce inflammation, improve jaw function, and promote healing.

Q: How many osteopathic sessions are usually required for TMJ and jaw pain treatment?

A: The number of osteopathic sessions required for TMJ and jaw pain treatment can vary depending on the severity of the condition and the individual’s response to treatment. Some individuals may experience relief after a few sessions, while others may require ongoing treatment over a longer period. The osteopath will assess your specific condition and develop a treatment plan tailored to your needs.

Q: Are there any side effects or risks associated with osteopathic treatment for TMJ and jaw pain?

A: Osteopathic treatment for TMJ and jaw pain is generally safe and well-tolerated. However, as with any manual therapy, some individuals may experience mild soreness or discomfort following treatment. These effects are typically temporary and resolve within a short period. It’s important to communicate any concerns or unusual symptoms with your osteopath during the treatment process.

osteopathy treatment questions typically asked

Q: Can lifestyle modifications help in managing TMJ and jaw pain?

A: Yes, lifestyle modifications can play a supportive role in managing TMJ and jaw pain. Some helpful modifications may include practicing stress management techniques, avoiding excessive jaw movements (such as chewing gum), practicing good posture, avoiding hard or chewy foods, and applying heat or cold packs to the affected area. Your osteopath can provide specific recommendations based on your condition and lifestyle.

Q: Can TMJ and jaw pain be completely cured with osteopathic treatment?

A: The effectiveness of osteopathic treatment for TMJ and jaw pain varies from person to person. While some individuals may experience significant relief and improvement, others may find that symptoms are better managed but not completely eliminated. Osteopathic treatment aims to reduce pain, improve function, and enhance overall well-being. It’s important to have realistic expectations and work closely with your osteopath to achieve the best possible outcome.

Q: Can children receive osteopathic treatment for TMJ and jaw pain?

A: Yes, children can receive osteopathic treatment for TMJ and jaw pain. Osteopathic techniques can be adapted to suit the age and condition of the child, providing gentle and effective relief. It’s important to consult with an experienced pediatric osteopath who specialises in treating children to ensure safe and appropriate care.