Connective tissue is found throughout the body, providing support, protection, and structure. In the Ehlers-Danlos syndromes (EDS), this tissue is more fragile and stretchy than usual, meaning the body’s natural support systems don’t always work as efficiently as they should. The pelvic floor is made up of muscles and connective tissue that support the bladder, uterus, and bowel. When that connective tissue is lax, as it often is in EDS, the muscles have to work overtime to keep everything suppo
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FacebookThe Ehlers-Danlos Society
Hypermobile Ehlers-Danlos syndrome (hEDS) is a heritable connective tissue disorder that causes generalized joint hypermobility, joint instability, and chronic pain. hEDS is also associated with a variety of other symptoms and related conditions that affect many different areas of the body. Learn more about signs and symptoms of hEDS and diagnosis at https://www.ehlers-danlos.com/heds/ | The Ehlers-Danlos Society
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Hypermobile Ehlers-Danlos syndrome (hEDS) is a heritable co…
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FacebookThe Ehlers-Danlos Society
The Ehlers-Danlos syndromes (EDS) are a group of 13 heritable connective tissue disorders. The conditions are caused by genetic changes that affect connective tissue. Connective tissue is found throughout the body, where it provides support, protection, and structure to other parts of the body. Connective tissue disorders are caused by issues that prevent connective tissue from functioning properly. Collagen is the primary component of connective tissue. There are different types of collagens wi
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FacebookThe Ehlers-Danlos Society
What are Connective Tissue and Collagen? | Ehlers-Danlos Syndromes | The Ehlers-Danlos Society
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"What if your joints were super flexible, but it came with constant pain and exhaustion? That’s life with #EhlersDanlosSyndrome (#EDS). 🦓🤍 "EDS affects the entire body—connective tissue, joints, skin, and even blood vessels don’t work as they should. Daily pain, dislocations, and fatigue are common, but the hardest part? Many, even doctors, don’t understand it. 💔 But The Ehlers-Danlos Society is changing this. Talking about EDS makes #InvisibleIllness visible. By sharing, we help others feel
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