Ehlers-Danlos Syndromes: Types and Diagnostic Criteria | The Ehlers-Danlos Society posted on the topic | LinkedIn
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Many women with Lipedema are surprised to learn they also have symptoms of EDS (Ehlers-Danlos Syndrome) — and it’s not just a coincidence. Both conditions involve weak connective tissue and altered collagen structure, which can cause: ✨ Joint hypermobility (your joints move beyond the normal range) ✨ Easy bruising and fragile skin ✨ Chronic pain or instability in the joints ✨ Poor lymphatic flow ✨ Tissue that feels soft, doughy, or easily injured Because Lipedema and certain types of EDS share o
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🔎 EDS (Ehlers-Danlos Syndrome) is a genetic disorder of collagen that affects each person differently.⁣⁣ Living with EDS can mean living with pain every single day, not the occasional ache, but constant pain that usually sits between 5–10 on the pain scale. 🦓 Why can EDS hurt so much? 🔹 Joint instability & subluxations 🔹 Micro tears & tissue fragility 🔹 Mild demyelination 🔹 Overworked muscles from constant compensation … and more. 💙 Chronic pain is often invisible, but it affects millions
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