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FacebookDr. Jen Caudle
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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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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“I was diagnosed at 12. Eighteen years later, a doctor told me EDS is only found in European women.” Sabra was diagnosed with Ehlers-Danlos syndrome (EDS) as a child. Years later, a provider questioned her diagnosis, not because of new evidence, but because of a belief that EDS “isn’t seen in Black patients.” This is what systemic gaps look like in practice. When medical education does not reflect the full diversity of people with EDS and HSD, Black people are treated as exceptions. Diagnoses ar
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Lucinda Ritchie has Ehlers-Danlos syndrome, a condition that affects the joints; functional neurological disorder, which impacts her mobility; Addison's disease, a hormonal disorder; and epilepsy. She was studying for a Master's in sustainability at Southampton University, as well as acting as a charity ambassador and keynote speaker. #DisabilityAwareness #EDS #SouthamptonUniversity #Sussex #BBCNews
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