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0:39
...but they might not want to. 🦓The current diagnostic criteria for Hypermobile Ehlers Danlos Syndrome (hEDS) by @ehlers.danlos states: 📣“This diagnostic checklist is for doctors across all disciplines to be able to diagnose EDS” 👉We’re often referred to genetics, rheumatology, or other specialists. 💥 But your primary care doctor, NP, or PA can diagnose #hEDS too! 🤔They may not be comfortable doing so because they aren’t familiar enough with the condition or simply because they aren’t aware
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In this video I will go through the diagnostic criteria for h-EDS in the simplest and most easily digestible way I can. Many are suffering with the symptoms of Hypermobile Ehlers Danlos Syndrome and being met with nothing but dismissal and medical gaslighting by their doctors. Some of the things people have told me their doctors have told them in an attempt to dismiss their concerns and daily battles with this disorder are deeply upsetting and often just down right medical neglect. I hope this v
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❣️Comment “EDS” to get my free guide “How to Get a Hypermobile Ehlers Danlos Syndrome (hEDS) Diagnosis”👇🏻 I wasn’t diagnosed until a few years ago, though I’d had symptoms my whole life. I never knew EDS was even a thing! It took a friend who specializes in EDS to assess & diagnose me with not only EDS but with MCAS & POTS too. 😳 She had seen my complicated breast cancer journey (including several hernias & infections & breast implant illness) & knew these were underlying it all. Getting a di
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