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This is a support sub for those with ?

A place for those diagnosed with, or seeking diagnosis of, Hypermobile Ehlers-Danlos Sy?

It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! This is the most common sub-type of Ehlers-Danlos, which is a rare (probably not so rare) genetic condition that affects collagen made in the body. This has been the difference between horrible and pretty good medical care for me. EDS in general has been getting more and more research in the past ten years- who’s to say what will happen in the next ten? :) without being too cheesy, be careful, keep up with your doctors, and stay positive. Start with going very extreme with health, and if it fixes your ED, start re-introducing some sugar, some fast food etc. are kye and lizzy still together 2023 If you’re struggling to find the motivation to clean your home, you can turn to specific methods, inspiration, and. We would like to show you a description here but the site won’t allow us. in person discussion sections are chill. Ehlers Danlos Syndrome (EDS) is a underdiagnosed connective tissue disorder characterized by a genetic fault in collagen. average raise 2023 So this mainstream article is written by (edit my mistake about) an ex orthopedic trainee who seems to be doing a private EDS clinic as far as I can tell. They quickly fell in love, met each other’s families and started to build a life. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. In today’s digital age, having a strong online presence is crucial for the success of any website. So I guess my first "worrisome" EDS symptom was the rolling of my ankles, knee dislocations and shoulder dislocations that started in grade school Ehlers Danlos Syndrome (EDS) is a underdiagnosed connective tissue disorder characterized by a genetic fault in collagen. sherwin willliams The thoughts and experiences of violet are so unique to people with EDS and other chronic illnesses that they seem to pass over the heads of other people sometimes, but their true value to us, as the community being represented is absolutely incredible. ….

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