![]() One thing to watch out for is compression vs graduated compression. ![]() I'd buy several more if I could afford it. My insurance paid for two pair initially and then one pair every three months after that.so pretty much a pair to wash and a pair to wear (Juzo recommends replacing stockings every six months because the compression weakens over time). Juzo isn't cheap but you might be able to convince your insurance company to help pay for them if your doctor will write a prescription. I can't wear footless because my ankles get strangled when fluid pools in my feet, and I have some swelling/pooling above knee highs so I need something taller. I've had good experiences with both the closed toe and open toe versions. I like Juzo's Soft line because they're, well, soft and don't irritate my skin. I wear 20-30mmHg compression thigh highs daily for POTS type symptoms. NIH hEDS Information, Criteria & Management We cannot verify where the money is going, and to protect all parties, we do not allow these posts. This subreddit does not allow posts asking for financial help. If you want to post memes anytime, check out our sister subreddit /r/ZebraMemes. Any meme submitted as its own post will be removed. Please ONLY post memes into the weekly threads. This is a bannable offense and will not be tolerated. In order to avoid further bullying and harassment, it is now against subreddit rules to make comments regarding the morality of having children with EDS unless OP specifically asks. The decision to have children is an extremely personal one-Ehlers-Danlos syndrome or not. Sharing your failures or successes with treatments is fine. Soliciting or giving medical advice is not allowed in this subreddit. It is best to avoid giving medical advice over the internet in general. NOBODY HERE IS A VERIFIED MEDICAL PROFESSIONAL. Instead of making a "could I have EDS post?," read the resources provided here first! Please remember that only a doctor can diagnose you. The wiki has information on what Ehlers-Danlos syndrome is, the different subtypes, information on pursuing a diagnosis, and more! 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.Īccess the wiki index here. This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD-diagnosed or waiting to be diagnosed.
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