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Authorgreenteafairy
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Please do not listen to the person above. Eds pain and fibro pain are very different. Although there are some overlaps in conditions along with me and long covid too. With eds some of the pain comes from constant microtraumas of the joints over stretching of ligaments muscle misuses and muscle overuse. Among other conditions we have. This is very real and should be taken seriously. Please look up understanding hypermobile ehlers danloa syndrome by Claire Smith and fight to have your records be as corrects as possible. I was assessed for fibro and didn't meet the criteria but I have heds.
Reddit Linkhttps://www.reddit.com/r/glasgow/comments/nhsyf0/is_it_possible_to_get_a_gp_nhs_to_remove_a/gyzte4s/
CreatedFri 21st May 2021 11:25pm
Statusnormal ()

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