#im in year four or some shit of dealing with these Specific Neuro Symptoms
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hmm yet another experience of looking to see how other ppl deal w similar neuro symptoms to mine and finding endless "have you looked into eds?" comments followed by almost exclusively advice for treating eds symptoms and not my very much not eds neuro symptoms
#im just. annoyed.#like literally the only shit i can find rn is fucking therapy/self help bullshit and eds treatments#neither of which are relevant to my specific issues#i am very glad that eds is getting more awareness! yay! but it is not helpful to me to have anything potentially helpful drowned our#*out#like. i get it my neuro symptoms are not easily diagnosable#im in year four or some shit of dealing with these Specific Neuro Symptoms#and when NO doctors are useful (shoutout to the neuro who really wants me to get brain surgery i do not need and the other neuro who thinks#all my issues were bc im trans)#and NO online resources are helpful because of the overrepresentation of eds#i get. frustrated.#anyways. personal rant done
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