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hannahmurg reblogged your post piningjohn: Ok quick survey who would... and added:
You do realise that Europe is a bloody big place right? Please specify which country.
this is a rough idea now, if we do make it work you'll be the first one to know
Do you mind me using your slytherin period idea to put into a fanfiction if I credit you as inspiring me?
ha i don’t mind in the slightest! pls send me a link if you end up doing it because i am rather intrigued
Out Of Arendelle
Also, I know this is super cheeky of me, but can you guys follow hannahmurg because she is one of the single most gorgeous human beings I have ever had the pleasure to know and be friends with, but she's going through an unbelievably hard time right now and it makes me sad. Please show my baby some love! <3 :*
I have been diagnosed with hypermobility, but they said nothing about me having Ehler-Danlos, they just said I have hypermobility. I frequently dislocate joints. Do you know if I have ehler-danlos or not? I have been diagnosed with it for four years, and I am only just being sent to the hospital. Do you think they will tell me at the hospital? Thanks xx
Hi there! I only just saw this message – I never got a notification for it – so I’m sorry if this is very delayed.
I don’t know if you have EDS or not; I don’t know your symptoms or your history. In my experience, doctors can’t/won’t diagnose EDS simply because they’ve never heard of it. If you want the diagnosis, you’re going to have to find a doctor who’s familiar enough with it. I more or less self-diagnosed months before I found the geneticist who gave me my “official” one. You can check the list of symptoms here and see how many you match up with - it’s not official or perfect, but it should give you a good idea of whether you have it or not. If you’re frequently dislocating (or subluxating), then there’s definitely a chance you do have it.
I hope your hospital visit went okay and that you do get the answers you want. Good luck!!
