@spencerfrog 

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spencerfrog

hi….

hey so i had my first relapse november 2020 and was working at the time and literally couldn’t feel my hand and i had optic neuritis during my driving test and somehow passed but i’ve not been driving since. i had my first relapse at 21 and finally diagnosed at 22 after many mris but my neurologist at the time told me its probably ms over the phone lmaooo at the time i didn’t know much about it at all i didn’t know what was happening to me but yup ms! i struggle with fatigue, migraines, neuropathic pain uhhhh idk just looking for others out there been anxious to post on here or just anxious in general. does anyone else struggle with mental health because i’m mega depressed might be because of colder times but its hard talking to ppl uhhhhh also i’m trans if any other msers are trans or gay !! also hard of hearing from birth 🍇🦩🪱🧠🌈 have a great day my brain is scrambled so thats why this is all other the place oh forgot i like doing candles and art!
@marychvz7

@spencerfrog I’m so sorry I know it’s hard to digest when you are first diagnosed. I’m sure here you will find support and a lot of people who can help you understand what’s happening to you and give you great advice. Stay strong I used to think that what people say “What doesn’t kill you makes you stronger”!!! Was BS but living with RRMS, LUPUS and Sjögrens syndrome I can honestly say it’s true. Welcome I’m new here as well but everyone is very nice. Stay strong feel free to message me anytime ok

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@spencerfrog

thank you 🫡🫡