doctor wasn’t able to answer all my questions as he didn’t have the scan on his computer (rahh!) but he’s going to refer me to an MS specialist.
IT still hasn’t hit me yet as apart from a bit of eye pain (not enough for me to bother with paracetamol even!) i have no other symptoms. i had 3 lesions in my brain and one was active so i may have had symptoms before and dismissed them as somthing else but I can’t remember anything!
Hello I was diagnosed yesterday after a year of tests and different symptoms was sort of expecting this but I’m still in shock sending a hug as I need one too x
I’m not going to say welcome lovely, let’s be fair, nobody want’s to have MS. On a good note, you have come to an awesome forum & everyone is absolutely priceless. We are all members of a right shitty club, but we have each other. Nice to meet you, albeit in nasty circumstances, any questions or support you need, just ask, there is always someone on here that can & will help. I am not usually a huggy person, but I send you 1, you are now officially not alone & a part of our unique gang, take care Tracey xxxx
Ice queenly & dexie, welcome & big big siber hugs. Please both focus on getting onto a DMD which will
give you the best chance.
i hold onto my nearlologist’s way of telling me. ’ even five years ago this would be something to be worried
about, but with treatments available & resurch being done, don’t worry.’
this fourum is great. But remember when you are reading things that a lot of people have had ms for a long
time before development in treatment.
also… Only read ‘caring for someone with ms’ if you either want a self pity moment, or you want to get cross !
(OK, the reality is probably that people are posting who have not yet come to terms with their relative having ms & those who have had ms pre developments.)