i'm also fed up of people telling me it's all in my head, you wouldn't be saying that if you woke up feeling dizzy, or if you couldn't feel your leg, i get that most people don't get it, and that's fine, but please don't belittle me and tell me i'm imagining it, because believe me i wish i was.
i found this description on facebook and thought it was pretty accurate, i don't suffer from all of these symptoms and they aren't there 100% of the time, but the joys of Multiple Sclerosis is that you don't know when a symptom is going to hit and how long it's going to last.
now that i have had my rant i will go to something more positive...
I AM ALMOST 7 MONTHS RELAPSE FREE!!
this is a massive deal for me, since getting my diagnosis almost 2 years ago the longest i have been relapse free is 7 months, i am so close to beating that so i am feeling positive. :D
since i last posted i have also been discharged from my neuro physiotherapist this was daunting for me at first, but i have now realised that it is a good thing, i have been given a number to ring if i ever need to get in touch again but he said that he'd done all he could for me and that he could see improvements and i just needed to keep at it :)
