I’m guessing I’m not the only one who is lying in bed being British moaning about the hot weather and not being able to sleep. This heats amazing, but for us MS’ers it can really play havoc…think I mentioned how if I get too hot my eyes just go all blurry and I can’t see…it […] Read more…
20. Reality check for Rach
I’m not ashamed to admit that one of my biggest faults is putting things I don’t want to deal with in an imaginary box, putting the imaginary lid on it and forgetting about it. I’ve had a great few months, holidays, good times with lovely people and most importantly no relapses. I’ve actually felt the […] Read more…
19. NOT TO BE MISSED! MS Research Event, 21st June. NW England.
One of the most frustrating things I have found since being diagnosed with MS is that access to resources and up to date reliable research is few or far between. Don’t get me wrong, I read the articles that are published on a weekly basis which claim “The MS Cure is on its Way”, but […] Read more…