I just wanted to say thanks for being out there to listen and understand. I’ve had ms for 17 years and for most of them I’ve been in denial! Last year was horrible, I went through having a SPC fitted and didn’t think to seek support from here. It was a dark time and whilst my waterworks are on an even keel everything else feels a bit too unpredictable at the moment. I hate the way ms comes along when you least expect it and bites you!
I was heavily ‘encouraged’ to join the ms society by wheelchair services. I’m in the process of upgrading my manual chair to power and this is bringing lots of ‘stuff’ up to deal with and I don’t like it one little bit. I’m so glad I did, what a great bunch of people you are
So, thanks everyone for being out there. x