Folks, my partner has remitting MS. I was to be as aware and supportive as possible. Can anyone recommend some reading or tips please. I have some experience with MS through my uncle. Many thanks,
So my wife of 31 years was diagnosed with RRMS in 1995. In that time she has tried many many medications. Nothing has stopped or even slowed her progression into secondary progressive MS. We travelled to Poland 2010 for CCSVI treatment. Still her MS progressed. She has been using a wheelchair now fo...
Hi everyone, I thought I'd just share this short clip explaining very simply how stress causes inflammation and fuels MS. This is from a documentary called "The Connection", very well worth watching.
http://youtu.be/qP1d4tqmSuk
I’ve had RRMS for 4 years and I’ve had 2 rounds of Lemtrada.
For years I’ve suffered with extreme sweating and after Lemtrada it’s gotten worse!
I literally can’t leave the house as I’ve only got to move and The sweat is pouring off me. I take small electric fans everywhere with me and I have a fa...
Hello
Just wanted to ask the community for any feedback / experience.
Redundant 14 months now. Just secured some freelance work 2 days per week, ongoing. In my industry and for a good company. Will not pay the bills but I am hoping it will lead to a full time job and will buy me more time from my...
Hello There,
Long time no speak. Or type in this case. I just wanted some advice on how to manage work and MS. I have really struggled the past couple of months with my MS and going back to work. I work in hospitality and have been lucky with furlough but also the place I work for has been super bu...