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Honesty..... People tell me to be honest about where I am with my ms. I try to do that, but my problem just now is being honest with myself. I am struggling with work. My colleagues are very supportive and they say that they understand, but my thinking is how can they understand when I don't unde...

For those of you who regularly read my blog, I offer my sincere apology for my long absence from this site. At the very least, I should have posted that I was going to be gone for a while. I didn’t, and for that I am truly sorry. This past summer was…hectic and for a lot of people it was truly awful...

I don't know why Birmingham was not in the list when signing up to this site. Am looking to see if there are any support groups In Birmingham as there used to be one that did regularly meet at the Garden House pub on the Hagley Rd Egbaston

It is 7.25pm on a Saturday evening and I have just done some ironing. I guess boredom can sometimes kick in. But nothing a glass of Prosecco won't sort. And the supporting match was won. Y.N.W A. Sorry if you're not into footy.

Hello friends, My name is Austin & my recent diagnosis has my brain completely twisted up. I am really hoping to find knowledge and support through this forum. I know not how to handle such a curveball in life… google can only say so much to me… i hope to find peoples with personal experiences t...

I was diagnosed about a year ago with RRMS. I'm interested to find out what kind of accommodations your employers have given you to help you continue working with MS. For nearly twenty years, I have worked as a software project manager. This means I am in a leadership position with constantly changi...

Good morning, Yes, I too take my vitamins, Calcium, D3, Boron, Zinc, Vitamin C, B Complex. I will be meeting with this Doctor on the 27th, we will see what she says, I am not going to allow anyone to use me as a demonstration. I need to be capable of working in the next week.

Hi there! 👏🏾 Have been reading a few of your posts and commenting here and there but this is my first post - it is really nice to find this community and see how supportive of one another so many of you are. I was diagnosed last year, after optical neuritis in 2019 and a few MRIs... Have been taki...

Not long now til my skydive for MS Society! I still have a little bit to go! Any donations would be amazing! I think everyone on here would agree we have all needed support at some point through our MS journey and I would love to give MS Society a good donation to help for the future of MS. Help...

Hi thanks for your support, I will let you know how I get on with taking Kesimpta on Thursday!