Ey up MSdebators Just wondering if anyone has managed to set up a blog while juggling work, kids and msdebating. I’m struggling to find time to do it and also being a finicky pants about the design of it all. Iv been paying for the bloody thing for o er a year now and I’m not even close to ope…

Has anyone ever experienced sudden, temporary weakness and loss of coordination in their extremities? While loading the washer today I had sudden weakness in both arms with lack of coordination. Then went to make coffee and it was a challenge to hold my empty cup, put in the k-pod, even fumbled wit…

I’ll be 10 years diagnosed in December, and I’m wondering how on earth I’m going to get my own place to live. My skills are wide and varied, as are my anxieties around moving out on my own. Clearly however, if I am to realise my full potential, I will have to find a source of inco…

hi! i completed my first year of treatment in jan + feb this year and sadly, i’m not having the best experience. i’m keen to hear from anyone else who has been on cladribine and what sort of side effects you had. thank you! lauren

Do you keep a thermometer handy to know if you are coming down with something? What thermometer do you recommend?

Over the past few weeks my left wrist has felt really weak, I’ve got a cane for walking around the house with because my balance hasn’t been great either but I’m thinking just around my daily routine to wear some sort of wrist splint for the support but more so, so I don’t do anything to sp…

Does anyone else find the idea of waiting until sicker before stepping up treatment rather odd? I am getting v. slowly increasingly frustrated with the attitude that in order to access the most efficacious MS treatment (HSCT – Stem Cells) I have to decline to a certain point degree of disabil…

This has been suggested to me by a friend. Has anyone tried it and if so was it a waste of money or a possible therapy.

Anyone tried any of these? Yeah I know its mainly for cancer but the way it works on the immune system seems to have had positive effects on MS too. I had a look at the GcMaf website, and apparently NICE closed down the UK facility where they were giving away the treatment in Jersey to cancer suff…

Does anyone follow the ketegenic diet and want to share its experience with it? I started about two weeks ago, but my fatigue increased so much that it affected my walking. I wonder if this is just in the beginning or if it will get better.