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I have a relatively decent diet and try to look after myself the very best way I can, but when JUSTEAT comes knocking on my brain, I surrender in purchasing everything I see. Mexican, Chinese, Indian. I can be quite the pig when it comes down to it, yet I can't put the weight on. :( Have a great ni...

Hi , I am new to forum, I have had Ms for 20+ years, about 8 month ago I started having problems with swelling on my left leg and foot (this is the side MS effects me) I have been back and forth to my doctors who just tell me to use support socks, but they do not work. The swelling effects my walkin...

Hi everyone! Three months ago I delivered my baby girl via C-section. Scar has healed very well but since the catheter was taken out the day after I have had problems with my waterworks on and off. Some days I have no pain or urge to go and other days the urge will be there all day sometimes and...

Hello Just thought I would say hi and try to reach out to anyone who are successfully managing their MS and are fortunate to be their own boss. I feel that I need to start to work for myself as whenever I have been in employment I seem to get unlucky and hit problems. Mainly down to having MS and...

Hi! I am hoping to get some feedback. I am dx RRMS. Doing pretty well, on Glatopa (copaxone) about three years. Anyway, I am having serious joint pain in both hands and mainly thumbs. Maybe carpal tunnel but I have much joint pain in other areas like knees and feet. But the hands are the worst. An...

Hi I’m so sorry if this is inappropriate but I’m just upset and don’t have anyone I feel will understand to talk to. I have just come off a telephone consultation with my (very nice) GP. I had an MRI as I have been having symptoms that my GP agreed sound like MS for ages - even years. I’m 36yrs old....

Need to get something off my chest....... so fed up, diagnosed 24th March 2020. Still no communication, phone calls or anything else from any health care professional. I keep reading about asking your ms nurse for advice - think I’m losing it cos I’m still waiting.

Hi all, I am seriously new to all of this, My RRMS journey has been a whirlwind. I had the MRI and got diagnosed literally overnight. Multiple MS occurences all at once. After a huge course of steriods Methylprednisolone 1000mg 5 days. My flares have calmed down. Not gone away, I my hands are numb a...

Hi everyone! I'm just coming back to check in as I realise I've not been around for a while. I had NEDA (No Evidence of Disease Activity) on my last MRI and have been feeling fine since then *touch wood* I became friends with an amazing woman who also has MS and hosts a podcast about living with a...

Is anyone worried about the whole coronavirus I’m starting to worry I already have a weak Immune system due to my MS treatment... would that make me variable to the virus because of that or am I just overthinking this?!? Get back to me in the comments what’s your opinion