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Hello people I am a little new at this posting questions. But I thought I’d give it a go. Who better to ask than the ma community. I was diagnosed with ms after having optic neuritis About 8-9 years ago. Since then I have very few symptoms. I do suffer what I Describe as a ice cold feeling/ pain ...

Hi, I have rrms. I have been having stomach and lower back pains, for a couple of days. It doesn't hurt when I go to the toilet. Anyway doctor gave me 3 days of antibiotics, half way through and still have pain. I also have a fibroid. Could this be due to ms ??? Any advise please ???

Hi all, hope you are keeping well and safe in these unusual times. I am newly diagnosed in March, first symptoms 18 months ago and 1 minor relapse 6 months ago. Other than that I am lucky not to have any symptoms of note. I discussed with my MS nurse DMT drugs early March and my neurologist recom...

Hi guys. I've got epilepsy because of a lesion (yay), and talking to my gp, hes said that when I do start trying for kids, to discuss with him first because of my lamotrigine. So, obviously, I've looked on the bnf (a very good resource for looking at meds, and its what health professionals use) and ...

My name is karen. I was born in England. I will be 43, this year. I had three older siblings. All of them were born three years apart... Five years later I was born. Back in 2002-03, my second oldest sister started having symptoms. It took along time for her diagnosis. By 2020, and my sister can do...

Hi all, if anyone could comment on this before 11 am Thurs: I'm taking part in a focus group with MS Society to discuss how these guidelines have affected MSers, or if anyone could suggest what could be put in place to make you feel more confident about venturing out. Please let me know if you have ...

Been waiting 2 years to start on Ocreus now, had blood test after blood test its like the doc always finds some thing to stop me starting on it. I've not heard from the ms team since the being of March and that was a letter about my last blood test. feel like im banging my head on a wall.

Been waiting 2 years to start on Ocreus now, had blood test after blood test its like the doc always finds some thing to stop me starting on it. I've not heard from the ms team since the being of March and that was a letter about my last blood test. feel like im banging my head on a wall.

https://www.youtube.com/watch?v=MM-6kNE4YYw&list=PLVUOB-ZqvZOGuy6t95B67vi5A6nQTY0BS Progression is often the elephant in the room, serving to build fear and trepidation for people who are living with MS. Through investigative conversations that unpick the human side of the topic, ‘Is my MS progres...

Calling all aspiring actors! I am casting the third series of a very successful Netflix show. Please do take a look at the brief below and get in touch if you are interested: Roland is in his 40s. Warm, cheeky, sharp, witty. He has MS with mobility and fatigue symptoms. He lives on his own with ...