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Im new on here and wanted to ask your opinions and advise for travelling. Im going to Australia next month and I'm traveling alone with my 6 year old son to met my husband out there. Im fine with planes but I am a terrible sleeper and wanted to ask if anyone ha staken rescue remedy before to help t...

Hi i will start treatment with ponvory. Who here is on this treatment and how it efects your life side effects.....?😁 Tnx

I am just 20 years old. I was diagnosed with MS 8 months ago but I've experiencing MS symptoms way back when I was still 18 years old, those symptoms are numbing of my hands, feet, and blurry vision but those symptoms come and go. I was already checked by different doctors and they always tell me th...

Hi my name is Anne I’m new here I was diagnosed with ms in October 2018 went through so many treatments finally I’m on Ocrevus and I’m surprised 😮 it is slowing it down

What do you expect next? I had to put my love one and a nursing home. She is on a feeding tube now and can’t walk

I have MS and I am new to this group.

I was wondering whether anybody had tried the Alinker, I bought this a short while ago and thought I would start using it now the warm weather is on its way. apparently, there is one in my area (Southend) and is bright yellow, so I am sure I would’ve seen it somewhere, but not seen it. if you have s...

I'm Marta and I live in Lisbon, Portugal. I have my diagnosis since 2007 when I was 21 years old. I'm a midwife and have two great kids. I'm currently on occrevus

New here so thought I'd introduce myself. Call me Elz. Diagnosed Oct 22. Currently on Copaxone. Main symptoms: Vertigo, numbness in feet and nerve pain in arm.

Hi I have many symptoms and have been referred to a Neurologist in May this year. I just wondered people's experiences, like, what does the Neurologist do? Do they do tests or just look at symptoms? I'm trying to jot down the symptoms in a diary so I don't forget them. I've read a little about the ...