Looking for
something specific?

Has anyone ever tried the Stem Cell treatment? I keep getting advertisements and was wondering if anyone has tried this treatment. Thanks in advance for any feedback.

Hey, I was diagnosed with Ms at the start of this year, recently just had another scan and I have more lesions on the brain so now I qualify for the treatment and I don’t know how to feel about that, is anyone on treatment for ms, has it made you feel any different? Xx

My neurologist suggest me to start treatment with frexalimb injection. Need your opinion guys. Aslo if anyone already on this and have any side effects please suggest. Thanks..

I wonder so people change their MS treatment after a length of time? I’m on Gilenya 11 years

Hello, starting my first infusion on Friday with briumvi. I know everyone is different but wondering if on briumvi how has your experience been like?

Has anyone been given duloxetine 30mg for numbing, tingling and burning pain for ms? I’m awaiting diagnosis following my mri two weeks ago and the doctor has prescribed these for now, until confirmed. The numbing, tingling, burning pain is constant.

Hi all, I have a question. Is there anybody on a treatment that is working well for them and they can see and feel a good improvement in their situation. Personally I'm not on any medication at the moment only a daily vitimum d supliment tab. KESIMPTA OR OCREVUS ANY GOOD?? Good days and bad days ar...

7th ocrevus tomorrow morning

It’s my first dose of Ocrevus tomorrow. I have the iPad charged, snacks and food sorted. Luckily I love meeting and talking to new people so I’ll make friends ☺️

Can I please ask, those of you in the uk that have been diagnosed a while but not on treatment, what is the reason for this? NHS or a personal choice ?