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Migraines….still

Hey guys!!! So before I had posted about my migraines. Im on A bunch of stuff that has helped with blocking the migraines but I still have headaches on the daily. Its more of a pressure in my head all over. I'm getting really frustrated with it at this point. I have an appt with my neurologist on th...

@ncm22 

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ncm22

Tecfidera

Hi, I will run out of tecfidera on monday morning, as my new prescription hasn't been sent through. It will probably take a number of days to get some more. Does anyone know how long it takes for tecfidera to get out of your system ? Thanks X

@MiaPi 

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MiaPi

Copaxone switch to Tecfidera

Hello all, So I have been on Copaxone for 3 years. 1st year all good no relapse or new MRI lesions. Second year I got one new lesion but since it was also small my dr said let’s stay on Copaxone. Now my latest MRI showed one new lesion but at the same time I got lipoatrophy on my thigh from the Cop...

@NicciS 

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NicciS

In need of some positive words!

Hi, feeling fed up. I'm just about to move on to my 4th DMT in 5 years. So far I've done Tecfidera, Gilenya, Aubagio and now on to Ocrevus. Any positive stories anyone can throw at me would be gratefully received right now!

@katiecog 

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katiecog

Starting Tecfidera in Ireland

Hi there, does anybody here have advice for starting Tecfidera? Is it a matter of just taking the drug and getting on with it or is there a support network available in Ireland? Thanks :)

@Henrietta 

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Henrietta

Diagnosis - the long and winding road

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...

Newly diagnosed - advice please!

I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...

Newly diagnosed - UK MSers advice please

I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...

Newly diagnosed - UK MSers advice please

I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...

@mscyclist 

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mscyclist

tec and exercise

Morning all, I've been med free for 15+ years since diagnosis but a couple of recent relapses (including my first learning to walk again episode) have put me on a treatment plan. I'm due to start taking tecfidera soon and wondered how it may affect my exercising? I currently cycle on a static trai...