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hello shift.msers, does anyone else on here use aubagio please? I started it 2 weeks ago, haven't noticed anything YET but I assume it'll be building up inside me still and side effects may start. After self-injecting Rebif for 13+ years I am finding it difficult to break my routine. Injection nigh...

I live in Wales but was just wondering whether anyone in the UK has been offered it yet? I asked at my last appointment and originally I was told it would be available from 22nd April but now I've been told it could be a few more months.

I'm fed up with Tecfidera, 2 tablets a day, so I asked MS nurse about 'once a day' tablets, She suggested looking up Aubagio. Any comments appreciated, thanks, Oskar

Did anyone take Aubagio and had really bad side effects? Cause I did! That’s why I switch to Ocrevus

hello, everyone. about a year ago I tested positive for JCV & then the connections with Gilenya came out. I stopped taking the meds & went on Dr. Jelinek's "Overcoming MS Diet". I lost 30lbs in 6 months & felt great. I have not been so great with the diet over the past several months...

Hi everyone, Just wondering if anyone here is on Aubagio and could share their experience of it with me? I've been having stomach problems on tecfidera and have been offered that instead but I'm hesitant from what I've read about its efficacy. From what I understand it has a lower relapse reduction...

Hey All, I have been taking Aubagio for a couple of years with all the usual side effects I.e additional non ms based pins/needles, hair loss,anxiety etc but lately I have been experiencing some additional side effects such as sciatica, increased nerve pain/ spasticity etc Has anyone also experienc...

Hey guys! Haven’t been on this for some time and hope everyone is doing great (besides the mess we deal with)! I started Aubagio in the start of the pandemic & there were definitely a few changes. I dealt with the hair thinning/loss, acne on my face 😞, low WBCs, and weight loss. I lost a great...

Someone has experience with this?

Anyone have any experience of this? Been told I may have to come off Tecfidera due to low lymphocytes and this has been mentioned as a possible alternative? Any views? Thanks