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Hey Everyone! My name is Manel and I live in the Algarve, south of Portugal. I Started taking Aubagio 4 months ago and I am having problems sleeping. Also feel more anxious, my mood os not on its best SIDE and dont have a lot of pacience. In general, i feel more stressed and cant get a good night sl...

hello, im kinda new here.. My question is does anybody else have problems with wound healing. I had a total hysterectomy October 2020, and have had a variety of issues all dealing with the fact that it just wont heal. Had a 2nd surgery to remove scar tissue that was turning gangrene September 2021,...

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

Hiya, I was diagnosed in 2003 and have been on Copaxone and now on Gilenya but neurologist wants me to switch to Aubagio. He seemd fine with me on Gilenya for almost 6 years until I got shingles on the left side of my face and now he feels I need to change medication to Aubagio. I've bee kinda sca...

Someone has experience with this?

Hi everybody. I have been diagnosed with RRMS in summer 2021 and have had Aubagio therapy for 13 months. What is your experience with it and with MS after/during the therapy?

Hello. I've been on tecfidera since diagnosis last year. But blood count is too low to be allowed to continue. Had a rough few weeks starting with tecfidera but have since been ok with minimal to no side effects. Now need to change and MS nurse has recommended aubagio. Side effects of one round of h...

Hello everybody, just found out about this site and very relieved it exists. So, I will begin by saying that I’m 20 and I was diagnosed with RRMS November last year. My neurologist decided to put me on Tecfidera. Unfortunately, I couldn’t cope with the side effects (burning stomach). However, my MS ...

I was diagnosed 01/2021. Started taking aubagio 03/2021. Had 30 different side-effects, but they gradually passed. It took up to 8 months for it tho. Now, after being side-effect free for almost a year, they started again. Especially the hair loss. I had really thick hair, lost half ofmy hair. Peop...

For context I’m on the Gemini trial. I’m either taking Aubagio, or Tolebrutinib (not fda approved). I’m curious if anyone here takes aubagio and if so, what have been you biggest side effects?

Hope you guys are well! I would like to find out if anyone has had any side effects when taking aubagio … or has their MS progressed? I have not started my treatment as yet but Aubagio is the planned treatment for me. I am a bit worried as the only real symptom of ever had of MS is my optic neuritis...

Hi All I was diagnosed about 7 years ago and have been using Avonex since, but am now considering a change to either Tecfidera or Aubagio. Is there anyone out there who has made a similar switch? I currently experience flu like symptoms the day after my injection and have noticed an increase in peri...

This isn't a good or bad thing but is interesting if you are on Aubagio (terifluonimide) or are considering it. https://multiple-sclerosis-research.org/2022/07/does-teriflunomide-as-a-dmt-warrant-discussion/

Hi everyone! Haven’t been here for a while. A lot of things have happened since my last post here. The war started and my family had to flee from the southern part of Ukraine. Women and kinds had a chance to be here with me in Finland for a while. I’ve had so much stress over the last couple of mont...

Please could people who currently take Aubagio - share their experiences with me? I had my first batch delivered today and the 'Common' side effects have made me VERY nervous! Thanks!

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...

Does anyone have positive experiences of Aubagio? I've been offered it for my latest DMT. I was previously taking Copaxone but had to stop due to lipoatrophy. I then went on to Tecfidera but had to stop as I was vomiting more or less every day and this was after several weeks and only on the low dos...

I injected myself for 14 years with Rebif and have finally been able to switch to Aubagio tablets..... what a pleasure! Anyone wondering about switching/possible side effects - I am happy to share!

I am starting on Aubagio tomorrow and wanted to ask peoples experience? I took Avonex for 10 years, ( luckily no progression? Just hated injecting myself so am giving Aubagio a go. My main concern is the hair loss, how thin does it get, I'm 40 and proud to have thick hair, sorry if that sounds vain.

Hi. I have done nearly 2 weeks on aubagio. I stated with stomach ache, then back ache, by day 4 I was hit with really bad vertigo, room spinning, puking every time I moved. Phoned Ms nurse who advised me to continue. However I am now totally disorientated, off balance, right arm and leg feel numb an...