Hey All, I’ve been diagnosed with Ms within the last couple of weeks. Today was my DMT appointment, my MS nurse and I have narrowed treatment down to either Tecfidera or Aubagio. I see from older posts that some people have experienced hot flushes as a side effect of the drugs so I wondered …

Hi, I’m new to shift ms and just wanted to share my experience after completing my course of Lemtrada. As Lemtrada is the leukaemia chemotherapy drug, it was quite scary to think I was putting Chemotherapy into my body to destroy the T and B cells that are responsible for giving MS. After about…

Hi everyone, Thank you for the lovely and useful comments you left on my post two months ago (“Newly diagnosed teacher”). I apologise for not responding – I wasn’t sure if there was a function for directly replying to comments – and I was also busy with many things, including mov…

Hiya, I’m moving to the Netherlands from the UK for a year pretty soon, which as you can imagine, is a clusterf*ck from a medication point of view. My neurologist recommended I stay registered as a patient in the UK, and keep getting my Tec from the company in the UK, with my family here shi…

Hi all, Following on from my new lesion, I’ve decided to try gilenya. I’ve been off tecfodera for four days now and I feel really sick. Has anyone else come off Tecfidera? If so, did you have any side effects like nausea or headaches?

Hi, I was recently diagnosed with relapsing MS. My main symptom is dizziness. I am looking for anyone who also suffers form dizziness and can give me any suggestions on how to avoid it. I had a flare up this week. I was in bed all week long and couldn’t even move my head. I started Tecfidera…