Looking for
something specific?

Updates and in case you didnt know... Cladribine - https://msra.org.au/news/relapsing-ms-treatment-cladribine-comeback/ It is an oral medication that selectively targets immune cells called lymphocytes. These immune cells are a type of white blood cell that are believed to play a central role in MS...

Hi I know I have posted about this before but it crosses my mind many a time, and with the CCSVI it would make sense for us all to eat lots of garlic to thin the blood in our jugulars so we encourage good blood supply in our hands and toes, I really suffer from this (raynauds) I have no problem eati...

Hi, this has crossed my mind many a time, and with the CCSVI it would make sense for us all to eat lots of garlic to thin the blood in our jugulars so we encourage good blood supply in our hands and toes, I really suffer from this (raynauds) I have no problem eating lots of garlic but it is usually ...

Hey there, I just joined shift.ms today and I hope it's okay to ask that question here and that maybe some of you can help me with this question. Btw sorry if I make too many mistakes in English; it's not my mother tongue. My question is: I have been diagnosed with RRMS in 2015/6 and only had some...

So I'm having to change from vumerity to the above medication as it made me flush so badly. Just wondered what side affects people had with this.imnonly diagnosed since March wasn't on vumerity long.

Im being admitted in the hospital again for the 2nd time in 5 weeks. Im having a really bad flare that my body is having a really hard time recovering from ive had m.s fot 10 years but have never had a flare quite this bad. My symptoms are as bad as they've ever been and i dont seem to be bouncing ...

Most of the time I just wanna give up on life but I am not one to take the easy way out. I will become a great environmental graphic designer in an amazing architectural firm and have a successful business in my spare time. Dreams can come true and I will pave my own way. Getting braces and underbit...

So can I share this..I'm not sure, but I'll give it a try For the last few months I have been attending or failing to attend a monthly group meet up at a pub in Walsall. As the group I used to attend near Wolverhampton is no longer running, this is a welcome relief. Just to have a chat face to face...

Hello! I'm cynthia I'm new to ms. I have the rrms. I am 34 and I'm learning to navigate through this.'im in the hospital for 2nd relapse in less than 6 months. I having bad vision. Any encouragement advice would be helpful in this time that I am uncertain and have to work and want to have a family a...