#thisisms - Shift.ms

13 Jan 2020 09:30

FYI

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...

@loulou

15 Aug 2012 15:15Last reply 15 Aug 2012 17:40

Garlic

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...

@loulou

15 May 2012 08:36Last reply 15 May 2012 13:25

Should we all eat lots of Garlic???

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 ...

Deleted

@Charlotte85

25 Aug 2025 15:47Last reply 26 Aug 2025 16:35

Hi everyone. I have totally neglected myself and my life really including my MS with how utterly rubbish it all is for me atm. Im trying so hard to work out my marriage and its just too hard. I have noone to talk to as I dont want ppl I know finding out. Me n my kids aren't homeless anymore...we have a home now. But I am really really becoming depressed and having such bad thoughts. I want my husband so much as I love him but he isn't even a nice person 80% of the time. I dont even no why im putting this...im just needing to talk or It will end up killing me. Ive had 2 small flare ups since June because of all this. I live with 3hours sleep and constantly throwing up from stress and pain more than normal. I just dont know what to do anymore. Im a mum to an autistic 15yr old in yr 11 and a 4yr old starting school. I have almost nothing left in me. I dont know how to either work the marriage out or walk away...I need peace and I wont ever have it with him but it felt like it was worth it but now I dont know if it is. Sorry im just so upset xx

First posted on the Shift.ms app

@mumof6

27 Aug 2025 13:51Last reply 27 Aug 2025 14:37

Teriflunomide (Aubagio

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.

First posted on the Shift.ms app

@H4ndsomeHaz3

26 Feb 2025 18:19Last reply 26 Feb 2025 23:20

2nd time in 5 weeks

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 ...

First posted on the Shift.ms app

@kzohina

2 Jul 2023 02:57Last reply 2 Jul 2023 15:56

Invisible

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...

League City, United States

@Haynesy

28 Feb 2023 10:43

Walsall MS meet up tonight

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...

@crussell

1 Dec 2019 15:41Last reply 2 Dec 2019 16:49

New to ms

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...

@greasycanadian

24 Jan 2019 16:38Last reply 10 Apr 2019 17:47

Ocrevus

I have been taking this IV chemo drug for almost a year now, and have had styes, acne and a wicked rash on my belly. Given the side effects from the other medication I have tried, I have been putting up with these, but no Dr. believes me when I say that they are a side effect of Ocrevus..."Oh, you m...

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