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So am divorced from my ex, which is fine! But now he has taken our children, 2 boys, off me because apparently I am an unfit mother! Yes, I have m.s, yes I like an alcoholic beverage occasionally but HE has dictated to all, that disabled people shouldn't drink! Aaarrrggghhh! Court case online on tue...

A meeting will be held at the Holiday Inn Bromsgrove B61 9AB hopefully this will go ahead and any spike in this virus will not affect us like before Any MSer is welcome as the last one was informative and fun it will start at 12 but your welcome to come early. Also take a read of my recently posted ...

Hey guys I’m in need of urgent help! I’ve had extreme bloating and abdominal discomfort for as long as I can remember ! The doctors have ran all the tests and don’t know what’s wrong :( I was wondering if anyone follows a certain diet that might help with this because I have a feeling it’s connected...

I’ve just started Copaxone and did my first injection with the MS Nurse a few days ago. I just wanted to share some of the advice she gave me in case it’s of use to anyone else, as some of it I hadn’t seen mentioned before. Firstly, she said she doesn’t like the CSYNC autoinjector because it leave...

Please VOTE for Shift.ms to win ➡️ https://buff.ly/2CcRgUc ⬅️ 'Best non-fiction' at Webfest Berlin. The 'Animated Symptoms' series has been nominated - a series that shows real stories & experiences told by people living with symptoms of MS. You can watch it here: https://www.youtube.com/playli...

Hi! I’m Jenny-May,I’m 21 and I’ve recently been diagnosed with relapsing remitting MS. I’ve been advised to join because I’m quite ‘lonely’ as my therapist says 🤦🏼

After nearly 3 years of searching for answers to my wife's rapid cognitive decline, multiple tests and MRIs and second opinions it is clear she has a the syndrome of Dementia. Our local neurologist as well as the team at UCLA agree that the cause is MS. Images show significant brain atrophy. I ...

Does anyone else get the terrible MS related toe pain ? Omg it is awful 😔

I was diagnosed with RRMS last week. The neuro gave me some options in regards to treatment; I'm to take a week to educate myself and hopefully come to a decision. Tomorrow will be one week. I'm leaning towards Tecfidera, but I'm absolutely terrified. I'm terrified about all of this, but in regards ...

I'm going to be on ocrevus in a few weeks, what are the best options for treatment so far?