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Life swallows you up and you forget you're seriously ill until you have another relapse. I have to laugh otherwise I'll cry. Luckily, it's nowhere near as severe as my last just incredibly uncomfortable and is making work and study difficult. I'm also going to be starting my DMDs soon, I'm going to ...

I applied for PIP in November. I went for an assessment in January and failed to qualify - scoring 2 0's. I reapplied (sorry can't think of the proper word :D) after failing and someone from the DWP called me on Monday and spent 25 minutes on the phone with me going through how MS affects my day t...

Hi all! Can anyone share how life is after having the immune system prevented from working as effective as it should be? Do you get lots of colds or infections? I’m thinking to start either Ocrevus or kesimpta (there are pretty much the same really). I work as a primary school teacher and I’m a bit ...

This is just a little rant... PIP. What a waste of time! My decision letter arrived and the report wasn't even close to what I wrote and spoke about in the assessment. It doesn't even reflect the letter I sent in supporting evidence from my neurologist. It's left me feeling like I've been complete...

Have you ever felt like you've backed your self into a corner with no way out? I've been officially told I'm now spms...no great shock I have been for years but neuro always told me I was rrms so I could still have DMT (tec). I've been NEDA since I started, now that mayzent has been approved he wan...

I have just had to accept that I need to give up a well paid job that I loved because of the impact of ms on my cognitive ability. 23 years of working soo hard and it comes to this. Perhaps it’s the new start I need.

I had physio today hard work but worth it I'm sure I always think it's best to push for excellence but stop when you get tired!😁

Saying hello, first time on Shift. Took me 6 months to be diagnosed after years of symptoms and a bit of medical gaslighting thrown in. I've been on Copaxone, Gilenya and currently on Tysabri. Having a difficult time the last couple of months in work with my boss, which is not helping my fatigue or ...

The CBT practice variant which interest me the most is mindfulness-based cognitive therapy (MBCT). Why? Because I know from personal experience that it works. In our first course we were tasked with developing a safe and effective use of self (SASE) program and I chose to research mindfulness-based ...

yesterday at work we had a contractor in doing maintenance (I work in a cafeteria style kitchen for the military). Being in limbo I have no cause for why I'm struggling to walk and just carry on as best as I can. My co-workers and management are supportive and understanding (thankfully no longer pan...

Hello, My name is Dennis and I have RRMS since 2004. I have used some medication untill now Started with monthly Tysabri infusions for several years until I had JC in my system and switched to the oral Fingolimod medication. I did everything again with the Fingolimod, sport, long walks etc. After...

I had a really bad day yesterday with fatigue and brain fog. Everything was a battle, but I still had to go to work and just get through it somehow. I got home, my husband asked how my day was and I told him how I had really struggled. He said "oh I get that too sometimes". Like...no. I love my ...

Hi, Can anyone suggest how to tackle information retention and memory issue in MS? I have difficulty understanding and retaining information at work. I cannot write down everything.

I recently got distracted this past December. After dealing with symptoms...speech issues...feeling my head tense up/roller coaster...using a walker. And now I went from being a school manager to being a stay st home mom (1 and 4) now I'm considered legally blind and just feel so stuck. Don't get m...

I've been on Tysabri for 6 months and my MRI results came back looking good. I have been feeling unwell for 2 days and this makes me spiral down into dark thoughts and what ifs🥺 does it usually work for a long time?!

Shortly after my diagnosis, I had to make a decision, whether or not I wanted to continue, try working, or apply for disability and see what happened. I made the decision to continue working, it was extremely hard, trying to do jobs as a disabled man. Constantly trying to figure out creative ways to...

Shortly after my diagnosis, I had to make a decision, whether or not I wanted to continue, try working, or apply for disability and see what happened. I made the decision to continue working, it was extremely hard, trying to do jobs as a disabled man. Constantly trying to figure out creative ways to...

So a lot of us have bladder issues, and there's plenty of advice on how to help (more water, plan ahead, etc) , but sometimes you just need to go and there's no planning to stop it. My question to you all is what do you do for events like weddings, funerals, school meetings, etc? In general I tr...

Hi, I have not visited Shift for a few years now, like another member said 'trying' to get on and lead a normal life without my head being consumed with MSsy things! I had HSCT at Kings College Hospital transplant date 14th Feb 2018, Ive two birthdays like the Queen only I wish I could walk as well ...

How is everyone getting on with manual jobs. I am a roofer just looking to hear how different people cope with work.