Looking for
something specific?

Hello, Today I received my first appointment with the neurologist in finding out what has been going on for me recently. I had no expectation of when I would receive this, and fully expected to be waiting a while before I would hear anything. However, now that I know the date, I feel incredibly an...

I used to be really active pre diagnosis, with lots of Bikram yoga, hiking and running. Due to life these have all gone by the wayside for nearly a year and a half now. I want to get back into running, with some complimentary strength building on the side, but I'm worried about having lack of motiva...

Hello all, I know that talking about long term prognosis with ms is like asking how long a piece of string is, but I'm going to try and pick your collective brains anyway! I was diagnosed at 16 years old (rrns) and my ms probably started when I was 14 or so. I am 39 next month and although my ms i...

I started a new job a few weeks ago, I didnt tell anyone I had MS but today many people were off and I was alone with another coworkers. At the end of the day we started chatting and she mentionned she needed a steady job because of her illness and treatment, of course I asked what illness she had.....

Heya, I was wondering if anything be else had been diagnosed with MS and just felt alright? I've had a few relapses but, touch wood, nothing to write home about. I see an awful lot of people here that seem to be having such a rubbish time with everything, and I feel for them, it's just that, I don't...

Hi team, I hope everyone is well today! 🤞🏻 I'm so excited and just had to share; I've just finished the 4 week trial of Fampyra and had my assessed walk earlier. I HALVED the time it took me to walk 25ft in the initial assessment, and haven't stopped crying since! 😭🤣 I really needed this toda...

Hello, I have ms and under treatment with ocrevus. I’ve just got a question. I was abroad recently on summer holiday and caught a cold. I had a fever was doing really poorly for two days and then started becoming better. However my horrible cough has stayed and I’m constantly brining up phlegm. The ...

This article appearing in MS News Today, it hit a bit chord in me because I'm a great "What if" person. Take a look: https://multiplesclerosisnewstoday.com/columns/chairborne-a-column-by-ben-hofmeister/2024/09/12/what-if-i-ask-too-many-questions-about-multiple-sclerosis/?utm_source=MS&utm_campaign=...

Is anyone else having a really hard time with trying to do better health wise. After my diagnosis of RRMS I got so depressed. It seems like I cannot find even an ounce of motivation to get me to eat better or exercise. I just don’t even understand. With everything else I have to deal with, kids, inj...

I was diagnosed in June with RRMS after starting symptoms in Sept 2022. I'm trying to come to terms with my new normal. I'm struggling to return to work after being off since April. Today I went on site and trying to be mindful to not push it I used a mobility scooter for an outdoors meeting (the si...