Looking for
something specific?

I started Lemtrada June of 2018, completed May of 2019. It wasn’t an easy treatment. Ms for me began in 1995 (17 years old). Around 29 years of interferons…betaseron and then avonex. Then I stopped dmt’s and tried just diet…..bad idea.🤦🏼‍♂️. With my ms progressing and shouldering from RRMS to ...

Hi fellow MSers, I’m Anna, I’m a 28 yo from Italy but have been living in London for the last 6ish years. My story with ms is pretty new. In early June I woke up with all the right side affected by a sensation of numbness and tingling. After a couple of trips to the ER (where they told me I was st...

I have bought a bottle of fizzy orange pop, locally made mallorquin in a glass bottle (return the bottles to the shop and get 30 cents off the next bottle) with a plastic top. I can't get the top off, every time I open the fridge there it is laughing at me. Even my opener thingy won't make the top b...

Just wanted to share some good news. Lord knows we all could use it. I just had my 6 month MRI results after being on kesimpta come back and evidently my lesion number has gone from 7 to 3??? I'm a little bit blown away. My doctor wasn't 100% clear about what that means for me but it's got to be goo...

Hi all, I've been around for a while now. Dx 2009 if you can believe it. There's useful information in my old posts. Should be reasonably easy to find. I remember Prague in 2016. That was great fun. And then Bucharest in 2019. George might remember all those little bottles of Palinka. Fun times. ...

Does anyone take this as a supplement? I was in the health food store purchasing my vitamin d and omegas when the person helping me said that people with MS had been purchasing this recently. Very curious to know if anyone has been using this or finding it helpful.

Can anyone help with a definitive answer about whether ppms should or shouldn't take a vit c supplement? There's so much conflicting advice! I've read that it can trigger symptoms due to boosting the immune system, but when I recently started ocrevus lots of people were recommended it to prevent inf...

Hi all, hope you are all doing as well as you can be... I just wanted to say that my MS nurse referred me to a neuropsychologist, locally- I was waiting for about 7 months on NHS, and i saw him for my first session yesterday. I really didn't think that after 7 years of being diagnised that there was...

What are people’s thoughts about how the food you eat affects your ms? I have spms after RR diagnosed 2009. I have always til now been very active but now I am not. I sometimes try to go on strict diet’s cutting out processed food dairy and meat etc but I love all those things and there’s not much...

I hate my body, I hate this Constant fatigue. I hate being F A T dieting doesn't work for me. One more thing I hate complaining because there is a lot worse going on this world! Ms really suckssss! Rant over 😡😭 I feel angry and sad and incredibly lonely