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Hope everyone is well, I’m new to the app, I was diagnosed RRMS in 2004 been on DMDs ever since, rebif for 20yrs recently changed to Avonex 👋👋

I've been diagnosed with RRMS in 2020 and started Tysabri in 2021, everything went and is great, no relapses since but I just cannot stop thinking about Tysabri's side effects and what bad things does to my body. I wasn't sure I wanted to go with it in the first place and I'm stressed and frustrated...

Hey all, Wanted to get a perspective from everyone on how I can better support my spouse. My spouse was recently diagnosed with RRMS and began their infusions right away. So far, they have minimal lesions. However, morning depression and they feel they have lost in life has taken a burden. I liste...

I was diagnosed with RRMS in 2022. It’s been a journey in trying to educate myself and people close to me about MS. I wrote a blog post last week that friends tell me gave them a better insight into and understanding of MS. This isn’t a sales pitch, I understand hypnotherapy isn’t for everyone. Bu...

I’m new to the site. my name is Kimberley and I'm 41. CIS in 2001, diagnosed RRMS in 2018. I'm from the city of Nottingham and I don't get out enough. I wish I could drive. I also have ADHD and I'm autistic. I sometimes make wigs for fun. I have a little lovely cat but otherwise live alone. I'm life...

I had my annual check up with my consultant 2 hours ago at RUH Bath. Here is a brain dump of our discussion, while it's fresh in my mind, in case it helps anyone else with RRMS/SPMS who takes a T Cell based DMD: - Lymp count was 1.3 and right where they want it. - The very slow annual increase in...

I am originally from Alaska but moved to California and i was diagnosed with RRMS just after my son was born in 2023 found out that it was already progressed to what would normally be found in a 50 to 60 year-old and I am only 25. They said I had had it for a long time. I was also diagnosed with sev...

Hi, so a bit of background, I have RRMS, it’s been stable for a number of years (I think my last relapse was 2017). I went for my yearly brain and spine MRI recently and have just had a call from my MS nurse saying that something got flagged on my scan and so they are asking a neuro-radiographer to ...

Hi everyone, long time MSer, 1st time poster. Here's my story. In January I transitioned from RRMS to SPMS. It sent me into shock. For a time I was inconsolable. However after a period of grieving, I picked myself up and got to work. I cut dairy, gluten, eggs, most carbs, refined sugars and nightsh...

Hi all, this is my first post on here. Got diagnosed with rrms coming up 3 years ago. Wondering what kind of diets people are doing and how effective it is with ms symptoms. I’m not looking to lose any weight, was on a mainly sea food and veggie diet but thinking a steak now and again can’t hurt?