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Good morning MS community 🤗. I was diagnosed in July with relapsing ms and have had it for four years before diagnosis. I am due to start my injections once the nurse has visited to show me correctly how to do the injection. I had worries about medication (family all have died of liver cancer or p...

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 was diagnosed on January 6, 2020. I have a heavy disease burden with almost all of my lesions in my brain. I started taking Tecfidera shortly after. Every MRI I have had except one showed new brain lesions. So now I'm on Ocrevus. My memory has progressively become worse. I forget words, names, an...

Hi everyone. I have RRMS but I believe I might be progressing to different type. This disease can be so frustrating at times. I can't get an appointment with my neuro until next month and my symptoms are increasing. I don't currently take a DMT - I had a bad reaction to Copaxone and haven't wanted ...

Trigger warning ⚠️ Abuse. Me and my partner have been together 13 years, I'm 28. My oldest son is 12 (biologically not his) and we have a 2 year old together and I've also just fount out I'm pregnant now! 😥 I'm waiting on a diagnosis for MS My partner is extremely cruel to my children and I, he...

im 35 and had pretty stable MS since I started Ocrevus in 2018 now thinking about getting pregnant. Does this sound like a good idea I know there is a possibility of relapsing after having the baby I want to hear experiences from women that had their children already diagnosed with MS

Unfortunately I am having my first relapse in 2.5 years and I am still on tysabri (going into ocrevus in a few weeks) I feel angry as I was kind of in denial as everything was going to so great. My father passed away in May and I thought since I didn’t have a relapse then I’d be safe but here it is...

Hi everyone I’m Callum and I’m new to this site. My MS nurse advised me to join. I was diagnosed with MS last year and I thought I had processed the diagnosis well but it turns out I haven’t. I’ve developed a lot of fears about life and body functions and it’s effecting my daily life. My partner i...

I am still trying to get used to this site, so if I don't respond to you then I apologise in advance. Getting up this morning, making sure my son is up and ready for school, do other things like a bit of washing, tidying and things I can try an get done whilst husband is at work. Sometimes I feel...

Hey all, I'm fairly newly diagnosed (May 2023 I think), I started a new job a few weeks ago and I didn't tick the disabled box on my application for a few reasons: 1. I wanted to get the job on my own merit. 2. I didn't have many symptoms and was hoping it would stay that way for a while. However,...