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I was diagnosed with Relapsing Remitting MS in 2004. I am only taking Betmiga for my bladder control. I suffer with foot drop, poor balance, terrible fatigue, memory problems, vision issues, cognitive problems, dizziness. I feel like I have been forgotten! I’m due to see the MS nurse in April, so...

I am 42 and just been diagnosed with relapsing remitting,I am awaiting my meds to start with the injections,my main symptoms are balance and mobility abit of confusion and bad memory,I have 2 kids 6 and 3,I am having alot of mum guilt at moment as I can't do outdoor things with the kids,I at least n...

I've had ms for 18 yrs now got diagnosed when I was 27 im on tysabri excellent med I haven't had a relapse for about 10 yrs since I started it but if anyone has any questions I will trt and help I walk still just can't walk for long distance like walmart for that I use my manual wheelchair I'm prett...

I am a 25 year old man from Ireland. I was diagnosed with Relapsing Remitting MS in September 2015. I have been six treatments to choose from 1) Tecfidera 2) Plegridy 3) Avonex 4) Rebif 5)Copaxone 6) Betaferon. If anybody is on any of these and has any advice or recommendations I would be delighted ...

Hi all, We've got Prof Alan Thompson from the Institute of Neurology in London lined up to respond to your questions about the transition from Relapsing Remitting MS to Secondary Progressive MS. Professor Thompson is a world leader when it comes to progressive MS and this is your chance to ask...

I’m having difficulty with my fatigue I was on provigal and know I’m on Ritalin. I’m going to be trying a time release Ritalin. Ugh. I want aderall. I have done my research. I’m terribly frustrated . I live in Erie Pennsylvania.

Good morning, I´m from Argentina and I have relapsing remitting MS since 2010 aprox. My employee has offered a job in the UK to start in February and they are requesting a Tier 2 Visa for me and my wife, we need to pay for the Healthcare Surcharge. Right now I´m taking Gilenya Fingolimod 0,5mg; do y...

Anyone have experience taking modafinil?

Temporary memory loss is common for me. I try to stay positive​. As a great post once said; Never admit to having an illness. Unfortunately the lack of admission only works when you feel good.

I was only recently diagnosed with MS and found to have this form, and must admit that I'm finding it hard to come to terms with. Does anyone know of any counselling support through the NHS that can help with this? e.g. MS nurses etc?

Hi all I’m new to the site but not new to MS I’ve had it for over 25 years Initially relapsing remitting but now chronic progressive, or like my neurologist diagnosed me relapsing progressive because even though chronic progressive was my dx I’ve had a few relapses which were treated with massive s...

Has anyone else experienced severe abdominal pain requiring you to go to hospital? I’ve had a lot of tests and even surgery to find out the problem but nothing is coming back. I was just wondering has anyone else ever experienced this type of issue: severe bloating, inability to eat, nausea, vomitin...

Hello, I’m new here, I’m 38 and I’m in the uk. I’ve been diagnosed for about 5 years with relapsing remitting. I generally get EVERY side effect (for example Tecfidera caused me to lose 2 stone) After my MRI at Christmas my neurologist described me as ‘moderately severe’ and after that things have...

Hi everyone👋🏻 I’m new in this community, but I felt an imminent need to share my ms story with other people. I was diagnosed with a relapsing-remitting ms at the age 19. But I had first symptoms a long time ago. My name is Elisa, I’m Italian and I study primary education sciences at university. My...

i only share with you the only thing i can do since i was diagnosed to depict the shock & the happiness i live in. by the day tomorrow i was diagnosed with MS. *open this in a code writter app

Hi MSers, Hope you are well. In the UK MS is a disability by law. Such as certain cancers and HIV, if you didn't know we are protected by the Equality Act. I have relapsing-remitting multiple sclerosis and I am not in a wheel chair. However, I have difficulties walking but you won't really notic...

Has anyone got any experience of this drug? My neurologist wants to switch from Ocrevus to this drug Mayzent as she thinks I have secondary progressive rather than relapsing remitting? Thanks Nathalie

Hi guys. Hoping you could share some of your advice on treatments and what has worked well for you ? What side affects, issues, you have form treatments etc. I have been diagnosed with relapsing remitting September last year and have appointment end of this month to discuss treatment. Any advice ...

I was diagnosed with relapsing remitting MS 1,5 year ago. The hypothesis of my neurologist was that i had it for at least 10 years before the diagnose because of the numbness, tingling and other symptoms that i was experiencing. They never were severe until 1,5 year ago (when we finally found out th...

Hi to all I am new in here. I have Relapsing remitting Multiple Sclerosis, on Tysabri infusion once a month in Stoke Hospital. Was diagnosed in 2019 I was married at that time but have since separated last year 2021. Quick questions how do people find relationships or is there anyone out there that...