Sort 2952 results by

Page 2


Last reply


Hi my name is Anne and I have relapsing remitting MS for 23 years.

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.


Last reply


Relapsing remitting MS (Tier 2 Visa)

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...


Last reply


25 Perth, relapsing remitting.

Anyone have experience taking modafinil?


Last reply


Relapsing, Remitting

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.


Last reply



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?


Last reply


First Post Here….

Hello all, My names Ryan. First post here. Hope you are all enjoying life as much as possible! I was diagnosed with Relapsing-Remitting this November. At the same time as this I had just started a new job, and moved house, so plenty of stress that has increased symptoms a bit. Now I know I have...


Last reply


First time post.

Hi everyone, First time poster. In late 2021 I was diagnosed with Relapsing Remitting Multiple Sclerosis. This is a very new diagnosis for me, and I’m learning every day. I learned is that connecting with people in the MS community is a powerful thing and I’ve decided to get out of my comfort zone ...


Last reply


Starting New Treatment

Hi my name is Lara and I am due to start new treatment tomorrow-Kesempta, for my relapsing remitting MS. Just wanted to know what side effects people may of had with it when they first started it as I was informed by my MS nurse that it may feel like I have the flu and just wondered how others that ...


Last reply


NHS Referral - wait time?

I was diagnosed with Rapidly evolving severe relapsing-remitting MS in September 2023. I am waiting my NHS referral appointment to discuss having the ocrelizumab infusion although on the urgent referral list, is there anyone else who has gone through the NHS and the processes that come with it?

Recently Diagnosed

Hello all I was recently diagnosed with relapsing/remitting MS on 12/11 and I am taking it one day at a time. After the MRIs and lumbar punctures my neurologist told me they caught it early and only a few lessions were spotted in my spine and brain. I have been on starter pack of Dimethyl Fumarate. ...