About the Relapsing Remitting MS category

Relapsing Remitting MS
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Meet others living with relapsing remitting MS. Share your experiences, get tips and speak to other people who understand.

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So, this is where all the cool kids hang out eh? :rofl:

I don’t really know much about this MS malarkey yet but, I suppose experience will build knowledge for me over time.

I know that I had quite a kick in 2023/24 and, they told me it was RRMS in March this year - no good boy sticker, no lolly pop, just a letter from my nice consultant. I do have changes that are here to stay - some can be quite comical at times the rest not so much.

I wouldn’t even know how to identify a relapse if it does happen :roll_eyes: I suppose I’ll figure that out over time aswell.

For now, I just try to keep active, not let boredom creep in and, see the funny stuff in life wherever I can. It works for me :+1:

Take care all x

Jon.

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Hi @jthatcher welcome in, lovely to meet you :waving_hand:

I can speak from experience having been diagnosed in 2021 myself. Over time you’ll build the knowledge and what a relapse looks like for you. But lean on the people here when you need to. They’re a super bunch.
We also have our wonderful team who work on the MS Help Hub and can be contacted on **0808 800 8000.
**
More detail about how we can support you can also be found here: MS Help | MS Society

Do take care of yourself and keep in touch with everyone here too.

Clare (MSS)

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I was diagnosed with RRMS about a year ago, hoping to connect with others!

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Hi @desdemonaduck :waving_hand:

Welcome aboard. I was also diagnosed with RRMS - about 5 months ago for me.You’ve joined a good forum with loads of good members​:+1:

There’s sub forums on here to chat about anything you’d like to. do, have a browse around and get stuck in mate :slightly_smiling_face:.

Jon.

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Hi everyone

My daughter, who is 36, was diagnosed with MS about 9 months ago. She already has a genetic condition and learning difficulties, and navigating this new world has been quite hard to say the least! If there are any other families/carers in a similar situation to ours it would be lovely to connect with them.

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Hi guys

My girlfriend who is 23 has RRMS. I would love to connect with people to see if anything I can do or be doing better to help her. Because at times I am lost in what I can do for her and also see what we can do together as a community no matter if it’s a big or small impact.

I was looking into a fundraiser or charity even to partake in soon if anyone has any information would really appreciate it.

Thanks for reading.

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I am 56 y.o. Diagnosed 6 years ago.I am ready to share any experience you would need or would like to ask, please donot hesitate.

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