# About the Relapsing Remitting MS category **URL:** \ **Category:** Relapsing Remitting MS\ **Created:** [19 August 2026 14:27 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628 "2026-08-19T14:27:31Z")\ **Posts on this page:** 8\ **Page:** 1
**Author:** ![ClareMSS](https://dub1.discourse-cdn.com/mssociety/user_avatar/forum.mssociety.org.uk/claremss/32/8661_2.png) [@ClareMSS](https://forum.mssociety.org.uk/u/ClareMSS)\ **Post date:** [19 August 2026 14:27 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/1 "2026-08-19T14:27:31Z")
Meet others living with relapsing remitting MS. Share your experiences, get tips and speak to other people who understand. ---
**Author:** ![jthatcher](https://avatars.discourse-cdn.com/v4/letter/j/46a35a/32.png) [@jthatcher](https://forum.mssociety.org.uk/u/jthatcher)\ **Post date:** [21 August 2026 14:45 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/2 "2026-08-21T14:45:26Z")
So, this is where all the cool kids hang out eh? 🤣 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 🙄 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 👍 Take care all x Jon. ---
**Author:** ![ClareMSS](https://dub1.discourse-cdn.com/mssociety/user_avatar/forum.mssociety.org.uk/claremss/32/8661_2.png) [@ClareMSS](https://forum.mssociety.org.uk/u/ClareMSS)\ **Post date:** [24 August 2026 14:03 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/3 "2026-08-24T14:03:58Z")
Hi @jthatcher welcome in, lovely to meet you 👋 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](https://08088008000/ "Opens in a new window"). \*\* More detail about how we can support you can also be found here: [MS Help | MS Society](https://www.mssociety.org.uk/support-and-community/ms-help-support-services) Do take care of yourself and keep in touch with everyone here too. Clare (MSS) ---
**Author:** ![desdemonaduck](https://avatars.discourse-cdn.com/v4/letter/d/bcef8e/32.png) [@desdemonaduck](https://forum.mssociety.org.uk/u/desdemonaduck)\ **Post date:** [31 August 2026 18:04 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/4 "2026-08-31T18:04:57Z")
I was diagnosed with RRMS about a year ago, hoping to connect with others! ---
**Author:** ![jthatcher](https://avatars.discourse-cdn.com/v4/letter/j/46a35a/32.png) [@jthatcher](https://forum.mssociety.org.uk/u/jthatcher)\ **Post date:** [31 August 2026 18:32 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/5 "2026-08-31T18:32:39Z")
Hi @desdemonaduck 👋 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​👍 There’s sub forums on here to chat about anything you’d like to. do, have a browse around and get stuck in mate 🙂. Jon. ---
**Author:** ![REB](https://avatars.discourse-cdn.com/v4/letter/r/51bf81/32.png) [@REB](https://forum.mssociety.org.uk/u/REB)\ **Post date:** [22 September 2026 08:02 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/6 "2026-09-22T08:02:43Z")
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. ---
**Author:** ![sanchezveron26](https://avatars.discourse-cdn.com/v4/letter/s/e9c0ed/32.png) [@sanchezveron26](https://forum.mssociety.org.uk/u/sanchezveron26)\ **Post date:** [28 September 2026 10:16 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/7 "2026-09-28T10:16:29Z")
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. ---
**Author:** ![imgrbag](https://avatars.discourse-cdn.com/v4/letter/i/53a042/32.png) [@imgrbag](https://forum.mssociety.org.uk/u/imgrbag)\ **Post date:** [28 September 2026 10:16 UTC](https://forum.mssociety.org.uk/t/about-the-relapsing-remitting-ms-category/81628/8 "2026-09-28T10:16:36Z")
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.