15-Year Journey: My Life with Multiple Sclerosis 

Thank you so much for your sharing. It means so much to me. I have Ms and just diagnosed 2023. Thank you so much.

Good to hear your update. I had a MRI again after 12 years and had no new lesions, old ones hadn't changed, normal brain volume loss for my age, 66. Still have it though. No real flare ups just gradual slowing of abilities, could just be getting older.. I don't take any MS meds, just for symptoms like spasms. Haven't been able to walk for about 18 years now and found life is more than walking. Life is so good.

That's great!! MS strong 💪🏼 🧡🧡🧡🧡🧡🧡🧡🧡🧡🧡

thank you for sharing your realistic and lived experience. i am 'newly diagnosed' 2.5 years ago. as a lady who was diagnosed 25 years ago said to me "there is life after MS" 💪🙌💓

I love when people say you "don't" look like you have MS...what does MS look like is my response. It's an invisible illness till it's not.

This was such a positive video, you have such a lovely mindset! I got diagnosed almost 2 years ago now (I'm also sharing my story on Kesimpta on my channel). Thank you for being such a positive light, I think keeping track of your MS over the years is really beneficial, especially going from 20 to 8 lesions - that's such a good motivator to keep going!! xxx

I'm glad the results were positive.👌

Keep up the positive attitude Laura, we need it 💪

You’re a bright light in this ms world Laura. Very happy for you about the mri results. I totally understand not wanting to have anymore!

Brilliant news Laura! I think we all have our own journey and you must do what's best for you. I am the same with my MS its part of me now but I cannot make it the foxus of my life. Luckily, I dont have to. 2 years in after originally being diagnosed with TM, was told it's 'MS... albeit at the benign end of the scale'. So onwards and forwards. Your videos have been very helpful. Thank you for all you do!

🧡 💪🏼🎗️ you are an amazing MS warrior, you continue to be a positive light through this journey MS places on. Thank you for sharing your journey and providing helpful tips. sending ❤ 💫🕊️ ❤️‍🩹 healing energy, love, strength and light.

HELLO BEAUTIFUL!!! I'm so glad to hear the great news regarding your last MRI. I totally understand you about future MRI, especially after 15years. My last visit with my neurologist a couple months ago I was told that because evey MRI I had since 2020 has been stable with some lesions slightly diminishing, that I would only need get one MRI a year instead of two. For a while I was thinking that they were trying to permanently turn me in to a glowing magnet.😂 I'm still going to continue with the Ocrevus treatments every 6 months for the time being, on my next visit with my neurologist Im going to ask her what she thinks about me ditching the Baclofen that I'm taking 3x a day just to see how I get on without it. I'm reminded pretty much ever day that I have MS and that I'll aways have MS but as you said, "It is what it is." So lets just live our best life possible. Thanks again Laura for your videos. For what it worth they helped me get passed a couple of rough years after my official diagnosis.🙏 STAY GORGEOUS!!! 😘

I finally watched the video...8 lesions from 20...that's a really great result. That would seem to show the treatment has worked fairly well. I have had ms for 39 years plus...have never had it treated and an MRI from a few months ago (4th) is showing no lesions on my spine...mild brain atrophy, and several multi centimeter lesions on parts of the brain and moderate demylination of the optic nerve. Code is G35. So who wins? Hard to say...I guess it depends on how you look at it. Hey...have you ever considered resetting your immune system? Pain in the butt apparently...but some have claimed it cured their ms. Decisions decisions...

I was diagnosed with PPMS about 18 years ago, I haven't bothered with seeing any Neurologist's, or having any more MRI scans or anything else ever since then..I really couldn't see any point once I found out they had no cure to offer. I have tested out things like the Wahls diet without any noticeable changes, I have also been going through the entire list of vitamins and supplements' over the years to see if any particular one has any noticeable effect but so far I have found nothing...I am completely wheelchair bound now

What is Campath how often do you take it hun? And can I ask for ? And congratulations that’s ur mri come back good xxx

Hi Laura, thanks for the video. Do you have a twin sister? I wanna marry her 😅😅😅 all the best for you, pretty ❤

I think it's important you do scans and report on them, not just for yourself but others that are going through the same thing. I understand it's hard and scary, but what is the meaning of these things we're going through if not to help other people? Maybe I'm a bit projecting, a bit 😊

Morning all, Q? Did anyone with MS had knee buckling as a symptom Cant stand on tip toes or on heels Due to weakness and balance issues Regards in advance

Relapsed? You seem so normal!