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S C O T T

@rrms-sucks

Tattooed | RRMS dx2006 | Never give up

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27.11.2025
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Latest posts by S C O T T @rrms-sucks

Absolute beaut!! πŸ‘ŠπŸΌ I wish I could still run, my intention is to try and start again this year. #PrayForScott πŸ˜‚πŸ€£

12.03.2026 09:23 πŸ‘ 1 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

You have such a way with words! πŸ˜‚πŸ˜Š I glad the cold benefits your symptoms. -1C is like hell for me, I need 25C to be comfortable. It's incredible to me how unique we are all with this car crash of a disease πŸ€¦πŸ»β€β™‚οΈ

11.03.2026 16:50 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

Step 2 of aHSCT planning/implementation in the diary. New immune system please πŸ™πŸΌ #MS #AHSCT

09.03.2026 17:48 πŸ‘ 1 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

Dr Gretchen Hawley, MSCS and PT in the US, promotes increasing neuroplasticity repair through her #MSing link book/program. It's brilliant.

08.03.2026 12:38 πŸ‘ 0 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0
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Winter Paralympics 2026: Nina Sparks on being Great Britain's first female Paralympic snowboarder When Nina Sparks was diagnosed with multiple sclerosis in 2021, she decided it was going to be the making of her - now she's competing at the Winter Paralympics.

Representing #MS at the Paralympics! πŸ‘ŠπŸΌ

Meet GB's first female Paralympic snowboarder www.bbc.co.uk/sport/articl...

06.03.2026 16:45 πŸ‘ 5 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

πŸŽ‰ πŸ₯³ 🎈 🍻 πŸ₯‚ πŸ₯ƒ

06.03.2026 16:37 πŸ‘ 0 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

So good to hear. We have a very thin wire to tread and having a professional we get on with reduces the burden on everyone, for short bursts at least.

03.03.2026 21:01 πŸ‘ 1 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

Brain Stem compromise. Vagus nerve involvement. Bollocks.

#MS #MultipleSclerosis #CranialNerve10 #CNX

03.03.2026 18:56 πŸ‘ 2 πŸ” 0 πŸ’¬ 2 πŸ“Œ 0

Same. My neuro has been a 'mate' for 21 years for me. I call him by his first name, like he does me! 🀣 Glad you have that place to feel safe and content, no matter how the World is burning around you.

03.03.2026 18:53 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0
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B cell targeted CAR-T therapy for autoimmune diseases Chimeric antigen receptor T (CAR-T) cell therapy has emerged as a transformative approach in modern medicine, demonstrating remarkable efficacy in targeting pathogenic B-cell lineages with unprecedent...

B cell targeted CAR-T therapy for autoimmune diseases
www.eurekalert.org/news-release...

03.03.2026 08:04 πŸ‘ 3 πŸ” 1 πŸ’¬ 0 πŸ“Œ 0

Ordered it this morning too, arriving Friday hopefully πŸ™πŸΌ

03.03.2026 10:33 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

This is an incredible read. What a woman. With everything she has been through she still shows up. There are no words. #MS #Cancer #Survivor #NeverGiveUp

02.03.2026 18:54 πŸ‘ 4 πŸ” 1 πŸ’¬ 1 πŸ“Œ 0
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Spring news - good news Fenebrutinib pulverizes teriflunomide in relapsing multiple sclerosis

#MS_Selfie Spring news - good news

Fenebrutinib pulverises teriflunomide in relapsing multiple sclerosis gavingiovannoni.substack.com/p/spring-new...

02.03.2026 09:52 πŸ‘ 3 πŸ” 2 πŸ’¬ 0 πŸ“Œ 0
Video thumbnail

Energy management is medical, not optional.

More at livewithms.com

#MSFacts #LiveWithMS #MSFatigue

28.02.2026 22:31 πŸ‘ 2 πŸ” 1 πŸ’¬ 0 πŸ“Œ 0
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Myelin-targeting drug Lucid-MS inches closer to testing in patients Quantum Biopharma expects data from two now-completed, FDA-requested toxicology studies to support clinical testing of its Lucid-MS therapy.

Lucid-MS Phase 2 Trial imminent. Reduce myelin loss and promote myelin repair. Two phrases I like the sound of a lot!

multiplesclerosisnewstoday.com/news-posts/2...

27.02.2026 18:46 πŸ‘ 1 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

Yes it's #dysphonia, yes that's a term (in plain English) used for trouble with speaking. Yes, I have weak vocal chords!! What of it? What's it to you?! 🀣 Vocal physio is now the order of the day. I'll be a baritone before you know! πŸ˜‚πŸ€£

27.02.2026 08:52 πŸ‘ 2 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0
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Christina Applegate’s Unflinching Honesty on Life With MS Resonates After Eric Dane’s ALS Death Christina Applegate, multiple sclerosis, MS awareness, Eric Dane, ALS community, chronic illness, disability advocacy, health news, All Angles UK

Christina Applegate has long been admired for her candour, but her recent reflections on living with multiple sclerosis offer an especially stark window into the realities faced by many people with chronic neurological illness...Read moreπŸ‘‡ #news #Hollywood #MS
www.allangles.co.uk/2026/02/chri...

25.02.2026 18:13 πŸ‘ 6 πŸ” 1 πŸ’¬ 0 πŸ“Œ 0

You are allowed to grieve who you were β€”
without giving up on who you can become.

Confidence after diagnosis is not denial.
It’s integration.

More at livewithms.com

#MultipleSclerosis #LiveWithMS #ChronicIllnessJourney

23.02.2026 20:30 πŸ‘ 1 πŸ” 1 πŸ’¬ 0 πŸ“Œ 0

Had MRI's for aHSCT prep almost 4 weeks ago now. Heard nowt. I'll contact Radiology next week for the scans to make my own assessment. It's usually yearly for me, but had 12 in 2024 πŸ€¦πŸ»β€β™‚οΈand 4 in 2025. Lucky me.

20.02.2026 21:05 πŸ‘ 1 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

It's gone! πŸ˜‚

20.02.2026 18:31 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

Sorry to hear of your plight. I hope you recover as quickly as possible

18.02.2026 15:36 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

It's taking 4 days so far to recover. 4 days of watching the Olympics and no work! Could be worse πŸ˜‚ Totally worth it to see my wife graduate. 100%

17.02.2026 10:54 πŸ‘ 1 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

Crushed by #MS #fatigue today. Full day at the wife's MSc graduation ceremony has put me on my ass all day. Love the delayed onset of it all. Love it I do!! 🀬🀬😩

14.02.2026 18:49 πŸ‘ 3 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

Strong response of, does a bear shit in the woods?! πŸ˜‚πŸ€£

13.02.2026 19:03 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

Just got home after spending the day attending my wife's MSc graduation event! It's been an awesome (but exhausting) day! 😊

Hope yours has been decent too!

13.02.2026 16:02 πŸ‘ 1 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

I wish you well, I really do.
PALS where I am were very helpful with me a week or so back, I hope they're forward leaning with you where you are too πŸ™πŸΌ

12.02.2026 21:02 πŸ‘ 2 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0

That is bullshit! My friend got taken off Tysabri, after 14years, and put on Tyruko (the biosimilar) with no conversation, notification or choice. She was just put on it. Her quality of life deteriorated badly. Such poor decisions by those who control our health. Hoping you get to a better place.

12.02.2026 20:11 πŸ‘ 2 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

Not a truer word spoken πŸ™πŸΌ
I'm currently on 48hr rest to try and get my walking ability back. MS sucks! 🀬😭😩

11.02.2026 17:48 πŸ‘ 2 πŸ” 0 πŸ’¬ 1 πŸ“Œ 0

Living with MS means:
Planning carefully.
Canceling unexpectedly.
Adapting constantly.

That’s not inconsistency.
That’s awareness.

06.02.2026 15:30 πŸ‘ 3 πŸ” 1 πŸ’¬ 0 πŸ“Œ 0

Voice and breathing complaints are more than likely because of #MS brainstem lesions in the pons and medulla oblongata. 11th cranial nerve involvement. That's why ENT don't care. Nowt to do with them! All Neurology's deal! πŸ€¦πŸ»β€β™‚οΈπŸ€¬

06.02.2026 17:41 πŸ‘ 2 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0