Apparently today was World MS Day with a theme of “my MS diagnosis”. Well, as I’ve basically missed the day entirely, I’ll keep this short: symptoms 2005, diagnosis 4 years later after a lumbar puncture. It sucks, but it’s honestly made me stronger.
Now watch this beautiful film they made for World MS Day 15 years ago. It gets me every time.

https://youtu.be/pXWihqmEjO0

#MS #MultipleSclerosis #WorldMSDay

Beautiful Day - World MS Day Video U2

YouTube
#WorldMSDay - Accept the diagnosis, but not the prognosis… never give up! I live 20 years with MS and I am stronger than ever.
#MShero #despiteMS #mentalstrength #MSisNotTheEnd

🧠⚡ World #MultipleSclerosis Day and @gregoryMS brings hope!

Our latest upgrade, co-built with Nova SBE, delivers sharper algorithms, multi-subject support & per-topic models (“MS + DMTs”, “MS + Myelin”). Less noise & quicker insights for researchers, clinicians, patients & carers.

Please boost so more people hear on #WorldMSDay.
Details ➡️ https://gregory-ms.com/post/gregory-ai-update-better-algorithms-ms-researchers/
Support ➡️ https://lnkd.in/df3aZkeH

#MSResearch #AIforGood #BotsFightMS #mschat

Today we stand in solidarity for #WorldMSDay! 🧡 Let's raise awareness, share stories, and support the incredible strength of everyone affected by multiple sclerosis. 💪 Together, we can make a difference. #MSAwareness #MultipleSclerosis #MSCommunity #StrongerTogether
Oggi è la Giornata Mondiale della Sclerosi Multipla. Mi sembra un buon momento per ripostare la mia guida un poco cretina alla #sclerosimultipla. (continua nei commenti)
#WorldMSDay #GiornataMondialeSclerosiMultipla AISM - Associazione Italiana Sclerosi Multipla

𝗪𝗼𝗿𝗹𝗱 𝗠𝘂𝗹𝘁𝗶𝗽𝗹𝗲 𝗦𝗰𝗹𝗲𝗿𝗼𝘀𝗶𝘀 𝗗𝗮𝘆 | 𝟯𝟬 𝗠𝗮𝘆 𝟮𝟬𝟮𝟱
Today, we stand together to raise awareness about Multiple Sclerosis (MS), a chronic autoimmune disease affecting the central nervous system. MS disrupts communication between the brain and body by damaging the myelin sheath around nerve fibers, leading to various physical and cognitive challenges.

𝗪𝗵𝘆 𝗶𝘁 𝗺𝗮𝘁𝘁𝗲𝗿𝘀:
- MS primarily affects people in their most productive years, impacting lives and communities worldwide.
- Around 2.8 million people globally live with MS.
- Early diagnosis and access to treatment can improve outcomes but challenges remain.

𝟮𝟬𝟮𝟱 𝗧𝗵𝗲𝗺𝗲: “𝗠𝘆 𝗠𝗦 𝗗𝗶𝗮𝗴𝗻𝗼𝘀𝗶𝘀”
This year focuses on breaking down barriers to early and accurate diagnosis, promoting better diagnostic tools, clinical training, and fair access to care everywhere. Sharing real stories helps build understanding and supportive communities.

Let's support those living with MS by spreading awareness, encouraging research, and fostering inclusion.

#WorldMSDay #MultipleSclerosis #MyMSDiagnosis #MSAwareness #AutoimmuneDisease #CentralNervousSystem #EarlyDiagnosis #SupportMSPatients #HealthcareForAll #MSResearch #SCABPharmacy #InvisibleIllness #ChronicIllnessAwareness #DisabilityInclusion

Swansea family to scale Principality Stadium roof in daredevil fundraiser for MS Society Cymru

To mark World MS Day (30 May), Sharon Hier, Group Coordinator for MS Society Swansea and District Group, and her family will take on the ‘Scale the Stadium’ challenge at Cardiff’s iconic Principality Stadium on the 1st of June in an adrenaline-filled fundraising challenge to support people living with Multiple Sclerosis (MS) across Wales.

The challenge will see Sharon, supported by her husband and daughters, climb to the roof of the 75,000-capacity stadium, traverse the roof edge with a bird’s-eye view of Cardiff and the pitch below, before scaling the stadium’s mast and zip-wiring across the canopy. The heart-stopping finale will see them descend back to Earth via ‘The Drop’. For Sharon, a proud Ospreys Rugby supporter, the challenge is particularly daunting due to her fear of heights, but her family’s support is giving her the courage to take on this incredible feat.

Sharon, who was diagnosed with relapsing remitting Multiple Sclerosis in 2014, has been a dedicated volunteer with MS Society Cymru, running information stands at public events including the Wales Air Show and Swansea and Llanelli Pride to raise awareness and support others living with the condition.

MS is a lifelong neurological condition where the immune system attacks the nerves, causing symptoms that can significantly impact daily life. With an estimated 6,111 people living with MS in Wales, MS Society Cymru provides vital support services and funds essential research to find treatments and ultimately stop MS for good.

Sharon Hier, Group Coordinator for MS Society Swansea and District Group, said:

“Volunteering has shown me the power of community. Our weekly socials are a lifeline, especially for those living alone. We laugh – a lot – and that laughter brings strength, connection, and hope.

“When my wonderful family volunteered to support me in taking on this incredible challenge, I was overwhelmed by their support. Every penny raised will help us support more people with MS, bring more smiles, and make sure no one feels they have to face this condition alone.”

They won’t be alone in their efforts, Sharon and her family will be joined by 20 others taking part in the daring fundraiser, each with their own connection to MS.

Among them are Marie Nixon, wife of MS Ambassador Stuart Nixon, and Daf Wyn, MS Society Ambassador and Cymru Council member and TV presenter on the popular Welsh language show Heno, who will be tackling the challenge with his family. Their collective efforts reflect the strength and solidarity of the MS community in Wales.

Shelley Elgin, Director of MS Society Cymru, said:

“Sharon’s dedication to supporting our MS community in Swansea and across Wales is truly inspiring. Her family’s willingness to support her in taking on such an exhilarating challenge demonstrates the incredible spirit and determination we see throughout our MS community.

“Fundraising challenges like ‘Scale the Stadium’ are vital in helping us continue our work supporting people living with MS and funding the research that will one day lead to treatments and a cure. We’re incredibly grateful to Sharon and all the other fundraisers for their courage and commitment to making a difference.”

The fundraising challenge supports MS Society Cymru’s ongoing work providing support services, advocacy, and funding vital research. The organisation runs support groups, information services, and community events across Wales to ensure no one faces MS alone.

To support the Sharon’s challenge, donations can be made at: https://www.justgiving.com/page/sharon-hier-54

[Lead image: MS Society Cymru]

#MSSocietyCymru #PrincipalityStadium #WorldMSDay

This week Christina Applegate and Jamie-Lynn Sigler promoted their podcast (https://www.messythepodcast.com) and general MS/Chronic Illness/Disability advocacy on Conan O’Brien’s podcast (https://teamcoco.com/podcasts/conan-obrien-needs-a-friend/episodes/christina-applegate-and-jamie-lynn-sigler) with Christina joining in “Work from Bed”-style
#MusComEnt #WorldMSDay #Disability #MultipleSclerosis #ChristinaApplegate #JamieLynnSigler
MeSsy

MeSsy
During the filming of “Dead to Me” in 2018 Christina Applegate began to experience symptoms that were later diagnosed as #MultipleSclerosis in early 2021. She went public with her diagnosis later that year. She has since retired from acting due to MS but now has a wonderful podcast with fellow MS-diagnosed actress Jamie-Lynn Sigler (https://www.messythepodcast.com)
#MusComEnt #WorldMSDay #DontTellMomTheBabysittersDead
#ChristinaAppleGate #JamieLynnSigler
MeSsy

MeSsy
Join me Wednesday @ 6pm EST/5pm CST when #MusComEnt jointly honors #MothersDay AND #WorldMSDay with the Christina Applegate classic “Don’t Tell Mom the Babysitter’s Dead” (1991). Available on AMC+, Cinemax and for free here (https://tinyurl.com/4tf6vz8y)
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ASA 🎥📽🎬 Don't Tell Mom The Babysitter's Dead (1991) a film directed by Stephen Herek with Christina Applegate, Joanna Cassidy, John Getz, Josh Charle

Don't Tell Mom The Babysitter's Dead (1991) Synopsis / Plot Five kids are left home when their mother leaves town on a three-month vacation, only to have their geriatric babysitter die of a heart attack, leading to the eldest teen, Sue Ellen, to scam her way into taking a job at a hip Los Angeles fashion company to feed and support her needy siblings.

OK.RU