#mscommunity 搜索结果
Living with MS doesn’t only impact physical health. It’s just as important to support your mental health 🧡 Have you connected with others on our forum? Talking to people with similar experiences can make a big difference. Find out more: mssoc.uk/3PBvzQ2 #MSCommunity
The findings show neurologists who receive payments from a company are significantly more likely to prescribe that company’s drugs to their patients. Review the findings in detail: bit.ly/4piTtjF #MSCommunity #MSAwareness #PharmaInfluence #Transparency #HealthcareEthics
We’re celebrating Black History Month! Meet Nikoma, who lives with MS, and his wife Simone 🧡 They share how important it is to change the belief that MS only affects White people. And how much it matters to feel seen! Read more: mssoc.uk/4pWf6Xn #bhmuk #MSCommunity
Are you coming to one of our MS Walks? Scott Mills joined our MS Walk in Birmingham! He tells us about the MS Walks we have planned for September 🧡 And why our MS Walks can make a difference to people living with MS. Find out more: mssoc.uk/4cAPrNS #MSCommunity
Full room "Career in cybersecurity: where to start? " by @JasminAzemovic @MSCommunityBiH #mscommunitybih #mscommunity
On Saturday, we were joined by staff and members of our MS community to march in Pride in London! We want to say a big thank you to everyone who came together to celebrate the LGBTQ+ MS community 🧡 #MSCommunity #PrideInLondon
Pretends she doesn’t have a chronic illness, does too much, ignores the symptoms and ends up comatose in bed for the day. Who can relate? #ms #mscommunity
"Azure Virtual Desktop vs. Windows 365" and packed room! #MScommunity #MScommunitybih @MSCommunityBiH @ddamirMVP
Our MS Helpline is back open! If MS is on your mind and you need information or emotional support, we’re here for you 🧡 You can contact us on 0808 800 8000 or send us an email at [email protected]. #MSCommunity
Meet Scott 👋 He tells us how he had to adjust after his MS diagnosis. And how he had to learn to ask for help when he needed it. He shares his treatment journey and how hopeful he is for the future of MS research. Read Scott’s story: mssoc.uk/3VpZFsM #MSCommunity
As a part of #MSAwarenessMonth, we want to give a s/o to these wonderful organizations we're so proud to work w/: @MSassociation, @MS_Focus, @mssociety, and the AFMS Foundation. Check out these resources and the excellent programs they have available to support the #MSCommunity!
Say hello to Yvette 👋 She was diagnosed with MS in 2016, but has lived with symptoms for longer. She tells us how she wanted to gain more control of her health 🧡 And how she discovered adaptive rowing! Read Yvette’s story: mssoc.uk/45VbEDa #MSCommunity
If you’re feeling like the fate of each day is in the hands of your Mighty MS, know that you’re not alone. 🫶 bit.ly/3IjBUiY #MS #MSCommunity #MSAwareness #LivingWithMS #SpoonieLife
Breaking the taboo: s*x & MS. It's normal to feel embarrassed, but don't feel ashamed of any sexual issues caused by MS. Ask for help, support & find ways to enjoy intimacy. Share your challenges & tips for a fulfilling s*x life #MSCommunity #SexAndMS www.s…
Dating with MS can be tricky. Say hello to Becky 👋 She lives with MS. She tells us how she felt about dating when she got her diagnosis. She shares how she believes it's important to stay single instead of being miserable with the wrong person 🧡 #MSCommunity
The world’s largest meeting on MS has begun, and we’re bringing you all you need to know! Stay tuned right here for our coverage of all the latest news. And learn more about the 41st congress here: bit.ly/47UfFKX #ECTRIMS2025 #MSResearch #MSCommunity #MSNews #Bionews
Say hello to Dave 👋 Dave lives with relapsing remitting MS and experiences balance issues. They tell us how dizziness affects them. And how they’ve learned to adapt to protect themselves from falls and injuries 🧡 Read Dave’s story here: mssoc.uk/4gtj2L8 #MSCommunity
On #WorldMentalHealthDay, we invite you to take part in a conversation that starts where many journeys begin - our minds. This session is open to everyone in the #MSCommunity across the UAE and beyond. Register now: bit.ly/4h9aoSi
We’re celebrating Black History Month! Meet Nikoma, who lives with MS, and his wife Simone 🧡 They share how important it is to change the belief that MS only affects White people. And how much it matters to feel seen! Read more: mssoc.uk/4pWf6Xn #bhmuk #MSCommunity
The McDonald Criteria are the international guidelines doctors use to diagnose multiple sclerosis (MS). With the latest 2024 updates, diagnosis can now be made earlier and with greater accuracy, a milestone for the #MSCommunity. #MSSocietyUAE
What’s a common misconception about MS that you wish more people understood? 🧡 Share in the comments! #MSAwareness #MSCommunity
MS Perspectives brings real voices, expert insights, and practical tips that meet people living with MS where they are. Tap in, learn, and share. ➡️ msperspectives.com/issues #MultipleSclerosis #MSCommunity #patients #MSCare #MSAwareness #Art
The world’s largest meeting on MS has begun, and we’re bringing you all you need to know! Stay tuned right here for our coverage of all the latest news. And learn more about the 41st congress here: bit.ly/47UfFKX #ECTRIMS2025 #MSResearch #MSCommunity #MSNews #Bionews
Great to be celebrating the fantastic work of unpaid carers at @carerswales lecture tonight. Do check out our offer to unpaid carers supporting people living with MS through our #BreathingSpace project. #UnpaidCarers #MSCommunity
Meet Scott 👋 He tells us how he had to adjust after his MS diagnosis. And how he had to learn to ask for help when he needed it. He shares his treatment journey and how hopeful he is for the future of MS research. Read Scott’s story: mssoc.uk/3VpZFsM #MSCommunity
Say hello to Dave 👋 Dave lives with relapsing remitting MS and experiences balance issues. They tell us how dizziness affects them. And how they’ve learned to adapt to protect themselves from falls and injuries 🧡 Read Dave’s story here: mssoc.uk/4gtj2L8 #MSCommunity
Thanks to MS' unpredictability, a bucket list may seem illogical. But for some, a list represents forward momentum, even in the face of a sometimes impossible disease. Which side do you fall on? bit.ly/46mWqXY #MS #LivingWithMS #MSCommunity #BucketList
What’s a common misconception about MS that you wish more people understood? 🧡 Share in the comments! #MSAwareness #MSCommunity
Exciting times are ahead in Singapore! 🇸🇬 Dive into our packed line-up of speakers, sessions, and unique venues for the aMS event 🙌 All details live on the site: amssingapore.com #aMSSingapore #MSCommunity
As #MSAwarenessMonth comes to an end, we invite the #MSCommunity to take advantage of two amazing resources. Both the @MSassociation & the @MS_Focus have established free programs for body cooling products which can improve quality of life. Discover more: bit.ly/ms_coolingprog…
Pretends she doesn’t have a chronic illness, does too much, ignores the symptoms and ends up comatose in bed for the day. Who can relate? #ms #mscommunity
As a part of #MSAwarenessMonth, we want to give a s/o to these wonderful organizations we're so proud to work w/: @MSassociation, @MS_Focus, @mssociety, and the AFMS Foundation. Check out these resources and the excellent programs they have available to support the #MSCommunity!
Say hello to Yvette 👋 She was diagnosed with MS in 2016, but has lived with symptoms for longer. She tells us how she wanted to gain more control of her health 🧡 And how she discovered adaptive rowing! Read Yvette’s story: mssoc.uk/45VbEDa #MSCommunity
Educate yourself and others about Multiple Sclerosis to help create a more understanding and supportive world for those with MS. #MSAwareness #MSCommunity #SpreadKnowledge #KailashHospital #MultipleSclerosis
"Azure Virtual Desktop vs. Windows 365" and packed room! #MScommunity #MScommunitybih @MSCommunityBiH @ddamirMVP
#MSconnections #MSNetwork #MSCommunity #WeHaveMS #URNotAlone #ShiftMS #CureMS #chronicillness #WeGetIt #ThisIsMS I am in constant invisible pain. You might not be able to see it but that doesn't mean that it's not real #FuckMS
The MS journey can be unpredictable. Empathy and understanding go a long way in supporting those navigating this complex condition. #MSCommunity #SupportMatters
Full room "Career in cybersecurity: where to start? " by @JasminAzemovic @MSCommunityBiH #mscommunitybih #mscommunity
The findings show neurologists who receive payments from a company are significantly more likely to prescribe that company’s drugs to their patients. Review the findings in detail: bit.ly/4piTtjF #MSCommunity #MSAwareness #PharmaInfluence #Transparency #HealthcareEthics
The world’s largest meeting on MS has begun, and we’re bringing you all you need to know! Stay tuned right here for our coverage of all the latest news. And learn more about the 41st congress here: bit.ly/47UfFKX #ECTRIMS2025 #MSResearch #MSCommunity #MSNews #Bionews
Thanks to MS' unpredictability, a bucket list may seem illogical. But for some, a list represents forward momentum, even in the face of a sometimes impossible disease. Which side do you fall on? bit.ly/46mWqXY #MS #LivingWithMS #MSCommunity #BucketList
Meet Scott 👋 He tells us how he had to adjust after his MS diagnosis. And how he had to learn to ask for help when he needed it. He shares his treatment journey and how hopeful he is for the future of MS research. Read Scott’s story: mssoc.uk/3VpZFsM #MSCommunity
If you’re feeling like the fate of each day is in the hands of your Mighty MS, know that you’re not alone. 🫶 bit.ly/3IjBUiY #MS #MSCommunity #MSAwareness #LivingWithMS #SpoonieLife
May is #MSAwarenessMonth & I was delighted to meet with MS Canada representatives in Ottawa yesterday. We're committed to building upon our 75-year history of supporting the #MScommunity and advocating for those affected by #multiplesclerosis #EndMS #MSResearch #MSCanada
Today, My MSAA Community recognizes 7 YEARS of offering a safe, supportive place to connect with other members of the MS community. This free online forum makes it possible to find and provide #MSsupport with members of the #MScommunity who have shared experiences.
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