MS caregiving is a journeyβone thatβs too often unsupported.
Thatβs why ACP and RealTalk MS launched the MS Care Partner Connection: a one-stop site for resources, caregiver guides, and even an AI-powered support bot.
READ: www.acceleratedcure.org/april-2025-i... #MultipleSclerosis
21.05.2025 18:34 β π 1 π 0 π¬ 0 π 0
Help Us Fast Track the Cure! | Accelerated Cure Project
Imagine a world without MS. ACP is on a mission to make that vision a reality, & you can be a part of it!
People with #MS aren't just subjects of researchβtheyβre the driving force behind it.
iConquerMS has already powered over 30 studies, contributed to 16 publications, and built tools that help researchers better understand MS.
Help us do even more:
www.acceleratedcure.org/help-us-fast...
14.05.2025 16:10 β π 1 π 0 π¬ 0 π 0
Each year, Haileeβs family runs a pumpkin patch in memory of their dad, who passed from progressive MS.
A portion of proceeds supports MS research through the Accelerated Cure Project. Read how they're turning love and loss into impact:
www.acceleratedcure.org/picking-pump...
12.05.2025 13:28 β π 1 π 0 π¬ 0 π 0
I totally get that. For many, itβs a chance to share their MS experiences on their* terms and reach people who rarely engage with the MS community.
It's all about increasing visibility, connection, and change. Regardless, we appreciate your voice, whether during βawareness monthsβ or anytime!
31.03.2025 16:54 β π 2 π 0 π¬ 1 π 0
#MSAwarenessWeek has ended, but the need for #MS advocacy and research remains. π§‘
A huge thank you to the people living with MS, care partners, and researchers who make iConquerMS possible!
π¬ What stuck with you the most from MS Awareness Week?
16.03.2025 17:12 β π 4 π 0 π¬ 1 π 0
#MSAwarenessWeek is about real voices, real experiences. Sharing your MS story can help others feel less alone and bring more awareness to the challenges of living with MS.β¨π¬ Whatβs something you wish people understood about MS? Share your thoughts in the comments! #MSVoices #MultipleSclerosis
15.03.2025 18:00 β π 2 π 0 π¬ 0 π 0
YouTube video by iConquerMSβ’
Chat with Chat Episode 10
#MSAwarenessWeek: Managing insurance with MS can feel impossible. In Chat with Chat, Dr. Deborah Miller discusses the five key types of insurance that matter most for people with MS and the biggest challenges in getting the coverage you need.β¨πΊ Watch: youtu.be/Uc9xBIlNd1o?... #HealthInsurance #MS
15.03.2025 17:00 β π 0 π 0 π¬ 0 π 0
iConquerMS:Β A Personal Touch | Accelerated Cure Project
Join us as we dive into the personal stories of three iConquerMS RIDE Council members and how the initiative is making a difference.
As #MSAwarenessWeek ends, weβre highlighting the Voices of People with #MS. iConquerMS is ensuring all voices are heard in researchβespecially those that are too often underrepresented.
Read about DeLisa, Dimika, and Veronicaβs inspiring advocacy: www.acceleratedcure.org/iconquerms-a... #MSResearch
15.03.2025 16:01 β π 3 π 0 π¬ 0 π 0
Sharing knowledge is key to driving MS research forward. iConquerMS works with leading MS research organizations to turn real-world findings into breakthroughs.
What MS research has impacted your journey?β¨#MSAwarenessWeek #MSResearch #MultipleSclerosis @mssociety.bsky.social
14.03.2025 17:59 β π 1 π 0 π¬ 0 π 0
YouTube video by iConquerMSβ’
Chat with Chat Episode 6
How much do you really know about your MRI scans? Chat with Chat explores MRI in MS, from brain volume loss to standardized scan protocols. Watch now and join the conversation!
π₯β¨youtu.be/8XIATrQCLYo?...β¨#MSAwarenessWeek #MS #MRI @mssociety.bsky.social
14.03.2025 17:00 β π 0 π 0 π¬ 0 π 0
June 2024 iConquerMS Spotlight | Accelerated Cure Project
Discover the benefits of exercise and other relevant topics for people with MS through our Chat with Chat webinar series!
A study using REAL MS Wellness & Diet survey data explored the effects of exercise, diet, and wellness choices. What wellness strategies have made a difference in your life? π§‘
Read more: www.acceleratedcure.org/june-2024-ic... #MSAwarenessWeek #MultipleSclerosis #MRI @mssociety.bsky.social
14.03.2025 16:00 β π 0 π 0 π¬ 0 π 0
On Day 5 of MS Awareness Week, weβre talking about the importance of inclusive research. Whatβs something about MS that you think is often overlooked? Letβs discuss! π§‘
#MSAwarenessWeek #WelcomingAll #MSResearch #MS @nationalmssociety.bsky.social
13.03.2025 17:00 β π 0 π 0 π¬ 0 π 0
#MSAwarenessWeek Day 5: Fatigue affects ~70% of people with #MS, yet treatment options are limited. A past study explored digital therapy as a non-medication approach.
How do you manage MS #fatigue? Letβs discuss. π¨
π www.acceleratedcure.org/july-2024-ic...
@nationalmssociety.bsky.social
13.03.2025 16:00 β π 0 π 0 π¬ 0 π 0
#MS research is strongest when those affected by MS help shape studies. By sharing their insights, people with MS ensure research reflects real needs. π‘
On Day 4 of #MSAwarenessWeek, weβre celebrating #PeoplePoweredResearch! What role should patients play in shaping MS studies?
#MSAwarenessWeek
12.03.2025 17:36 β π 0 π 0 π¬ 0 π 0
On Day 4 of MS Awareness Week, weβre celebrating people-powered research! Learn more about how the Our Questions Have Power program is making MS research more patient-driven.
π Read more: www.acceleratedcure.org/january-2025...
#MSAwarenessWeek #PeoplePoweredResearch #MSResearch
12.03.2025 16:25 β π 0 π 0 π¬ 0 π 0
Patient-Powered Research Networks (PPRNs) let people with MS contribute from homeβremoving barriers like travel and clinic visits.
On Day 3 of MS Awareness Week, letβs discuss inclusive engagement in MS research. What barriers do you think need to be addressed next? π§‘
#MSAwarenessWeek
11.03.2025 17:47 β π 0 π 0 π¬ 0 π 0
People from historically marginalized communities are underrepresented in MS research.
On Day 3 of MS Awareness Week, letβs talk about inclusivity in research. What barriers still need to be addressed? π§‘
www.acceleratedcure.org/november-202...
#MSAwarenessWeek
11.03.2025 16:41 β π 0 π 0 π¬ 0 π 0
YouTube video by iConquerMSβ’
Chat with Chat Webinar Series Episode 1
π‘ Whatβs the real cost of MS treatment? Access, affordability & patient choices all shape MS care. Dr. Chatβs research explores these challenges & why people-powered research is the future.
π₯ Watch: www.youtube.com/watch?v=Ykqi...
#MSAwarenessWeek
@nationalmssociety.bsky.social
10.03.2025 19:25 β π 1 π 0 π¬ 0 π 0
π‘ Did you know? People with #MS can participate in mMS research from home thanks to people-powered research! π‘π» No travel, no clinic visitsβjust accessible research.
This #MSAwarenessWeek, what do you think about remote research? Share the comments below!
@nationalmssociety.bsky.social
10.03.2025 16:00 β π 2 π 0 π¬ 0 π 0
𧬠Todayβs MS Awareness Week theme: Transcriptomics! Researchers are exploring how genes respond to MS, unlocking insights that could lead to new treatments. π Learn more about this exciting field:
π www.acceleratedcure.org/transcriptom...
@nationalmssociety.bsky.social
#MSAwarenessWeek
10.03.2025 14:45 β π 0 π 0 π¬ 0 π 0
MS is unique to each personβno two experiences are alike. Thatβs why patient-centered research is key to shaping the future of MS.
This MS Awareness Week, letβs highlight how real-life MS experiences inform research. π§‘ What areas of MS research need more attention? Comment below!
#MSAwarenessWeek
09.03.2025 17:00 β π 0 π 0 π¬ 0 π 0
π§‘ MS Awareness Week starts TOMORROW! π§‘
Each day from March 9β15, weβll share key areas of MS research & the role of the MS community in advancing progress.
Join us for discussions, polls & insightsβyour voice matters!
#MSAwarenessWeek
08.03.2025 16:11 β π 1 π 0 π¬ 0 π 0
Do you have MS? Our researchers want to hear your views and experiences!
Share your views on a range of topics, including health and care, and you could win Β£200.
Find the links to take part in our thread π§΅
27.02.2025 14:12 β π 1 π 1 π¬ 1 π 0
Are you living with an autoimmune disease? Your experience matters!
Share your views on health and care as part of our study and you could win Β£200.
Find the links to take part in our thread π§΅
27.02.2025 09:05 β π 2 π 3 π¬ 2 π 0
A new trial is investigating CAR T cell therapy for MS! Plus, learn about the link between MS & anxiety in this monthβs Research Spotlight.
Read more: www.acceleratedcure.org/january-2025...
#MultipleSclerosis #MS #MSresearch
17.02.2025 18:19 β π 1 π 0 π¬ 0 π 0
The January 2025 iConquerMS Spotlight dives into how the "Our Questions Have Power" program is helping patients drive MS research. Through iConquerMS, you can submit & vote on research questions that matter most. π§‘
π Read more: www.acceleratedcure.org/january-2025...
#MSResearch #MS
13.02.2025 16:49 β π 0 π 0 π¬ 0 π 0
ποΈ For people with MS, creativity isnβt just an outletβit can be a form of healing.
Art, music, and writing can help manage symptoms and build resilience. Read about the connection between creativity and MS in ACPβs latest newsletter:
π www.acceleratedcure.org/creative-hea...
#MS #CreativityHeals
07.02.2025 14:15 β π 3 π 0 π¬ 0 π 0
MS research should include everyone affected by MS! π iConquerMS is leading the way in making research more inclusive & patient-driven.
Learn how your voice can help drive change: www.acceleratedcure.org/research-for...
#MultipleSclerosis #MSResearch #ResearchForAll
05.02.2025 13:59 β π 1 π 0 π¬ 0 π 1
Empowering people affected by MS to live their best lives
The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS.
The Navigating Your Journey Program is on January 23, 7:30β9 PM EST! Teens with MS and their families are invited to join this virtual event to learn about Pediatric MS research from experts, including the Accelerated Cure Project. Register here: www.nationalmssociety.org/understandin...
22.01.2025 14:30 β π 0 π 0 π¬ 0 π 0
Empowering people affected by MS to live their best lives
The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS.
Donβt miss the βNavigating Your Journey Programβ on Jan 23, 7:30β9 PM EST. Designed for teens with MS and their families, featuring Pediatric MS research insights from leading experts. Register: www.nationalmssociety.org/understandin...
#PediatricMS #MS
20.01.2025 13:35 β π 0 π 0 π¬ 0 π 0
We partner with pharmaceutical and medical device developers to provide critical strategy and integrated evidence generation throughout product development lifecycles. www.rtihs.org
CTO @icometrix & researcher University of Brussels | #neuroradiology #AI #alzheimer #multiplesclerosis
Global Healthcare Services Manager @ Hyland | Passionate about healthcare, digital health, AI & cloud | BSc, PRINCE2, MSP, L6Ο Green Belt | Opinions are my own | https://linktr.ee/paulcochrane
A source of multiple sclerosis and related news, views and research
https://patienttalk.org/category/multiple-sclerosis-2/
Hold your plans lightly in your hands
Reversing uphill in Devon lanes since time immemorial so you donβt have to
Full of wit. Wit, I said
#95%Dartmoor #5%civilised
#MS #formerlawyer #TheArchers #dementiacarer #FitsofRageβ’οΈ
No DMs
π
#ElbowsUp
Retired - Boomer
Happily married, father, friend
Coffee Lover!
Dog Lover!
"Living with MS" since 1998 #MS, #MultipleSclerosis
πππ’π³ππ§ π’π§π¬π©π’π«ππ
#VancouverCanucks, #BCLions, #VancouverWhitecaps FC, #TorontoBlueJays, #Seahawks
A sheep raising, #horror movie loving guy that somehow lives with Multiple Sclerosis.
Fuck ICE.
Living with RRMS since 2018.
UK
#advocate #disability #equity #inclusion #DoTheWork #Baltimore
Smart Patients - a peer-to-peer support forum where patients learn from each other about treatments, challenges, and how it all fits into the context of their experience.
www.smartpatients.com
https://linktr.ee/smartpatients
Transforming brain scans into confidence. Empowering radiologists with actionable insights for better care.
https://icometrix.com/
https://www.equipforchildren.org/
Pediatric disability equipment reuse organization serving Maryland, DC, and North Virginia for free. #disability #reuse #AbilityAdvocate #LoanCloset
www.abilityalliance.org #Baltimore!
#disability #DisabilityAwareness #AbilityAdvocate #BeKind #HelpOthers
Disabled USMC Vet | Widow | Living with DDD & #MS | Joomla Dev | Grave Digger | Sarcastic AF (blame the MS)
MS Sucks: A snarky journal to track your MS bullshit & snarky MS apparel
mssucks.co/links
Podcast host for Overcoming MS. DX with MS 2015. Lemtrada since 2018. From Essex to Devon via London.
#MS, #MultipleSclerosis
@geoffallix on Twitter
A Chicago #Cubs fan. Suffering from #MultipleSclerosis for 30 years. F-CK the Orange King! He will prevent any life-changing medical breakthroughs to keep me alive. I am the #marxist #communist, #wokeAF #liberal you hear about.
π€¬I WILL NOT BE SILENCED! π‘
Mum, Wife, retired ICU nurse, MS, Carer of hubby, Lewy Body Dementia.
Lover of Nature, Rescue animals, books, travel if I could, meeting new peeps and experiences. Above all try and be a good human βΊοΈx
I'm a politically engaged disabled cosplayer, sci-fi aficionado, lover of books, cats, trivia, and tea. Kinkster, Dom, some NSFW comments likely! . MS sufferer since 2014. Tories, Republicans, etc. get short shrift from me.
#Resister. #PoliticalJunkie, bleed #Dem blue. #AntiMAGA. #MultipleSclerosis warrior, mom of MS fighter. π§‘ #AshevilleNC strong. π― for women, human, civil, & equal rights. Mama, Baba, #DogMom. #CA born, #CO lived, #NC home. I block sketchy!
We are at the forefront of #mentalhealth & #neuroscience #research. We collaborate across industries & disciplines to find answers to global #health challenges.