National MS Society HCP
@mssocietyHCP
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Official @mssociety healthcare provider account. For professionals working to ensure access to comprehensive high-quality care for everyone living with MS.
Joined October 2020
I’m excited to announce that @mssociety is now a partner of the National Rural Health Association to raise awareness about #MS among rural health professionals and equip them with resources to drive high quality care!
nationalmssociety.org
The National MS Society has partnered with the National Rural Health Association (NRHA) to expand access to MS care in rural areas. Learn more about this partnership.
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👉Check out the interview live on our site now: https://t.co/JbxoRaSDMb
#MultipleSclerosis #MS #Medicare
neurologylive.com
The senior director of clinical resources and programming at National MS Society discussed the significant updates to Medicare Part D in 2025 that will cap annual out-of-pocket costs and introduce a...
Recently, @iciccone7 had a conversation with Sarah Anderson, PharmD, NBC-HWC, of @mssociety, who spoke about what clinicians should know about the big changes coming in 2025 for patients with #MS who are on Medicare Part D or Medicare Advantage plans. Stay tuned! 🎥🧡
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#ECTRIMS2024 | That's a wrap! This year’s congress may be over, BUT the sharing of knowledge is definitely not 👇 👇 👇 The ECTRIMS 2024 Best of Slide Deck is now available. Download & share this valuable information with your colleagues and peers ➡️ https://t.co/LjcyuPdJfg
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"We can accelerate collaboration and imagination!" 👏🏻 Perfect description from @tim_coetzee @mssociety of what we achieve as the global #MultipleSclerosis community working together 🌍 #ECTRIMS2024 @ECTRIMS patient community day
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Join us on National Voter Registration Day, September 17that 2 https://t.co/2jf8MfAeFO 1 p.m. CT/ 12 p.m. MT/ 11 a.m. PT, for an empowering webinar where you will learn more about voting laws, election accessibility and creating an informed voting plan.
p2a.co
Enter your information to register
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🆕 Glatopa now available on https://t.co/DbEuAEZQYV! Thanks to the National MS Society @mssocietyHCP for helping us identify and prioritize crucial medications to include in our offerings. We now offer: Glatopa Subcutaneous Solution Prefilled Syringe 20 MG/ML: $1,228.25 ↪️
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The National MS Society funds 2 MS clinical care fellowships - the MS Clinical Care Physician Fellowship grants and the Institutional Clinician Training Awards. Pre-applications are now open! https://t.co/KsBBQKd6NN
@mssociety
#multiplesclerosis
lnkd.in
This link will take you to a page that’s not on LinkedIn
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The National MS Society funds 2 MS clinical care fellowships - the MS Clinical Care Physician Fellowship grants and the Institutional Clinician Training Awards. Pre-applications are now open! https://t.co/KsBBQKd6NN
@mssociety
#multiplesclerosis
lnkd.in
This link will take you to a page that’s not on LinkedIn
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Bryant Robinson, senior manager of government relations at the National MS Society, discussed how telehealth access has become vital for patients with multiple sclerosis who often lack nearby specialist care. https://t.co/EKnnFlp7EZ
@neurology_live
neurologylive.com
Bryant Robinson, senior manager of government relations at the National MS Society, discussed how telehealth access has become vital for patients with multiple sclerosis who often lack nearby...
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The National MS Society funds 2 MS clinical care fellowships - the MS Clinical Care Physician Fellowship grants and the Institutional Clinician Training Awards. Pre-applications are now open! https://t.co/KsBBQKd6NN
@mssociety #multiplesclerosis
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The #InflationReductionAct is keeping pharmacists like Mike busy! Certain vaccines like shingles and RSV are now free for seniors and people with disabilities with Medicare Part D. See Mike's story here: https://t.co/bRcTGwhFu1
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The National MS Society funds 2 MS clinical care fellowships - the MS Clinical Care Physician Fellowship grants and the Institutional Clinician Training Awards. Pre-applications are now open! https://t.co/KsBBQKd6NN
@mssociety #multiplesclerosis
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It’s @WorldMSDay! With your help, we’re shining a light on what life is like with MS. Each story is as varied and unique as the people living it. Your diagnosis story reminds us that we’re in this together.
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Bruce Bebo, EVP of Research at the @mssociety talked about the Dystel Prize which was presented at AAN last week. Congrats to Dr. Rhonda Voskuhl who was the 2024 recipient! https://t.co/tpxEDLcM0y
#research #MultipleSclerosis
neurologylive.com
The executive vice president of research at National MS Society talked about the Dystel Prize which is presented at AAN to a recognized individual who promotes further advancements in understanding...
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Wanting to learn more about the impact health literacy has on PwMS? Curious how the @mssociety strives to be a health literate organization? Wondering what you can do? Advancing Equity and Inclusion: Health Literacy for the MS Community and Beyond ( https://t.co/zKI3A7IPWc)
#MS
neurologylive.com
NeurologyLive is your direct connection to the latest neurology news and interviews with expert neurologists in multimedia formats.
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Congratulations to Dr. Rhonda Voskuhl on being selected as the recipient of the 2024 John Dystel Prize for MS research. https://t.co/vMtlE8SoaY
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Check-out NeurologyLive® Clinician of the Month Spotlight: Scott Newsome, DO, MSCS, FAAN, FANA https://t.co/YJMMaGvo1M
#multiplesclerosis
neurologylive.com
As part of our monthly clinician spotlight, NeurologyLive® highlighted multiple sclerosis expert Scott Newsome, DO, MSCS, FAAN, FANA, director of the Stiff Person Syndrome Center and professor of...
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It’s MS Awareness Week! Stories of life with MS are often portrayed through the everyday moments that people with MS experience. This MS Awareness Week, share your MS Moment with us: https://t.co/xm09a9Dnao
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1 million people in the U.S. still live with the uncertainty of MS. I won’t stop spreading #MSawareness until the moment we’re all waiting for – the one when we finally find a cure for multiple sclerosis. I’m proud to be part of this movement, join me
nationalmssociety.org
We will keep talking back and standing up to MS until we end MS for good. See how you can help us raise awareness, create community and ensure MS ends with us.
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Join us for our upcoming Clinical Discussion Call on the topic of Living Loss: Identifying Grief and Building Resilience in Caregivers on Thursday, March 21, 2 p.m. ET. To be added to our regular distribution list, register here: https://t.co/HWPlFGUmF9
#MentalHealthMatters
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