(1/7) Nearly 100,000 CDNs are living with #MultipleSclerosis, and many face limited treatment options for progressive disease.
For #MSAwarenessMonth, we’re shining a light on researchers like Dr. Anastassia Voronova, who is working to unlock the brain’s potential to repair itself in progressive MS.
For #MSAwarenessMonth, we’re shining a light on researchers like Dr. Anastassia Voronova, who is working to unlock the brain’s potential to repair itself in progressive MS.
Neurological diseases and disorders - Stem Cell Network
Neurological Diseases and Disorders Neurological diseases and disorders affect the brain, the spinal cord, and nerves that form an intricate and complex network. These conditions are often difficult t...
stemcellnetwork.ca
May 26, 2026 at 3:03 PM
(1/7) Nearly 100,000 CDNs are living with #MultipleSclerosis, and many face limited treatment options for progressive disease.
For #MSAwarenessMonth, we’re shining a light on researchers like Dr. Anastassia Voronova, who is working to unlock the brain’s potential to repair itself in progressive MS.
For #MSAwarenessMonth, we’re shining a light on researchers like Dr. Anastassia Voronova, who is working to unlock the brain’s potential to repair itself in progressive MS.
May is #MSAwarenessMonth
With $224 Million invested, #Canada is a leader in MS research.
As part of the MS Canada campaign, I’ll be pinning a digital carnation!
Let’s #TakeActionForMS
Learn more: mscanada.ca
#ableg #abpoli
With $224 Million invested, #Canada is a leader in MS research.
As part of the MS Canada campaign, I’ll be pinning a digital carnation!
Let’s #TakeActionForMS
Learn more: mscanada.ca
#ableg #abpoli
May 6, 2026 at 6:05 PM
May is #MSAwarenessMonth
With $224 Million invested, #Canada is a leader in MS research.
As part of the MS Canada campaign, I’ll be pinning a digital carnation!
Let’s #TakeActionForMS
Learn more: mscanada.ca
#ableg #abpoli
With $224 Million invested, #Canada is a leader in MS research.
As part of the MS Canada campaign, I’ll be pinning a digital carnation!
Let’s #TakeActionForMS
Learn more: mscanada.ca
#ableg #abpoli
May is #MSAwarenessMonth ❤️
We stand in solidarity with everyone affected by MS. Your resilience and courage are a powerful reminder that even in the face of uncertainty, hope endures, you are not alone.
Let’s keep moving forward together.
#TakeActionForMS
We stand in solidarity with everyone affected by MS. Your resilience and courage are a powerful reminder that even in the face of uncertainty, hope endures, you are not alone.
Let’s keep moving forward together.
#TakeActionForMS
May 6, 2026 at 4:36 PM
May is #MSAwarenessMonth ❤️
We stand in solidarity with everyone affected by MS. Your resilience and courage are a powerful reminder that even in the face of uncertainty, hope endures, you are not alone.
Let’s keep moving forward together.
#TakeActionForMS
We stand in solidarity with everyone affected by MS. Your resilience and courage are a powerful reminder that even in the face of uncertainty, hope endures, you are not alone.
Let’s keep moving forward together.
#TakeActionForMS
I'm one of more than 90,000 Canadians living with MS. For over 50 years, the carnation has been a symbol of hope and support for the MS community.
Every post shared reminds Canadians affected by MS that an entire community stands behind us.
#TakeActionForMS #MultipleSclerosis #MS #MSAwarenessMonth
Every post shared reminds Canadians affected by MS that an entire community stands behind us.
#TakeActionForMS #MultipleSclerosis #MS #MSAwarenessMonth
May 6, 2026 at 3:59 PM
I'm one of more than 90,000 Canadians living with MS. For over 50 years, the carnation has been a symbol of hope and support for the MS community.
Every post shared reminds Canadians affected by MS that an entire community stands behind us.
#TakeActionForMS #MultipleSclerosis #MS #MSAwarenessMonth
Every post shared reminds Canadians affected by MS that an entire community stands behind us.
#TakeActionForMS #MultipleSclerosis #MS #MSAwarenessMonth
Raising awareness. Advancing care.
Recognizing Multiple Sclerosis Awareness Month
Visit to know more: ACRM.org/neurodegenerative-diseases-networking-group
#ACRM #MultipleSclerosis #MSAwarenessMonth #NeurodegenerativeDiseases #Rehabilitation #NeuroRehab #HealthcareCommunity #ClinicalResearch #NDNG
Recognizing Multiple Sclerosis Awareness Month
Visit to know more: ACRM.org/neurodegenerative-diseases-networking-group
#ACRM #MultipleSclerosis #MSAwarenessMonth #NeurodegenerativeDiseases #Rehabilitation #NeuroRehab #HealthcareCommunity #ClinicalResearch #NDNG
March 30, 2026 at 7:05 PM
Raising awareness. Advancing care.
Recognizing Multiple Sclerosis Awareness Month
Visit to know more: ACRM.org/neurodegenerative-diseases-networking-group
#ACRM #MultipleSclerosis #MSAwarenessMonth #NeurodegenerativeDiseases #Rehabilitation #NeuroRehab #HealthcareCommunity #ClinicalResearch #NDNG
Recognizing Multiple Sclerosis Awareness Month
Visit to know more: ACRM.org/neurodegenerative-diseases-networking-group
#ACRM #MultipleSclerosis #MSAwarenessMonth #NeurodegenerativeDiseases #Rehabilitation #NeuroRehab #HealthcareCommunity #ClinicalResearch #NDNG
It’s #MSAwarenessMonth. We’re partnering with a National MS Society self-help group to offer our Tele Tai Chi program. Learn more about this accessible, socially engaging virtual exercise program.
🔗https://ow.ly/GJ0U50Yyc4u
Center for Inclusive Design and Innovation at Georgia Tech
#NMSEAM2026
🔗https://ow.ly/GJ0U50Yyc4u
Center for Inclusive Design and Innovation at Georgia Tech
#NMSEAM2026
March 30, 2026 at 11:00 AM
It’s #MSAwarenessMonth. We’re partnering with a National MS Society self-help group to offer our Tele Tai Chi program. Learn more about this accessible, socially engaging virtual exercise program.
🔗https://ow.ly/GJ0U50Yyc4u
Center for Inclusive Design and Innovation at Georgia Tech
#NMSEAM2026
🔗https://ow.ly/GJ0U50Yyc4u
Center for Inclusive Design and Innovation at Georgia Tech
#NMSEAM2026
March is apparently #MSAwarenessMonth.
I have MS and didn't know about #MSAwarenessMonth until today... Not like we can march and type. We sure as shit can't organize an awareness campaign lol.
I have MS and didn't know about #MSAwarenessMonth until today... Not like we can march and type. We sure as shit can't organize an awareness campaign lol.
a woman with the word the on her eye
ALT: a woman with the word the on her eye
media.tenor.com
March 27, 2026 at 7:10 PM
March is apparently #MSAwarenessMonth.
I have MS and didn't know about #MSAwarenessMonth until today... Not like we can march and type. We sure as shit can't organize an awareness campaign lol.
I have MS and didn't know about #MSAwarenessMonth until today... Not like we can march and type. We sure as shit can't organize an awareness campaign lol.
MS doesn't always look like anything, but it feels like everything. So much is under the surface #msawarenessmonth #invisibleillness #multiplesclerosis
March 27, 2026 at 3:12 PM
MS doesn't always look like anything, but it feels like everything. So much is under the surface #msawarenessmonth #invisibleillness #multiplesclerosis
It’s National Multiple Sclerosis Education & Awareness Month! Time to educate, unite, & empower the MS community. Over a million people in the U.S. live with MS. Let’s advocate for them & their families. Show your support: wear orange, donate & attend MS events. #MSAwarenessMonth
March 27, 2026 at 12:07 PM
It’s National Multiple Sclerosis Education & Awareness Month! Time to educate, unite, & empower the MS community. Over a million people in the U.S. live with MS. Let’s advocate for them & their families. Show your support: wear orange, donate & attend MS events. #MSAwarenessMonth
#DisabledVet #PVA #MS #MSawarenessmonth #Adaptivesports #femalevets
augustagoodnews.com/adaptive-spo...
augustagoodnews.com/adaptive-spo...
Adaptive sports and PVA give Grovetown veteran community and independence - Augusta Good News
An Air Force veteran who was diagnosed with multiple sclerosis (MS) in 2014, Dotson found a supportive community and leads a life of relative independence due in large part to the Paralyzed Veterans o...
augustagoodnews.com
March 26, 2026 at 8:04 PM
Living with MS every day means struggling in ways some may never see. Managing tradeoffs between work and rest, independence and support, and hope and fear is a daily reality.
Let’s end MS together.
#SLCo #PublicHealth #MSAwarenessMonth
Let’s end MS together.
#SLCo #PublicHealth #MSAwarenessMonth
March 25, 2026 at 6:01 PM
Living with MS every day means struggling in ways some may never see. Managing tradeoffs between work and rest, independence and support, and hope and fear is a daily reality.
Let’s end MS together.
#SLCo #PublicHealth #MSAwarenessMonth
Let’s end MS together.
#SLCo #PublicHealth #MSAwarenessMonth
It's #MSAwarenessMonth 🧡
Wear your orange and join a Walk MS event to support people living with multiple sclerosis.
Find a walk near you: https://events.nationalmssociety.org/pages/2039?eventID=2525
Wear your orange and join a Walk MS event to support people living with multiple sclerosis.
Find a walk near you: https://events.nationalmssociety.org/pages/2039?eventID=2525
March 23, 2026 at 11:00 AM
It's #MSAwarenessMonth 🧡
Wear your orange and join a Walk MS event to support people living with multiple sclerosis.
Find a walk near you: https://events.nationalmssociety.org/pages/2039?eventID=2525
Wear your orange and join a Walk MS event to support people living with multiple sclerosis.
Find a walk near you: https://events.nationalmssociety.org/pages/2039?eventID=2525
Cecelia didn’t give up aerial arts after her MS diagnosis — she adapted.
This #MSAwarenessMonth, read her story.
https://www.healthywomen.org/real-women-real-stories/im-an-aerial-artist-even-with-multiple-sclerosis
This #MSAwarenessMonth, read her story.
https://www.healthywomen.org/real-women-real-stories/im-an-aerial-artist-even-with-multiple-sclerosis
Aerial Arts Taught Me to Fly. Even With Multiple Sclerosis, I’m Still Hanging On.
My artistry looks different with MS, but I’m determined to practice as long as I can
www.healthywomen.org
March 19, 2026 at 10:19 PM
Cecelia didn’t give up aerial arts after her MS diagnosis — she adapted.
This #MSAwarenessMonth, read her story.
https://www.healthywomen.org/real-women-real-stories/im-an-aerial-artist-even-with-multiple-sclerosis
This #MSAwarenessMonth, read her story.
https://www.healthywomen.org/real-women-real-stories/im-an-aerial-artist-even-with-multiple-sclerosis
When I was diagnosed w/ #MultipleSclerosis so many drs & nurses warned me to be prepared because way too many marriages end when the wife gets sick 😧
I’m so lucky to have a husband who is 💯 here for the good & the bad days
#MSWarrior 🧡
#PartnerWarrior ♾️
#MSAwarenessMonth
@kimmgaillard.bsky.social
I’m so lucky to have a husband who is 💯 here for the good & the bad days
#MSWarrior 🧡
#PartnerWarrior ♾️
#MSAwarenessMonth
@kimmgaillard.bsky.social
March 17, 2026 at 12:13 PM
When I was diagnosed w/ #MultipleSclerosis so many drs & nurses warned me to be prepared because way too many marriages end when the wife gets sick 😧
I’m so lucky to have a husband who is 💯 here for the good & the bad days
#MSWarrior 🧡
#PartnerWarrior ♾️
#MSAwarenessMonth
@kimmgaillard.bsky.social
I’m so lucky to have a husband who is 💯 here for the good & the bad days
#MSWarrior 🧡
#PartnerWarrior ♾️
#MSAwarenessMonth
@kimmgaillard.bsky.social
Did you know that Multiple Sclerosis (MS) is an invisible disease?
Many of its most debilitating symptoms are not apparent to others.
I used to think MS just affected people physically. Boy was I wrong!
A huge shout out to my MS warrior, @ms-motorcyclemama.bsky.social 🧡
#MSAwarenessMonth
Many of its most debilitating symptoms are not apparent to others.
I used to think MS just affected people physically. Boy was I wrong!
A huge shout out to my MS warrior, @ms-motorcyclemama.bsky.social 🧡
#MSAwarenessMonth
March 14, 2026 at 4:23 AM
Did you know that Multiple Sclerosis (MS) is an invisible disease?
Many of its most debilitating symptoms are not apparent to others.
I used to think MS just affected people physically. Boy was I wrong!
A huge shout out to my MS warrior, @ms-motorcyclemama.bsky.social 🧡
#MSAwarenessMonth
Many of its most debilitating symptoms are not apparent to others.
I used to think MS just affected people physically. Boy was I wrong!
A huge shout out to my MS warrior, @ms-motorcyclemama.bsky.social 🧡
#MSAwarenessMonth
"Not ready yet." For many people with MS, those three words echo for months or years while symptoms progress. This MS Awareness Month, we're sharing what it feels like to live in that diagnostic wilderness: https://research.smartpatients.com/resources
#MSAwarenessMonth #AutoimmuneDisease
#MSAwarenessMonth #AutoimmuneDisease
March 7, 2026 at 10:00 PM
"Not ready yet." For many people with MS, those three words echo for months or years while symptoms progress. This MS Awareness Month, we're sharing what it feels like to live in that diagnostic wilderness: https://research.smartpatients.com/resources
#MSAwarenessMonth #AutoimmuneDisease
#MSAwarenessMonth #AutoimmuneDisease
March is also Multiple Sclerosis Awareness Month.
I had a feeling that I had #MS in 2018 but I just ignored it until I couldn't anymore. I was officially diagnosed in August of 2021.
#multiplesclerosis #msawarenessmonth #nervepain #facialpain #chronicillness
I had a feeling that I had #MS in 2018 but I just ignored it until I couldn't anymore. I was officially diagnosed in August of 2021.
#multiplesclerosis #msawarenessmonth #nervepain #facialpain #chronicillness
March 6, 2026 at 5:01 PM
March is also Multiple Sclerosis Awareness Month.
I had a feeling that I had #MS in 2018 but I just ignored it until I couldn't anymore. I was officially diagnosed in August of 2021.
#multiplesclerosis #msawarenessmonth #nervepain #facialpain #chronicillness
I had a feeling that I had #MS in 2018 but I just ignored it until I couldn't anymore. I was officially diagnosed in August of 2021.
#multiplesclerosis #msawarenessmonth #nervepain #facialpain #chronicillness
Understanding triggers is part of managing MS.
Learn more at livewithms.com
#MSFacts #MSAwarenessMonth #HeatSensitivity #MultipleSclerosis #LiveWithMS
Learn more at livewithms.com
#MSFacts #MSAwarenessMonth #HeatSensitivity #MultipleSclerosis #LiveWithMS
March 5, 2026 at 10:31 PM
Understanding triggers is part of managing MS.
Learn more at livewithms.com
#MSFacts #MSAwarenessMonth #HeatSensitivity #MultipleSclerosis #LiveWithMS
Learn more at livewithms.com
#MSFacts #MSAwarenessMonth #HeatSensitivity #MultipleSclerosis #LiveWithMS
March 5, 2026 at 3:58 AM
That’s not weakness.
That’s biology.
livewithms.com
#MSAwarenessMonth #MSFatigue #LiveWithMS #MultipleSclerosis
That’s biology.
livewithms.com
#MSAwarenessMonth #MSFatigue #LiveWithMS #MultipleSclerosis
March 4, 2026 at 3:31 PM
That’s not weakness.
That’s biology.
livewithms.com
#MSAwarenessMonth #MSFatigue #LiveWithMS #MultipleSclerosis
That’s biology.
livewithms.com
#MSAwarenessMonth #MSFatigue #LiveWithMS #MultipleSclerosis
Each year the #MultipleSclerosisAssociationOfAmerica launches their new #ArtShowcase during #MSAwarenessMonth. I've submitted a few pieces you can see here alongside an array of fantastic work by others living with #MultipleSclerosis🎗
#MS #MSAA #MSAwareness #ThisIsMS
#MS #MSAA #MSAwareness #ThisIsMS
Art Showcase 2026 | MSAA
MSAA is very proud to present our 2026 MSAA Art Showcase, celebrating the work of artists affected by MS.
mymsaa.org
March 4, 2026 at 1:36 PM
Each year the #MultipleSclerosisAssociationOfAmerica launches their new #ArtShowcase during #MSAwarenessMonth. I've submitted a few pieces you can see here alongside an array of fantastic work by others living with #MultipleSclerosis🎗
#MS #MSAA #MSAwareness #ThisIsMS
#MS #MSAA #MSAwareness #ThisIsMS
17 years 6 months 19 days from my first symptom identified by a neurologist to my official diagnosis 🧡
#MultipleSclerosis
#SPMS #RRMS #PPMS
#MSAwareness
#MSAwarenessMonth
#MSWarrior #MSWontStopMe
#MS #MSEndsWithUs
#MultipleSclerosis
#SPMS #RRMS #PPMS
#MSAwareness
#MSAwarenessMonth
#MSWarrior #MSWontStopMe
#MS #MSEndsWithUs
March 3, 2026 at 5:00 AM
17 years 6 months 19 days from my first symptom identified by a neurologist to my official diagnosis 🧡
#MultipleSclerosis
#SPMS #RRMS #PPMS
#MSAwareness
#MSAwarenessMonth
#MSWarrior #MSWontStopMe
#MS #MSEndsWithUs
#MultipleSclerosis
#SPMS #RRMS #PPMS
#MSAwareness
#MSAwarenessMonth
#MSWarrior #MSWontStopMe
#MS #MSEndsWithUs
Did you know that, on average, someone is diagnosed with Multiple Sclerosis every 5 minutes?
This MS Awareness Month, explore our list of top-rated charities working on support, prevention and finding a cure: https://bit.ly/4aF1ZEH
#MS #MultipleSclerosis #MSAwarenessMonth #MSCharities
This MS Awareness Month, explore our list of top-rated charities working on support, prevention and finding a cure: https://bit.ly/4aF1ZEH
#MS #MultipleSclerosis #MSAwarenessMonth #MSCharities
March 1, 2026 at 6:41 PM
Did you know that, on average, someone is diagnosed with Multiple Sclerosis every 5 minutes?
This MS Awareness Month, explore our list of top-rated charities working on support, prevention and finding a cure: https://bit.ly/4aF1ZEH
#MS #MultipleSclerosis #MSAwarenessMonth #MSCharities
This MS Awareness Month, explore our list of top-rated charities working on support, prevention and finding a cure: https://bit.ly/4aF1ZEH
#MS #MultipleSclerosis #MSAwarenessMonth #MSCharities
Today is World MS Day. As someone who lives with MS every day, I’m sharing this digital carnation to #TakeActionForMS. #MS @mscanofficial #MSAwarenessMonth #NavigatingMSTogether #MultipleSclerosis
May 30, 2025 at 7:31 PM
Today is World MS Day. As someone who lives with MS every day, I’m sharing this digital carnation to #TakeActionForMS. #MS @mscanofficial #MSAwarenessMonth #NavigatingMSTogether #MultipleSclerosis
Dr. Sarah Morrow of @sunnybrookhsc.bsky.social's study on recovery of demyelinating optic neuritis after treatment with equivalent high doses of oral vs. intravenous corticosteroids: a randomized single blinded clinical trial: www.psifoundation.org/funded-resea.... #MSAwarenessMonth #WorldMSDay
Funded Research - PSI Foundation
List of projects funded by PSI Foundation.
www.psifoundation.org
May 30, 2025 at 5:20 PM
Dr. Sarah Morrow of @sunnybrookhsc.bsky.social's study on recovery of demyelinating optic neuritis after treatment with equivalent high doses of oral vs. intravenous corticosteroids: a randomized single blinded clinical trial: www.psifoundation.org/funded-resea.... #MSAwarenessMonth #WorldMSDay