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National MS Society

@mssociety66k followers

For 80 years the National MS Society has reshaped the story of MS. Now we intend to finish it.

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3Dec 1, '15.@amyschumer gives in honor of her dad, Gordon Schumer. Why do you give? #GivingTuesday #MyGivingStory #endMS6.2×06801460
4Aug 10, '21Thank you, Christina, for your courage in opening up about living with MS. We all appreciate the awareness that you are bringing to the disease. Please know that we at the MS Socie5.8×06441211
5Mar 10, '19It’s MS Awareness Week! Each day, people living with MS do whatever it takes to move their lives forward despite the challenges of #MS. Read and watch inspiring stories at and shar5.1×02972182
6Apr 21, '23Multiple sclerosis is a chronic, unpredictable disease of the nervous system that affects nearly 1 million people in the US. Here are 5 facts to know about MS 👇4.2×26k117476
7Mar 12, '18“Multiple sclerosis may be a part of who you are, but it doesn’t define you.” Every day, people do whatever it takes to move their lives forward despite #MS. This MS Awareness Week4.1×02291731
8Mar 9, '20It is MS Awareness Week. RT this video to your followers to help them better understand #MultipleSclerosis. #ThisIsMS #MSAwareness3.9×01841937
9Feb 26, '24"When I got the news I gave my fiancée (now wife) the option to leave me because of all the unknowns that could pop up in my life...because of her, I push through, and find ways to3.8×23k13760
10May 30, '24It’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 th3.4×21k148648
12May 15, '19“MS fatigue is horrible, it’s not what ‘normal’ tired is. It’s as if someone has stuck a tube inside you and sucked every ounce of life out of you. MS is a lot of asking is this no3.0×0273821
13May 30, '18It’s @WorldMSDay! Research is bringing us closer to ending MS. As a global community, we’re celebrating what we’ve achieved in MS research so far and sharing our hopes for the futu2.9×01371420
14Mar 11, '24What is MS? Multiple sclerosis is a disease that impacts the brain, spinal cord and optic nerves, which make up the central nervous system and controls everything we do. Watch this2.8×17k1328027
15Mar 19, '24From coast to coast, cities across the nation lit up in orange for MS Awareness Week 🧡 In order: 1. Times Square, New York City 2. Sunshine Skyway, Tampa, FL 3. Hoan Bridge, Milwa2.7×17k107323
16Oct 21, '18Thank you, Selma, for your courage in opening up about your #MultipleSclerosis diagnosis. We all appreciate the awareness that you are bringing to the disease.2.7×0249740
17Jan 11, '21Medical experts convened by the National MS Society agree the COVID-19 vaccines are safe and should be administered to people with MS. Read the full guidance on the Society’s COVID2.6×0174831
18Mar 11, '18It’s MS Awareness Week! Each day, people living with MS do whatever it takes to move their lives forward despite the challenges of #MS. Read and watch inspiring stories at and shar2.5×01361230
19Oct 3, '23The ADA signified a milestone toward inclusivity for those living with disabilities. Thank you, @SelmaBlair, for your continued advocacy and for shedding light on life with MS 🧡2.4×15k148310
20Mar 14, '18It's MS Awareness Week! We're thankful for the many ways people are raising awareness of multiple sclerosis and doing whatever it takes to change the world for people with MS! #Thi2.4×01691030
21May 28, '19"For those who don’t understand why someone ‘like me’ might have a disability permit...I might look well, but I’m going through hell on the inside - head pain, nerve pain, vertigo,2.4×0209660
22Mar 9, '20Orange light illuminated Niagara Falls last night to kick off #MSawareness Week! #multiplesclerosis #MS2.4×0200830
23Mar 1, '20Mark your calendars – next week is MS Awareness Week! Together, we’ll bring awareness to #MultipleSclerosis as we do whatever it takes to change the world for the nearly 1 million 2.3×01591020
24Mar 8, '18Mark your calendars – next week is MS Awareness Week! Together, we’ll bring awareness to multiple sclerosis as we do whatever it takes to change the world for people with MS. #This2.3×01381040
25Nov 9, '18We are a movement by and for people affected by #MultipleSclerosis. Until we end this disease forever, we will do whatever it takes to accelerate breakthroughs. We are calling on y2.2×0186570
26Feb 27, '23Beautiful 🧡 We are so proud of Christina (@1capplegate) and everyone else with MS - whether that's showing up or just taking it day by day. We are here for you.2.1×13k173211
27Mar 2, '23“I was diagnosed with MS when I was 14. Living with MS has taught me many life lessons. One of the biggest is to never take anything for granted; especially the little things and t2.1×13k270170
28Jun 14, '19"I’d like for everyone without #MultipleSclerosis to know that sometimes for people with chronic illnesses, such as MS, the symptoms can be invisible. Those of us living with the d2.1×0181661
29Mar 9, '24Symptoms like brain fog, double vision and chronic pain can mark a person's MS experience. Tomorrow is the first day of MS Awareness Week – help us raise awareness by sharing your 2.0×13k111355
30Mar 8, '20"The hardest part about having #MultipleSclerosis is not being able to explain how you feel. I wish I could write I have MS somewhere on my body because people are so judgmental wh2.0×0172601
31May 12, '22"MS is referred to as an invisible disease, because most often you cannot see the pain, the shaky balance, the loss of words, the darkened vision, the dizziness, the fatigue, or th2.0×0199520
32Mar 9, '20Niagara Falls was lit up in orange last night for #MSawareness Week! One of our top Walk MS fundraisers and volunteers, Denise Jarosch, coordinated with the team in charge of light1.9×0183600
33Jan 18, '18Sometimes, you just need some words of encouragement. Happy Winnie the Pooh Day! #WinnieThePoohDay1.9×0147761
34Sep 19, '17Ask your Senators to oppose the Graham-Cassidy Bill and instead, continue bipartisan efforts to improve access:1.9×090920
35Mar 6, '21Multiple sclerosis and the MS movement become better known each year. But more must be done to spread the word. Let’s amplify our collective voices next week during MS Awareness We1.9×0132761
36Mar 29, '17Last night the FDA approved the first and only treatment for both primary progressive and relapsing forms of #MS:1.9×0113820
37Dec 2, '18Check out the shoes on Tampa Bay @buccaneers head coach Dirk Koetter! Dirk is wearing these special shoes during today's game in honor of his mother and sister who are living with 1.9×0169560
38Oct 18, '20"Being diagnosed with an incurable, life long disease so young felt like my life was already over before it begun. I felt alone and scared about my future. However I have come to r1.8×0212292
39Aug 20, '20"'You don’t look sick' is something that many people living with MS hear. Many of our symptoms are not visible for others to see and not every person experiences the same symptoms.1.8×0155571
40May 29, '19MS symptoms are variable and unpredictable – and many of these symptoms are invisible. Tomorrow, @WorldMSDay, people around the world are bringing awareness to the invisible side o1.7×0121720
41Mar 10, '21It is MS Awareness Week. Show this video to your family and friends to help them better understand #MultipleSclerosis. #ThisIsMS1.7×0113654
42Sep 24, '23"Daily reminder that you don’t always know what is going on in someone’s life and that not all illnesses and disabilities are visible. So what is it they say? In a world where you 1.7×10k171461
43Dec 13, '18American entertainer Richard Pryor died 13 years ago this week. After his diagnosis, he often joked that #MS stood for "More Sh*t." Let’s hope that we can all work together to erad1.7×0132610
44Jun 3, '20We are outraged by the injustice and violence that led to the death of George Floyd and too many others in our country. This is not OK. Not today or any day. We realize that our he1.6×0147510
45Mar 4, '21Mark your calendars – next week is MS Awareness Week! Together, we’ll bring awareness to #MultipleSclerosis as we do whatever it takes to change the world for the nearly 1 million 1.6×0123640
46Dec 6, '18The Cleveland @Browns ' @MylesLGarrett chose these special cleats for his grandmother, Pauline White Johnson, who was diagnosed with #MultipleSclerosis. Video by Cleveland Browns. 1.6×0124520
47Mar 10, '20"I painted my MRI that had confirmed my #MultipleSclerosis diagnosis. It was deeply therapeutic, and somehow made everything less scary. The lesions became colorful instead of clin1.5×0158372
48Mar 7, '21This is MS Awareness Week. There is no more powerful way to demonstrate the urgency of our work than through the voices of those directly affected by MS. Join us this week as we ex1.5×0114550
49Dec 11, '20"Can you tell which eye is affected by a flare-up right now? Or which eye has permanent damage because of an optic neuritis? And that's the point (healthy) people don't get. We mig1.5×0144280
50May 30, '25Today is @WorldMSDay, a global moment to honor the courage of those living with multiple sclerosis and reaffirm our commitment to ensuring that MS ends with us. Whether you live wi1.5×9.4k137732
51Sep 11, '17Thank you, @jamiebenn14, for your help in creating a world free of MS!1.5×0173340
53Oct 18, '22.@SelmaBlair, Your journey on @officialdwts might have come to end, but you continue to inspire the nearly 1 million people with MS in U.S. and countless millions around the world.1.4×0162280
54May 30, '19“You can’t see what’s going on in a person’s body.” Chloe stumbles due to invisible symptoms of MS, so she got a service dog to help show the world that she was disabled and not dr1.4×0113510
55Jul 10, '15Meet @amyschumer - Comedian, Writer, Actor and #MSactivist Extraordinaire:1.4×0114540
56Mar 30, '23"When you live a life full of random pains & aches, you get REALLY good at identifying it, where it is, and how to rate it from 1-10. Except sometimes, not everyone believes yo1.4×8.7k128200
57Apr 12, '21"I have finally fully accepted my MS. There is not a known cure but I plan on fighting this with everything in me. So if you see me walking funny or see me fall pick me up and we c1.4×0172152
58Jan 21, '19"If you can't fly then run, if you can't run then walk, if you can't walk then crawl, but whatever you do, you have to keep moving forward." – Dr. Martin Luther King, Jr #MLK1.4×0118480
59Dec 3, '17Thank you, @ChadSlade62, for bringing awareness to MS!1.4×0117480
60Mar 8, '19For #InternationalWomensDay we celebrate Sylvia Lawry who founded the National MS Society in 1947. She was committed to do whatever it took to find solutions for her brother and ev1.3×0119482
61Aug 17, '21"I have finally fully accepted my MS. There is not a known cure but I plan on fighting this with everything in me. So if you see me walking funny or see me fall pick me up and we c1.3×0165180
62Jan 13, '20"I’m done feeling sorry for not responding to text messages promptly, for taking days off work, for canceling plans, for saying this sucks a lot, for being selfish...Because I’m li1.3×0155222
63Feb 9, '20"One year ago I was diagnosed with #MultipleSclerosis. I’d like to be able to say that I am thriving and have everything under control, but the truth of it is, I have good days and1.3×0158140
64Jul 31, '18"Once you become fearless, life becomes limitless." ~ Instagram user mel.safel sharing the inspiration behind her tattoo after she was diagnosed with #MS. Do you have an MS-inspire1.3×0132242
65Jun 28, '19"Looks can be incredibly deceiving. What’s that old saying? Don’t judge a book by its cover. I may appear fine in person & photos, but that doesn’t mean I FEEL fine. I may look1.2×0116360
66Sep 3, '21"Every morning I get out of bed I thank my lucky stars that I can feel my legs, my hands, that I can play with my kids and go to work. Things must people don't think twice about." 1.2×0154170
67May 11, '24"We don't talk about what it feels like to not have children because of MS...I know I cannot be the only woman with a chronic illness who has made this decision and who struggles w1.2×7.6k11773
68Jan 1, '19Wishing you all a very Happy New Year! Thank you for being a part of the MS Movement. Together, we are stronger. TOGETHER, WE WILL BREAKTHROUGH MS.1.2×0116360
69Sep 14, '21"The hardest part about having MS is not being able to explain how you feel. Just because I can look like this picture doesn’t mean I am free from this disease or always okay. Hopi1.2×0144222
70Mar 28, '19Thanks to @mtv, @SiestaKey and @thekelseyowens for a great event and for helping raise awareness for Kelsey's mom and everyone affected by MS. Nearly 1 million people live with MS 1.2×0148210
71Nov 2, '22Christina Applegate (@1capplegate) opens up about her journey with MS. Thank you for your vulnerability & honesty in sharing your story, Christina. We appreciate you raising aw1.2×0122303
72Jul 6, '23"Tonight I’ll probably go to bed with the same questions as every night. How will my life look in the future? Will I wake up with new symptoms? What will I still be able to do in a1.2×7.4k110193
73Dec 16, '18"My dad has had MS since 2004, and I've seen the transformation firsthand and how it has impacted his life. I want to bring awareness to this disease." ~ @D7_Reed #MyCauseMyCleats 1.2×0110360
74Apr 9, '20"Remember staying home helps our seniors and those with underlying conditions! Thank you to my hubby for insisting he works from home as we middle through this crisis as best we ca1.2×0130260
75May 6, '18To all of the special nurses helping those with MS live their best lives possible – we thank you! #NursesDay1.2×0120270
76Feb 18, '20"So today I had to accept the fact that I have to officially give up HEELS. So I’m saying Goodbye to my beloved heels. Not because I’m giving up on myself, but because I care about1.2×0133111
77Sep 21, '18You just never know who you will meet at Walk MS – actor Bill Murray. According to team members, Bill asked what they were doing attired in their team T-shirts. After hearing about1.2×0125280
78Aug 26, '19"It can feel overwhelming. I have to tell myself slow down, it’s ok if the kids are still in their pjs. It’s ok to eat breakfast for dinner. It's ok to feel like this. This day wil1.1×0133181
79Sep 14, '20"Living with #MultipleSclerosis is a pain. But it does not define me. Gotta lay down for a while? Talking a little funny today? Using the wheelchair today? Still the same me. It's 1.1×0123250
80Sep 24, '18.@DanelleUmstead, a Paralympian who is visually impaired and living with #MS, is competing on Dancing with the Stars. Tune in tonight to @ABCNetwork @DancingABC to watch Danelle, w1.1×0106331
81Jul 9, '18Tune in tonight to watch @ninjawarrior's feature on @lancepekus & his wife Heather, who is living with #MS. Lance, the Cowboy Ninja, says, “It’s going to be very emotional to g1.1×0125260
82Jan 5, '20"Four years ago, I started experiencing vision changes that I had no answers for. I never would’ve imagined hearing a #MultipleSclerosis diagnosis. Unpredictable changes can always1.1×0122220
83May 2, '19"This is my year. It will be my 7 year diagnosis anniversary...this is my 1st ever Bike MS event. I’ve never been physically capable to do something like this and this is my year n1.1×0134160
84Apr 23, '24"When people say it is the invisible illness, it truly is. I look fine...but I'm not always. You may not get it and sometimes, neither do I. When I go to bed I never know what's go1.1×6.9k155202
85Nov 6, '18Shout-out to our amazing Walk MS volunteers! Walk MS is possible because of YOU and we thank you for making our 2018 Walk MS event season such a success! #walkMS1.1×0120190
86Jul 24, '20"If there is something good that can come from a disease like MS, it is that it has taught me how strong I am and how incredibly blessed I am to be surrounded by the most amazing, 1.1×0123151
88Sep 21, '21"Can you tell which eye is affected by a flare-up right now? Or which eye has permanent damage because of an optic neuritis? And that's the point (healthy) people don't get. We mig1.1×0125180
89Sep 6, '24The goals: 🛑 Stop MS 💪 Restore lost function ❌ End MS forever1.1×6.6k144273
90Jul 28, '19"I don’t believe in always being grateful things aren’t worse. However. Today, I will focus on being grateful for every slow, unsteady step I take. I can feel sad tomorrow, but tod1.1×0117191
91Dec 19, '19"I am lucky that many of my symptoms have been mild & I have been able to live a fairly normal life. But there are times that it feels like my body is not my own, that my mind 1.0×0114190
92Sep 7, '23"We all have something we are dealing with, whether you can see it from the outside or not. Having MS sucks! There is no sugarcoating it! However, I chose to live my life with grat1.0×6.2k133100
94Aug 14, '19"Every hospital visit, every dr appointment, every needle poke and test, and every literal step forward was for this moment...smelling the salty sea, feeling the sand on my toes, s1.0×0109201
95Jul 6, '19"Big Girl Panties Day. It's my first time using a cane at work. I should have done this months ago, but denied I was having problems. I know this heat wave is impacting me, so I'm 0.9×0112110
96Oct 23, '20"I (try) almost everyday to go for walks because walking is something I don’t take for granted. And that's pretty much how my life goes with #MultipleSclerosis, not taking life for0.9×0114130
97Jul 11, '24What you see versus what you don't — there is a lot beneath the surface of MS. MS, much like an iceberg, has an unseen side to it that can be very frustrating. Everyone's experienc0.9×5.3k112406

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