'Now that I’ve become a mother, I think ahead a lot. Although I know that so much is out of my control, I continue to do the best I can in advocating and caring for myself in spaces that don’t encounter people like me.'

~Fatima, @ fatiszafari_bjj on IG, #ThisIsMS

The new Walk MS is an unforgettable display of the support and love surrounding people with MS 💚 It takes a whole community to end this disease.

Be a part of that community: ntlms.org/WalkHomepage

Any gift to support people living with MS is valuable, but if you give before May 16, all gifts will be MATCHED by our extraordinary donors, up to $75,000.

Make an impact at ntlms.org/OSOC_MayMatch

At Walk MS, Neelesh proudly holds up a green circle — representing that he loves and supports a person living with MS. Discover why he walks.

If you have multiple prescriptions, it can be difficult to keep track of them all. Taking your medications and following your treatment plan are key to managing MS.

Learn more tips for medication management here: ntlms.org/3Uw3wVa

'I don’t ever wish to be solely identified as 'the girl with MS' and most certainly will never allow it to define me...However, I do hope to be able to make those of you (us) out there feel a little less alone & a little more understood.'

~Sarah, @ sarahmgosnell on IG, #ThisisMS

Cooking in warmer weather can be difficult whether or not one has heat intolerance. Additionally, any positive diet changes are likely to help your overall health and wellbeing.

This delicious salad recipe can be thrown together in just a few minutes: ntlms.org/43sokQm

'Your body still does millions of things right for you to be here each and every day, even though it got some things wrong.'

Kylin shares her experience living with MS with those who are newly diagnosed on May 14 during New to MS: Navigating Your Journey: ntlms.org/NewToMS

Low-dose naltrexone, or LDN, is an 'off-label' treatment doctors may prescribe to help treat MS symptoms like pain, fatigue, and cognitive issues. We want to know: Have you used, or considered using LDN? If so, what was your experience? Share your story in the comments below 👇

#MSNews : 35 groups welcome and celebrate the President Biden's new rule that will better protect patients from short-term, limited-duration health plans, a risky form of low-quality health coverage.

Read more: ntlms.org/3xOSgKP

At 12 ET/11 CT TODAY I'll be sharing #wellness strategies to live your best life with #MS - and other chronic conditions - on National MS Society 's Ask An MS Expert. Hope you'll tune in! #multiplesclerosis

Wellness in MS: Positive Lifestyle Changes youtube.com/live/cDaZ3F8Hl… via YouTube

#MSNews 📰: When it comes to children and teens living with MS, studies show starting treatment with highly effective DMTs is the way to go. Discover how these therapies work to control disease activity and offer hope for a brighter future ➡ ntlms.org/44pa1wk

Match alert! 🧡 Generous supporters are MATCHING all gifts, dollar-for-dollar, up to $75,000, until May 16. Give now to make 2x the difference toward a cure for MS.

Help advance research and increase access to quality MS care. Every dollar counts: ntlms.org/OSOC_MayMatch

The new Walk MS brings the MS community together in a powerful demonstration of our strength 💪

'Life is a ride, having MS just makes it a little more crazy lol if anyone is going through some tough things just know you are not alone and it gets so much better! Even if it’s not overnight just hang in there!'

~Danielle, @ danimarie0827 on IG, #ThisIsMS

Nate, a longtime rider with Bike MS, gets himself into a 'hairy' situation each year! His unique strategy for fundraising has not only given others laughs, but it's helped him to make an impact.

Find ideas for your next fundraiser at ntlms.org/48ZHi2C.

It's #NationalSuperheroDay , and every single person living with MS lives with a variety of superpowers, from perseverance to resilience to adaptability. What's your superpower?

Read more of Traci's story of MS superpowers here: ntlms.org/3JwqPIc

Every winter, Adam visits the Adirondack Mountains to cross another mountain off his hiking list. They kicked off MS Awareness Week in March with a snowshoe trip to the summit of Mt. Van Hovenburg.

Learn more about DIY fundraisers here: ntlms.org/diyMS

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We are ONE DAY away from the National MS Society MS Activist Rally! Find out how you can sign up. On RealTalk MS #MultipleSclerosis #MSActivist

'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 going to happen overnight or what condition I'm going to be in the next morning.'

~Chyanne, #ThisIsMS