#MemorialDay : Today, we remember and honor the individuals who made the ultimate sacrifice for our country.

What’s your #MyMSMoment ? Everyone’s MS story is unique – starting from diagnosis. For World MS Day this year, join us as we share the varied MS diagnosis stories.

Share your own diagnosis story here: ntlms.org/WorldMSDay_MyM…

.World MS Day – a day to celebrate global solidarity and hope for a cure – is in just one week. This year, we invite you to raise awareness for MS diagnoses by shining a spotlight on your stories.

Share your story using the #MyMSMoment creator: ntlms.org/WorldMSDay_MyM…

A biosimilar is a medication that, though produced differently, is very similar to an existing biologic medication. It's given at the same strength, dose and form as the reference.

Tyruko, the first FDA-approved biosimilar DMT, will be available for MS: ntlms.org/3UZE8Yf

The National MS Society Black MS Experience Summit is more than a gathering — it's a space for our community to share our experiences, uplift each other & gain insights into living with MS. Join me on June 12-13 to be part of this empowering experience. Sign up: ntlms.org/bmses24registr…

From dinner to dancing, our Climbers know how to celebrate after showing the stairs who's boss! ➡

'I still have to be a mother, a wife and now a Warrior. I’m an MS activist who now tells people don’t ignore your body. My vision left and now it came back…I’m going to hold strong as long as I can!!'

~ Sophia, @mrs_sophs on IG, #ThisisMS

Kenneth struggled with telling his employer about his MS after his symptoms started to become more regular. When he finally disclosed, he was met with encouragement - and years later, at his retirement, he was flooded with deeply moving comments: ntlms.org/MyRetirementPa…

'The anxiety and depression can set in as you never know for sure what is going to happen. But, that is life right? We never know what’s around the corner. I just continue to believe in my strength, my doctors and my fight.'

~ Missy, @swissmelis on IG, #ThisisMS

✅ Advance vital research
✅ Increase access to quality care
✅ Support people living with MS

One gift accomplishes so much. Today is your LAST CHANCE for all donations to be MATCHED by our extraordinary donors, up to $75,000: ntlms.org/OSOC_MayMatch

👀 Have you seen the news?! There’s a new place for everyone affected by MS.

Our new website is your one-stop shop for understanding and managing MS, finding the resources you need, learning how to help the cause, and exploring all the work we’re doing.
ntlms.org/NationalHomepa…

New experience, same mission. Check out the new Walk MS: ntlms.org/WalkHomepage

#MSNews : Researchers unearth clues to MS development by mapping cells within brain lesions. The team learned important information about how different cell types are arranged and how they interact with each other.

Read more: ntlms.org/CluesToMSDevel…

“Fundraising for Walk MS is important to me because I would love to see a cure for MS in my lifetime.” — Jackie, diagnosed in 2018

We need you to join us because a cure is on the line. Register today: ntlms.org/WalkHomepage

It's #NationalHospitalAwarenessWeek - did you know the Society has a tool for finding MS doctors and resources near you?

Check it out here: ntlms.org/FDR

Photographer Sara J. Winston captures what managing motherhood & MS is like through photos with her daughter.

This Mother's Day, we honor the mothers with MS, the mothers of children with MS, and mother figures who deal with MS every day. 🧡

Read more: ntlms.org/3PYq7qP

'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 with this loss.'

~Justine, @ runwithms on IG, #ThisIsMS

'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