Walk MS Team Alex

Walk MS Team Alex We walk for Alexandria, and for everyone living with Multiple Sclerosis. Thank you for standing with us.🧡

Our team is united in hope, strength, and determination to fuel research, support families, and move closer to a cure.

National MS Society Walk MS Portland, OR🧡I promised my grandchildren that every year I would attend their local Walk MS ...
05/30/2026

National MS Society Walk MS Portland, OR🧡

I promised my grandchildren that every year I would attend their local Walk MS in Portland, Oregon. It’s so important to me that they grow up knowing the community that supports their mom. We had a soccer game rescheduled and arrived a little late, but we made it and even dodged the rain. It was a beautiful day. Thank you to the incredible volunteers and community members who make this event possible year after year.

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05/30/2026

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was created to help raise awareness across the globe about the experiences of people living with MS, as well as their caregivers, healthcare providers, and loved ones. How are you spreading awareness today?

05/09/2026

One week until Walk MS Portland! 🧡

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05/05/2026

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The future of MS research and care depends on the decisions Congress is making right now.

On May 14 at 12:00 p.m. ET, the National MS Society will host its next MS Activist Webinar, "Make it Count Now: Mobilizing for Federal Funding in a Changing Policy Landscape." You'll learn more about the Society's advocacy efforts to protect funding across the federal budget, including for the MS Research Program, the National Institutes of Health, the Centers for Disease Control and the Food and Drug Administration.

Your voice can drive the funding, research and care that will shape the future for everyone affected by MS. Register now and to learn how you can help fuel progress: https://ntlms.org/AdvcWebinarMay14

🧡Walk MS Chicago🧡It was a beautiful day in the city. Thank you to everyone who showed up, supported, donated, and cheere...
04/26/2026

🧡Walk MS Chicago🧡
It was a beautiful day in the city. Thank you to everyone who showed up, supported, donated, and cheered us on. Your support means more than you know. We’re so grateful.

04/26/2026

Today is WALK MS Chicago!!!🧡🧡🧡🧡

Walk MS Chicago is in TWO days!!!! 🧡Dalia found the sunshine, the lilacs, and her favorite bandana… now we just need Sun...
04/24/2026

Walk MS Chicago is in TWO days!!!! 🧡
Dalia found the sunshine, the lilacs, and her favorite bandana… now we just need Sunday to get here!

🧡🧡 It’s WALK WEEK! 🧡🧡  Rain in the forecast, so bring your ponchos and come ready for a good time. 🌦️☔️ A little rain wo...
04/20/2026

🧡🧡 It’s WALK WEEK! 🧡🧡

Rain in the forecast, so bring your ponchos and come ready for a good time. 🌦️☔️

A little rain won’t stop us. See you at Walk MS Chicago!!

Did you know?
04/15/2026

Did you know?

Weather changes don’t cause new MS damage, but they can absolutely make symptoms surge, often quickly, dramatically, and temporarily. People with MS have been saying for years that storms, heat waves, cold snaps, and pressure drops hit their bodies harder than the average person, and the science increasingly supports what lived experience has always known. MS nerves operate on a razor‑thin margin, and when the environment shifts, that margin gets even thinner.

Heat is the most common trigger. Around 60–80% of people with MS are heat‑sensitive, and even a tiny rise in body temperature can make symptoms flare. This is classic Uhthoff’s phenomenon. Demyelinated nerves struggle to conduct electrical signals when the body warms up, so symptoms like blurry vision, weakness, fatigue, balance issues, and cognitive fog can intensify within minutes. It feels like a relapse, but it’s actually a pseudo‑exacerbation, miserable, but not causing new inflammation or damage.

Cold can be just as disruptive, though it’s talked about far less. For many, cold weather increases stiffness, spasticity, nerve pain, and the MS hug. When temperatures drop, blood vessels constrict, and in MS, that overreaction can amplify discomfort and make movement feel heavier and more effortful. Some people feel like their whole body locks up the moment the temperature dips.

Storms and barometric pressure changes are another major trigger. Many people with MS describe themselves as “human weather radars,” noticing symptom shifts before the forecast even updates. Falling pressure can subtly change how tissues behave, irritating already‑damaged nerves.

Storm systems also bring humidity, which traps heat and forces the body to work harder to cool itself. The result is often a spike in fatigue, pain, tingling, migraines, or balance issues.
Science hasn’t fully mapped the mechanism yet, but patient reports are consistent and impossible to ignore. Rapid temperature swings, those weeks where it’s 80 degrees one day and snowing the next, which has been the weather here in Nebraska the last few weeks can be especially rough.
Research shows that MS clinic visits increase on days with large temperature fluctuations. The nervous system likes stability. Weather rarely cooperates. There’s no perfect climate for MS, but many people do better in mild, cooler, less humid environments. Hot, humid climates tend to worsen symptoms for most, while very cold climates can increase stiffness and pain. The sweet spot is often somewhere in the middle, where the body isn’t constantly fighting extremes.
Does your body react to weather changes?
I know my body has a sweet spot, I dont know the specific temperature range but I should track it.

Less than 2 weeks until Walk MS Chicago!
04/14/2026

Less than 2 weeks until Walk MS Chicago!

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Chicago, IL

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