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    Multiple sclerosis overview
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  • Living with
    Living with MS
    Mental health
    McDonald criteria
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    MS hug
    Cannabis and MS
    MS spasticity
    Heat sensitivity
    MS in men
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    Support and resources
  • Community
    Perspectives
    • Authentically Human – Desiree Lama
    • Balancing Grit and Grace – Ahna Crum
    • Chairborne — Ben Hofmeister
    • Delicate Balance – Leigh Anne Nelson
    • Rhythms and Routines – Susan Payrovi, MD
    Archived Columns
    • A Life in Letters — Jamie Hughes
    • DISabled to ENabled — Jessie Ace
    • Dive to Fight MS – Mike Parker
    • Fall Down, Get Up Again — John Connor
    • Goldilochs — Stephen De Marzo
    • Patiently Awakened — Teresa Wright-Johnson
    • The MS Wire — Ed Tobias
    • Silver Linings — Jennifer Powell
    In memoriam
    • Through the Looking Glass — Beth Shorthouse-Ullah
    Guest Voices
  • News
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    Expert voices
    • Exercise
    • Pain management
    • Cannabis use
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    • Managing fatigue
    • Sleeping well
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    Video & Podcasts
    • Get Tough on Multiple Sclerosis Video Series
    • Get Tough on Multiple Sclerosis Podcast
    • The Multiple Sclerosis Podcast
    • Video: MS caregiving journey
    • Video: MS life changes
    Featured Topics
    • Newly diagnosed guide
    • MS pathways
    • Living strong
    Advocacy partners

Throughout March, Multiple Sclerosis News Today is recognizing Multiple Sclerosis (MS) Awareness Month through a variety of stories representing different perspectives on life with MS. These stories highlight some of the unique challenges of living with MS, as well as stories of hope, inspiration, and other topics that help to generate awareness among the MS community. Follow along with the series here or visit us on Facebook, Instagram, X, or Pinterest using the hashtag #MSSpotlight.

My niece’s diagnosis of MS brought us closer together

From left, Adela Puente and her niece, Desiree Lama, spend time together in downtown San Antonio. (Photos courtesy of Desiree Lama) Day 31 of 31 This is Adela Puente’s story: Lama and Puente share a hug at Desiree’s college graduation. Being the youngest of six, I always wished…

Having RRMS has taught me how to live one moment at a time

Ross smiles for a photo. (Photos courtesy of Ross) Day 21 of 31 This is Ross’ story: I was diagnosed with relapsing-remitting multiple sclerosis (RRMS) in 2007 when I was a senior in college. I had been very sick with vertigo and gastrointestinal issues for a year…

Learning from others in the MS community empowers me

Jenn Powell wears her MS ambassador shirt with pride. (Photos courtesy of Jenn Powell) Day 20 of 31 This is Jenn Powell’s story: Hosting The Multiple Sclerosis Podcast has been eye-opening, exposing me to the diverse and inspiring voices within the multiple sclerosis (MS) community. Every guest I…

How I’ve embraced a holistic approach to living with MS

Latifa Janahi takes a five-day course of corticosteroids to reduce inflammation in her body. (Photos courtesy of Latifa Janahi) Day 19 of 31 This is Latifa Janahi’s story: I am a woman from Bahrain Island who’s passionate about technology and baking. After working in the tech field for 10…

Food fights and alien languages: Finding humor in life with MS

Dee Ecklund, riding her Alinker, finishes a Turkey Trot on Thanksgiving 2024. (Photos courtesy of Dee Ecklund) Day 18 of 31 This is Dee Ecklund’s story: I am a firm believer everything happens for a reason. Maybe we have some things to learn, teach, or even both. With the…

I imagine MS as the uninvited guest permanently at my dinner table

Ronald Harris shows off his new power wheelchair. (Photos courtesy of Ronald Harris) Day 17 of 31 This is Ronald Harris’ story: Harris is seen working from home, using a desk that accommodates his power chair. My journey with multiple sclerosis (MS) began with an unexpected diagnosis…

Sharing my truth as one of many stars in the MS universe

Tom Anderson, 67, was diagnosed with multiple sclerosis at about 30 years old. (Photos courtesy of Tom Anderson) Day 16 of 31 This is Tom Anderson’s story: I may be the dimmest star, but don’t get all hokey on me. There are lots of us. The following are the…

My dad with MS teaches me to live wholeheartedly

Sterling Hofmeister is pictured here at 6 months, carried in a backpack by his father Ben Hofmeister. (Photos courtesy of Ben Hofmeister) Day 15 of 31 This is Sterling Hofmeister’s story: Sterling Hofmeister, far right, is pictured with his brothers and father in 2018. My name is Sterling…

Prioritizing mental and physical health after an MS diagnosis

Yara Essam takes a selfie in a mirror during one of her many gym sessions. (Photos courtesy of Yara Essam) Day 14 of 31 This is Yara Essam’s story: I’d always been fairly healthy as a child — barely getting sick, eating well, and constantly moving my body. That’s…

With or without MS, we are all unique people — from A to Z

Christy Hoffman poses for a picture with her husband Mike, who has MS. (Photos courtesy of Christy Hoffman) Day 13 of 31 This is Christy Hoffman’s story: Anxious. Blessed. Curious. Daring. Excited. Frustrated. Gregarious. Happy. Isolated. Jovial. Kind. Loving. Moody. Numb. Opinionated. Pumped. Quiet. Restless. Strong. Trusting. Underrated. Valiant.

Finding workarounds makes it easier to navigate an MS flare

Nanette Lai locks eyes with her chihuahua Fanny. Lai says mutual gazing between humans and dogs can cause synchronization in areas of the brain. (Photos courtesy of Nanette Lai) Day 12 of 31 This is Nanette Lai’s story: My name is Nanette, and I have lived with relapsing-remitting…

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Recent Posts

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