About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

Recipe for Mind-Body Wellness

By Doug Ankerman

Wee-Ha!  Phew, it has been crayzee celebrating MS Awareness Month! Wait, what?  You want MY recipe for mind/body wellness? Oh, I don’t know, we are all so very different.  What works for ME might not work for YOU.

Celebrating Mind Body WellnessIt’s like a recipe for chocolate chip cookies—everyone makes them a tad bit differently. Well, sure.  If you are okay with it, here is my personal recipe for mind/body Continue reading

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Blame it on the Brain…

By Scott Cremeans

The knee bone is connected to the thigh bone; the thigh bone is connected to the hip bone, and it is all connected to the brain bone. Ok, so the brain is not a bone, but that line sounds better poetically. The mind-body connection is often ignored and overlooked, especially if there is nothing wrong. When something does go wrong, many people bury it deep in their psyche, like a squirrel that hides his nuts for the winter. This disguise over Continue reading

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Rock Climbing and MS

By Amanda Bastien, PT, DPT

Exercise is medicine. As a physical therapist, I believe that, and I teach my patients the benefits and opportunities that exercise can grant them daily. As a person with MS, I am grateful that I am able to exercise unencumbered by symptoms at this time. I know that someday, that might change, but for now, I’ll enjoy every minute of it.

I started rock climbing the year I was diagnosed with MS, which was also the hardest year of my life in school. Climbing was Continue reading

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A Healing Mindset

By Alene Brennan

When I was diagnosed with multiple sclerosis, I immediately went into action in changing my diet. As a nutrition coach, it’s how I knew how to heal.

That approached served me well. It helped me to significantly reduce my symptoms – specifically brain fog and fatigue.

However, what I mistakenly overlooked was the way Continue reading

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Coronavirus, Multiple Sclerosis, Health Fears, and Lessons

By Stacie Prada

With the current coronavirus spreading, wellness is at the forefront of the news. I live in Washington state where the first confirmed cases and deaths from COVID-19 (the coronavirus) in the United States occurred. My neurologist’s office is in Kirkland, the epicenter of the US outbreak. We have a confirmed case in my community, and others are pending test results.

I’m writing this on March 8, 2020, and news updates are frequent. By the time I hit publish on this post, Continue reading

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10 Tips for Planning an Accessible Vacation

MSAA recently asked Founder and Executive Director for Open Doors Organization, Eric Lipp, for advice on how to research and plan a wheelchair accessible trip. Read below for his 10 tips for planning an accessible vacation.

This is a great question and if you’re thinking about traveling this spring or summer, now is the time to start planning. You can never do enough due diligence! Also, I’ve never heard from a traveler, “I was over prepared!” Don’t be afraid to start at Continue reading

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The New You

By Doug Ankerman

Here is my car. My loyal steed. Thirteen years old with 145,000 hard-earned miles on the odometer. Showing more than its share of bumps and scrapes. Door dings. And a couple of rust spots. Inside the carpet is worn in places while the driver’s seat has a stain of a long, forgotten fast-food burger.

Acceptance, they call it.“Wait a minute, what does this have to do with MS?” you ask.

Well hear me out. Continue reading

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A Life with Multiple Sclerosis Has Taught Me the Importance of Letting Go of Yesterday

Life with multiple sclerosis means letting go.

By Penelope Conway

I have a problem with expecting too much from myself which in turn hurts me more than helps. This year I have made it my purpose to evaluate my life and simplify everything I’m doing as much as I can. Is that even possible? There are things I want to do, things I need to do, and things I need to let go of. Multiple sclerosis has definitely changed my perspective about everything in life.

Some of the top priorities for me are Continue reading

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The Changes in Me Since My MS Diagnosis: Kinship and Nurturing My Well-Being

By Stacie Prada

Experiencing life events and trauma can change a person. We all experience life milestones and challenges, yet they are so personal and timed differently for each of us that how we react or change is never the same. Losing a loved one or experiencing an illness is different when experienced as a child, a young adult or as an older adult. Our expectations and life skills are different at each point in our life, and what may be life changing for one may be life affirming for another.

As I reflect on how being diagnosed with multiple sclerosis and living with symptoms has affected me, it’s difficult for me to Continue reading

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Old and New Me

By Lauren Kovacs

If you are like me, I try. Everyday is new. We have a “new me” daily. Some days we are the broken car in the garage and some days we are a strong engine.

On days your engine won’t turn over, don’t beat yourself up. We all have bad days. Some have really bad days. Try to hold on to something. Chocolate is meaty, but it makes things better.

I have had days that Continue reading

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