GUESS WHO NOW HAS HOME FIELD IN THE ALDS Comerica Park will be an absolute ZOO on Wednesday #RepDetroit

I just registered for the upcoming #MSActivist Webinar: "Voting Without Barriers!" I hope you'll join me for the virtual event! Register today at:

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This is a good reminder for myself and hopefully for others living with Multiple Sclerosis. We are needed and valuable. https://t.co/a3wDYTBlvU

A recording from the Tuesday, June 25, AnCan MS group. A good session where we talked about caregiver burnout, home modifications, NMSS navigators and quite a bit more. #PeerSupport is what AnCan does best!! #MS https://t.co/PVqSRfDdiE

.@RepMoolenaar @SenStabenow @SenGaryPeters Can Dan and I count on you to pass the FY25 spending bills? These bills help fund critical #MSResearch as well as programs and services that people with MS rely on to live their best lives. #MSActivist

Dan and I had a great MS State Action Day. We met fellow #MSActivists and learned about Step therapy and access to MS medications. To advocate for Michigan’s HB 5339 follow this link and connect with your legislator: https://t.co/9CBQcHQaqi

Tomorrow, May 21, is the day for those of us in Michigan living with, or caring about, Multiple Sclerosis. It is MS State Action Day and this is your opportunity to advocate for the MS community. Interested? Follow this link and make your voice heard. https://t.co/hxSwL9QRKl

Thank you! 🧡

"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

https://t.co/JHOYItTnso Today, there are more people living with MS who are over the age of 65 than there are people living with MS under the age of 45. That's why this week's episode of RealTalk MS is all about aging with MS. #MultipleSclerosis

I just published an op-ed in @sfchronicle to share my experience with a copay accumulator. It’s time for CA legislators to take action and support AB 2180 to ban these harmful practices! Read here: https://t.co/Tx22WDrR0U #MSActivist

I just registered for Virtual MS State Action Day in Michigan! Join me in taking action for people affected by MS: https://t.co/cEYnHlMh23 #MSActivist

Dan and I always learn a lot and are reenergized as we gather with others in our MS community. #MSactivist

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.@RepMoolenaar @SenStabenow @SenGaryPeters can I count on you to support #MSResearch funding at the #NIH and #MSRP in fiscal year 2025? Together - we hope to find a cure for MS! #MSactivist

How many MS patients does it take to screw in a lightbulb? None, because they keeps dropping it, get distracted, have to take a pee break, or forget what they are doing in the first place.

❤️❤️ what a way for me to celebrate my turning 50! Thank you, @DanJenDig Loved Bruce. Love you!! Epic Show!!!

So much about MS can make me feel powerless, but advocacy and sharing my story has helped me reclaim some strength to manage and live with the disease. I hope you’ll check out my essay and discover the power of your voice. #MSactivist https://t.co/KzVL5nHYsQ

I just took action for @MSSociety to help protect and expand access to #telehealth! Join me: https://t.co/nIbPycNGcE #MSActivist