Jennifer Digmann
@JenniferDigmann
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Happily married and living with Multiple Sclerosis. Inconceivable, but possible.
Mount Pleasant, MI
Joined March 2016
RT @JimCosta_: GUESS WHO NOW HAS HOME FIELD IN THE ALDS . Comerica Park will be an absolute ZOO on Wednesday . #RepDetroit .
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I just registered for the upcoming #MSActivist Webinar: "Voting Without Barriers!" I hope you'll join me for the virtual event! Register today at:
p2a.co
Enter your information to register
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This is a good reminder for myself and hopefully for others living with Multiple Sclerosis. We are needed and valuable.
multiplesclerosis.net
Just because I have multiple sclerosis doesnāt mean that people donāt depend on me or benefit from the help I can provide. There is so much I still can do.
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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 .
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.@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.
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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 Michiganās HB 5339 follow this link and connect with your legislator: .
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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.
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Thank you! š§”.
āļøFAA Reauthorization is now "taking flight" with some new accessibility provisions!. Thank you to #Congress and @POTUS for prioritizing people living with disabilities - as we all deserve the ability to travel with ease. Check it outā”ļø #MSActivist.
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RT @mssociety: "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 chroniā¦.
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RT @RealTalkMS_jon: Today, there are more people living with MS who are over the age of 65 than there are people liā¦.
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RT @MargueriteC_MS: I just published an op-ed in @sfchronicle to share my experience with a copay accumulator. Itās time for CA legislatorsā¦.
sfchronicle.com
Copay accumulators are harmful policies that place an immense and unnecessary burden on...
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I just registered for Virtual MS State Action Day in Michigan! Join me in taking action for people affected by MS: #MSActivist.
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Dan and I always learn a lot and are reenergized as we gather with others in our MS community. #MSactivist
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šš¤š.
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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.
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RT @PositiveWithMS: How many MS patients does it take to screw in a lightbulb? None, because they keeps dropping it, get distracted, have tā¦.
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ā¤ļøā¤ļø what a way for me to celebrate my turning 50! Thank you, @DanJenDig . Loved Bruce. Love you!! Epic Show!!!.
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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 youāll check out my essay and discover the power of your voice. #MSactivist.
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I just took action for @MSSociety to help protect and expand access to #telehealth! Join me: #MSActivist.
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