Dan & Jen Digmann @DanJenDig
We are A Couple Takes on MS. He’s walking. She’s rolling. Together, we’re moving forward. Engaging public speakers, authors, MS activists acoupletakesonms.com Mount Pleasant, Michigan Joined July 2009-
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Dan & Jen Digmann retweeted
MULTIPLE SCLEROSIS: Need to be around people who ACTUALLY understand your #MS? We got you 🙌 Join other peers as we all chat about life with #multiplesclerosis 2nd Tuesdays 8:30pm ET Drop in: gotomeet.me/AnswerCancer @DanJenDig #MSwarrior
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We figuratively have nearly $150K riding on the Nov. 5 election — that’s the estimated annual cost of our MS therapies. When candidates talk about lowering drug prices, we’re listening. The solution? It starts w/Pharmacy Benefit Manager reform. bit.ly/47NbrT6 #msactivist
Dan & Jen Digmann retweeted
Mind over MS: Strategies for Staying Positive New MS Living Well Podcast🎙️with @tripping_onair & @tcspeaks32 bit.ly/3zOja6P🍎apple.co/3ZLoAu1 @DanJenDig @LisaEmrich @TheGirlWithMS @DrAmyBSullivan @Montel_Williams @narologist @napolineuro @MarTintore @CathyChes
Dan & Jen Digmann retweeted
Women are 6 times more likely to be separated or divorced soon after a diagnosis of cancer or multiple sclerosis than if a man is the patient—a sad truth. Cheers to the majority who commit to the journey. #MS #lifewithMS #chronicillness #MSwarrior #perseverance #hope
Thx to @AdamMGrant & @rafi_kohan for their conversation about the value of trash talking. It makes me feel better that I’ve found strength in trash talking MS in my competition with the disease these past 25 years. msfocusmagazine.org/Magazine/Magaz…
Dan & Jen Digmann retweeted
Disrespect doesn’t just make people feel bad. It leads them to perform worse. Evidence from medical teams: Even a single insult decreases the quality of diagnoses and procedures. Rudeness disrupts focus and undermines collaboration. Civility is not optional. It’s vital.
Dan & Jen Digmann retweeted
Cadense Adaptive is revolutionizing the way the world thinks about adaptive footwear. We chatted w/its Chief Technology Officer and founder Tyler Susko about its game-changing shoes in our latest episode. Listen here or where you get your podcasts. #MS bit.ly/3M9LUcV
Dan & Jen Digmann retweeted
Not all disappointing outcomes are failures. Some lead to improvements in your process. Success is about more than the results you achieve. It's also about the growth you attain. Progress is more than how close you come to your goal. It's how far you've come from your start.
Life-changing medicine never works if patients can’t afford it. Thanks to Colette from @SenGaryPeters’ office for taking the time to meet with us today to talk about legislation related to comprehensive Pharmacy Benefit Manager Reform. #msactivist
Dan & Jen Digmann retweeted
Medications can only work if people can afford and access them. PBMs are getting in the way and the @mssociety supports reform focused on getting patients the medications they need. #MSActivist #PBMReform
Medications can only work if people can afford and access them. PBMs are getting in the way and the @mssociety supports reform focused on getting patients the medications they need. #MSActivist #PBMReform
Dan & Jen Digmann retweeted
This is a good reminder for myself and hopefully for others living with Multiple Sclerosis. We are needed and valuable. multiplesclerosis.net/living-with-ms…
Dan & Jen Digmann retweeted
@DanJenDig had a life-changing moment at 2:34 a.m. while walking through his house. He came to terms with the true effects of his MS that he had been avoiding. This awakening prompted him to confront his MS head-on. Read Dan's full story: msfocus.us/noexceptions
Dan & Jen Digmann retweeted
Uncommon MS Symptoms🎧New MS Living Well Podcast! ⚡️Shocks🦵Spasms 🫂MS Hug 🌪️Spinning 👀Shaky Vision 💩Bowel Issues bit.ly/4a9cmwH 🍎apple.co/3UuorqA @themsguide @TheGirlWithMS @MarkWebb_ @DanJenDig @Brandon_Beaber @RachelHorne19 @TrishnaBharadia @deedubs57
I just registered for Virtual MS State Action Day in Michigan! Join me in taking action for people affected by MS: p2a.co/sALXay2 #MSActivist
Dan & Jen Digmann retweeted
It's #NationalSuperheroDay, and every single person living with MS lives with a variety of superpowers, from perseverance to resilience to adaptability. What's your superpower? Read more of Traci's story of MS superpowers here: ntlms.org/3JwqPIc
Dan & Jen Digmann retweeted
.@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
Dan & Jen Digmann retweeted
❤️❤️ what a way for me to celebrate my turning 50! Thank you, @DanJenDig Loved Bruce. Love you!! Epic Show!!!
❤️❤️ what a way for me to celebrate my turning 50! Thank you, @DanJenDig Loved Bruce. Love you!! Epic Show!!!
Dan & Jen Digmann retweeted
Thank you @HouseCommerce for highlighting the need to expand and protect access to telehealth services. Join fellow MS Activists by contacting your Members of Congress and urge them to support #telehealth today: p2a.co/rrFXtXh #MSActivist
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