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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

Joined July 2009
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We’re going beyond New Year’s resolutions in 2023. Who’s with us? Join us here or wherever you listen to your podcasts as we delve into starting the new year with the challenge to build on the momentum we started the final weeks of 2022. bit.ly/3vjvPJk


Dan & Jen Digmann Reposted

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

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Dan & Jen Digmann Reposted
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Dan & Jen Digmann Reposted

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 Reposted

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.

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Dan & Jen Digmann Reposted

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

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Dan & Jen Digmann Reposted

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.

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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

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Dan & Jen Digmann Reposted

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

I asked the CVS Caremark CEO how much he’s charging for a $16 drug for multiple sclerosis. Answer: $6,229. Yeah, that‘s a 38,000% markup from this Fortune 10 PBM.



Dan & Jen Digmann Reposted

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 Reposted

@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

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Dan & Jen Digmann Reposted

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

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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: p2a.co/sALXay2 #MSActivist


Dan & Jen Digmann Reposted

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

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Dan & Jen Digmann Reposted

.@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 Reposted

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


Dan & Jen Digmann Reposted

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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