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
- Tweets 8,416
- Following 2,266
- Followers 2,320
- Likes 8,651
594 Photos and videos
Pinned Tweet
28 Dec 2022
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
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Dan & Jen Digmann retweeted
8 Oct 2024
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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1 Oct 2024
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 retweeted
1 Oct 2024
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
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Dan & Jen Digmann retweeted
26 Aug 2024
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
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24 Aug 2024
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…
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Dan & Jen Digmann retweeted
23 Aug 2024
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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19 Aug 2024
I’ll give you 113,015 reasons for Congress to act on pharmacy benefit manager reform. That’s how much it costs for my MS disease-modifying therapy each year. Thanks to Jacob Bennett from @RepDanKildee’s office for meeting with us to talk about PBM reform. #msactivist
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19 Aug 2024
Thanks for sharing this, and thanks for always being there to support our efforts, @McgheeCorbin!
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Dan & Jen Digmann retweeted
17 Aug 2024
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 retweeted
8 Aug 2024
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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8 Aug 2024
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 retweeted
30 Jul 2024
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
25 Jul 2024
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.
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Dan & Jen Digmann retweeted
16 Jul 2024
This is a good reminder for myself and hopefully for others living with Multiple Sclerosis. We are needed and valuable.
multiplesclerosis.net/living…
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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
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Dan & Jen Digmann retweeted
7 May 2024
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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30 Apr 2024
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
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Dan & Jen Digmann retweeted
28 Apr 2024
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
ALT A comic book-style quote that says: "From the moment of my diagnosis, I was determined not to let MS defeat me. We all have superpowers. I have come to realize that my true strength is not in the ability to bounce back, but in the belief that I can." - Traci, diagnosed in 2002
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Dan & Jen Digmann retweeted
25 Apr 2024
.@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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Dan & Jen Digmann retweeted
22 Apr 2024
❤️❤️ what a way for me to celebrate my turning 50! Thank you, @DanJenDig
Loved Bruce. Love you!! Epic Show!!!
22 Apr 2024
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Dan & Jen Digmann retweeted
10 Apr 2024
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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