Dan & Jen Digmann

We are A Couple Takes on MS. He’s walking. She’s rolling. Together, we’re moving forward. Engaging public speakers, authors, MS activists

[Dan & Jen Digmann @DanJenDig]

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.
https://t.co/xLpcCx3wGo

[AnCan Foundation @ancan501c3]

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: https://t.co/r4H8hFOIQZ

@DanJenDig #MSwarrior

[Dan & Jen Digmann @DanJenDig]

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. https://t.co/4I6olSFE85
#msactivist

[Barry Singer MD 🧠 @drbarrysinger]

Mind over MS: Strategies for Staying Positive
New MS Living Well Podcast🎙️with @tripping_onair & @tcspeaks32
https://t.co/rSBxGAYCQO🍎https://t.co/U7gaT9JaPJ
@DanJenDig @LisaEmrich @TheGirlWithMS @DrAmyBSullivan @Montel_Williams @narologist @napolineuro @MarTintore @CathyChes

[kenthemser @kenthemser]

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

[Dan & Jen Digmann @DanJenDig]

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. https://t.co/yaZYEo3YrK

[Adam Grant @AdamMGrant]

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 @DanJenDig]

Thanks for sharing this, and thanks for always being there to support our efforts, @McgheeCorbin!

[Dan & Jen Digmann @DanJenDig]

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

[coupletakesonms @CoupleTakesOnMS]

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

https://t.co/rUv3s962Lk

[Adam Grant @AdamMGrant]

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.

[Dan & Jen Digmann @DanJenDig]

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

[MS Activist @MSactivist]

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

[Jennifer Digmann @JenniferDigmann]

This is a good reminder for myself and hopefully for others living with Multiple Sclerosis. We are needed and valuable.

https://t.co/a3wDYTBlvU

[MS Focus: The Multiple Sclerosis Foundation @MS_Focus]

@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: https://t.co/ll3JMno1Wv

[Barry Singer MD 🧠 @drbarrysinger]

Uncommon MS Symptoms🎧New MS Living Well Podcast! ⚡️Shocks🦵Spasms 🫂MS Hug
🌪️Spinning 👀Shaky Vision 💩Bowel Issues
https://t.co/jB07YlHUhj 🍎https://t.co/Sdv7r7hs8p
@themsguide @TheGirlWithMS @MarkWebb_ @DanJenDig @Brandon_Beaber @RachelHorne19 @TrishnaBharadia @deedubs57

[Dan & Jen Digmann @DanJenDig]

I just registered for Virtual MS State Action Day in Michigan! Join me in taking action for people affected by MS: https://t.co/Jas2TTRjvo #MSActivist

[National MS Society @mssociety]

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: https://t.co/hEv1TTsYTn

[Jennifer Digmann @JenniferDigmann]

.@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 @DanJenDig]

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

[Jennifer Digmann @JenniferDigmann]

❤️❤️ what a way for me to celebrate my turning 50! Thank you, @DanJenDig

Loved Bruce. Love you!! Epic Show!!!