We are A Couple Takes on MS. He’s walking. She’s rolling. Together, we’re moving forward. Engaging public speakers, authors, MS activists
Mount Pleasant, Michigan
Joined July 2009
- Tweets8.4K
- Following2.3K
- Followers2.3K
- Likes8.6K
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
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
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.
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
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…
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
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
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
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!!!
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
Dan & Jen Digmann retweeted
Our Caregiving.com podcast features inspiring stories and practical advice from caregivers just like you. Tune in for support and solidarity. 🎧
Listen now: [youtube.com/@Caregiving]
#caregiving #realtalk #caregivers
Dan & Jen Digmann retweeted
Harnessing #AI: Transforming #MS Care. New MS Living Well Podcast🎧: Profs. Arbel🇨🇦 & Barnett 🇦🇺
bit.ly/3vKz2Fu🍏apple.co/3Jap6bl
@MustStopMS @TheGirlWithMS @narologist @Ali_SyedRaza @jsabatino37 @DrJim4MS @CathyChes @TheMSKittylady @JeffreyDunnMD
Dan & Jen Digmann retweeted
Telehealth isn't just convenient — it makes it easier for people living with MS to get the care they need.
Today at 10 AM ET @MSActivist Jeanette will testify before the @HouseCommerce committee on the importance of this crucial service.
Watch Live: ntlms.org/3JcVhqN
Dan & Jen Digmann retweeted
Navigating #MS with Other Medical Conditions? 🎧NEW MS Living Well Podcast. Prof Marrie & Dr. Cascione.
bit.ly/49WLLnf🍎apple.co/3PrjnBv
@RachelHorne19 @MustStopMS @themsguide @TheMSKittylady @DanJenDig @MarkWebb_ @MS_Stumbling @MSCanOfficial @TheGirlWithMS
Dan & Jen Digmann retweeted
Thank you for your ongoing advocacy for those of us living with #MultipleSclerosis You guys are indefatigable, continually making a difference as you raise awareness and promote positive action for supporting, treating and ultimately curing people from this pernicious disease. 🙏
Dan & Jen Digmann retweeted
Brad Allen should not leave the stadium with his whistle. Fired on the spot, no compensation the remainder of the year. #OnePride
