Jennifer and Dan Digmann have been married since 2005 and have lived with Multiple Sclerosis throughout their relationship - Jennifer was diagnosed in 1997, Dan in the year 2000. They met at a National Multiple Sclerosis Society event in 2002, and since then, they have dedicated their lives to MS activism and helping others to live their best lives. 

In the final part of this two-part interview, Dan & Jennifer talk about the effect that COVID has had on their advocacy work, and their plans for the future, including their podcast and YouTube channel. We also chat about the difficulty of finding support and the opportunities that are available for younger generations with regards to advocacy.

DISCLAIMER

The information contained in this podcast is for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare providers with any questions you may have regarding a medical condition or treatment.

Visit A Couple Takes on MS and listen to the podcast 
Visit Dan & Jennifer's YouTube channel 
Email [email protected] 

If you're interested in having Kathy speak at your event, learn more here

Find out more about the DMAT Fitness Training program

Visit MS Disrupted

You can find Kathy Chester at:
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[email protected]
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