MS Diagnosis Journey

In the chronic disease arena, most everyone is more than willing to share their story for their own benefit and that of others. At the core of each story is the diagnosis. Everyone has a story to tell, and every storyteller needs an audience. We invite you to join us for the Multiple Sclerosis Diagnosis Journey podcast and listen to these unique stories. There's much to learn from each other by listening to these stories of diagnosis. By sharing their experiences with others, the MS Diagnosis journey podcast will serve as a vehicle for healing and empowerment for the storyteller. Support of this project is made possible through the generosity of Janssen Pharmaceutical Companies of Johnson & Johnson.

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MS Diagnosis Journey

DeLisa French: "Your Medical Team Works For You!"

August 25, 2022 • Episode 23

It took DeLisa French ten years from the onset of her symptoms before she got a diagnosis of Multiple Sclerosis. She now sees MS as a blessing and a curse, and although it might slow her down, she won't let it stop her.

DeLisa is another guest to advise people to advocate for themselves on their own diagnosis journeys. As she says, whether you're covered by Medicaid, Medicare, or Health Insurance, your doctors are paid by YOU. So make sure they know what you're dealing with!

DeLisa's MS has now been classified as Secondary Progressive, but she continues to look forward to the future with positivity.

Interview by Laura Kolaczkowski
Edited by Steve Woodward at The Podcasting Editor
Podcast artwork by Jackie Zimmerman at Queen of GSD
Background Music is “Old Photos” by Olexy

Support of this project is made possible through the generosity of Janssen Pharmaceutical Companies of Johnson & Johnson.