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

Nohora Gutierrez: "I want to see my lesions!"

July 07, 2022 • Laura Kolaczkowski • Episode 16

When she was first diagnosed, Nohora Gutierrez was told by her (former) neurologist to stay away from MS Support Groups. She was even told which drug she was going to take.

As a trainer, Nohorra is naturally drawn to learning as much as possible and sharing her knowledge with people. Looking back now, she sees that she was dismissed and wishes that she could have advocated for herself better.

In this interview, Nohorra wants anyone who is newly diagnosed to know that they have more treatment options than ever before. And that support groups are out there to help you along your journey.

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.