For the final episode of the MS Diagnosis Journey podcast, regular host Laura Kolaczkowski and editor Steve Woodward reflect on the stories that they've heard throughout the series. In this chat, Laura and Steve look back on what they found most interesting in previous interviews. Mostly what they take away from the series is the generosity with which guests have shared their own personal stories. Thank you to them and to everyone who has listened to and shared the MS Diagnosis Journey podcas...
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For the final episode of the MS Diagnosis Journey podcast, regular host Laura Kolaczkowski and editor Steve Woodward reflect on the stories that they've heard throughout the series. In this chat, Laura and Steve look back on what they found most interesting in previous interviews. Mostly what they take away from the series is the generosity with which guests have shared their own personal stories. Thank you to them and to everyone who has listened to and shared the MS Diagnosis Journey podcas...
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...
MS Diagnosis Journey
For the final episode of the MS Diagnosis Journey podcast, regular host Laura Kolaczkowski and editor Steve Woodward reflect on the stories that they've heard throughout the series. In this chat, Laura and Steve look back on what they found most interesting in previous interviews. Mostly what they take away from the series is the generosity with which guests have shared their own personal stories. Thank you to them and to everyone who has listened to and shared the MS Diagnosis Journey podcas...
