The msacrusaders’s Podcast
.David and Daisy are both patients with Multiple System Atrophy who want to create Awareness for this rare terminal neurological disorder for other patients, caregivers and medical staff to help become more knowledgeable of the disorder **While this podcast features discussions with medical experts, it is important to note that the information provided is for general informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Listeners are encouraged to consult with qualified healthcare professionals for personalized guidance* We want to create awareness for the rare disorder. David and Daisy are both patients of the disorder and will talk with other patients, Caregivers, physicians, therapists experienced with MSA
Episodes
Jul 5, 2024
Jul 5, 2024
1 hr 7 min
MSA Crusaders: PART TWO Seriously Sassy Sarah Returns to talk with us about Doctors, Treatments & More for MSA
Jun 28, 2024
Jun 28, 2024
1 hr 7 min
MSA Crusaders: PART ONE Seriously Sassy Sarah Returns to talk with us about Doctors, Treatments & More for MSA
Jun 21, 2024
Jun 21, 2024
1 hr 5 min
MSA Crusaders: Special Guest Denise Sutcliffe, Mother of Co-Host David Knox, Joins us LIVE
Jun 14, 2024
May 17, 2024
May 17, 2024
1 hr 9 min
MSA Crusaders: Susan Shares Lee's Journey, Joined by Daughter Danielle.
May 10, 2024
May 10, 2024
1 hr 4 min
MSA Crusaders: Aggie Returns to Update Us on her Clinical Trial and More!
May 3, 2024
May 3, 2024
1 hr 10 min
MSA Crusaders: Sarah Talks about Her Battle With MSA & Autonomic Failure. Repeat
Apr 26, 2024
Apr 26, 2024
54 min
MSA Crusaders: Daisy's Mother Jolie, Joins Us To Talk About MSA & Parkinson's as a Nurse, Mother and Wife
Apr 12, 2024
Apr 5, 2024
Apr 5, 2024
1 hr 7 min
MSA Crusaders: Danielle Marano Shares Her Journey From Cerebellum Ataxia to Multiple System Atrophy.