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
Mar 31, 2024
Feb 23, 2024
Feb 23, 2024
55 min
MSA Crusaders: Sisters Jennifer Frost & Andrea O'Neil Share Their Mother MSA Angel, Edith Huzar, Journey
Feb 16, 2024
Feb 16, 2024
1 hr 5 min
MSA Crusaders: Caroline and Her Son Jacob From Australia Share Their Personal Journey With Multiple System Atrophy.
Feb 9, 2024
Feb 9, 2024
1 hr 1 min
MSA Crusaders: John MacDonald From New Zealand, Shares His Personal Journey With Multiple System Atrophy.
Jan 26, 2024
Jan 26, 2024
40 min
MSA Crusaders: Physical Therapist Ryan Schaeffer Shares His Experiences With Multiple System Atrophy.
Jan 19, 2024
Jan 19, 2024
46 min
MSA Crusaders: RAW & Unedited, David & Daisy Share Their Updates with Multiple System Atrophy.
Jan 12, 2024
Jan 12, 2024
59 min
MSA Crusaders: Suzy Knox (Wife of host David), Shares Her Journey with her husband's Multiple System Atrophy.
Jan 5, 2024
Jan 5, 2024
43 min
MSA Crusaders: Clinical Trial Participant, Gary Troutman Shares his Journey with Multiple System Atrophy.
Dec 22, 2023
Dec 15, 2023