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
.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

May 6, 2026
May 6, 2026
22 min
Most people don’t realize how crucial cooling technology can be for managing conditions like multiple system atrophy (MSA). In this eye-opening episode, David Knox dives deep into innovative, high-tech ways to stay cool — and why traditional fans just don’t cut it for those with autonomic dysfunction. If you or a loved one struggle with irregular sweating, temperature regulation, or just need better comfort on the go, this episode is the game-changer you've been waiting for.
May 6, 2026
22 min

Mar 13, 2026
MSA Crusaders: We're Back!
Mar 13, 2026
Mar 13, 2026
45 min
MSA Crusaders: We're Back!
Mar 13, 2026
45 min

Feb 21, 2026
Feb 21, 2026
1 hr 20 min
5th Anniversary of fighting MSA. Full 5 year review of progression
Feb 21, 2026
1 hr 20 min

Jan 7, 2026
Jan 7, 2026
22 min
Moments from dying from saliva pooling complications with Multiple System Atrophy.
Jan 7, 2026
22 min

Dec 19, 2025
Facing MSA: Insights from David Knox
Dec 19, 2025
Dec 19, 2025
23 min
Join David Knox as he shares his personal journey living with Multiple System Atrophy (MSA). In this episode, David opens up about the daily challenges he faces, the medical treatments he's undergone, and the lifestyle changes he's embraced to manage his condition. With a focus on resilience and adaptation, David's story offers valuable insights and inspiration for anyone navigating life with a chronic illness. Tune in to discover how he maintains hope and strength in the face of adversity.
Dec 19, 2025
23 min

Dec 13, 2025
Dec 13, 2025
18 min
https://www.nature.com/articles/s41531-025-01121-w?utm_source=chatgpt.com#citeas
Dec 13, 2025
18 min

Nov 27, 2025
Scientists Halt Toxic Brain Protein
Nov 27, 2025
Nov 27, 2025
14 min
Scientists Halt Toxic Brain Protein Behind Parkinson’s in Landmark Study
https://scitechdaily.com/scientists-halt-toxic-brain-protein-behind-parkinsons-in-landmark-study/
Nov 27, 2025
14 min

Oct 17, 2025
LIVE: Understanding Mild Oropharyngeal Dysphagia
Oct 17, 2025
Oct 17, 2025
36 min
LIVE: Understanding Mild Oropharyngeal Dysphagia
Oct 17, 2025
36 min

Oct 3, 2025
World MSA Day! Good & Bad Days Ahead!!
Oct 3, 2025
Oct 3, 2025
42 min
World MSA Day! Good & Bad Days Ahead!!
Oct 3, 2025
42 min

Aug 22, 2025
Aug 22, 2025
9 min
ATH434 AS A POTENTIAL TREATMENT FOR MULTIPLE SYSTEM ATROPHY
Aug 22, 2025
9 min







