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
Aug 15, 2025
Aug 15, 2025
17 min
“When the Voice Becomes a Clue: How MSA-P and MSA-C Change Speech Over Time”
Jul 18, 2025
Jun 27, 2025
Jun 27, 2025
52 min
Daisy talks to Carrie about starting the MASCOT clinical trial and to Sarah about her recent hospitalizations/ They talk about creating awareness with "The Purple Hat Society". It's a great way to start up a conversation to create awareness. It's also not just for women, men can wear purple hats too. Carrie and Daisy talk about creating awareness by collaborating their music to create awareness {look out for more to come!)
Jun 20, 2025
Jun 6, 2025
Jun 6, 2025
54 min
Paul Gibson Joins MSA CRUSADERS. Join Us As We Speak On Medical Fatigue and PTSD.
May 30, 2025
May 30, 2025
37 min
Mission MSA CEO, Joe Lindahl joins David & Daisy to talk about the Charity Organization & More!
May 16, 2025
May 9, 2025
Apr 25, 2025
Apr 19, 2025
Apr 19, 2025
35 min
M.S.A. Momma tells Daisy about her journey and how laughter is the best medicine.