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
Sep 22, 2023
Sep 15, 2023
Sep 15, 2023
34 min
Alison talks about her late husband, Jeffrey, and his fight with MSA. Please vote for Marco Gonzales to receive the Roberto Clemente Award for Community Activism. Marco has worked to raise MSA awareness and funds for MSA research. You can vote here https://www.mlb.com/community/roberto-clemente-award
Sep 8, 2023
Sep 8, 2023
33 min
Daisy & David, patients of Multiple System Atrophy, speak about their journey and battle with MSA.