← Return to Parkinson's plus Multiple System Atrophy (MSA)
DiscussionParkinson's plus Multiple System Atrophy (MSA)
Parkinson's Disease | Last Active: Dec 10, 2025 | Replies (63)Comment receiving replies
Replies to "Hello @pammettee Welcome to Mayo Connect. My name is Teresa and I am a volunteer mentor..."
My husband received this diagnosis this week at UT Southwestern Medical Center. His next step is to get an appointment at their MSA Clinic; he said to expect a two month wait. We would love to see posts regarding this rare disorder as this is new journey for both of us. This is my first post; I don’t know if it’s going to everyone or only one person. I’m hoping it’s going to the whole group.
Connect

Hello,
My husband was an MSA patient at Mayo Clinic. As his spouse of 32 years and caregiver for seven, I joined Defeat MSA Alliance as an advisor, in hope that I can help other families navigate their MSA journey. I have been charged with researching grants that may help MSA patients and their families. Can anyone at Mayo point me in the right direction.
Thank you,
Jodi O'Toole