The MSA Blog
The Multiple System Atrophy Coalition’s official blog. Find posts on MSA tips, caregiving, patient experience, fundraising, research updates, and more.
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The Loving Sacrifice of Caregiving
By Deborah Park Hello, my name is Deborah and I'm a 25-year-old daughter whose mother lost her fight to Multiple System Atrophy on September 11, 2021. My story of caregiving began in 2018 when my mom was diagnosed with MSA-C. As a sophomore in college, I was...
Learning to Navigate Life Changes
By Wendy McCullough April 27th, 2023 marked 25 years since my husband, Jason, and I said, "I do." We vowed to love and care for each other through all of life's changes, and yet, when you are in your mid-twenties, you do not know exactly what that will mean. Life's...
You Walk Away? | A Poem from an MSA Patient
By Teresa Baker I write a great deal of poetry in order to express feelings, ideas, and opinions which come from someplace deep inside which cannot be easily explained; but I also think and express myself using abstract ideas which come through better using poetry. I...
From Parkinson’s to MSA: My Path of Resilience and Faith
Hello, my name is Teresa Scruggs-Dyer, and I want to share some of my experiences with Multiple System Atrophy (MSA). There are 2 types of Multiple System Atrophy, MSA-P (parkinsonian) and MSA-C (cerebellar). In July 2021, I was diagnosed with MSA-P. In early 2018, I...
MSA Instruction Manual
By Amy Davis When my husband was diagnosed with MSA-P in 2017 and after the shock of what we would be dealing with, I immediately wished for an MSA instruction manual. Through all the numerous doctors’ appointments, nothing prepared me for the frightening symptoms my...
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