Tiffany Christensen, President

My name is Tiffany Christensen. I am a daughter, sister, mother of 5, friend, and advocate for the Multiple System Atrophy community. I am a self-proclaimed daddy’s girl and my dad, Kurt Williams, was diagnosed with Multiple System Atrophy in 2014 with it confirmed in 2015. His symptoms began in early 2013. He is the reason for this organization and for me and my family to pursue raising awareness of Multiple System Atrophy and to support patients, families, and care-givers who are going through this journey.

My dad lost his battle with MSA (Multiple System Atrophy) on August 21, 2020. He fought hard. My mom fought hard and cared with even more intensity. We love him and miss him dearly. Thank you for supporting us on our journey and as we strive to support those who are currently on the MSA journey.

To date Move Over MSA has raised over $95,000 for research of Multiple System Atrophy and we hope to continue to help support this research to find treatments and hopefully a cure. Dad was humble and always hoped his story would help others and we are striving to do just that.

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