UPCOMING EVENT:
Saturday, June 15th at 10:30 Support group for those with Atypical Parkinsons or anyone with a Movement Disorder. 

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​About our Organization

We are a family who loves BSU football, waterskiing, snow skiing, running 
together and our faith in Jesus Christ. In the spring of 2014 our father was diagnosed with Multiple System Atrophy--a rare neurodegenerative disorder.  During the past two years this disease has taken our father's ability to participate in the things we love as it attacks his balance, speech, fine motor skills and autonomic systems.  There are no treatments available and at the time of diagnosis the doctor gave him 5-7 years to live.  It is important for us to do something to help and so we have 
established this non-profit 501 (c)  association to raise awareness and money for research.  All of the money raised will be donated to the MSA Coalition. 

About MSA:

Multiple system atrophy (MSA) is a progressive neurodegenerative disorder characterized by a combination of symptoms that affect both the autonomic nervous system (the part of the nervous system that controls involuntary action such as blood pressure or digestion) 
and movement. The symptoms reflect the progressive loss of function and death of different types of nerve cells in the brain and spinal cord.
MSA is a rare disease, affecting potentially 15,000 to 50,000 Americans, including men and women and all racial groups. Symptoms tend to appear in a person’s 50s and advance rapidly over the course of 5 to 10 years, with progressive loss of motor function and 
eventual confinement to bed. While some of the symptoms of MSA can be treated with medications, currently there are no drugs that are able to slow disease progression and there is no cure.
Below are pictures from our Fourth Annual Race. Thanks for your support!
Play the slide shows below to see more great pictures from our October 2018 event.