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Scott Stafne is a passionate young father focused on living a full life despite the ill-fated impact of neuromuscular disease.
Scott grew up in Cottage Grove, Minnesota where his parents Gerry and Judy Stafne still live. He graduated from Park High School in 1990 and from the University of Minnesota Institute of Technology with a degree in Mechanical Engineering in 1995. He worked in information technology for Accenture in Minneapolis after graduation and later, for Guidant Corporation in St. Paul. In 2002 he married his wife Kirsten.
Scott was diagnosed with Amyotrophic Lateral Sclerosis (ALS) or Lou Gehrig's Disease in 2004, a few weeks after learning he and his wife Kirsten were expecting a baby. His daughter Eva, now 2 1/2 years old, brings light, energy and hope to Scott despite his steady disease progression.
Scott has taken a very serious and difficult disease and opted to do everything he can with the time he has available to educate and spread awareness of ALS. Scott and his family are working to raise over $100,000 for research through a variety of events and activities. Scott enjoys speaking at engagements to promote ALS awareness, as well as share his own experience with ALS. Scott finds taking proactive, positive action to educate others about ALS to be enormously meaningful and therapeutic.
No longer employed, Scott pursues his interests in writing and film by publishing a blog and recording and editing video as part of a legacy project for his daughter.
Scott and Kirsten are expecting another daughter in March 2008. Scott looks forward to enjoying life with his newly expanded family and friends. He and his family live in Woodbury, Minnesota.
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