A Letter from Clay and Carrie Mauritson
Our oldest son Brady was diagnosed with Down Syndrome in September, 2010 at the age of 2 ½. The diagnosis was emotionally devastating for our family. At the time, it felt as if every parent’s worst fears had come true. Little did we know what an incredible blessing this diagnosis would be and how it would profoundly change our lives.
That being said, I don’t know how we would have made it through those first couple of months without the tremendous support of the Down Syndrome Association, North Bay (DSANB). They provided desperately needed educational resources, medical recommendations, and emotional support.
Unfortunately, our story is not unique; the DSANB provides these resources to countless families in and around Sonoma County. Their mission is simple: To promote advocacy, raise awareness, further educational pursuits, and support research for people with Down Syndrome and their families.
While the group is derived of some of the most caring, passionate, and dedicated people I have ever met, they can only do so much with limited funds and the problem is getting worse: what little Federal and State funding that has been available is in jeopardy due to the current fiscal climate and economic crisis.
My wife and I are committed to raising awareness and advocating for all people with disabilities, especially those with Down Syndrome. Please join us for this fantastic Zinfandel event and help us raise money for an amazing cause. We hope to see you there.
—Clay and Carrie Mauritson