One Family's Hope for A Cure
Last October, our daughter, Megan, was complaining about double vision. What she thought would be quickly resolved with a trip to the eye doctor turned out to be so much more. A diagnosis of MS changed her life.
While she's been able to manage her MS with daily shots and has not experienced a second "episode", we are holding out for that day when an oral medication is available or better yet.... a cure!
|Megan and her father David|
We will walk as a team in Walk MS 2012 in Boulder for the first time. It just seems like a great way to rally people around this important cause.
Our fundraising efforts have gone quite well - not necessarily because people know Megan's story, but because they personally have a friend or family member who is afflicted with MS.
Everyone seems to have their own story of how MS has impacted their life. We will walk on May 19 for Megan and all the others who have connections to those who have joined our team or generously donated to our walk.
We are Craven-A-Cure!