Hoofing It: Walk MS 2008

Five years ago this month I believed that the numbness that began in my left shoulder was nothing more than a pinched nerve that would work itself out. As the weeks passed, the numbness enveloped everything from my left shoulder to the very tips of my left hand. The continued progression and intensity to a feeling of pins and needles accompanied by burning sensations ultimately led to a doctor’s visit. After countless tests I was diagnosed with Multiple Sclerosis. Even after five years the numbness, tingling, and burning still remain.

The reason I share this is because this weekend I and several friends will be joining thousands of other people across the country as we walk. We walk to fight Multiple Sclerosis. We walk that others might know the terrible effects that this disease inflicts upon individuals, families, and children. We walk to bring hope that researchers will find the cure to this disease. We walk for those that cannot.

The research, educational, and support programs that are funded by The National Multiple Sclerosis Society change the lives of people with MS. People like me. People like my father. When my father was diagnosed in 1982, there were very few of the treatments for Multiple Sclerosis that we have today. A diagnosis of Multiple Sclerosis was in essence a precursor to disability. Research funded by the MS Society has helped to discover the treatments that allow us to continue to live our lives, advance our careers, and build our families. The educational and support programs help us to understand what MS is, how it will affect our lives, and how it will affect those around us. It provides us with the tools and knowledge to keep moving despite the disease.

Unfortunately, none of these programs are possible without the necessary financial resources. It is my hope that you will join me in helping meet these financial needs. I realize that no one likes being asked to donate money to something. However, knowing firsthand the impact that the MS Society has empowers me to make this plea. It is also easy to advocate for an organization where nearly 80% of all income is directed to research and local programs.

You can make a donation/pledge online quickly and easily. I’m not asking for anything eye-popping. I’m hoping you’ll join me and support my team with a donation/pledge of just $20. Together, each of our $20 could be what makes the difference in finding a cure. Even if it doesn’t find a cure, I hope you’ll smile knowing you made a difference in the life of someone with MS!

Thanks in advance for your support of me and my team – the mooving hurd!!