Fight ALS.

Hi friends and family - this weekend I will be running in the ALS SuperHero Dash in memory of my father-in-law Kevin. As many of you know, ALS (Amyotrophic lateral sclerosis) is a devastating disease that affects individuals and their families in unimaginable ways.

The ALS Association is dedicated to assisting families throughout the most challenging times, offering vital resources and unwavering compassion. The McDevitt family experienced firsthand the tremendous support and care provided by this organization.

I am honored to help support them as they supported the McDevitt family.

If you can donate even a little it would be deeply appreciated. You can find more information on ALS and the event below:

Please Support Me...

On May 20th, I will be participating in the SuperHero 5K/10K Dash, an event designed to raise funds in support of those with living with ALS. I am reaching out to you because I need your help to reach my personal fundraising goal. Together, we can support those living with ALS while spreading awareness of the urgency to find treatments that will lead to a cure.  

This is a great time to get your family, friends, colleagues, and neighbors involved and become SuperHeroes! Please consider the difference that you might be able to make in the lives of people affected by this disease. Join me at Harriet Island on May 20th or make a donation!

Why Your Help Matters...

Also referred to as Lou Gehrig's Disease, amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly takes away the body's ability to walk, speak, swallow and breathe. There is currently no cure for the disease with life expectancy averaging 2 to 5 years from the time of diagnosis.

Due to the rapid progression of ALS, the needs of someone living with the disease evolve rapidly over a short period of time. Often times insurance does not cover durable medical equipment, so The ALS Association utilizes a loan pool that allows people to access equipment at no charge. Caregivers often need a break, so The ALS Association pays for skilled home care workers to give those caregivers time. The ALS Association also provides augmentative communication devices that are critical when someone's ability to speak has been compromised.  

All of these supports help individuals and families impacted by ALS live the fullest life possible, which is why I'm asking you to support my fundraising efforts. Help make a difference and donate today by clicking on the Donate key. Your gift will make you a hero in the lives of others.     

Thank You!