Bob's ALS Team

I walk in memory of my amazing husband, Bob, because he no longer can.

Bob was diagnosed with ALS in December 2019. He lost his fight with this terrible ruthless disease in August 2023 just 2 months shy of our 35th wedding anniversary.  My hope is that no one ever has to go through the horrible experience that we had to face. Bob's great attitude and awesome sense of humor got us through some of the worst days of our lives. I will never regret even one second of our time together. Hopefully others will never have to lose one second of time with their loved ones.

Please donate whatever you can. Every little bit will help someone with ALS in some sort of way. 

Thank you for visiting my fundraising page.  I'm participating in ALS United Connecticut's Walk ALS to raise funds that will support individuals and families affected by ALS.

Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of it's ability to walk, speak, swallow and breathe.  The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis.  ALS can strike anyone regardless of age, gender, nationality, or ethnicity, although it is primarily an adult-onset disease.  Currently there is no known cause or cure.

Being a part of ALS United Connecticut's Walk ALS is the number one way to unite and fundraise for those living with ALS.  Please consider supporting my efforts by donating through my fundraising page.

Your donation today will help fund resources and services to the local ALS community, help find new ALS treatments, and move us closer to a world without the disease.

Please feel free to send this page to any friend or family member who might be interested in donating!

Thank you!