Hello Family and Friends,
If you are here, you've found your way to one of the Nivlac V Ride and Rally pages. This fundraising program requires a personal page and a team page. We combine all of our donations into one family fundraising endeavor. Because I'm the team captain, the donation will show under Bethe Sullivan. Please feel free to donate (and join if you wish to) under the team page. Please feel free to either donate to the general donation page or join as a team member and your donation will show under your own name. Either way, your donation will be acknowledged on the Nivlac V donation scroll.
When you donate on either page, you will be donating in memory of Cal; loving husband to Rosemarie, inspiring father to Tom, Camille, Bethe, Patti and Peter, , welcoming father-in-law to Darlene and Tim, and doting grandfather to Robert, TJ, Katherine and Jonah. If you are here, you can navigate to the team page using http://web.alsa.org/goto/nivlacv22
Thanks and blessings to you all. Hope to see some of you at the Ride and Rally.
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its 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, and presently there is no known cause or cure.
That’s why I’m walking. To change the statistics. To bring help and hope to those living with the disease. To ensure that no one ever hears the words: “You Have ALS” again.
The past two years have brought incredible advancements in ALS research, expanded access to care for people living with ALS, and enabled legislation that impacts the quality of life of people with ALS and their families.
But, we can’t stop now. The key to a cure begins with you.
Please consider joining me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.