Robert Carty
ALS took my best friend and the best thing that ever happened to me
Event: | New Hampshire Walk |
Date: | October 1, 2023 |
Team: | Claire's Bears |
For those who have been through the battle, ALS is a terrible disease and it is a very lonely disease for the Patient, Caregiver and Family. We walk to help provide support to those who are currently fighting ALS so that we can find methods to contain ALS, make life more livable and to ultimately find a cure where Patients can get treatment and return to their families to live a normal life. Even in Today's hectic environment ALS will not stop and neither can we. We must continue the fight so that other good people will not have to deal with the terrible impact of ALS. Let us all work to achieve the objective.
Thank you for helping me reach my Walk to Defeat ALS® fundraising goal! This is an exciting opportunity for us to work together to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure.
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. WE CAN'T STOP NOW!
Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.
Why We Need Your Help
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 two to five years from the time of diagnosis.
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
ALS can strike anyone. Presently there is no known cause of the disease, though support is bringing researchers closer to an answer. In the meantime it costs an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to bring help and hope today!
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Robert's donors
joined the movement!
Bob Carty
$1,550.00
Joan and Bernie
$50.00
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