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Stacey Aronstein

Donate to me Join my team

$5,160.00

Raised

$5,000.00

Goal

Of Goal

An Opportunity to Support ALS Research in Honor of Ron Isroff

Event:	Northeast Ohio Walk - Cleveland
Date:	Sunday, September 12, 2021
Team:	Ronnie's Raiders

We are raising money for ALS in honor of my amazing dad, Ron Isroff, who was diagnosed with ALS in June 2018. While this disease has had a profound impact on our family, we want to do something to help my dad and others like him who have also been diagnosed with this devastating disease.

So many of you have been so generous to our family over the past three years, offering help, support and friendship, and we greatly appreciate it.

We are committed to raising money to support people with ALS and spreading awareness of the urgency to find treatment and a cure. Please consider donating to this cause.

Due to the pandemic, we will be walking in our own neighborhoods for this event. We hope you will consider sponsoring us by donating in honor of my amazing dad.

Thank you so much.

With Love,

Stacey & Marc Aronstein

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The past three 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 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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