An ALS Foundation - By The Youth - For The Future
Our team is committed to our mission of finding a cure for Amyotrophic Lateral Sclerosis (ALS or Lou Gherig’s Disease). At The Jimbo Foundation, we raise funds through events, sponsorships, and one-off donations from the community. Our donations go directly over to our partner(s) ALS TDI to help fund research & experiments that will get the world one step closer to curing ALS.
The Jimbo Foundation is in accordance with Section 501(c)(3) of the United States Internal Revenue Code.
On October 18th, 2020 - Jimbo was called home and ended his extremely hard-fought battle against ALS. During this fight - a promise was made that we were going to do our part to ensure ALS becomes treatable… Two years later - we are leveraging our platform at The Jimbo Foundation to make good on this promise.
”ALS is not an incurable disease - it’s just a severely underfunded one” - Anonymous
In Partnership With
Be apart of our journey.
Support us on this journey.
Our mission is to support ALS researchers in their hunt to find a cure for ALS.
How to get involved on our journey?
Reach out to thejimbofoundation@gmail.com to participate in upcoming campaigns!
Venmo: @Thejimbofoundation
Events.
The JIMBO Foundation is looking to sponsor or host events with individuals that are motivated to take down ALS just as much as we are. Please contact us at Thejimbofoundation@gmail.com
The latest on ALS Research.
Dr. Colin Quinn, MD and Dr. Lauren Elman, MD
(July 2, 2021) For perhaps the first time ever, there's optimism about the direction of amyotrophic lateral sclerosis (ALS) research. Read more…
ALS TDI lab
(June 7, 2021) We serve as a “drug-discovery engine” for ALS – meaning we utilize our experienced team and our established and innovative research programs to advance treatments into human clinical development. Read more …