The Jonah Finn Foundation is a 501(c)(3)non-profit organization started in 2018 following Jonah's diagnosis of ETMR.
We invite you to join our fight and contribute to our goals of raising awareness and money in support of much needed preclinical research in the areas of ETMR and other rare brain tumors of early childhood. All proceeds will go directly to support novel and focused preclinical research in these areas. With your generous contributions, we can help save precious children like Jonah. We can work together to offer a brighter and better tomorrow for children suffering with this disease now and in the future.
To learn more about Jonah's story, check out the Jonah Finn Foundation website: https://jonahfinnfoundation.org/