The highest priority of the foundation is funding research for potential treatments and cures of leukodystrophy.  In partnership with medical advisors, the board of directors will assess new and ongoing research efforts around the country.  We will fund promising research initiatives that hold the greatest potential to positively affect the lives of leukodystrophy patients. 


Public awareness is also key to winning the battle against leukodystrophy.  Given its rarity, the vast majority of the public is unaware of the disease, its severity, and impact on families.  Part of our efforts will focus on raising awareness through social media, community events, and local partnerships.


Resources and services for those affected by leukodystrophy is how we will come alongside families.  It shouldn’t have to be a challenge to find a support group, current clinical trials, medical resources, and information.  It is our goal to help ease a families’ journey and the many decisions that they will make along the way. 


It is our desire that you would join our vision in providing hope for what matters.

Please help enhance the lives of those affected by leukodystrophy by donating today.  There are two ways you can help us achieve our mission: either via PayPal or by mail.




Or mail checks to:

The Brooks Coleman White Foundation

PO BOX 141038

Broken Arrow, Oklahoma 74014

The Brooks Coleman White Foundation is a 501(c)(3) not-for-profit organization and all donations are tax deductible.  Please include your e-mail address with your donation, so that we may send you a giving receipt.

© 2018 The Brooks Coleman White Foundation, Inc.