Despite the effects of Chiari malformation, syringomyelia and related disorders on millions of Americans and people around the world, these disorders are not well-known, and there is limited public and private funding to support efforts to provide better therapies and, ultimately, to find a cure.
As we continue our fight against these debilitating conditions.
Whether you have a passion for supporting a 501(c)3 like Bobby Jones CSF or you are starting to think about leaving a legacy, setting up a donor advised fund or charitable giving fund may be the best option for you! Create a strategy that gives you control of your financial legacy.
LEARN MOREHost your own fundraiser or join in on an existing one! There are lots of different kinds of fundraisers and awareness events you can organize or contribute to with your friends, family and local communities. Check out this page for our upcoming calendar of fundraising and advocacy events!
LEARN MOREWe ask you and/or your company to become a member of our Corporate Sponsorship team. Sponsorships opportunities are available for our advocacy events, unite@night walks, signature fundraising events, and more! Check out this page for more information.
LEARN MORECan't give a large gift in one lump sum? Set up a multi-year pledge! Give monthly or yearly, like a payment plan for good. Learn more and set up your own pledge below.
LEARN MOREInvolve your company in giving to a great cause. Find out how to set up a matching gift and how you can donate through your company’s United Way Giving Campaign
LEARN MOREDonate, shop, or even search online to give! Find out how here.
LEARN MOREBobby Jones CSF is a participant in the National Combined Federal Campaign (CFC) and the New York City Combined Federal Campaign. If you work for the federal government in any capacity, request a CFC pledge form, please contact your local CFC office. Find out how here!
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