The FA Project is committed towards creating awareness of Friedreich's Ataxia, a life altering disease. We aim to educate the public by increasing the visibility of related information & resources and creating a support system for those afflicted with FA. Ultimately it is our goal to provide those living with FA the tools and resources necessary to lead the best life possible.

Frequently Asked Questions about The FA Project

1. What is The FA Project?
2. How does my donation help and where are the funds used?
3. When is the next fundraising and awareness event?
4. How can I get involved from a volunteer perspective?
5. What are some of the other FA advocacy organizations?

1. What is The FA Project?
A. The FA Project was inspired by an individual living with Friedreich's Ataxia. To read more about what inspires us click here. In an effort to help people living with FA live the best life possible a group of family and friends have come together to form a special support group. Many people affected with FA live a typical life but need some assistance at times. The FA project is here to help.

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2. How does my donation help & Where do the funds go?
A. The proceeds earned by the FA Project will be used in several different ways. First, the money will go directly to support those living with FA. Whether it is the installation of a shower grab bar, a ramp, or physical therapy your donation will have a positive effect!

A portion of the proceeds earned by the FA project are donated directly to the Friedreich's Ataxia Research Alliance. The Friedreich's Ataxia Research Alliance (FARA) is a national, public, 501(c)(3), non-profit, tax-exempt organization dedicated to curing Friedrech's ataxia (FA) through research.

Most recently, the FA Project has disbursed funds to support FARA via the Fuzzy Buzzy Charity Golf Tournament (all proceeds went to FARA for research). We are also reaching out to those with the disease to offer services where needed. Please visit our Support page to learn more about our application process.

You can also learn more about some of our past events, how much we've raised and how funds have been disbursed by visiting our Previous Events page.

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3. When is the next fundraising and awareness event?
A. We at The FA Project and our network of supporting friends would be honored to have you attend an upcoming fundraising and awareness raising event. Please visit our Events page to learn more.

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4. How can I get involved from a volunteer perspective?
A. We would greatly welcome anyone interested in volunteering with The FA Project's efforts. Many available opportunities exist from event assistance to marketing and fundraising support. Please contact Maria at maria@thefaproject.org to learn more.

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5. What are some of the other FA advocacy organizations?
A. The FA Project donates a portion of its proceeds to various FA advocacy organizations in an effort to diversify our attack on the disease and its ramifications. We are proud to call these groups friends and are very supportive of their efforts. Please feel free to visit the largest advocacy group, The Friedreich's Ataxia Research Alliance (FARA) to learn more about their wonderful efforts. We have also posted several other links to various organizations on Our Friends page.

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