"Our mission is to raise awareness and increase funding for research to find a treatment and cure for blindness, focusing on Leber's Congenital Amaurosis (LCA)." Gavin R. Stevens Foundation
501(c)(3) Non-Profit Organization
PO Box 2108
Chino, CA 91708
877.625.6505
E-mail: info@gavinsfoundation.org
Changing the lives of those who live with LCA, a form of blindness present at birth.
All donation amounts are welcome.
Together.... a Cure is in Sight.
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The Gavin R. Stevens Foundation!

BUNCO!  BUNCO!  BUNCO!

Friday Feb 17, 2012

  • - Friday Feburary 17, 2012 7pm
  • - El Prado Golf Course
    6555 Pine Ave Chino, CA
    Map     - Bunco Flyer
  • - $40 presale per person / $50 at the door
  • - 300 person capacity...MORE
Valentine’s Cookies
for a Cause Fundraiser
 Click here for More Info!
Thank you for being here and taking interest in our cause. Our son, Gavin, was born with a rare retina disease, called Leber’s Congenital Amaurosis. It is through our research, and knowing that a cure is in fact a possible reality, that we came to creating the Gavin R Stevens Foundation. We are driven to raise awareness, and increase funding in the area of LCA and gene therapy research. We are not just doing this for our son, Gavin. We are touched by all the faces of LCA, and all the individuals who are left in darkness due to blindness. It is our hope and mission that we can help with the financial aspect of research, and be able to help fund much needed clinical trials. We want treatment to be an option, and not just a dream!

There are so many ways you can help us. You can join us at an event. You can hold your own fundraising events (regardless of how big or small). You can sign up for our newsletter, to keep up to date with the latest news in our efforts of the foundation, as well as LCA research. You can purchase GRSF products, in which proceeds will benefit the foundation. Just by you being here, is us reaching out to one more person and informing you about this disease LCA. Since it is a rare disease, it takes organizations like ours to bring much needed awareness.

As a parent, there is nothing more precious than those who care for your children. We have been reminded of this, during one of the most difficult times in our lives, receiving Gavin’s diagnosis. It is through the support of family, friends and complete strangers that build our strength to move forward. Thank you to each and every one of you who have supported us! It is with you, that we will make a difference to those living with LCA.

Please contact one of us if you have any questions or suggestions. We would love to hear from you!

“There is no better way to thank God for your sight than by giving a helping hand to someone in the dark."
- Helen Keller

Sincerely ,
Troy & Jennifer Stevens
Parents of Gavin, and Founders of GRSF