Katie Starr is the 2011 face of the Foundation Fighting Blindness. Her image and story are on all of their membership materials. This was the letter from me that was enclosed with the membership package. If you would like to become a member of the Foundation Fighting Blindness and make a tax deductible contribution that will help aid the research towards treatment and possibly a cure for hereditary blindness, please go to Katie Starr's link. Every dollar counts....more than you will ever know!
Thank you, The Katie Starr Team
4 comments:
I received your letter today from ffb about your daughter. I have a 9 yr old little boy who was diagnosed with the same thing as your daughter. I would love to share with you. My email is bob_aimeewest@yahoo.com. It would be great to talk w someone that has the same situation.
Love the letter. Praying for you all.
Wishes from Australia, you and your girl are so very brave!
Yve
I stumbled upon your blog because my maiden name is "Starr." However, my two younger boys were diagnosed with Usher Syndrome (1B) a little over a year ago and we are also raising money for the FFB! We are doing a wine tasting in May and hope to raise a similar amount as you have done. Keep up the good work. My boys' site is ushers.kwilinski.org.
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