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Last year we served 752 children. Help us continue to make a difference!

As we prepare to celebrate our 35th anniversary, we know the next twelve months are critical and we need our VIPS supporters even more. Please help us during this challenging time by continuing your existing pledges or donations. If you are not a monthly donor--now would be a great time to initiate a monthly gift. The families we serve depend on our teachers and we depend on you to help us in our critical mission to provide early intervention to every child with blindness or low vision.

Learn more about how VIPS is moving forward with our services in spite of COVID-19.

Isaac sits in his stroller with mom, Traci, next to him, and siblings, Haddon and Noel smiling nearby.

On January 19th, I was on bed rest and about to go crazy. I was 4 cm, 80% effaced, and knew that Isaac could be born any day. That evening, as I was watching TV, I thought my water broke and it was finally time to go to the hospital and give a *natural* birth.…

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“Simone is joy and light, and the center of our family,” said Nicole, mother to VIPS child Simone. She is a busy little girl, always moving and thriving on attention. She spends her days playing, dancing, and exploring the outdoors; specifically, the trees and flowers. She especially loves doing so with her family.  Simone is…

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VIPS Board Member, Paul Frazier, at age 4.

VIPS board member, Paul Frazier, brings a lot to the table. He is the father of a preschooler, a former educator, a businessman and a natural advocate with a charismatic personality and a heart of gold. But one of the strongest qualities Paul brings to his board responsibility is the critical perspective he has as a…

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Wallace has several diagnoses and is our miracle boy, hence his middle name Braveheart. We went from planning his funeral at 33 weeks during my pregnancy, to 193 days in the NICU/CICU following his birth, to home and thriving. We were introduced to VIPS once we were home for a few months and started to receive…

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“I never imagined that my son’s first best friends or play dates would be with his therapists,” said Jeanette, mother to 19 month old Dallin, a child who currently receives services through VIPS. Dallin was born with a brain condition called Periventricular Leukomalacia (PVL) which is caused by the softening of white brain tissue. Because…

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Louisville, KY – November 10, 2020 Bria Byrd is a sophomore at Elizabethtown High School and an ambassador to Visually Impaired Preschool Services (VIPS), a nonprofit based in Louisville, focused on providing education and intervention services to children born with blindness or visual impairment in Kentucky or Indiana.  Byrd chose VIPS as the charity she…

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Craniosynostosis – a word Teresa never thought would be in her vocabulary, much less a part of her baby boy’s life. Teresa’s son, Elias, was born at 31 weeks of age and weighed just 3lbs 13oz. Elias was diagnosed with left craniosynostosis; which means some of the joints in his skull fused before his brain…

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He came into our lives with Gods Perfect Timing. But we soon learned our little boy had visual problems and was getting behind in developing. Therapy helped but the gap was getting larger in his development. We moved to Indiana just before he turned two and struggled with getting therapy started again. We were set…

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Elijah's Determination Overcomes Hurdles of Ocular Albinism

Elijah was first seen by our ophthalmologist in late February 2013. We noticed that his left eye was turning inward and felt it was necessary to have him evaluated. It was at the first appointment that he was diagnosed with Ocular Albinism, Strabismus (the turning in of his left eye) and Nystagmus. So many things…

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