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Helping families financially and emotionally affected by Lowe Syndrome.
Follow Waylon's Journey on FB.
Here is our son Waylon! He is the main reason we wanted to start the Foundation. He was diagnosed with Lowe Syndrome at 6 months old after having genetics testing due to being born with bilateral cataracts. This Foundation means so much to us. The Foundation will help other Lowe Syndrome families financially and emotionally. We want to be able to help lift some financial burdens if they shall arise such as medical supplies, medical bills, funeral expenses and some other unexpected financial burdens. Y'all please help us by donating to the Waylon Sullivan Foundation and by sharing our page to reach more people
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