To learn more about Violet’s condition or to make a donation, please contact: violetsvoice2012@gmail.com
Violet is now on social media as well. Request to join our page: Through her Eyes:Violets Voice
Playing barbies with her sister
Contact Information
violetsvoice.org 
Do you have a website to make donations or have you considered trying a fundraising website like youcaring.com for the people that cannot attend events?
thank you. This is something we are looking into.
The Thompsons
Hi! Your story touchs my heart. Our daughter was born with Agenisis of the Corpus Collasum. So far, no other issues so we feel extremly blessed. We make a visit to Milwaukee to talk with genetics in July so they can check that out as well. She will be 9 months on July 5. Your whole family is in our prayers. I hope to make it to one of your benefits.