Thank you for visiting my page! As you may or may not know, Keira was diagnosed with Prader-Willi syndrome (PWS) when she was 6 years old and we are taking one SMALL Step to help to raise funds for critical research to help eliminate the challenges of PWS. Most children are diagnosed at birth, we had to wait 6 years till we had diagnosis. That is OK though as God provided for us and continues to. Keira is who she is and we would never want her to be any other way.
Funds raised will be used to advance PWS research through the Foundation for Prader-Willi Research. You can learn more about PWS and the research that is underway at http://www.fpwr.org.
Please join me and donate now!