In 2005 our child was diagnosed with Tuberous Sclerosis. We started this foundation to raise money for research for Tuberous Sclerosis and its related diseases such as autism. Along the way we have learned so much about this disease and how to best advocate for our child. We hope our experiences can help you with your journey with your child.

The information contained on this website is for informational purposes only.  We are not medical or legal professionals.  Should you be interested in any of the information presented, you should consult your own medical and legal professionals to see if it is appropriate for you.

All contents on this website is © 2010 The Bayless Family Foundation.