Monday, February 18, 2013
Tea for NF
My daughter Tayler has been living with NF since birth. She was first diagnosed at 6 months old. Since then it has been a struggle at times but that amazing little girl has never lost her smile. Now at 9 1/2 she wants to talk to others about it so that other kids do not get picked on like she has. She also wants to do a fundraiser to raise money for my awareness and research. I am currently awaiting to hear back about how to set it up. She is super excited though so hopefully we will have some news about it soon so we can get started. Looking forward to this new adventure with her.