I am from a small town in Missouri, and I listen to you guys everyday on my way to and from work. I just want to take the time to say that I love what you do for the children with Special Needs. I was blessed to have a daughter by the name of Alexis in my life for 7 years, until she lost her life to pneumonia on December 24, 2004. She was born with Amniotic Band Syndrome, and wasn't expected to live at all. She touched so many lives around her. Being a young parent of a special needs child came easy for me because it was just about being a parent and taking the responsiblity of doing what needed to be done for my child. I love what you all do for them because "tomorrow is not promised" to no one, and to give that chance to those children is awesome. I look back on things and wish that my daughter had the same opportunity, but alot of the organizations that we were hooked up with had to be given specified reasons on why we, as her parents, felt that those wishes was what she would have wanted because she couldn't speak and we were her voice. Everytime I hear what you all do for Kidd's Kids, it just touches my heart in so many ways, and I know how those parents feel. You want so much for whatever "it" is to go away, but it doesn't and you have to learn to cope and do what is best for your child. These children are very special, in so many ways. Since going back to college, I have found myself being a speaker on special needs children because of my daughter. I speak to a class at the college I attend, and share my story about Alexis and the things we encountered in life with her. Now, I have been blessed with two other children, and talk with them constantly about their big sister! We take them to her graveside, look at her pictures, and just remember her on a daily basis. All I have to say is keep doing what you're doing because you guys are paying it forward and your blessings will come back to you in so many ways!! I could go on forever, but I won't. If you ever need someone to share their story with anyone...let me know because I love sharing my story and meeting new people and their families even though my little girl is gone, I just feel a connection with these children and their families although I may not know them. My heart goes out to them, and we just have to remember that God never puts on us what we cannot bear!! May God bless all of you!!

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Comment by Leanne Seeman on October 10, 2009 at 1:48pm
I'm so sorry to hear about your angel going to heaven early, however all the time when I'm asked how do I deal with two disabled children I tell them for some reason God gave me this responsibility and it's just what I must do and yes this is very special the Kidds Kids organization.

Welcome To Kidd's Kids

I founded Kidd's Kids in 1991 with the hope of making a difference in the lives of terminally and chronically ill children. Each year, Kidd's Kids offers five amazing days of suspended reality to
children whose lives have been ravaged by disease. Kidd's Kids children and their families are given the chance to experience the exuberance of being "normal." That is the gift that you and I can
offer by supporting the Kidd's Kids organization. Signed,

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