Kidd's Kids's Page

Hola Kidd,

I don't even know where to begin....We want to thank you from the bottom

of our hearts for the best 5 days ever in Marcos' life, really! He still cannot stop

talking about some aspect of the trip and I don't think he ever will. This trip

meant almost as much to me and my husband as to Marcos; for different

reasons. I have been a listener of yours since you were on KEGL and my

youngest sister has a picture of you and her when she was 12 (she… Continue

Dear Mr. Kraddick,



I truly commend you for what you are doing for sick children. It is people like you who really make a difference in the world. I saw you on the Doctors TV today, and was blown away by the help & generosity you provide for others. Could you please mail me a donation form? I was not able to open it from your web site. I do not have much, and have my own issues, but I do realize that there are many that are less fortunate that I am, and therefore I would like to… Continue

Growing up my childhood best friend was diagnosed with leukemia. We lived a simple life in Louisiana, and didn't have much. I just saw the episode of DR.s with Kidd's Kids on the show. I wish we would have known about this to nominate Larissa Keen for a trip of a lifetime. She was 13 when she died, with short hair (grown after treatment stopped) and long nails (from treatment.) She is on my mind every day, and I am now 21. I miss her so much and it is an inspiration to see so many children able… Continue

Hello Kidd
I saw you on the Dr's show today. I know you were concerned about your appearance. You did GREAT. You told the story about Kidd's Kids and made a awesome impression on your audience. You should be proud.
I would like to volunteer for Kidds kids. Please send me the email address so I can do that.
Thank you
Margaret Crabtree

I just saw your piece on The Doctors, and I just wanted to let you know how much it touched my heart to see groups like yours reach out to these children.



My 5-month-old daughter was just diagnosed with Gaucher's disease, a very rare metabolic disease, and at this pointo we don't know if it is type 1 (just physical symptoms) or type 3 (physical and neurological with a limited life expectancy of 20 years or so,, but she will have IV treatments every 2 weeks for life regardless of what… Continue