Gin

[anonymous]

Hello this is Kaitsmom, I would just like to tell you what a wonderful person you are, How thoughtful it is of you to help other people that are dealing with the loss of their loved one. I am a mother to a child with CF and it truly breaks my heart to know what alot of parents and spouses go through, I know how hard it is to see my daughter sick and how i wish that i could trade her places in a heartbeat, I know that all of us as parents would do that. I have honestly thought about Cody everyday since seeing her website and talking to you on the phone .
I know that you are doing all that you can to spread CF Awareness, and i would like to thank you for all of your efforts and support that you are giving to help others with CF.

Kaitsmom<img src="i/expressions/rose.gif" border="0">

 

[anonymous]

Hello this is Kaitsmom, I would just like to tell you what a wonderful person you are, How thoughtful it is of you to help other people that are dealing with the loss of their loved one. I am a mother to a child with CF and it truly breaks my heart to know what alot of parents and spouses go through, I know how hard it is to see my daughter sick and how i wish that i could trade her places in a heartbeat, I know that all of us as parents would do that. I have honestly thought about Cody everyday since seeing her website and talking to you on the phone .
I know that you are doing all that you can to spread CF Awareness, and i would like to thank you for all of your efforts and support that you are giving to help others with CF.

Kaitsmom<img src="i/expressions/rose.gif" border="0">

 

[gin]

thank you so much for your kind words.. I would have to thank Angie for her support in putting Cody's website in the CF forum for me and Anne fokaitsmomr putting the web site together as a gift to us for Cody's birthday. You guys are just as big a help to me. This has been a terribly tough time for us. I know no other way but to reach out and do what I can do, but it is people like you who have helped us get through this. Our tears flow daily for the loss of our Cody. With all of your support, we get through another day. Cody's website is beautiful and displays her life in an unforgettable way. She loved life like no other. Her message to all is Cystic Fibrosis is about "living, not dying" and she wanted parents to know there children are very special gifts and can accomplish lifes many goals. Thank you all for visiting our web site www.codydieruf.com

ginny

 

[gin]

thank you so much for your kind words.. I would have to thank Angie for her support in putting Cody's website in the CF forum for me and Anne fokaitsmomr putting the web site together as a gift to us for Cody's birthday. You guys are just as big a help to me. This has been a terribly tough time for us. I know no other way but to reach out and do what I can do, but it is people like you who have helped us get through this. Our tears flow daily for the loss of our Cody. With all of your support, we get through another day. Cody's website is beautiful and displays her life in an unforgettable way. She loved life like no other. Her message to all is Cystic Fibrosis is about "living, not dying" and she wanted parents to know there children are very special gifts and can accomplish lifes many goals. Thank you all for visiting our web site www.codydieruf.com

ginny

 

[gin]

kaitsmom

thank you so much for your kind words.. I would have to thank Angie for her support in putting Cody's website in the CF forum for me and Anne for putting the web site together as a gift to us for Cody's birthday. You guys are just as big a help to me. This has been a terribly tough time for us. I know no other way but to reach out and do what I can do, but it is people like you who have helped us get through this. Our tears flow daily for the loss of our Cody. With all of your support, we get through another day. Cody's website is beautiful and displays her life in an unforgettable way. She loved life like no other. Her message to all is Cystic Fibrosis is about "living, not dying" and she wanted parents to know there children are very special gifts and can accomplish lifes many goals. Thank you all for visiting our web site www.codydieruf.com

ginny

 

[gin]

kaitsmom

thank you so much for your kind words.. I would have to thank Angie for her support in putting Cody's website in the CF forum for me and Anne for putting the web site together as a gift to us for Cody's birthday. You guys are just as big a help to me. This has been a terribly tough time for us. I know no other way but to reach out and do what I can do, but it is people like you who have helped us get through this. Our tears flow daily for the loss of our Cody. With all of your support, we get through another day. Cody's website is beautiful and displays her life in an unforgettable way. She loved life like no other. Her message to all is Cystic Fibrosis is about "living, not dying" and she wanted parents to know there children are very special gifts and can accomplish lifes many goals. Thank you all for visiting our web site www.codydieruf.com

ginny

 

[gin]

kaitsmom

thank you so much for your kind words.. I would have to thank Angie for her support in putting Cody's website in the CF forum for me and Anne for putting the web site together as a gift to us for Cody's birthday. You guys are just as big a help to me. This has been a terribly tough time for us. I know no other way but to reach out and do what I can do, but it is people like you who have helped us get through this. Our tears flow daily for the loss of our Cody. With all of your support, we get through another day. Cody's website is beautiful and displays her life in an unforgettable way. She loved life like no other. Her message to all is Cystic Fibrosis is about "living, not dying" and she wanted parents to know there children are very special gifts and can accomplish lifes many goals. Thank you all for visiting our web site www.codydieruf.com

ginny

 

[gin]

kaitsmom

thank you so much for your kind words.. I would have to thank Angie for her support in putting Cody's website in the CF forum for me and Anne for putting the web site together as a gift to us for Cody's birthday. You guys are just as big a help to me. This has been a terribly tough time for us. I know no other way but to reach out and do what I can do, but it is people like you who have helped us get through this. Our tears flow daily for the loss of our Cody. With all of your support, we get through another day. Cody's website is beautiful and displays her life in an unforgettable way. She loved life like no other. Her message to all is Cystic Fibrosis is about "living, not dying" and she wanted parents to know there children are very special gifts and can accomplish lifes many goals. Thank you all for visiting our web site www.codydieruf.com

ginny