What a beautiful Website... Check it out!

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anonymous

New member
Angie

I can't thank you enough for sharing this web site with others. It is wonderful to know that other people can see how beautiful and wonderful Cody was. I am her mother and i thank you so much for sharing with others. I believe that we can make something good out of this with our benefit auction and memorial walk in May. Again, Angie, thank you

ginny dieruf
gdieruf@aol.com
<a target=new class=ftalternatingbarlinklarge href="mailto:dierufg@msn.com">null</a>
 
A

anonymous

New member
Angie

I can't thank you enough for sharing this web site with others. It is wonderful to know that other people can see how beautiful and wonderful Cody was. I am her mother and i thank you so much for sharing with others. I believe that we can make something good out of this with our benefit auction and memorial walk in May. Again, Angie, thank you

ginny dieruf
gdieruf@aol.com
<a target=new class=ftalternatingbarlinklarge href="mailto:dierufg@msn.com">null</a>
 
J

julie

New member
I just emailed the family, just a really short note about the website, and that it was posted on this CF forum. The wrote back already, I'm sure they'd love to hear from anyone else-knowing that even after her life is over, their daughter is very much "alive".
 
J

julie

New member
I just emailed the family, just a really short note about the website, and that it was posted on this CF forum. The wrote back already, I'm sure they'd love to hear from anyone else-knowing that even after her life is over, their daughter is very much "alive".
 
E

eli

New member
What a beautiful site and young girl.It made me cry and cry and cry.
Thank's heaps for sharing it.
 
E

eli

New member
What a beautiful site and young girl.It made me cry and cry and cry.
Thank's heaps for sharing it.
 
A

anonymous

New member
I too loved Cody's website. I have cried cried and cried some more but she is such a beautiful girl and it was a blessing to watch her video and read her website.

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

anonymous

New member
I too loved Cody's website. I have cried cried and cried some more but she is such a beautiful girl and it was a blessing to watch her video and read her website.

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

New member
What a wonderful site and a beautiful young lady! I got up this morning feeling tired and just wanting to go back to bed and not start the day. This made me get up and do the normal routine, except this morning I have out the camera, ready to get more photos of our family and my goal is to get all of our digitals printed which I haven't for over 2 YEARS! Pictures are worth so much! Thanks for sharing this site!AngieStep-Mom to Brittany 13 no cf Mom to Tyler 12 no cf, cf carrier Mom to Brady 4 with cf Mom to Taylor 3 no cf, but chromosome 9q 21.2 q 22.1 deletion 
 
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fourkidsmom

New member
What a wonderful site and a beautiful young lady! I got up this morning feeling tired and just wanting to go back to bed and not start the day. This made me get up and do the normal routine, except this morning I have out the camera, ready to get more photos of our family and my goal is to get all of our digitals printed which I haven't for over 2 YEARS! Pictures are worth so much! Thanks for sharing this site!AngieStep-Mom to Brittany 13 no cf Mom to Tyler 12 no cf, cf carrier Mom to Brady 4 with cf Mom to Taylor 3 no cf, but chromosome 9q 21.2 q 22.1 deletion 
 
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gin

New member
Thank you all for taking the time to see Cody Dieruf Web site. She truely was an inspiration to all. She still lives on. We are having a Benefit Auction/Cody Dieruf Memorial walk in May 2006, Bozeman, MT

Cody's motto, "Cystic Fibrosis is about LIVING not DYING. and that she did.

with much appreciation for watching the vidio and listening to the songs. They represent her life of dance, and education.

Ginny Dieruf
www.codydieruf.com
dierufg@msn.com
 
G

gin

New member
Thank you all for taking the time to see Cody Dieruf Web site. She truely was an inspiration to all. She still lives on. We are having a Benefit Auction/Cody Dieruf Memorial walk in May 2006, Bozeman, MT

Cody's motto, "Cystic Fibrosis is about LIVING not DYING. and that she did.

with much appreciation for watching the vidio and listening to the songs. They represent her life of dance, and education.

Ginny Dieruf
www.codydieruf.com
dierufg@msn.com
 
S

smoothdave

New member
i only read every thing on the site at work, i wanted to wait till i got home to watch the video, and i can truly say i never knew watchin a video could touch me so much, that is such a nice video, and i am stuck for words...... and i actually am..

Dave
 
S

smoothdave

New member
i only read every thing on the site at work, i wanted to wait till i got home to watch the video, and i can truly say i never knew watchin a video could touch me so much, that is such a nice video, and i am stuck for words...... and i actually am..

Dave
 
C

coltsfan715

New member
That is a wonderful site - I looked at it yesterday and think I about cried myself out of tears. Very touching. Thank you for sharing.


Lindsey
 
C

coltsfan715

New member
That is a wonderful site - I looked at it yesterday and think I about cried myself out of tears. Very touching. Thank you for sharing.


Lindsey
 
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