Please take a moment

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AngieM

New member
Hi guys. My friend, Ginny, lost her daughter, Cody, on April 28, 2005 to CF. It has been a hard year for the family and I know it has helped when she's heard from the "CF Community". I've posted Cody's website in the past, but here it is again. <a target=_blank class=ftalternatingbarlinklarge href="http://www.codydieruf.com">codydieruf.com</a>

Cody's family has put together the Cody Dieruf Foundation. Here's the website <a target=_blank class=ftalternatingbarlinklarge href="http://www.breathinisbelievin.org">breathinisbelievin.org</a> Ginny and family have planned a CF Benefit (Cody Dieruf Memorial Walk and Benefit Auction) on May 13, 2006 in Bozeman, MT. It has been a huge project and I think Ginny could use some kind, comforting words. Here's her email <a target=_blank class=ftalternatingbarlinklarge href="mailto:dierufg@msn.com">Ginny Dieruf</a>

Thanks for your help!

Angie
Step Mom to Hayley
11 yrs CF/CFRD
 
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Jane

Digital opinion leader
What a beautiful girl and a lovely biography. Very touching. Her family is in my thoughts.

Jane
 
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anonymous

New member
Angie

How nice of you to post Cody's website again...What a nice friend you are. Cody's website is on my favorites and my family and i visit it all of the time. My friends are forwarding her website to others that they know.

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

New member
Thank you all for taking the time to look at Cody's site. Kaitsmom.... Thankyou for the kind words! Again, please do not hesitate to send Cody's Mom, Ginny, a note <a target=_blank class=ftalternatingbarlinklarge href="mailto:dierufg@msn.com">Ginny Dieruf</a>

Angie
 
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anonymous

New member
A truly inspirational person. I only hope my little girl with CF is able to live her life to the full like you Cody. Thank you for sharing your life with us all.

Rest in Peace angel............
 
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anonymous

New member
It is a beautiful website! I have been e-mailing Gin for awhile now. I first met her on this website. I lost my son 3 months ago today. It is nice to talk to someone who has gone through the exact same thing. She is an amazing woman doing all she has done this past year. Thanks for making others aware of her and all she has done.

momofjosh
 
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anonymous

New member
Thank you Angie,for sharing our daughters website with the cf forum.. We are very touched. We miss Cody very much and are very touched by the response from all who have reviewed her site. Cody was amazing and she continues to touch many. Angie has become an advocate in our story. We appreciate you Angie. We don't even know each other , yet we have become friends. all of you out there in the CF world, if you find some one who understands and who cares, hold on to them. Angie has become a soul mate. Josh's mom has become a confidant. You all need each other,so know that you are all out there to help each other. this forum is good for you all.

love, ginny
cody's mom
www.codydieruf.com
breathinisbelievin.org
 
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anonymous

New member
to all of you who have clicked on to Cody's website. we are truly touched by all your kind words. This has been an extremely hard year, but we know that Cody is our force in getting the Cody Dieruf Benefit Foundation off the ground We hope to help other CF families in our area and surrounding area with this disease. Our families now have a support system amongst each other. Before Cody died, she asked me to help parents help there children reach there dreams, goals, and life's battle. She asked me to tell you all, there is hope out there for all, and to live each day and look forward to tomorrow. That with every down, there will be an up. So we all will hold our head up high and salute Cody on April 28th, and again on May 13th, when we have our Memorial Walk and Benefit Auction. We will have many balloons and at the end of the walk we will let them go and float upward as our salute. thank you all for all your kind words.

ginny dieruf
www.codydieruf.com
www.breathinisbelievin.org
 
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