--- We Will Love and Miss You Always  ---
The following is the story of Cody'slife as told in her own words
"I used to lie awake at night thinking of the futures I would never achieve -- graduate school, an established career, the archetypical house with the white picket fence and matching porch swing, Saturday morning cartoons with the kids and playing catch in the yard, even things like wrinkles, cellulite and the way my hands will spot and satin with age. I used to dwell on the "could-nots" and the "impossibles." Now, however, I dream about how I can make the time I have remaining as incredible and meaningful as is possible, and then more. I want to fill my life with as many experiences as my body will allow and to fill each day, each minute, with as much beauty as I can, because I know this body and these minutes are not for forever.
Also, I seem to feel as if every moment in my life now, not just the typical emblematic incidences, is a milestone, a turning point, to be marked as an epic event, as things have become so difficult and require so much energy. I am now trying to make each moment as special and memorable as I can, whatever it may be -- a new outfit for a first date, a sassy haircut at a stylish salon so that I can walk into a college party feeling like an edgy princess (Supercuts may be able to copy the do but not the attitude), taking my poor college friends out to dinner, or maybe even a triple latte instead of a single. Perhaps that sounds silly, but I have talked with elders in the past about what they would do differently if they had their lives to live over again. I have heard, "walk around barefoot," "be impulsive, extravagant, and spendthrift," "stay up past my bedtime," and "eat two helpings of dessert ... first."
Well, I guess you could say that I am approaching my old age now. Cystic fibrosis is my old age. No, I will never see the skin on my hands turn into wrinkled silk as they sleep in the hands of the one I love. However, I already have the aching joints, and the crepe paper lungs, the cough of an 80-year-old man laughing in my abdomen, snoring behind my sternum. My rib cage is every bit accommodating to the elder in house -- the body -- stretching and expanding, temporarily with each breath, permanently with each year and my spine shakes hands with gravity.  So I am lucky, I guess, to be simultaneously young and old. As a result, I won't look back on life and say, "If I had it to do over again, I would." It is funny, but it is almost as if I am living in the present and in the future and am thus conscious of what I want now and what I will want later in life. A perfect blend. No regrets.  Facing one's mortality can be a very scary and painful experience, but I also strongly believe that it can be beautiful, too. It is just hard to see sometimes. The sicker I get, the more difficult the little things become, but consequently, the more victories I have -- making it up a flight of stairs or down the block or through a slow dance with a close friend, without getting short of breath -- triumph! Before long, taking a breath will be the sweetest victory imaginable. But, all so beautiful. Perhaps I, we, should count ourselves fortunate to be able to find the grace, the splendor, the potential in the ordinary, the expected, the taken for granted.  Life."
Cody's family selected this beautiful essay, written by Cody herself, to use as her obituary.
Web Designer:
Our wonderful Cody lost her couragous battle with Cystic Fibrosis on April 28, 2005, with her loving family around her.  Cody was born on November 8, 1981 to George and Ginny Dieruf.  She is the beloved younger sister of Levi.
The love and happiness Cody so generously shared with her
family, friends, and everyone around her will live on forever in our hearts.  Her courage, grace, and determination are -- and always will be -- an inspiration.  We will never forget her shining personality, loving heart, and beautiful mind. 
To carry on Cody's beautiful legacy, her
family  has established the Cody Dieruf
Benefit Foundation to provide local support
to those suffering from Cystic Fibrosis. 

In Loving Memory of

Cody Nicole Dieruf
November 8, 1981 - April 28, 2005
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of Cody
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Foundation Memorial Walk
& Benefit Auction
2005 Great Strides Walk
Anne, Levi, Cody 
Cody & Dad
Cody & Mom 
Last updated
September 2008
Thank you for another successful Cody Dieruf Benefit Foundation Walk and Auction!!!
The very best daughter,
sister, granddaughter, niece,
and friend
we could have
hoped for!