GET TO KNOW CODY
About Dakota
Guestbook

Contact Information

About  our Foundation

ECMO & CDH
extracorporeal membrane oxygenation

Fetal Diaphragmatic Hernia

 
Children's memorial

Chicago Children's memorial hospital

Transport team

The NICU

Pulmonary hypertension

child life specialists

Respiratory care

Ronald McDonald House

 
Pictures 

Dogs walk For CDH "2010"

 
Our Logo/Shop

coming soon

 
 
 Follow us
Cody's foundation On FB

 
 
TIM McGraw's Page


Our Thank you to him

08/17/2010 03:07:03 PM

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 Cody's Foundation

Dakota was born 12-2-07 with Diaphragmatic Hernia He spent 9 months in Chicago Children's memorial Hospital. Dakota  got to come home for the first time on September 3rd 2008. We are now blessed with a happy toddler, who is smart, happy, has the biggest smile we have ever seen and  is the joy of our life's.. MY son Dakota (CODY) was born with Congenital Diaphragmatic Hernia. (CDH)

Welcome to my site

my name is Dakota  and I am a C.D.H. Survivor! Info about CDH below

UPDATES


SEP.3RD 2010 IS CODY'S 2 YEAR ANNIVERSARY BEING HOME.


AS OF JULY 2010 DAKOTA IS NOW OFF THE VENT ALL DAY!!! WITH ONLY 6 HOURS VENT SUPPORT DURING THE NIGHT. HE HAS A SLEEP STUDY 10-19-2010
AND IF ALL GOES GOOD, THE NEXT PULMONARY CLINIC HE'LL BE OFF THE VENT FOR GOOD!!!! WE THEN HOPE THE TRACH  IS  GONE FOR GOOD BY SPRING 2011.
 

 

Hearing Cody laugh for the 1st time at bubbles ( a passing muir valve over his trach)

 



Our Dog's Walk for CDH On 6-6-2010 raised 1,160.00  WOOO-HOOO

Our goal is 5,000.00  or more this year..

~~~~~~~

Cody's Foundation

 Autograph's we have been donated for our foundation

We will be  setting up a auction  by the end of the summer

Money from auction  will be added to all money we have raised for Chicago Children's memorial  for  Congenital Diaphragmatic Hernia Research

Date: info coming once we have all autograph's. we asked for

 

Money is being gave to Children's memorial in Sep 2010.

our Copyright on pictures below, not on actual item's

to see full size photos go to Cody's foundation Fan page be sure to click LIKE.

Autographed Tim McGraw Children's Book

Photo Signed by Miley Cyrus

Chicago Blackhawks Hockey Puck Signed by

 #82 "Tomas Kopecky"

Chicago Cubs

 Autographed picture of Tom Gorzelanny

Chicago White Sox

 Autographed picture of "Tony Pena"

Chicago Bears 4 autograph's

# 6 ---#33 -- #54 --# 23

coming soon

coming soon

   

coming soon

coming soon

   

Thank you to everyone who has supported our foundation

 

 Please read about CDH to understand why we are  raising money for CDH Research.  Thanks !!!!



What is Congenital Diaphragmatic Hernia?
Congenital Diaphragmatic Hernia occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth. Babies born with CDH often endure long hospitalizations and other complications such as pulmonary hypertension, infections, feeding issues, asthma and temporary developmental delay. Some babies develop worse complications and sadly, 50% of babies born with CDH do not survive. The cause of CDH is not known.

Congenital Diaphragmatic Hernia, is severe and often fatal birth defect that occurs as often as Cystic Fibrosis and Spina Bifida. Every 10 minutes a baby is born with CDH - adding up to over half a million babies since 2000
. Yet, CDH is given very little media attention.

Info on ECMO extracorporeal membrane oxygenation

Cody's foundation http://codysfoundation.com has been apart of a group of called CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. Cody's foundation is  to help spread the word of CDH and my son Dakota's fight to live. Our goal is to raise Money for Chicago children's Memorial for Congenital Diaphragmatic Hernia Research . We/ Cody's foundation do not have the help to do Congenital Diaphragmatic Hernia Research. Our mission is to get the word out about CDH.


For more info on and about CDH please visit http://www.cdhsupport.org

No money we get is going for Dakota's Medical Bills, Our HMO has paid close to 4 million and we have NO CAP! =)

All events and fundraisers are done by Cody's Foundation only. We have no other Foundation's helping.
****ʚϊɞ ʚϊɞ ****
Dakota's sites
http://dakota-cody.com
http://codysfoundation.com
 

Cody's fight to live.. birth-3 months

 

 

"Sponsor's" for our 6-6-10 event..

  Country Donuts

3091 US Highway 20 # 101
Elgin, IL 60124-3840
(847) 488-1900

Popeye's Chicken & Biscuits

(847) 622-0026

1616 Big Timber Rd
Elgin, IL 60123 42.0585 -88.316

Jewel- Osco

1250 West Main Street
West Dundee, IL 60118
(847) 428-3547
 

Jester's

96 Tyler Creek Plaza, Elgin, IL 60123

 

Tim McGraw Tickets Donated by:

US 99.5 Americas county station ( Chicago)


 

 

 

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All Rights Reserved http://www.codysfoundation.com 2007/2008/2009/2010

Site made by Mommy

All coding, graphics and designs within this site [http://www.codysfoundation.com] unless otherwise stated are Copyright © to our gift from god *DAKOTA* and may not be removed without our written permission. Please do not take anything from this site. A lot of hard work goes into creating everything, and it is all created especially for our gift from god *DAKOTA* . We would prefer that nobody asks to use any of our graphics, code or content for their own personal use.

 

Cody's Foundation To Raise Money for Children's  E.C.M.O & C.D.H..

 

No money we get is going for Dakota's Medical Bills, Our HMO has paid close to 4 million and we have NO CAP!

My son had a 4% chance to live once he was born. He was a strong willed baby. He told the Angel’s he did not need them to hold his hand. HE NEEDED MOMMY. TM.