I
want to thank everyone who has been here with us for this
long ride we have had since Cody was born.
He is a CDH survivor!!! and we are blessed.
I also want to thank all the people who know me from
my others websites I own and run.
The fantasy fights web site competition I have now owned for
more then 4 years now.
The hundreds of friends who have gave support to us for
Cody.
Cody’s many fans =)
Also to my fan site’s I have set up for Mikala and her
friends. I have seen hits coming
in from those sites to Cody’s site. I feel so blessed to
know I am also now getting
to spread the word about C.D.H!!
I have been trying hard to update all my sites, and add info
about C.D.H.
I have banners and links to Both of Cody’s sites..
My goals are to keep those hits coming in and to be sure my
sites have info..
Thank you
also to
www.cdhsupport.org.
the women there are the best!
and to the boards I am a member for Tracheostomy…
Let’s make 2009 a year to fight C.D.H!!! & get some
donations for
Children’s Memorial E.C.M.O & C.D.H. Research.
all money raised goes for
Dr. Reynolds
Research program
on
ECMO
& C.D.H.
at Chicago Children’s Memorial Hospital. in honor of
Cody’s Foundation.

please read this.
http://www.dakota-cody.com/about_dakota.htm
so you understand more about our
Mission.
Cody’s Foundation is a nonprofit organization
All Rights
Reserved © http://specialneedchildren.info/ 2007/2008/09
