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		Five and a half years ago,  during my second pregnancy, my child was 
diagnosed with a Congenital Diaphragmatic Hernia (CDH).  All I was told by my OB was that there was a hole in her diaphragm and that she would need surgery.  I went home and searched congenital diaphragmatic hernia and I found CHERUBS.  Almost everything I learned about CDH was due to CHERUBS.  Through their website and their information packet
I recieved in the mail.  This information gave me guidance as to what to ask the doctors at and what I need to know about CDH.  
There also is a need for research.  The fact that the medical community does not know what causes CDH shows there is a definite need for more research.
	 
 
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		CHERUBS is my new family, is the place I can go to cry or share or ask for prayers and there is always someone listening. CHERUBS is a place full of love, support and understanding. In CHERUBS I know I'm not alone and that my friends (because I have found so many wonderful friends) will always care for me and my family.
	 
 
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		When my son was diagnosed with CDH,during my pregnancy, I thought it was something simple that could be fixed with surgery once he was born. When he died I was so lost and alone, nobody really understood what CDH was even after I explained it over and over to them. Then I found CHERUBS and immediately I felt at home, everyone is there for me whenever I need them and most importantly I know I am not alone on my own journey of CDH, which makes all the difference!
	 
 
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		I thought when Colton was first diagnosed it was a one time thing. He's fixed and we were sent on our way. I went to our follow up thinking this is a waste of money. (not that I wouldn't of gone). But then the Dr, came in and said he had bad news. I was so confussed. I immediatly went home a started doing research. And I found my new friends and now I have a better understanding of what is happening. Not all the answers I was looking for. But I do understand it's not my fault. and Thank you for that.
	 
 
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		Lynne,
Brilliant post......... clap, clap, clap
Pen - love the new avator....
	 
 
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		Kimberly R - that photo is so gorgeous! I really love it!
	 
 
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		thanks shaz  :)  that was at the lake wednesday cole is a swimming freak !  loves it
	 
 
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		And yes, Lynne, that was a great post. thanks for including us too.
	 
 
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		I am so glad that you all did not mind me including you in it.  I wish I could have included everyone.  I hope everyone check's it out especially those who were menitoned and let's me know what they think and if they approve.  I love you guys so much!
	 
 
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		Lynne-your post was WONDERFUL!!!!
With all of us feeling SO strong about CHERUBS and ALL of us spreading CDH Awareness--we can do nothing but get the Awareness out there and with Awareness--means  MORE Research.
If we all bond together to keep spreading CDH Awareness--it will get into the public eye and we will stand strong for all we stand for.
Penny-love the new avatar.
Kimberly--I love your new avatar also!!!
Together we can accomplish GREAT things!