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Dear Members, It has been a long time since my last member e-mail but CHERUBS is still here, still going strong and we have tons of new services for CDH families! Our membership is now over 1900, including 1800 parents and 100 medical professionals. You can see all of our activities over the years at www.cdhsupport.org/about/timeline.php. There is quite a bit of news to fill you in on: We have a new web site! Our new site address is www.cdhsupport.org. Our new web site ...
This is me, Dawn. I am the person behind the logo doing the typing for this profile here - but I am only 1 of 2000 CDH parents who make up CHERUBS. [img:447519358a]http://www.shane-torrence.com/pics/93b.jpg[/img:447519358a] I am the founder of CHERUBS but I am also the Mom of Shane (1/28/93 - 9/11/99) Diagnosed at birth with left-sided CDH, polyhydramnios, 6 CDH repairs, ASD, Pulmonary Sequestration, Hypospadius, Undescended Testes, Microcephaly, Hospital- 300 days ...
More up-to-date posting at http://www.cdhsupport.org/about/timeline.php 1995 CHERUBS is founded with 2 members; Dawn Torrence, mom of Shane Torrence, and Rhonda Montague, mom of Preston Montague CHERUBS files for an Employee Identification Number, the first step to Non-Profit Status CHERUBS is granted an EIN and 501 (c) III Non-Profit Status CHERUBS Board of Directors is ...
About to post a whole lot of blogs here that we have posted on other places on the internet - just updates on what's new at CHERUBS! :)
What else is going on.... life is good. I am happy, in love with a wonderful man, have my health, my family... all the important things in life. I am at peace with my life and myself and that's not a easy thing to have after CDH! Shane's birthday is coming up next week... he would be 15 years old. 15 years old. The same age I was when I met his dad. I can't picture him at 15, I can only see him as 6. I miss him so much. I dream about him a lot lately and always feel ...
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