Stay Connected

View RSS Feed

Isabelle and Family

Introducing myself

Rate this Entry
Hello everyone! My name is Danielle Mason. I am a mom of a now heavenly angel. Her name is Isabelle May Mason. She was born on Nov. 29, 2007 and died Nov. 29, 2007. She was 2 and 1/2 hours old. She was diagnosed with CDH at 20 weeks. She had no other problems at all. Her heart was on the right side of her chest and had virtually no lungs. Yet she still managed to breath basically on her own for all that time. I also have 3 other children. None of which had CDH. My oldest is 7 his name is Cody. My second is Cayden and he is 5. My youngest child is Abbigail and she is 11 months. We had her after Isabelle passed. I joined this group after being a member of Breath of Hope. They were good support while I was pregnant but I soon had some disagreements with what they were doing so I removed myself from that group. The only thing I carry with me from them them is; I still register March 31 as CDH awareness day and I use tourqois ribbons to represent CDH. I wanted to join a group that could help me do fundraisers for CDH and help others become aware of it. I feel it is very important to inform others of this. One day I hope the awareness of CDH is as large as Breast Cancer. Of all the groups I looked at this was the only one that supported Living and non living babies of CDH and that was important to me. If you have any questions for me I will try to answer them the best I can. Thank you all for your time and God Bless our CDH babies!

Danielle Mason[size=9:2cd2147504][/size:2cd2147504][size=12:2cd2147504][/size:2cd2147504][size=24:2cd2147504][/size:2cd2147504][size=12:2cd2147504][/size:2cd2147504]
Tags: None Add / Edit Tags
Categories
Uncategorized

Comments

  1. JenniferTenney's Avatar
    I am so sorry for you loss. I am sure that your little angel is proud of her mama for wanting to spread awareness. I follow both groups as I think we are all just parents who love our children, want to understand what happened to them, and want to try to decrease the chance of it happening to anyone else. I love the range of topics that are discussed on this one and I get a lot more information and support here. I feel like good or bad, we all shared an experience and I am so glad to have the support and friendship of others who have been touched by CDH. Welcome!