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specialhearts · Special Hearts - A place to talk about cogenital heart defects
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Reply | Forward Message #28 of 333 |

I am a mother of a 3 year old beautiful little girl, she was born
with pulmonary stenosis and anamolous pulmonary venous return, she
has had a cath lab procedure, as well as open heart surgery. I am
just looking to talk to other people who understand how I am feeling
that I can help through the tough times and who can help me as well.
I don't talk about how I feel with friends or family as I feel they
do not understand or want to hear about it.






Thu Dec 2, 2004 5:51 am

janetk34
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Message #28 of 333 |
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I am a mother of a 3 year old beautiful little girl, she was born with pulmonary stenosis and anamolous pulmonary venous return, she has had a cath lab...
janet
janetk34
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Dec 2, 2004
5:52 am

hi janet, my name is lesley and i have a fourteen year old son with congenital heart defects his conditon is tricuspid atresia, ive lost count know of the...
lesley rowe
lesley37_2002
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Dec 2, 2004
11:15 pm

hi janet, my name is lesley and i have a fourteen year old son with congenital heart defects his conditon is tricuspid atresia, ive lost count know of the...
lesley rowe
lesley37_2002
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Dec 2, 2004
11:16 pm

Hi. i am Wendy. My 9 month old, Kyle, just had surgery & so we are 9hopefully) thru the bad times. His CHD is pretty mild compared to some out there. But I am...
Wendy Saintsing
pg02068
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Dec 3, 2004
2:39 am

Hey Janet, my names Cindy, mom to Molly (and her twin bro wayne, and big sis hayley). U name it, mo's got it, when people ask what her defect is, i tell them...
spencer davis
broodofsin
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Dec 15, 2004
5:08 am
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