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Hello New here   Message List  
Reply | Forward Message #524 of 908 |
Re: [noonan_support] Hello New here

Hi Madeline..my daughter had her sugery last May she was 2 1/2. They had tried to repair the ASD through catheritzation the previous Jan, but it didn't work. She was in hospital for 5 days home for 35hrs then back in for 2 days for complications. It really didn't take her long the recover. She was up and walking around two days post-op. She was still very tured for about a month but after that had all the energy in the world. We had never seen her with so much energy.
 
Oh! and her colour was great almost immdeiately..she wasn't blue anymore she was a wonderful colour of pink.
 
If you would like I can send you some post-op pictures. They are a little shocking, but we had seen pictures of other children and it did help with the recovery shock.
 
Thank you for the welcome and I would be happy to answer any questions you have.
 
Tracy

Madeline mckee <mckeefamily1@...> wrote:
Welcome, and congratulations on your recent delivery!  My name is Madeline and I have a 6yr. old daughter (no NS) and an 18mo. old boy with undiagnosed but highly probable NS.  He fits almost every mark, including the opinions of highly respected geneticists...but the blood work came back negative.  I guess that happens often.  How old was your daughter when she had her heart surgery?  How long was the recovery time?  We know Henry will need it at some point (between now and age 4...) and we are a bit nervous.  Well, thanks if you have the time to answer these questions...and again, welcome!

my2heartbabies <my2heartbabies@...> wrote:
Hello, I'm new here. I have two children with NS. A 3 year old
daughter, and 7wks old son. My daughter had open heart surgery to
repair an ASD and a few other problems with her heart. She has curly
hair, short hair line, feeding issues and weight gain issues,
behavioural issues, sleep issues. However, she is on the high end for
hieght for her age.

My son is having many feeding issues right now, slow weight gain.
Droopy eye lids, undecended testes, low set ears, and an ASD, VSD, and
PS.

I'm looking forward to meeting some people here, as we are going
through everything with both children.

My daughter will be starting school in September, hoping that the
transition into school will be successful.

Tracy





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Wed Apr 12, 2006 11:50 pm

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Message #524 of 908 |
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Hello, I'm new here. I have two children with NS. A 3 year old daughter, and 7wks old son. My daughter had open heart surgery to repair an ASD and a few other...
my2heartbabies
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Apr 11, 2006
12:35 am

Hi Tracy, My name is Amanda. I have a one year old son who has noonan's. He has heart issues, which is PS, ASD, and LVH. He also has issues with swallowing,...
Amanda Springer
dollgril0
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Apr 11, 2006
2:48 pm

Hello Tracy, My name is Wendy. My daughter Morgan is 7 and she has NS. She had surgery to correct her pulmonic stenosis when she was 18 months. She also has...
Jim Moseley
morgidsmom
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Apr 11, 2006
3:56 pm

Welcome, and congratulations on your recent delivery! My name is Madeline and I have a 6yr. old daughter (no NS) and an 18mo. old boy with undiagnosed but...
Madeline mckee
mckeefamily1
Offline Send Email
Apr 12, 2006
12:06 am

Hi Madeline..my daughter had her sugery last May she was 2 1/2. They had tried to repair the ASD through catheritzation the previous Jan, but it didn't work....
Tracy McIntyre
my2heartbabies
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Apr 12, 2006
11:50 pm

Hello, Im Katie, mom to 2 children. Jacob 3, probable Noonans and Kylie 2, who has Noonans. Kylie and Jacob show similiarities(sp?) so when we go back to...
Katie B.
andnowtheres2
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Apr 12, 2006
12:13 am

Hi Tracy, Welcome! - my name is Christina. I have a 15mo old son named Aaron. Last visit with cardiologist was told that he may have Noonans. We are going for...
Christina
red_lionfish
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Apr 12, 2006
4:38 pm
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