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| Comments by
Dionna
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Tuesday, October 25, 2005 |
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| My son is a survior of sct. he is now 8 yrs old. today im reading how many lives sct has affected. Wow.. I felt alone untill today
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| Comments by
Jane Bartosik
on
Tuesday, October 25, 2005 |
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| I'm so glad that everything turned out well. I am a research nuclear medicine technologist and was looking into teratomas when I found your website. Interesting medically and inspirational emotionally.
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| Comments by
Tracy
on
Tuesday, October 25, 2005 |
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| Thank you for this website. I have an 8 month old baby girl who was diagnosed at delivery with SCT. I have just received her first AFP result following surgery and I am unsure of how to interpret the result. Her surgeon is out of town and I am very scared. Thank you for all of the helpful information.
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| Comments by
michele chandler
on
Tuesday, October 25, 2005 |
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| Thank you for writting such a very personal story on the internet. My brother and his wife have just recieved the diagnosis of SCT at 20 weeks gestation and are having a hard time with it. Your story gives us hope and optimism along with the gifts that the lord can provide through prayer.
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| Comments by
Dear Rachel
on
Tuesday, October 25, 2005 |
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| Please email me at dad2elijah@yahoo.com so I can respond to you. Thanks, Michael
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| Comments by
Rachel Horrocks
on
Tuesday, October 25, 2005 |
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| I'm 7 months pregnant and my little girl has been diagonosed with SCT I have to deliver her at the university hospital in salt lake city. my dr. is having me visit once a week with ultrasounds every friday and non stress tests twice a week. we meet with the neonatologists on the 15th of this month to discuss what will happen after she is born and the surgical process. you said they remove the coccyx bone, what is that and do you have to hold your son differently than other babies due to the surgery and bone removal? special car seat needed any other special care required?
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| Comments by
charles G Parten
on
Tuesday, October 25, 2005 |
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| Thank you so much for your tribute to my Granddaughter Maia Grace Newland..it touched my heart as it will many others..God richly bless you and your family {Kara Newland is my daughter]
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| Comments by
Andrea O.
on
Tuesday, October 25, 2005 |
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| Thank you for putting together this website. I work at a Childrens hospital in their Hematology/Oncology unit and finding information for parents can be at times challenging. It is so wonderful to see a baby doing so well!
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| Comments by
Jackie VanderPol
on
Tuesday, October 25, 2005 |
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| The story of your difficult journey was artfully told. Love, strength, commitment, courage and faith.
I'm sure your website is an inspiration to others. Thank you for creating the site and sharing it.
Go gettum Elijah! The world is yours! Just don't let your beautiful sisters spoil you too much. What a lucky boy. :-)
A friend from the Literary Guild
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| Comments by
Stacie Alleger
on
Tuesday, October 25, 2005 |
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| Thank you for a wonderful site. I am currently 24 weeks pregnant with a baby girl that was diagnosed at 19 weeks with an SCT. Your site gives me hope and encouragement that she will survive this. God Bless you & your family.
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If you have any questions, suggestions or comments or otherwise want to talk,
please email me at dad2elijah@yahoo.com
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