This site was started when Silas was born on 04-10-06. He had complications and was placed on ECMO, a heart/lung bypass machine. He spent his first 7 weeks at Legacy Emanuel NICU in Portland, OR fighting for his life. This is his story of survival and the continuing saga of the Kyne's as told through the eyes of Mom and Grammy. To read from the beginning: scroll down, click on the May "archive", scroll down and start reading from the bottom. The most recent post is at the top.
Just a quick note to let everyone know that my nephew is okay; the medication worked and he is recovering from both the pox and MRSA. YEAH! Jerusha and Silas are on the mend as well and Jerusha went back to school today. Let me see... What crisis can I confront next?!?!?
posted by Tanaya @ 1:12 PM
2 comments
2 Comments:
Praise God! So glad that he is doing better and on the mend. Thinking of you and yours...
~Carole
I'm so glad that Silas is doing so well! Please know that if you have any questions or need to talk to other CDH families, CHERUBS is here.
Dawn
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support
Over 2000 CDH families and 150 CDH medical professionals, working together since 1995
http://www.cdhsupport.org
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