City of Le Sueur MN Graciously accepted my request to sign a CHD Awareness Week Proclamation. The mayor of the City sent me the proclamation, and a special note for Cameron.
He also let me know that The signed proclamation will be in the Le Sueur newspaper.
Cameron Chase was born October 7th 2009.
At our 21 week level II ultrasound, we learned that our precious baby boy would be born with a severe congenital heart defect, called Hypoplastic Left Heart Syndrome.
Hypoplastic Left Heart Syndrome (HLHS) is a heart defect where the left side of his heart didn't form properly in utero.
Without surgery it is 100% fatel.
There is NO cause for this CHD, and yet it occurs 4 in 10,000 babies.
In order for Cameron Chase to survive he will need to have three heart surgeries.
He has two out of three of the needed surgeries.
The first one was the hybrid norwood, he had that surgery at just 8 days old, and the bi-directional glenn at 6 1/2 months old.
Cameron still needs to have the stage three surgery which is the Fontan, the tentative plan is that he will have this surgery anywhere from the age of 2 to 3 years old.
Cameron's cardiologist Dr Gruenstien has sat us down already and told us that Cameron's heart will become tired and become worn out by the time he reaches his early to mid twenties, making a heart transplant his only option as to of staying alive.
We take everyday one day at a time, and do lots of praying that Cameron will survive and grow up and accomplish many great things in his life.
Please continue to lift Cameron up in your prayers as everyday is a a challange for him.
♥♥ mommy, daddy and big sisters love you so much Cameron, and everyday we have with you is truly a blessing from above.
Stay strong monkey, we will make it thru this with you ♥♥
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