Taylor had another echo on her heart yesterday. Thankfully, nothing has changed and her heart remains stable. She will continue to be watched monthly and will need to have these ultra sound pictures done every 1 to 2 months. As long as Taylor remains stable, the doctors are good with that. There is no way to know when she would need her next surgery to receive a replacement valve. Her body will let us know.
Our girl has such a little trooper and does a great job with all her tests. All of these things which seemed so huge to us once upon a time, have become routine and minor. God is good. She just gets cuter and cuter with each new month, smiling and even giggling at times. She's rolling all over the place, trying to put everything in her mouth. With therapy and practice we're continuing to work on her stomach strength. It won't be too much longer till she's sitting up.
4 comments:
Bless our little precious gift...I am continually reminded of God's grace and mercy in the life of Taylor and your beautifl family ~ There are no words to describe the love & thankfulness I feel as her Nana that she is in our lives & the love I have for her faithful mommy, daddy and sisters!!
Thank you for the update. I will continue to hold your family up before Our Lord and Savior. There is so much to be thankful for in this little life and that of her sisters that He has entrusted into your hands. I am blessed to know you and I thank God for you.
She is doing great! I have been out of the blogging scene for a while... trying to come back. Happy Down syndrome awareness month!
ohhhh sweet Taylor. What a litte cutie. I am so glad that our families have connected. We look forward to many Jocelyn and Taylor pladates:) Thanks for getting the photographer for Santa Day! Should be a good time.
xo
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