But those who wait on the Lord shall renew their strength; They shall mount up with wings like eagles, They shall run and not be weary, They shall walk and not faint.
ISAIAH 40:31
On September 21/05 we were blessed with a beautiful son. Born with a chromosome 12q deletion (q15q21.2), the challenges were many...cleft lip/palate, complex feeding issues, developmental delays, failure to thrive, multiple infections, blood clots, asthma, sleep apnea, GI and pulmonary bleeds, TPN dependency and kidney issues. Noah embraced life and taught us how to love. On July 29/09, Noah's journey ended, leaving us on a new journey...this journey on the pathway of grief...
4 comments:
It must be so frustrating to feel like you're taking 1 step forward and 2 steps back. I know God is still in the center of Noah's life and his health situation so we'll continue to pray that he will strengthen and encourage you for the days to come. I hope that you will still be able to make it out to BC in the next few weeks. We're anxious to see all of you!
we are praying for you Noah. Only God knows what is in store for you little guy and I know you guys have the comfort of knowing that.
I came across your blog awhile back and just wanted to say that your family has truly been an inspiration to me. We have a handicapped 15 month old little girl named Rebecca, and I can so very much relate to much of what you have written. An entry from last month really spoke to me, where you wrote "And as much as we desire to have control and map out the days ahead, we know that we must continue to trust in God's perfect plan." Our daughter's future is uncertain too, but I know that He gave her to us for a reason and she is our special gift from God.
God bless,
Monika
My family and I are praying for Noah. He's such a strong lil guy and God is taking care of HIS child. I love all the posting about Noah. I really like that picture of him in the lil dump truck. That's too sweet.
God bless you all!
~Rissa
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