On February 15, 2010...
we took our first breath.
We had an answer.
Finally.
A year of testing.
Test after test after test.
Confusion that led to more confusion.
Until now.
We. can. move. on.
To our life.
To our life of raising a son.
A special needs son.
A special needs son with cerebral palsy.
Hypotonic Cerebral Palsy.
To bring awareness.
To ourselves.
To our family.
To our friends.
And other parents who may need support.
Like us.
Because everyone needs help now and then.
Just like us.
But most of all, we remember.
When there is a rainbow...
there is hope.
1 comments:
He is an absolutely beautiful little boy - a gift from God.
Praying as you guys figure out how to parent to such a little special gift.
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