That Hannah does not carry the CMS gene mutation.
I got the email several days ago and wanted to post this as I know some of you were not aware.
My heart: Uggh, my heart. Well, I got sad. Then, I got sadder. Started thinking of 'well, she would have been healthy if it were not for downs'. Etc, etc. Lots of thoughts.
Many of you have said "I'm speechless". Well, know that we feel the same way still off and on. Just speechless and walking each day out.
I must say, she's incredibly strong. Very healthy. Just like a naturally healthy newborn. It's radical actually. Aside from the label of down syndrome, you would never really know.
I'm going to be bold and speak my mothers' intuition. She's going to be fine. She's going to be bright, smart and high functioning beyond what anyone could possibly see now.
I see it in her eyes when she looks at me. Just like when our little Luke could not move very much and a past therapist we had early on claimed he had neurological problems..."I boldly rebuked it, fired her and then said 'no, my child is in there..I know it, I see it, he has the will, God has shown me in his eyes'.
By God's grace and mercy...Luke is exactly what God showed me! Smart, bright and learning by the day.
I claim and profess boldly the same intuition that God gave me over my Hannah. She's going to be amazing. No specialists needed for momma.
Love you blog family...thanks for listening.
To God be the Glory,
A
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