Woo hoo! So glad that the GSF made it to the Top 6. I bet Brady's FB friends are glad to stop seeing messages and post from me. I can finally relax this weekend.
This is a snap shot of our life with Spinal Muscular Atrophy. After we found out that our son Joseph (Jojo) had SMA, we grieved. We grieved for all the motor milestones that he would never meet, and for the life that we dreamed and visualized for him. It is tragic to see our child not being able to move much, and then to watch as he progressively loses even those minimal movements and skills that he was born with. But we learn to adjust and keep the focus away from our grief. Because really, he is not fundamentally different from kids his own age: he learns stuff, he knows what he wants, he rationalizes, he whines and occasionally throws a tantrum, and he knows how to wrap his Mom and especially his Dad around his little finger.
I was praying they would win but being in the top 6 is still great.
ReplyDeleteHi Maria, feel free to use any of the ideas on the adaptions blog.
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