He won't be able to sit up, hold his head up, talk, eat, or walk. Those are things we were told for so long. No, not anymore. Past docs that see Logan now are amazed by the strength of this boy. How inspiring is that? It's amazing how inspiring a 12 month old can be!
Logan got his theratog vest on Friday, and I was amazed by how much it helps him. For the first time EVER, I could hold Logan just supporting his back a little bit and didn't have to hold his head up. He actually loves it too! This could eventually be the key to Logan sitting up on his own.
Logan Jay Forbis was born on 2/6/12 with a rare neuromuscular disease called Myotubular Myopathy. The past 8 months have been full of ups and downs, but now that Logan is trached and is on the vent 24/7, he quality of life is much better. We are blessed with an amazing little boy!
Monday, February 25, 2013
Never say never
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