This, guy right here is still not walking yet. This recovery from necrotizing pneumonia is taking way to long. I thought he would be walking by now. It has been six months now altogether. Therapy is going okay but it takes 20 minutes for him to get warmed up. I am so mad at the doctors at John Hopkins for taking so long to diagnose him.
This guy has an appointment tomorrow at the feeding clinic at Kennedy kreiger! I hope they give us some good news about the nasal gastric tube and his feedings. The news I, wish for is that he doesn’t have to have it anymore because it has become a pain in the butt. Especially when he pulls it out, then it takes me awhile to get it back in. He does everything he can to hinder it from going back in. He will bite it, he won’t swollow it and he thinks it funny the whole time. Another reason ,I don’t like it is because he always ends up sick for a couple a days.
Dylan is starting to feel better so, he was snuggling with his niece last night. He rolled over closer to her. The cat also had to get in one of the pictures too. We finally got air mattress from my moms house. Thanks so much for letting us use it sis. It is better then trying to take Dylan upstairs ever night. He still refuses to do his physical therapy. He has an appointment at cypress creek Saturday, hopefully he does work then.
This handsome guy will be sixteen Monday. He has not been feeling to good lately, he has a sinus infection, cough and post nasal grip. So, he will not even be able to enjoy Birthday cake. I wish things would get better for him. He is still doing PT, OT, and speech but since he has not been feeling good he did not do any this week. He has an appointment with his neurologist next Thursday and a appointment with cypress creek physical therapy next Saturday because the in home therapy is not effective enough for him because they do not have the equipment needed.
So Superman had an appointment with his pediatrician today and he was put on more medication for his breathing. This guy has never had any problems with his breathing until his long hospitalization. Oh not mention the ambulance rides to and from his appointments because he is still not cleared for car rides yet. His progress is slowly coming along. He ot,pt, and speech a couple times a week. His will start coming out soon for school. So, I have been busy since he has been home. Next week he has two appointments a follow up with the pediatrician and one at the feeding at Kennedy kreiger out patient. Please continue to pray for Superman and send positive thoughts. Superman says thanks for all the love, prayers, and well wishes.
Superman has been doing awesome in therapy. He has been do well in his OP therapy, I think this is favorite therapy, because he gets to eat. They have been taking it slow with feeding. He has been getting a couple ounces a day of yogurt, applesauce, and pudding. In PT he has been working different things, like arm strength, walking and crawling. He is doing okay with this. He struggles with this part though but he giving his all. I am so proud of how far he has come since he has been here. The only problem is his sleeping pattern. It seems like every two days he will not sleep all night and he will stay up for 2 days and sleep all day the next day. When he does this he has an increase in his seizures, the only good thing is they don’t last longer then 20-45 seconds.Please continue to pray for my Superman. I would like to say thank you for your prayers and positive thoughts. Superman loves you all.
So, Superman has been doing some walking in rehab with the help of a lift. He also has the ball in the picture that motivates him to move. On Friday he did a lot of walking with mine and his PT assistant. I am proud of the progress he making.