Day 30- Post transplant

The amount of food Brody is eating now is so much, that his little tummy is getting bigger and he looks like a little Buddha, you can rub his tummy for Good luck! LOL

We did the normal stuff again today, Blood tests, painting, drawing, school work, nurse checks, medications, clean sheets, shower, doctors, Tv and DVD's, DS, and eating and more eating.

The young doctor come into me today and said that Brody is pretty good for a Autism child. Oh how mother's with Autism dislike when people say that. People only see what they see in front of them there and then not 24/7. It really puts the parent down as we have done some hard work with the children to get them to be the way they are. Also in Brody's case the chemo has help to slow him down and this experience has forced him into the way he is now.

Unless you really know the child, you shouldn't say anything. As when Brody was diagnosed i had a very hard time with him and i was doing it by myself. Even Grandma and GRandpa notice the difference from when we lived with them before he was diagnosed to him beaning diagnosed with Autism. His teachers had a hard time too, to the level were they couldn't take him anymore, and after you go through a couple of day care centres you really wonder how he will fit into normal life when he can't fit into Day care. Its very stressful, and when people say he seems normal, and alright you just want to say, WE here you take him for a week and tell me then how normal you think he is. So please if you know someone with a Autism child don't say they seem alright!!!!! Thanks

Not much will happen over the weekend so will right one post on Sunday for the weekend.
Thanks again to my family and friends for all your help and support xoxoox