Up and moving

They finally moved Taylor to the neurological floor. My mom was excited for this to happen because she just pretty much did nothing too exciting while she was on the pediatrics floor. Now that she is in neuro she is up and hopping. They get her up and dressed every morning which was difficult at first because the clothes she had just fell off of her. She is so skinny so Kristen had to go and buy her some new stuff so she would be descent. They do physical therapy and voice therapy 2 times each day. Yesterday they had her in a wheel chair and she was moving herself up and down the hall using her feet. She also walked a little holding herself up on bars and with someone spotting her of course. So far she is doing well with the physical stuff but is still having a hard time with the vocal. They got her to move her mouth with some of the words but that was about it. She will swallow water but not food. They say that she will have to relearn that food is a good thing and that she likes it because she is not so sure about it right now. By the end of her therapy my mom said she was exhausted and went right to sleep. She seems to want to do that most of the time.
I had a dream last night that when I went to see Taylor that she was walking and talking and I was so overcome with emotion. I hope this is a sign of things to come. I can't wait.