Day 96 – quotes to remember

Hi Everyone, It was a quiet night for Miss Corey. She had a new cast put on today pushing the extension further; however, she was uncomfortable and trying to cope with the new casting. We are hoping the regiment of Tylenol will help with the discomfort. Despite her...

Day 95 – Friends are a gift

I thought I’d share a funny story with you. I used to say to my mother, “the day I lose my sense of humor and stop laughing is the day you all better worry about me!” As you know, I’ve been a gypsy since the accident. I haven’t been staying at home except for a rare...

Day 94 – You ask me how I do this?

Hi Everyone, This carepage is a vital resource for communication and a tool in our recovery from this tragedy. I come to the computer each night and the first thing I do is read the posts you all have sent. Each day I gain strength from reading your words of...

Day 93 – We’ll take the bone

Hi Everyone, Corey had a full day of therapy and a late afternoon follow-up appointment with the Neurosurgeon. Neurosurgeons and Neurologists are not warm and fuzzy doctors. They also do not commit to any definitive answer when it comes to the brain. Quite frankly,...

Day 92 – Corey you Sparkle!

Hi Everyone, It is very exciting to see each new change building upon the movements we saw from the previous day. I want to share three of today’s highlights. I “won the prize” a few days ago when Corey opened her mouth for the cold spoon exercise. Twice today, she...