Every day there are small improvements that are a big accomplishment for Emily and really add up over time.
Yesterday, Emily had a fairly productive hour or so with her occupational therapist. Angela is such a dynamo (and a dear) - she's so gentle with Emily and so supportive of me. Since Emily seems to have adopted that "teen sleeping thing" that she was never able to as a member of the WP Freestyle team, Angela is constantly fighting Emily's drowsiness in the mornings. Still, she's visually tracking, counting on her fingers - I've seen her do that on her own at least twice since Angela introduced it yesterday, and working on saying "yes" by putting her thumb up. Today, minutes after Angela gave up keeping her awake, I looked at Emily's left hand and the thumb could not have been more up.
Yesterday she did side-of-the-bed with her physical therapist while her speech therapist was working with her. She ate ice chips, apple sauce and tried her hardest to drink from a glass. She's very good at moving her head from left to right to track things visually, but still struggles with holding it up. One interesting side note - the whole time she's sitting up on the side of her bed her left leg is swinging front to back just like we all do when we're sitting on a stool or bench that doesn't allow us to touch the floor. Today she did over 20 minutes on the slant board making it to 30-degrees without any problem - compared to just 5 minutes last Friday! Since she'd slept all morning, she was still alert and responsive when Terry came in to do speech therapy. She continued her ice chip work, learning to hold a spoon and guide it to her mouth, and drinking, which was much better today. We got Terry's approval to give her ice chips when she's awake. Imagine how good that must taste!
Ken and I have the assignment of playing thumb wars, working with her to make a fist, and trying to ask her simple questions that she can answer with "yes" and a thumbs up. I'm going to meet with the Director of Nursing first thing tomorrow to work on her schedule, so that we have consistent times for everything.
Please don't forget - visitors are welcome Mon-Fri, 5-7, and Sat & Sun, 1-3 and 5-7. The specified times are to give her time to rest and eliminate stimulation for a couple of hours - following high stimulation, like visitors and therapy, with low stimulation, will help her brain heal.
Special side note to our friends at Metro: Holy smokes! Are there any snacks left at WalMart? Hannah thinks she's died and gone to heaven - she's never seen this many cookies and chips in this house. It took our neighbor Julie, her two sons, and her next door neighbor to get it all to our house.
Tuesday, May 8, 2007
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5 comments:
Sounds like she's doing so much better... Ice chips must taste absolutely fantastic after having a whole bunch of tubes down your throat. Yikes...
I bet it's alot better than a feed tube, too. I hope I can have a conversation with her next time I see her... something like
Brendan:"so I bet just lying there got pretty boring."
Emily: *holds thumb up*
Brendan "I bet you've eaten alot of ice chips."
Emily:*thumb still up*
Brendan: "...want some?"
Emily: *thrusts thumbs straight down to imply "For god's sake, no! I've eaten like forty billion of those things!"*
Brendan: "Sorry."
Dear Ken,Barb,Emily,and Hannah;
We are so elated to hear that Emily is making such great progress towards the long journey that still lays ahead for her, and her full recovery. We are all still here for all of you. Emily is always in our thoughts and prayers daily as is the rest of the family. We miss you all very dearly and cannot wait until we are able to see all of you. We want to Thank every person that has had a hand in Emily's care from the begining until present. If it weren't for all of you, and the special care that Emily has received from you, her present condition may not be the same. For this we want to thank you all from the bottom of our hearts. We consider you our "Angels on Earth". If it weren't for you, our precious Emily may not be in the same condition that she is presently. We also want to thank the numerous friends, colleagues, and family members that have supported Ken,Barb,Emily,and Hannah thorough this difficult time. May God Bless each and every one of you. Emily is a very special individual that has taught us lessons even in her time of need. If any thing is to be learned it is: Never give up in the face of adversity, always treasure every minute you have with the people that mean the most to you, always let the people you love know that you love them, and never take for granted a day with someone you care about, because life can be turned upside down and change in a blink of an eye.
We Love and Miss you all.
Love;
Uncle Richard, Aunt Tammy, Kimberly, Junior, Jennifer, and Baby Matthew
It is so wonderful to hear about Emily's progress! It is also wonderful that you are keeping track of her gains! Each day is another wonderful day of her in our lives.
I am so glad to see that Emily is progressing. I know it's baby steps but it's all cumulative. Ask them if they have the lemon swaps. They are a nice alternative to ice because they actually have some flavor. We will be by to visit. Just giving Em some time to adjust to the new surroundings.
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