Jenny has a new laptop that contains a software program that speaks what she types. This is something we have waited a long time to happen. It has wireless capabilities so she can drive around the house with her lap top. I downloaded all our digital pics on it and a few hundred songs that she could enjoy. I transfered her Word documents so she can continue with her writings and all. This is a great boost since traveling use to leave her unable to do anything- as well as being able to speak to the kids- who are still learning ASL. Jenny was even able to participate more in our primary class at church. She asked the questions to the kids and chose who would answer. As I suspected, the children were more attentive as they tried to hear what the computer voice was saying (the voice is not always the easiest to understand). I never saw more attentive kids in my life. It is still new and not always the easiest to use since it has to be on her lap or tray. She prefers the larger screened computer that is hooked up to the television, but she does well on the lap top. Best of all, the laptop is a Mac so it does not crash all the time like the Windows computers do. This is highly frustrating to her since she is unable to fix the crashes on her own. Taking care of this little problem is actually a huge thing for her.
News
April 4, 2005
We have returned from two consecutive trips out of town. Jenny continues to become more excited about our move to Austin since returning and seeing it again. The kids like all the new things and their new neighborhood. It is difficult to travel because there are so many things that most people would not think about that we have to address throughout the day. Jenny likes being back with her power chair and computer. Otherwise, she is at the mercy of others to move and entertain her. Jenny has made some really good voice sounds lately. She does best when laying down, so I usually hear more since I am with her when she is going to bed and is waking up. I am hopeful that this is part of her gradual improvements as well. Travels also interfere with our home physical therapy, but Jenny seems to do well from the rest and has demonstrated improvements regardless.
March 23, 2005
Jenny’s progress continues- slow and steady. She is now to the point that she can do some exercises without anyone needing to position her or set up a piece of equiptment. She is typing more, and getting a bit faster. She researches anything everything and has signed herself up on a stroke support e-group site. I get e-mails concerning cool/helpful things that Jenny looks up. She definately has a vast knowlegde of resources that are available and knows how to access them.
I finally beat Jenny in Mancalla (best 2 out of 3). We have not played in over a month or two and she is much stronger and has better dexterity. I think I caught her in a weak moment.
March 16th, 2005
Today marks one year since Jenny’s stroke. I was not very sure how to address this obvious anniversary with Jenny. I asked how she was feeling about today and she surprised me. She did not appear sad, but more of a empowered state of being. Jenny told me that she wanted to mark this day by sharing with me her writings, that she has been diligently working on, concerning the first few days after her stroke. She had worked so hard and wanted to have them completed by today. We have spoke little concerning specifics of those days due to our initial barriers with communication and reluctance to dwell on some of the more difficult memories. I have read her thoughts that she has typed out and I forgot for a short while that Jenny could not use her voice. Her thinking and writing style have remained the same and I heard her loud and clear for these few pages.
As for the last year- it has been a struggle for us all, but mixed with a lot of wonderful blessings. Jenny has had difficult days were she has needed to rely on friends and family to get her through it, but overall, I am so very proud of her. She truely has grown more than she may have without this kind of a trial. I am pleased with her physical progress as well. In the first days after her stroke, we were told that she would most likely die, or at best be “locked-in” without ever moving anything more than her eye lids (Depending on who we talked to, being “locked-in” was the worst thing that could have happened). I have seen Jenny’s scans and there is severe damage to the areas of the brain where muscle movement is controlled. I planned for a life of no communication, constant infections, and complete helplessness. She was to never be off a trache, breathing tube, catheter, or feeding tube. Heavenly Father has truely been watching over and blessing Jenny and our whole family. She surpassed what she was suppose to do and she continues to get stronger. I want to thank everyone who has been supportive in words, deeds, thoughts, and prayers. We look forward to another year, with even greater advances.
March 14, 2005
Our internet connection has been disabled for a few days for some unknown reason and I did not realize how nice it is to have the internet in Jenny’s situation. It brings a great sense of independence and provides a way that she can do so many things without the help of others.
Our whole family is slowly picking up more sign language every day. Sophia is most impressive and it is true that it helps reduce tantrums since she can sign easier than speak when she is upset. Jenny is the worst when it comes to using the signs. She claims that she forgets and ends up spelling out words. Of course, she has to modifiy some signs for her limited range of motion. We have lots of good friends who are helping with these adaptions, so we are quite lucky.
Jenny continues to progress, but it is not always in the same areas at the same time. Previously strong muscle groups show less movement, and other new movements pop out of no where. These movements are definately meaningful and do not seem to have any reason for coming or going- but they do cycle in and out. Her legs are getting stronger when it comes to supporting herself and doing independent leg bends on the tilt table, but have decreased in strength on a similar motion while laying on her back.
I sometimes fear that with so many areas to address, we are unable to fully work all that needs attention. It was much easier when all she could do was move her thumb and toes- but I prefer having too much to address than too little. Jenny has days when she is weak for no appearant reason. on these days, Jenny can barely hold herself up in her chair. The next day could end up being her most progressive ever. It does not make much sense, but I still look a the big picture and see continual progress.