Established in 1989, the (William Lang) nonprofit foundation is dedicated to improving the quality of life of those suffering Spinal Cord Injury (SCI). Foundation resources are also used to fund research and practical therapies toward the cure for SCI.We are so grateful to those who thru life changing circumstances have chosen to help others that find themselves in the same situation. We truly hope that at some point we will be able to repay those efforts.
"The onset of paralysis triggers both physical and emotional upheaval. Coping with the loss of movement, coupled with being dependent on others for their daily living is devastating. Every SCI individual undergoes transformations, sometimes completely making over their life goals. Employment opportunities are problematic. Relationships with all family, friends and acquaintances are reevaluated and made over based upon each individual's response to the injured, and their new physiological makeup. Adding to these challenges is the enormous expenses incurred, just to provide any kind of quality of life to the afflicted. The main goal of the foundation is to return purpose, motivation and an improved quality of life to the paralyzed. We, as caring human beings, can and must provide the tools to help the unfortunate." - Billy Lang
We took a ride on the Polar Express! The Durango/Silverton Narrow Gauge Railroad took us to the “North Pole” where Santa greeted us and handed out sleigh bells. When we made the reservations we conveyed our need to have wheelchair access to the railcar. We told the reservation agent that Ryan’s chair was just like Christopher Reeve’s chair. We have found that it helps to give a visual as to what his chair is like; being that almost everyone knows Christopher Reeve, that is a good comparison. After a long wait of being placed on “hold” we were told that there would be no problem; the train would be able to accommodate us. We are always a little skeptical when we are told that access is available; however, when we got there we were pleasantly surprised. They had a lift, albeit somewhat rusty, and Ryan was able to “load.” Because the railcar windows are so high, Ryan was able to see out rather well. As the train made its way to the “North Pole” we listened to the story of the Polar Express, ate cookies, drank hot chocolate and then on the way back home, sang Christmas carols. There wasn’t any snow, but it was fun to see all the Christmas lights along the way. The “North Pole” is awesome for those who haven’t been there!!
Ryan started running a fever late Friday night and wasn’t feeling well. I think that he has some congestion in his lungs and has had for some time but because of the antibiotics for the UTI the possible lung infection has been masked. His fever reached 101.7° again; we continued to monitor it as it fluctuated between 100° and 101° finally dropping this afternoon. After opening up his presents, then attending Sacrament Meeting he couldn’t do much more and went back to bed around 3:00pm. He hasn’t had a fever this evening, but still doesn’t feel good. We hope tomorrow will be a better day!!
We hope that he gets to feeling better as we have planned to go down to Gallup for a couple of days – if he is up to it. It will be good to have a change of scenery and see our family down there.
We are so grateful to our Savior; his birth and his atoning sacrifice for each one of us. As you may have read from the last blog, Ryan’s testimony is strong. It took him several days to write that blog, as he became very emotional several times. He is getting better and better at using the voice recognition software. We have also just learned of a “speaking valve” that may help his voice; we are going to be talking to a physician about that after the first of the year. Even though he has “bad” days, his outlook on this injury is unbelievable. He is such a strength to us.
We love you all and wish each of you a very Merry Christmas and a Blessed and Happy New Year.
Love,
Dean, Terry and Ryan