A Rainbow of Words

A Crazy Fun Life With 3 Kids

Tuesday, July 21, 2009

Moved

Well I decided 14 months in Utah was long enough. So I drove to TX and meet up with Michael (left the kids in UT) and we got the keys to our house and moved in! We got a house on base at Fort Hood. Its a 4 bedroom 2 and 1/2 bathroom house with a backyard and a living room as well as a family room. We decided to let the kids have the living room as there playroom. The kids have not seen the new house yet. We are unpacking and setting up everything before we leave back to UT to go get them and bring them to TX. Michael is resigning his contract with the Army for a few more years. While in he is going to the LPN year long training. Peyton will start her 2nd year of Special Education Preschool in a few short weeks. While we are here in TX she is going to go San Antonio and get seen by the institute the is one of the leading researchers for children with Peyton unique set of disorders. We are hoping that they will be able to give us some new information about her disorder, as well as new things to try to help her learn around her set of disorders. In other news I finally was allowed out of the my shoulder brace but still am not allowed to start physical therapy or really do anything with my arm or anything. They are still making up there mind about a 2nd surgery to fix my joint where the sternum and collarbone meet. After they figure that out they then have to figure out why I lose feeling in my whole shoulder they say it would have something to do with my spine and that would be a surgery of it own to fix that problem. So I have no idea when I will actually get to really use that arm as a normal person would use there arm. The longer this goes the longer it will be till my lawyer can settle with the people's insurance for the lady that so stupidly decided to not stop at the red light. They unfortunately said they can't settle till the Doctors say that this is the best my arm is going to be for the rest of my life and the Doctors are not ready to throw the towel in yet they keep making me do all these weird excersises hoping that it might help or they tell me to not use the arm hoping longer amounts of time without movement will make the problem correct itself. Its rather very frustrating and painful. I have to take sleeping pills now just so I can sleep cause the pain is enough to keep me awake at night. Currently my arm can only go to shoulder height in front of me and to my side I cant lift it over my head or behind my body. I am hoping with just having had the internet and everything setup and being in my own domain that I have more control over that my blogging skill will increase. I guess we shall see.

Slid down the rainbow at 3:57 PM

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