Day #11 Wednesday January 6,2010
Well,today didn't start off well at all. The problem is that I didn't sleep much last night. Kari didn't sleep much either. I don't know what was keeping me awake but, it messed with we all night. Kari tried rubbing my back, which usually works, but nothing seemed to work. I hate when that happens. Kari reminded me this morning that I had run out of one of my meds. This medicine is one that is used to help me sleep so...... no more explaination needed I guess. My appointments have now moved over to a really good time to go over to Portland. My RT is now at 11am until the end. We let a little early and when we got there the tech said they were running late. After the RT I looked at my schedule and saw that I was supposed to be there at 10:10am this morning but, hey , because they were late, they never noticed me being late. Funny how you get to know other patients waiting for treatment. I am not much of a talker in the area ( those of you who know me find that hard to believe) so I just look at people.I am still amazed at how many people are being treated for Cancer just at this hospital. My doctors were worried about how my scelroderma would be affected by the radiation. By the looks of my neck and face, they should use RT as a treatment for scelroderma. I am sure they have tried it but, my skin really looks better now than it did a few months ago. I will keep you posted in case there are any changes to that. Okay, Kari and I are feeling good about my progress and we are counting the days to the end of the treatment. Treatment today was uneventful. Laid on table for 22 minutes and all was done for another day.
I must say this again to all of you. The number of cards, emails, gifts and phone callsthat I have recieved has been incredible. I want you to know that these things really help us to get through everyday if this struggle. I try to talk and be as positive as I can when writing this blog. Also when talking to any of you . But, I must admit that sometimes my emotions get the best of me. It is all the cards, emails, and phone calls from all of you that helps keep Kari and I going. Thanks to all of you. In closing I must remind you......... Day #11 11 Down and 24 To Go
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Hi Donnie, Larke and I just read your blog and were so happy to hear that the doctor said your face and neck had improved with the RT. Keep the courage going. You're the greatest!! We're going to keep the prayers, novenas, etc. going for lesser side effects and more improvement of your skin. Good luck Kari with your surgery on Friday and will be keeping you in our prayers also. Lots of love to you both!! God Bless You!! Love you lots, Auntie D and Larke
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