This is not a pity party nor am I’m trying to cast gloom on the holiday season with this post.
I started on my OSA therapy on Jan 3, 2005, so it has been almost 1 year now. I cannot say that I have had the big increase in energy that some of you have had, and wish that I had. I have had good nights and days and not so good nights and days. But, I had those before I started used my CPAP. As we know, it isn’t any “fun” being tethered to a CPAP, but I will survive and continue to prosper in spite of this. Neither the CPAP nor the hose really bother me. It’s that hard plastic thing that I must strap to my face where the hose terminates that bothers me at times. But, I can do nothing about it other than not use it.
I don’t want to think about the consequences that that could bring.
Part of this could be from wondering about my mother-in-law and father-in-law. They are both elderly and not in the best of health.
Enough of this lamenting, in closing I want to wish everyone a Merry Christmas and the Happiest of New Years that you have ever seen. I know that 2006 will be better for each one of us.
Harold
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Harold
Until later, stay safe, be nice, sleep well and keep on papin'

