Guest guest Posted March 27, 2009 Report Share Posted March 27, 2009 Yes, she is still insanely cool. There are 4 teenage boys living in her house and 1 in Iraq for 9 more weeks. She has a small collection of boys from around the world. I remember reading a comment on this board sometime or other that basically said I am not defined by my disease. And I'm not. I adjust and move on. I had decided one night last week while Sherman was out of town that I was going to allow an entire night of pity party. Got a pint of Cherries and everything. It worries Sherman if he thinks something is wrong and I figured I had earned it. Just about the time I got my jammies on and got comfy with the ice cream I got called into work. The power in the building had gone off - not cool for my servers anytime but especially not this close to April 15. And I heard the voice of God say OH NO YOU ARE NOT - get off your butt and get on with it. So I did. We keep on keeping on. And thank God I don't have a collection of teenage boys around! S, Lubbock, TX NSIP w/PF 12/2006 et al > > > > > > Ok....I know to some, especially newcomers, this is an insane topic. > > > But, I know there are many ways in which the diagnosis and > subsequent > > > events have actually made my life better. I know things I've gained. > I'm > > > going to reserve my list a bit and just want to hear others answer. > > > While none of us would have chosen to have PF, I think it's > important to > > > remind ourselves of the good aspects of our lives and to instill > among > > > the newcomers the hope, not of a cure, but of a good life. So, what > have > > > you gained or what is better than before or what have you done since > > > diagnosis that you might not have otherwise? > > > > > > Quote Link to comment Share on other sites More sharing options...
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