Guest guest Posted September 11, 2005 Report Share Posted September 11, 2005 Wow Walt, You sure did describe parts of my life! Isn't it really sad to think about & looking back at how life was before this disease? I use to play softball 4 nights a week, and in tourney's every weekend! And now look at me...I am a single mom trying to raise 3 teenage daughters who can't stay out of bed long enough to do much of anything. It sure doesn't seem fair at all. If only I could change things.............. Lots of Hugs, ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ --- " walt " wrote: I can really relate! Yet the hardest thing for me is the waiting in line or sitting waiting for my name to be called. I have a hard enough time driving to an appointment. Lately doing laundry is a chore. I take part of the clothes then come back for more and then the laundry soap. I do everything in parts anymore. I remember the days of mountain bike riding for 15 miles out in the country for hours on end. It is so much different and how in a couple of years so much has changed. Walt Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2005 Report Share Posted September 11, 2005 Boy does this his home, what Walt said, what 's son is going through too. I used to run, work out with weights,Damn I looked good. :-p I was a massage therapist with a growing, busy clientele. I backpacked the NJ/PA Appalachian Trail, just loved being physically active. Now, I have to recover from taking a shower. There is a documentary movie out called " I Remember Me " . It was done by someone who has CFS?FMS but anyone could relate to it who has a chronic illness. The title alone, the first time I saw it, made me weep. It is a grieving, a mourning for the person we used to be. Eileen Quote Link to comment Share on other sites More sharing options...
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