Cement Signage for CCC Campsite Photograph by Sharon
Part 2
As we left home and Copper, I could tell The Chief was not taking a direct route. This is quite like him...to take the path unknown. Sometimes I'm not happy about such diversions, but I soon relaxed into the rural beauty and small communities we drove through. We had not mapped out our route and so, enjoyed many other diversions (er, we got a little lost).
We arrived a bit after sunset, checked in as I rode "Rosebud" my electric scooter into the lobby. Admittedly I was pooped. The last two days had used up all my spoons. (People who have Fibromyalgia know the "spoon" concept. For you who don't know, it has to do with allocating energy. If you use up all your spoons you are pooped.)
A nice, clean and recently renovated motel. I had reserved a designated wheelchair room with one king bed. The bathroom was extra large to allow for a wheelchair. The best thing was the free Wi-Fi. The Chief had his laptop and I had my iPad2. (We were set to get us some bear, so to speak.)
When I woke up the next morning I couldn't move. Packing my suitcase had done me in. Again, part of having Fibromyalgia means that "using all one's spoons" in one day carries over into the next day or two. Activities need to be planned.
So, I stayed in the King size bed enjoyed being on-line and watched news and movies. This was the way I spent most of my time during the retreat. I'm not complaining, really. I mostly stay at home doing the same thing and I enjoy it. I have fun and learn things and write a blog (um, this one).
When I look back at my life so far I did a lot of things, active things, good things, bad things, exciting things, all the while working very hard. I don't have any regrets, at least not in that regard. I'm enjoying retirement the best way I can. Before Fibromyalgia I volunteered and gave my time to my community. I became interested in local politics, speaking out at public hearings. Then Fibro set in. I had to stop volunteering. BUT, I have computers, a PC in my office and an iPad2 in the bedroom. I'm always working on something. Finally, found a medicine that helps with pain. There are so many different parts of Fibromyalgia. So far the one I dislike the most is called "Fibro Fog." There are times I get confused, lose words, ask the same question again. Working on my blog has become more difficult because my fingers will at times type a totally different word than what I thought I typed. And, my mind wanders on paper. Oh, well. Starved Rock Outlook Photograph by Sharon
Stay tuned for Part 3, which will come just when you think I forgot about it.



