
Yeah, I have been depressed about not being able to run, walk, play tennis, bike, do yoga and go boating.
I am trying not to complain at all (or maybe “not so much”)
This was a comment on one of my whiney FB posts:
Darlene I am so sorry you are still enduring all of this. I hope it is not too painful and you’re up and at ’em soon… makes me sad that you are tied down like this ~ I know how much you love to move!!!
This is from a former co-worker who has Cystic Fibrosis. She is in and out of the hospital. Tied to an IV most of the time. Can hardly ever leave the house. Needs a lung transplant if she wants to live much longer. But she always has a smile on her face and enjoys every day that she is still alive.
So I am thankful that:
- I have 4 days off from work
- I can walk/limp/shuffle without crutches
- I am not in any pain
- I have great friends
- My hubby sticks by me through ALL my ups and downs
- I have a job and co-workers that I like
- I have a boat on Lake George
- I know that I will run and play tennis again
I will again celebrate the holiday on Lake George. Moving around will be more difficult than past years but I’ll try not to complain.



Nice post. There is always something to put it into perspective.
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