I see my ME/CFS doc today down at the U. Miami center that Dr Nancy Klimas runs. I'm crossing my fingers that one of the visits will bring a supplement or whatever I can tolerate that will increase my quality of life just that wee more. I always can find out the latest in research when I go, too, before it's public since my doctor and Nancy Klimas are good friends and she's kept up to speed.
The long ride down and the wait, visit, half my blood drawn out (kidding) and the ride back all make for a pooped kid when I get home even though I have pillows and lie down in the back each way. It's all that shaking and bumping around that makes me dizzier and tired, but sitting up doesn't change it and I can at least semi-doze.
Pris
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