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hi guys & dolls,

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Keeping it brief. Exhausisting catching up on six years, pleasant

luch with Eva (mum-in-law), my sone and myself. Lots of chatter,

couldn't eat much, most of the space gets taken up by swallowed

air. Feeling big as ahouse right now, all air. My son went

home after wards and Eva and I sat and talked and talked, at the end we

were both starting to fall sideways, neither of us willing to call it

quits. Funny we should both be hypotense. Sons do marry their

mothers. I've missed her. Tomorrow we go to meet my daughter,

Sunday she's visiting her step daughter, so I have a day off to de-gas

and rest up.

Glad so many think the collected plain language bit is worth doing.

I'll cheerfully commit to it starting next Tuesday.

Question: what if any data has been collected comparing SDS (not PD+)

patients treated with anti-Parkinson's meds versus those who took none

(morbidity, decline etc.) So far I've only been treated for SDS

symptoms, is there really any reason to take them considering a poor

response is the best expectation - doc does not see the point in putting

me through a trial?

aletta mes

vancouver, bc

Canada

web:

http://aletta.0catch.com

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