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Barbara writes:


>Has anyone tried Annetta's PD treatment using liquid deprenyl?
>
>What do we know about liquid deprenyl, is it better than tablets?
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I find the liquid deprenyl to be MUCH stronger than the tablets, don't know
if that means better. My tolerance for the liquid topped out at about 4 mgs
a day to prevent too much sleep disturbance.

When I checked out Annetta's regimen I discovered I was already using many
of the same supplements. I added DHEA and still take it, I used the liquid
deprenyl for a while and would use it again, I never did get the Cell Guard,
and probably should. I think she also uses Sun Chlorella, which I love but
don't take with any regularity mainly because my threshhold for pill-popping
was crossed many moons ago, and you have to eat lots of those little green
pills.

I believe her program has definite merit although I don't think I would be
able to discontinue sinemet as she did. I would also have trouble with the
huge volume of pills/supplements and the required religious dosing, probably
a character flaw on my part.

BTW, we just caught the tail end of a news documentary on nutrition and
down's syndrome...studies showing that the down's babies main deficiency is
an inability to properly assimilate nutrients, causing ever-increasing
damage due to basically malnutrition. Some very convincing shots of down's
kids who are using a high-nutrient formula, very rich in amino acids, doing
really well compared to their degenerating counterparts.

I for one am making a New Year's resolution to be more diligent in the
taking of my supplements, and wiser about dietary choices. I noted a BBB
article stating that they have found a way to get chemo drugs into the brain
past the barrier by injecting sugar (manitol) into the brain, it creates a
very brief window of time that the blood brain barrier sorta relaxes and the
chemo drugs can pass. Makes me wonder how my excessive use of sugar as my
main food group has compromised my neurological health.

Kathie Tollifson
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