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MCS symptoms

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I've been chelating with dmps 30mg and ALA 50mg for about 22

months now (only at about round 45 though). My mild MCS

recently got dramatically worse.

Wondering if anyone out there has experienced this themselves,

or with their children, and has some advice. Is it possible it is

just a healing crisis and will go away, or more likely permanent

symptoms that I have to learn to live with?

Thanks,

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