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Re: No specific ratio

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Hi all

We've been on this new plan for a while not, started off with low

doses, equal ratios and have gradually raised it. From the time we

started and slowly raised it every few weeks, things have been the

same....really bad. The symptoms aren't going, if anything more of

them keep coming. The dryness of the joints have increased tenfold, I

have started having tremors racing up my right arm *something like an

electric buzz that I swear sounds as if it's humming* hair loss still

the same, my sister's bones seem to be convoluting all over the place

ie. her hands are starting to resemble an old woman's with arthritis.

We've been trying to take thyroid support, pregnenolone for the

cortisol levels but things are just the same or worse. - not sure what

to do. My levels of ALA:DMSA - 60:60, my sister's 50:50

Mentally I've regressed, I can't seem to gather my thoughts and hold

onto them. If i don't write them down immediately I forget the very

thing i was thinking. absolutely nothing has changed - any advise ?

Many thanks and best regards

Fatimah

P.S Hi (maribob)

I'd just been reading the messages again and noticed that you said

you'd write. Not sure if I'd gotten your email, If I didn't write

back, was probably because the mail ended up in the junkmail section

which i never check *you wouldn't believe how many of my emails are

ending up there, started checking it this past week. Apologies if I

seemed rude but I'd appreciate it your info if you'd care to send it

again.

>

> > > the ratio

> > of dmsa 50-100 mg and ala 50-200 mg

>

> There is no specific ratio, or range of ratios. Use reasonable

amounts of each that work for

> you. Don't worry about how the amount of one relates to the amount

of the other.

>

> Andy

>

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Guest guest

>

> Hi all

>

> We've been on this new plan for a while not, started off with low

> doses, equal ratios and have gradually raised it. From the time we

> started and slowly raised it every few weeks, things have been the

> same....really bad.

TK--- lower dosages down to what does not cause intollerable side

effects and do not just keep raising them every few weeks - please

read through the general suggestions in the files section so you do

not hurt yourself.

The symptoms aren't going, if anything more of

> them keep coming.

TK--- this is probably because you keep increasing dosage when your

body can not handle what you were using.

The dryness of the joints have increased tenfold, I

> have started having tremors racing up my right arm *something like

an

> electric buzz that I swear sounds as if it's humming* hair loss

still

> the same, my sister's bones seem to be convoluting all over the

place

> ie. her hands are starting to resemble an old woman's with

arthritis.

> We've been trying to take thyroid support, pregnenolone for the

> cortisol levels but things are just the same or worse. - not sure

what

> to do. My levels of ALA:DMSA - 60:60, my sister's 50:50

> Mentally I've regressed, I can't seem to gather my thoughts and hold

> onto them. If i don't write them down immediately I forget the very

> thing i was thinking. absolutely nothing has changed - any advise ?

TK--- you are both using too much - suggestion - both of you reduce

dosage to 12.5mg of dmsa only. then see what happens and report back.

read and follow general suggestions in files section

>

> Many thanks and best regards

> Fatimah

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