DANA, what do you think

[Guest guest]

I have been chelating Jack for 4 years, once a month for the last

year and I have been really treating yeast very hard this year. I

hate waking up all of the time. What was the schedule you used?.

Jack just start being able to do the hand movements for head

shoulders, knees and toes (without difficulty) and yesterday he

signed " eat ice pop " He is still progressing but langauge is slow.

This leads me to believe removing metals is still helpful but it is

still hard on the gut. I am hoping since I have tried diflucan it

may kill off yeast that I had been unable to get to w/ GSE,

biocidin, monolaurin, OLE, ect..

Any thoughts?

Thanks,

Marainne

> > Andy

> >

> > I was taken by your comment in the post below that " real

wellness

> > for autism kids is something more like 100-300 rounds. "

> >

> > If one does a chelation round every weekend then the timetable

> > equates to 2-6 years of chelation!!

> >

> > Do you really mean it will take this long?

>

>

> I chelated my kids with ALA basically every weekend for over 2

years.

> I went 84 rounds, but round 84 was four weeks long. So this

approx

> equals 100 rounds.

>

> Now I do maintenance rounds about once per month.

>

>

> > My boy is now 7 and I have chelated, as per your protocol, for

> > around 2 years and he is a long way from recovered. That said,

he

> > has shown a lot of improvements – more affectionate, good eye

> > contact, less repetitive behaviours and a whole lot happier.

> > However, no speech and very limited receptive language.

>

>

> My son also needed anti-viral and a few supplements.

>

>

> > However, it seems to me that progress would be slow for a child

that

> > has been VERY poisoned. My boy developed normally up until 18

> > months. However, he had not acquired speech in that time. I

wonder

> > if this therefore means that chelation progress would be a lot

> > slower compared to a child that developed speech but then lost

it.

>

>

> My son never developed at all. And he was severely low-functioning

> before chelation and anti-viral. So yes, he might have much

further

> to go than the " typical autistic kid " .

>

>

> > Do you think I should persevere with chelation?

>

>

> Personally, I would. My kids lost all their gut issues at my round

> 84, so if your child still has gut issues, I would suspect he still

> might have metal issues. He also might need certain supplements.

>

> Dana

[Guest guest]

> I have been chelating Jack for 4 years, once a month for the last

> year and I have been really treating yeast very hard this year. I

> hate waking up all of the time. What was the schedule you used?.

I started with giving ALA every 8 hours. When my kids showed no

problems with that, I slowly migrated to giving it 3x per day with

meals. Not all kids will do okay with this protocol, but fortunately

for me, mine have had no problems with it.

> Jack just start being able to do the hand movements for head

> shoulders, knees and toes (without difficulty) and yesterday he

> signed " eat ice pop "

Hey that is good news!

>> He is still progressing but langauge is slow.

Yes, my son's only remaining issue is language. I made a supplement

change yesterday, so far *seems* to be working okay.

> This leads me to believe removing metals is still helpful but it is

> still hard on the gut. I am hoping since I have tried diflucan it

> may kill off yeast that I had been unable to get to w/ GSE,

> biocidin, monolaurin, OLE, ect..

> Any thoughts?

Monolaurin [Lauricidin] causes nasty yeast for my son, I believe

because of viral die-off. If you drop the monolaurin, do you notice

any difference?

With Lauricidin, my son needs GSE, oil of oregano, AND uva ursi to

keep the yeast away. This is not the same as gut-yeast [my term]

because my kids lost their gut-yeast issues with chelation.

Dana