hello karla and others.advice

[Guest guest]

The only thing stopping us from chelation right now is my sons contipation.Dan

dr suggested PGX fiber.........but my son is having a hard time taking it

What did you guys successfully do for this

Thanks

Laila

From: wiersmak <wiersmak@...>

Subject: [ ] Re: Irene--Turning a corner: thoughts on amazing gains

and the AC protocol

Received: Saturday, August 28, 2010, 9:31 PM

 

ALA I get from Kirkman, the smallest dose they sell is 25 mg, so I split

it into 5 doses. I dont use DMSA (we use DMPS),but most get it from vrp.com.

Dont lose hope.

Karla

> > >

> > > > > >

> > >

> > > > > > I posted on this on another forum. I apologize for the length. But I

> >think my

> >

> > >

> > > > >experience with my son, bears posting here as well, to give hope and

> > >

> > > > >encouragement to those just starting out and to those perhaps further

> >along who

> >

> > >

> > > > >are in a stall or have hit a bump with the AC protocol.

> > >

> > > > > >

> > >

> > > > > > My son is 5 now. We are coming up on round 96. We have been doing

the

> >AC

> >

> > >

> > > > >protocol for 2 years. My son got 26 shots in his first 18 months of

life,

>

> > >

> > > > >including several flu shots and one in utero. My boy lost his skills

> >starting

> >

> > >

> > > > >with a Hep A shot at age one, and with all the ensuing shots down to

age

> >18

> >

> > >

> > > > >months, before we stopped the madness. My boy was loaded with metals,

> >needless

> >

> > >

> > > > >to say and was in a terrible way. Early Intervention in our state came

in

> >at 19

> >

> > >

> > > > >months and intimated we were dealing with a case of severe autism. We

got

> >an

> >

> > >

> > > > >appt with a neurodevelopmental ped - but that appt we had to wait 6

months

> >for.

> >

> > >

> > > > >During this time we discovered biomed - started gfcf, omega 3 oils,

yeast

>

> > >

> > > > >fighters and probiotics. By the time of our appt, we got a dx of high

> > >

> > > > >functioning PDD-nos. Whatever, labels meant nothing - my boy was vax

> >injured.

> >

> > >

> > > > >His gut was still a mess and he could not function or communicate

> >properly. For

> >

> > >

> > > > >the first several rounds of dmsa we saw lots of gains. Then we added

ALA -

> >this

> >

> > >

> > > > >was very tough, stressed his adrenals out, and we could only give him

3mg

> >or so

> >

> > >

> > > > >for half a year. At 25 rounds we hit a stall, that lasted 8 months, 8

> >long, long

> >

> > >

> > > > >months where there was even regression. We tried everything people tout

> >here as

> >

> > >

> > > > >miraculous - Enhansa, high dose vitamin A, antivirals, vinpocetine,

> >gingko,, b

> >

> > >

> > > > >vites, you name it. Nothing worked or mattered. We persevered. By round

50

> >we

> >

> > >

> > > > >were able to up ALA and were at more weight appropriate doses. We saw

some

> >

> > >

> > > > >satisfying gains, then nothing for a few months. At round 66 we saw

some

> >good

> >

> > >

> > > > >gains again, then nothing.

> > >

> > > > > >

> > >

> > > > > > At this time my son's gut was basically healing - no more yeast or

> >parasites

> >

> > >

> > > > >for months, formed stools, he could eat many things, corn eggs, some

> >dairy, etc,

> >

> > >

> > > > >and he loved to try lots of new foods. His seasonal allergies were gone

> >and food

> >

> > >

> > > > >allergies starting to abate. Still he spoke like a cave man and had

> >limited

> >

> > >

> > > > >receptive understanding. Cognition lagged way behind. We just kept

> >chelating. My

> >

> > >

> > > > >dh and I went round and round on whether an EEG was necessary. My dh

said

> >no, no

> >

> > >

> > > > >EEGS or Pharma rx meds, lets just chelate and eventually we will have

> >enough

> >

> > >

> > > > >rounds and it will get better. He prevailed and we waited.

> > >

> > > > >

> > >

> > > > > >

> > >

> > > > > > In the last 2 weeks it is like someone flipped a switch. My son

talks,

> >and

> >

> > >

> > > > >talks and talks, and seems to understand everything. He plays word

games,

> >makes

> >

> > >

> > > > >jokes. He seems to be 100% present for the first time in his life. The

> >teacher

> >

> > >

> > > > >reports he greets peers and plays with them on the playground instead

of

> >merely

> >

> > >

> > > > >running around the perimeter as is his habit. He is by no means

recovered

> >or age

> >

> > >

> > > > >appropriate yet - but he is starting to be on his way there. It is like

he

> >can't

> >

> > >

> > > > >tell me enough things - like he is uncorked or something. The other

night

> >he

> >

> > >

> > > > >would not go to sleep, it was 11 pm and he is a good sleeper. He had a

> >place mat

> >

> > >

> > > > >with the presidents on it and he was hell bent on showing me that he

knew

> >all

> >

> > >

> > > > >their names from Washington onward. He even told me, " you know,

> > >

> > > > >Washington even has his own bridge. " I almost fell over laughing. I

> >finally

> >

> > >

> > > > >uttered words I thought I would never say, but I had to... " sweetie,

please

> >be

> >

> > >

> > > > >quiet, stop talking, it is time to go to sleep. " We have done nothing

> >really,

> >

> > >

> > > > >other than what we have for the last 2 years. In fact, we have recently

> >lowered

> >

> > >

> > > > >all of his supplements considerably. He takes nothing but the most

basic

> >mins

> >

> > >

> > > > >and vites, a few amino acids, liver support, fish oils, antioxidants,

and

>

> > >

> > > > >probiotics. I even hesitated to post this, for fear of jinxing it

somehow.

> >

> > >

> > > > >

> > >

> > > > > >

> > >

> > > > > > I posted this basically to say, there is one miracle supplement only

in

> >my

> >

> > >

> > > > >view: AC chelation - dmsa and ala, week after week, after tedious

> >sleepless

> >

> > >

> > > > >week. To anyone doubting it or having a hard time of it, do not give

up!

> >We have

> >

> > >

> > > > >had stall after stall and regression, and at times I wanted to throw in

> >the

> >

> > >

> > > > >towel, thinking my boy is damaged beyond repair. But with the support

of

> >people

> >

> > >

> > > > >here on the boards and Andy, and my spouse, we just forged on, and on

and

> >on.

> >

> > >

> > > > >And I believe we have another 200 rounds to go, for full recovery. But

I

> >believe

> >

> > >

> > > > >in my heart it is truly possible. We have only one child, and for the

> >first

> >

> > >

> > > > >time, I feel his presence, his true presence as another person with

> >opinions and

> >

> > >

> > > > >ideas, fully present living in our house. It is a beautiful thing.

> > >

> > > > >

> > >

> > > > > >

> > >

> > > > > > I want to close my post with an inspirational saying my late mother,

a

>

> > >

> > > > >relentless optimist, kept by her bed side even as she lay dying of

breast

>

> > >

> > > > >cancer:

> > >

> > > > >

> > >

> > > > > >

> > >

> > > > > > Keep your heart open to dreams, for as long as there is a dream,

there

> >is

> >

> > >

> > > > >hope, and as long as there is hope, there is joy in living.

> > >

> > > > > >

> > >

> > > > > > She lived this and believed this, and she was very right. I have

hope,

> >and

> >

> > >

> > > > >joy now.

> > >

> > > > > >

> > >

> > > > > > Irene

> > >

> > > > > > 5 year old, 95 rounds

> > >

> > > > > >

> > >

> > > > >

> > >

> > > >

> > >

> > > >

> > >

> > > >

> > >

> > > >

> > >

> > > >

> > >

> > > >

> > >

> > > >

> > >

> > > >