LETTER FROM MY FRIEND WHO REVERSED SONS AUTISIM

[Guest guest]

Dear Group,

I cannot share Pamelas email address here, but I am willing to

share any information she shares with me, and says it's ok to share

with the group. You may also email me and I will then set you up

with her email address. She is very willing to help anyone who has a

son, daughter, grandchild, etc, who has autism.

 

So here is the letter I sent to Pamela this morning, and her reply

follows.

 

 

 

 

 

GOOD MORNING PAMELA,

I JUST READ A LETTER ON ONE OF MY FOR ALTERNATIVE

MEDICINE. A LADY NAMED MICHELLE IS ASKING IF ANYONE HAS INFORMATION

TO HELP HER FRIEND, WHOS 19 MONTH OLD BABY HAS AUTISIM NOW, DUE TO

VACCINES HE RECEIVED AT AGE 2 MONTHS. SHE SAID HE HAS NOT BEEN THE

SAME SINCE THOSE VACCINES. IS IT OK TO HAVE THE MOM GET IN TOUCH

WITH YOU THROUGH EMAIL PAMELA?

LYNN

 

HI there Lynn,

You bet! Of course you can give her my email address. I continue to

work with families each week and help them find the tools needed to

help get their precious kids on the road to recovery. I am getting

information together now to help a Mother who was sent to me

yesterday. Tell her there is a LOT of hope and not to believe the

doom and gloom out there. More then ever she will have to become a

survivor and fight for her child instead of a her child instead of

allowing the system to victimize her whole family.

 

So that I will know who she is please tell her to tell me in the

email that You sent her to me.

 

While I never practice medicine, or recommend drugs (as we never used

them for our son) I do represent a huge threat to the multi billion

dollar industry they have created that was designed to keep these

kids IN the system. IE: The ineffective robot training they push on

parents to put their child into that does not teach them instead

it " trains " them.

 

Remember my report this year about my son whereas we saw several

children in a class for " special " kids who were the SAME children my

son went to school with just two years earlier in a so-called award

winning STATE school? Our son is now thriving and overcoming ALL the

afflictions of the labels they tried to put on him. He sat in on that

class, with his old classmates, and excelled beyond their belief in

every question they asked him while the other precious children

struggled with even talking. It just broke my heart to see them still

suffering when I know first hand through my own child's progress what

is really possible for recovery.

 

Also remember, that After all the state testing we allowed them to

conduct on our son again, (this year) they reluctantly had to REMOVE

ALL labels from him. Meanwhile those precious children, still in the

system, were NO better two years later then when I last saw them. One

little boy in particular was a LOT worse. He had that familiar glassy

eye'd look of a child they heavily drugged into submission. That was

the fate of our child too if we would have left him in the care of

the state and followed their ill-fated directives. He would have been

NO better either. It really breaks my heart that they think nothing

of creating the disability via these toxic vaccines, then shamelessly

setting up a bogus system for a profit on that suffering.

 

And you know it is for a huge profit. The special schools for the

vaccine injured, they have via State and private industry, are

equally ineffective, and they cost the family $3000.00 to $5000.00 a

month-to which they now have all levels of so-called education (grade

school through highschool-special schools) What is the significance

of having all levels of so-called education for vaccine injured kids?

It means they have ZERO incentive of helping these children

mainstream with their peers and develop to the level of their non-

injured peers. Mainstreaming them means no more monthly hefty tuition

for those schools when the child overcomes the disability and they

will not let go of those profits unless parents force them to and use

what really works.

 

The unbearable truth is that they WANT to keep them disabled because

a LOT of money rides on them staying disabled. Last but not least the

killer drug industry that reaps millions of dollars for giving

useless allergy shots for life, and strong drugs that only cause more

damage, have a huge stake in making sure the child stays disabled

too. There are literally billions of funds on the line should parents

all find the true ways to help these kids recover from vaccine

injuries. Public schools have received more money for speech

therapists, more psychologists, etc. This is the new scam Cancer

society we are seeing in the creation phases. This beast needs to be

stopped now. If it truly helped these kids remove the labels, and

recover, it would be one thing, but it does NOT. It only dashes all

hopes and brainwashes the families into thinking they have to learn

to COPE with disabilities, instead of beating them.

 

All of these elemental steps they took to give the appearance they

were addressing vaccine injuries were conducted under the guise to so-

call help these precious vaccine injured children and they do the

opposite. They do ONE thing, they ensure the child does NOT recover,

and they make sure that sweet child continues to bring them a profit

for the rest of their life on NEEDLESS suffering.

 

Knowing all this, I know what I am up against in my efforts to help

families find real help, I try to err on the side of safety and that

is why I need to know who is writing me so I am not set up by this

industry that wants to silence the information that truly helps these

children.

 

I want to point out a serious note here. The only time these methods

and therapies we used will NOT work is when they are NOT used.

Unfortunately, I have come across other parents who were desperate

for help with vaccine injuries but they were still brainwashed into

believing mainstream was the only answer. Sadly they had to go

through the thousands of dollars in useless tests, doctors,

ineffective schools, and treatments, to only come back to me and ask

again what we did. That really breaks my heart to see. But I am

always open to help again. They just have to be ready to do what will

work. For as I said, it's never too late.

 

Parents can decide today to make choices to really help their little

ones. They just need to be prepared for their family, and community,(

who is still indoctrinated into believing in mainstream medicine) to

NOT be supportive, like my family and community was, UNTIL they saw

the irrefutable good results in our son. NOW that he is better they

are ALL praising what we did, but it was a Huge, lonely, up hill

battle. Having a family filled with mainstream practitioners, why

would I have ever expected any less? Anyway, tell her to wipe away

the tears because there IS hope and she has many wonderful choices.

Please do send her my way dear friend. There are no coincidences are

there? >warm smile<

 

God Bless

Pamela

[Guest guest]

--- Could you possibly set me up with her email address. My email is

mpmcox. My sisters grandson has autism and I would like to

get the information so they can help him. Thank You, Marjorie.

 

In , " dippitydodahff "

<MRSCM4871@A...> wrote:

>

>

> Dear Group,

> I cannot share Pamelas email address here, but I am willing

to

> share any information she shares with me, and says it's ok to

share

> with the group. You may also email me and I will then set you up

> with her email address. She is very willing to help anyone who

has a

> son, daughter, grandchild, etc, who has autism.

>

> So here is the letter I sent to Pamela this morning, and her reply

> follows.

>

>

>

>

>

> GOOD MORNING PAMELA,

> I JUST READ A LETTER ON ONE OF MY FOR

ALTERNATIVE

> MEDICINE. A LADY NAMED MICHELLE IS ASKING IF ANYONE HAS

INFORMATION

> TO HELP HER FRIEND, WHOS 19 MONTH OLD BABY HAS AUTISIM NOW, DUE TO

> VACCINES HE RECEIVED AT AGE 2 MONTHS. SHE SAID HE HAS NOT BEEN

THE

> SAME SINCE THOSE VACCINES. IS IT OK TO HAVE THE MOM GET IN TOUCH

> WITH YOU THROUGH EMAIL PAMELA?

> LYNN

>

> HI there Lynn,

> You bet! Of course you can give her my email address. I continue

to

> work with families each week and help them find the tools needed

to

> help get their precious kids on the road to recovery. I am getting

> information together now to help a Mother who was sent to me

> yesterday. Tell her there is a LOT of hope and not to believe the

> doom and gloom out there. More then ever she will have to become a

> survivor and fight for her child instead of a her child instead of

> allowing the system to victimize her whole family.

>

> So that I will know who she is please tell her to tell me in the

> email that You sent her to me.

>

> While I never practice medicine, or recommend drugs (as we never

used

> them for our son) I do represent a huge threat to the multi

billion

> dollar industry they have created that was designed to keep these

> kids IN the system. IE: The ineffective robot training they push

on

> parents to put their child into that does not teach them instead

> it " trains " them.

>

> Remember my report this year about my son whereas we saw several

> children in a class for " special " kids who were the SAME children

my

> son went to school with just two years earlier in a so-called

award

> winning STATE school? Our son is now thriving and overcoming ALL

the

> afflictions of the labels they tried to put on him. He sat in on

that

> class, with his old classmates, and excelled beyond their belief

in

> every question they asked him while the other precious children

> struggled with even talking. It just broke my heart to see them

still

> suffering when I know first hand through my own child's progress

what

> is really possible for recovery.

>

> Also remember, that After all the state testing we allowed them to

> conduct on our son again, (this year) they reluctantly had to

REMOVE

> ALL labels from him. Meanwhile those precious children, still in

the

> system, were NO better two years later then when I last saw them.

One

> little boy in particular was a LOT worse. He had that familiar

glassy

> eye'd look of a child they heavily drugged into submission. That

was

> the fate of our child too if we would have left him in the care of

> the state and followed their ill-fated directives. He would have

been

> NO better either. It really breaks my heart that they think

nothing

> of creating the disability via these toxic vaccines, then

shamelessly

> setting up a bogus system for a profit on that suffering.

>

> And you know it is for a huge profit. The special schools for the

> vaccine injured, they have via State and private industry, are

> equally ineffective, and they cost the family $3000.00 to $5000.00

a

> month-to which they now have all levels of so-called education

(grade

> school through highschool-special schools) What is the

significance

> of having all levels of so-called education for vaccine injured

kids?

> It means they have ZERO incentive of helping these children

> mainstream with their peers and develop to the level of their non-

> injured peers. Mainstreaming them means no more monthly hefty

tuition

> for those schools when the child overcomes the disability and they

> will not let go of those profits unless parents force them to and

use

> what really works.

>

> The unbearable truth is that they WANT to keep them disabled

because

> a LOT of money rides on them staying disabled. Last but not least

the

> killer drug industry that reaps millions of dollars for giving

> useless allergy shots for life, and strong drugs that only cause

more

> damage, have a huge stake in making sure the child stays disabled

> too. There are literally billions of funds on the line should

parents

> all find the true ways to help these kids recover from vaccine

> injuries. Public schools have received more money for speech

> therapists, more psychologists, etc. This is the new scam Cancer

> society we are seeing in the creation phases. This beast needs to

be

> stopped now. If it truly helped these kids remove the labels, and

> recover, it would be one thing, but it does NOT. It only dashes

all

> hopes and brainwashes the families into thinking they have to

learn

> to COPE with disabilities, instead of beating them.

>

> All of these elemental steps they took to give the appearance they

> were addressing vaccine injuries were conducted under the guise to

so-

> call help these precious vaccine injured children and they do the

> opposite. They do ONE thing, they ensure the child does NOT

recover,

> and they make sure that sweet child continues to bring them a

profit

> for the rest of their life on NEEDLESS suffering.

>

> Knowing all this, I know what I am up against in my efforts to

help

> families find real help, I try to err on the side of safety and

that

> is why I need to know who is writing me so I am not set up by this

> industry that wants to silence the information that truly helps

these

> children.

>

> I want to point out a serious note here. The only time these

methods

> and therapies we used will NOT work is when they are NOT used.

> Unfortunately, I have come across other parents who were desperate

> for help with vaccine injuries but they were still brainwashed

into

> believing mainstream was the only answer. Sadly they had to go

> through the thousands of dollars in useless tests, doctors,

> ineffective schools, and treatments, to only come back to me and

ask

> again what we did. That really breaks my heart to see. But I am

> always open to help again. They just have to be ready to do what

will

> work. For as I said, it's never too late.

>

> Parents can decide today to make choices to really help their

little

> ones. They just need to be prepared for their family, and

community,(

> who is still indoctrinated into believing in mainstream medicine)

to

> NOT be supportive, like my family and community was, UNTIL they

saw

> the irrefutable good results in our son. NOW that he is better

they

> are ALL praising what we did, but it was a Huge, lonely, up hill

> battle. Having a family filled with mainstream practitioners, why

> would I have ever expected any less? Anyway, tell her to wipe

away

> the tears because there IS hope and she has many wonderful

choices.

> Please do send her my way dear friend. There are no coincidences

are

> there? >warm smile<

>

> God Bless

> Pamela

[Guest guest]

I am new to this group, but old to the world of autism. Would it be

possible to share that email address with me also?

Thanks in advance,

Quinsmum

doyouhavebob

 

 

, " dippitydodahff "

<MRSCM4871@A...> wrote:

>

>

> Dear Group,

> I cannot share Pamelas email address here, but I am willing to

> share any information she shares with me, and says it's ok to share

> with the group. You may also email me and I will then set you up

> with her email address. She is very willing to help anyone who has

a

> son, daughter, grandchild, etc, who has autism.

>

> So here is the letter I sent to Pamela this morning, and her reply

> follows.

>

>

>

>

>

> GOOD MORNING PAMELA,

> I JUST READ A LETTER ON ONE OF MY FOR ALTERNATIVE

> MEDICINE. A LADY NAMED MICHELLE IS ASKING IF ANYONE HAS

INFORMATION

> TO HELP HER FRIEND, WHOS 19 MONTH OLD BABY HAS AUTISIM NOW, DUE TO

> VACCINES HE RECEIVED AT AGE 2 MONTHS. SHE SAID HE HAS NOT BEEN THE

> SAME SINCE THOSE VACCINES. IS IT OK TO HAVE THE MOM GET IN TOUCH

> WITH YOU THROUGH EMAIL PAMELA?

> LYNN

>

> HI there Lynn,

> You bet! Of course you can give her my email address. I continue to

> work with families each week and help them find the tools needed to

> help get their precious kids on the road to recovery. I am getting

> information together now to help a Mother who was sent to me

> yesterday. Tell her there is a LOT of hope and not to believe the

> doom and gloom out there. More then ever she will have to become a

> survivor and fight for her child instead of a her child instead of

> allowing the system to victimize her whole family.

>

> So that I will know who she is please tell her to tell me in the

> email that You sent her to me.

>

> While I never practice medicine, or recommend drugs (as we never

used

> them for our son) I do represent a huge threat to the multi billion

> dollar industry they have created that was designed to keep these

> kids IN the system. IE: The ineffective robot training they push on

> parents to put their child into that does not teach them instead

> it " trains " them.

>

> Remember my report this year about my son whereas we saw several

> children in a class for " special " kids who were the SAME children

my

> son went to school with just two years earlier in a so-called award

> winning STATE school? Our son is now thriving and overcoming ALL

the

> afflictions of the labels they tried to put on him. He sat in on

that

> class, with his old classmates, and excelled beyond their belief in

> every question they asked him while the other precious children

> struggled with even talking. It just broke my heart to see them

still

> suffering when I know first hand through my own child's progress

what

> is really possible for recovery.

>

> Also remember, that After all the state testing we allowed them to

> conduct on our son again, (this year) they reluctantly had to

REMOVE

> ALL labels from him. Meanwhile those precious children, still in

the

> system, were NO better two years later then when I last saw them.

One

> little boy in particular was a LOT worse. He had that familiar

glassy

> eye'd look of a child they heavily drugged into submission. That

was

> the fate of our child too if we would have left him in the care of

> the state and followed their ill-fated directives. He would have

been

> NO better either. It really breaks my heart that they think nothing

> of creating the disability via these toxic vaccines, then

shamelessly

> setting up a bogus system for a profit on that suffering.

>

> And you know it is for a huge profit. The special schools for the

> vaccine injured, they have via State and private industry, are

> equally ineffective, and they cost the family $3000.00 to $5000.00

a

> month-to which they now have all levels of so-called education

(grade

> school through highschool-special schools) What is the significance

> of having all levels of so-called education for vaccine injured

kids?

> It means they have ZERO incentive of helping these children

> mainstream with their peers and develop to the level of their non-

> injured peers. Mainstreaming them means no more monthly hefty

tuition

> for those schools when the child overcomes the disability and they

> will not let go of those profits unless parents force them to and

use

> what really works.

>

> The unbearable truth is that they WANT to keep them disabled

because

> a LOT of money rides on them staying disabled. Last but not least

the

> killer drug industry that reaps millions of dollars for giving

> useless allergy shots for life, and strong drugs that only cause

more

> damage, have a huge stake in making sure the child stays disabled

> too. There are literally billions of funds on the line should

parents

> all find the true ways to help these kids recover from vaccine

> injuries. Public schools have received more money for speech

> therapists, more psychologists, etc. This is the new scam Cancer

> society we are seeing in the creation phases. This beast needs to

be

> stopped now. If it truly helped these kids remove the labels, and

> recover, it would be one thing, but it does NOT. It only dashes all

> hopes and brainwashes the families into thinking they have to learn

> to COPE with disabilities, instead of beating them.

>

> All of these elemental steps they took to give the appearance they

> were addressing vaccine injuries were conducted under the guise to

so-

> call help these precious vaccine injured children and they do the

> opposite. They do ONE thing, they ensure the child does NOT

recover,

> and they make sure that sweet child continues to bring them a

profit

> for the rest of their life on NEEDLESS suffering.

>

> Knowing all this, I know what I am up against in my efforts to help

> families find real help, I try to err on the side of safety and

that

> is why I need to know who is writing me so I am not set up by this

> industry that wants to silence the information that truly helps

these

> children.

>

> I want to point out a serious note here. The only time these

methods

> and therapies we used will NOT work is when they are NOT used.

> Unfortunately, I have come across other parents who were desperate

> for help with vaccine injuries but they were still brainwashed into

> believing mainstream was the only answer. Sadly they had to go

> through the thousands of dollars in useless tests, doctors,

> ineffective schools, and treatments, to only come back to me and

ask

> again what we did. That really breaks my heart to see. But I am

> always open to help again. They just have to be ready to do what

will

> work. For as I said, it's never too late.

>

> Parents can decide today to make choices to really help their

little

> ones. They just need to be prepared for their family, and community,

(

> who is still indoctrinated into believing in mainstream medicine)

to

> NOT be supportive, like my family and community was, UNTIL they saw

> the irrefutable good results in our son. NOW that he is better they

> are ALL praising what we did, but it was a Huge, lonely, up hill

> battle. Having a family filled with mainstream practitioners, why

> would I have ever expected any less? Anyway, tell her to wipe away

> the tears because there IS hope and she has many wonderful choices.

> Please do send her my way dear friend. There are no coincidences

are

> there? >warm smile<

>

> God Bless

> Pamela