Several Yasko Test Questions....& B-12 intolerance

[Guest guest]

Hello Everyone!

I am hoping that someone can help answer a few questions for me about

Yasko Testing.

First, Should ALL Genetic Dr's be able to help with this protocol

after learning from Amy's website??

My son goes to his genetics Dr. for a re-check & he hasn't seen her

in 2 yrs. He just turned 5 & was sent to her from his neurologist to

check for mitochondrial problems, due to him showing autistic

tendencies, but something not being right (extemely affectionate w/

people,good eye contact, but stimming (w/ hands, vocally & visually)

covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!). His 2

MRI's both came back showing low myelin in the brain but not

deteriorating, just low/normal.

Nothing came back from the blood work showing mitochondrial issues at

all. We haven't seen either his neurologist or Genetics since

learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST, Metals

(he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in MARCH

of THIS yr.The earlies his gentics Dr. can work him in is April 2nd.

DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC

MEDICAID, WHO " KNOWS " THIS PROTOCOL??

We live between Asheville, NC & Spartanburg/Greenville SC.

I have read several times that after getting this test results, that

there were kids that couldn't tolerate the B-12. My son had

practically NO cobalt on his hair test, & he getting shots now, just

curious if there is a way to KNOW they can't tolerate it, before

getting the tests....

Is there ANYTHING else anyone would like to share about this??

We are waiting on a french urine test so we can do this next.

Thanks so much for any help anyone can give me!!!

Michele

[Guest guest]

I've had people the Yasko testing said should have lots of B-12 do very poorly

on it.

I think any real genetics doctor would realize that what is on the Yasko website

mostly

does not make sense and can't be so. However most genetic doctors would be too

prejudiced by the mainstream medical religion to really look into it and form a

reasoned

opinion - and thus might miss some things that would actually help.

Recall that all heavy metal intoxications are mitochondrial disorders - they

impair

mitochondrial ATP production - and that doctors usually tell you tests are

normal when

the tests come back abnormal in a way the doctor doesn't understand. The only

way to

have real information is to get actual photoicopies of the test results from the

lab yourself

and go over them.

Andy

> Hello Everyone!

> I am hoping that someone can help answer a few questions for me about

> Yasko Testing.

> First, Should ALL Genetic Dr's be able to help with this protocol

> after learning from Amy's website??

> My son goes to his genetics Dr. for a re-check & he hasn't seen her

> in 2 yrs. He just turned 5 & was sent to her from his neurologist to

> check for mitochondrial problems, due to him showing autistic

> tendencies, but something not being right (extemely affectionate w/

> people,good eye contact, but stimming (w/ hands, vocally & visually)

> covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!). His 2

> MRI's both came back showing low myelin in the brain but not

> deteriorating, just low/normal.

> Nothing came back from the blood work showing mitochondrial issues at

> all. We haven't seen either his neurologist or Genetics since

> learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST, Metals

> (he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in MARCH

> of THIS yr.The earlies his gentics Dr. can work him in is April 2nd.

>

> DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC

> MEDICAID, WHO " KNOWS " THIS PROTOCOL??

> We live between Asheville, NC & Spartanburg/Greenville SC.

>

> I have read several times that after getting this test results, that

> there were kids that couldn't tolerate the B-12. My son had

> practically NO cobalt on his hair test, & he getting shots now, just

> curious if there is a way to KNOW they can't tolerate it, before

> getting the tests....

>

> Is there ANYTHING else anyone would like to share about this??

> We are waiting on a french urine test so we can do this next.

>

> Thanks so much for any help anyone can give me!!!

> Michele

>

[Guest guest]

>

> I've had people the Yasko testing said should have lots of B-12 do

very poorly on it.

>

> I think any real genetics doctor would realize that what is on the

Yasko website mostly

> does not make sense and can't be so. However most genetic doctors

would be too

> prejudiced by the mainstream medical religion to really look into

it and form a reasoned

> opinion - and thus might miss some things that would actually help.

>

I APPOLOGIZE IF I MISUNDERSTOOD THIS, BUT IS THIS TO MEAN THAT THE

YASKO'S PROTOCOL... " CAN'T BE SO " ??? I AM VERY INTERESTED TO KNOW

ANYONES OPINION ON THIS, BEFORE WE SPEND A LOT OF $ THAT WE DON'T

HAVE. IT WAS MY UNDERSTANDING, IT WILL TELL WHAT SUPPS, ETC. THAT

EACH CHILD CAN/CAN NOT TOLERATE & NEEDS/DOESN'T NEED. I

> Recall that all heavy metal intoxications are mitochondrial

disorders - they impair

> mitochondrial ATP production - and that doctors usually tell you

tests are normal when

> the tests come back abnormal in a way the doctor doesn't

understand. The only way to

> have real information is to get actual photoicopies of the test

results from the lab yourself

> and go over them.

> I WISH I COULD DO THIS....I TOOK MY SON IN & THEY DREW 5 LITTLE

TUBES OF BLOOD FROM HIM, THAT TOOK 4 OF US TO HOLD HIM & 8 STRAIGHT

MINUTES OF h***!! TO GET THAT BLOOD, THEN I WAS CONTACTED & SAID THEY

LOST IT..I WAS REALLY UPSET & THE GENETICS DOC TOLD ME THAT IF HE

HAD'VE HAD ANY MITOCHONDRIAL ISSUES THEY WOULD ALL COME FROM ME (MOM)

SO THEY SAID FOR ME TO COME UP & GIVE MY BLOOD & IT WAS TESTED... SO

I WOULDN'T HAVE ANY TESTS LIKE THIS, ON HIM. SO, IF IT WAS CAUSED BY

METAL POISONING, THAT WOULDN'T SHOW UP ON ME ANYWAY,HUH.

THANKS FOR YOUR REPLY, ANDY. I AM STILL VERY NEW & TRYING TO LEARN

EVERYDAY TO HELP MY SON. THANKS FOR ANY MORE ADVICE OR SUGGESTIONS!

MICHELE

>

Andy

>

> > Hello Everyone!

> > I am hoping that someone can help answer a few questions for me

about

> > Yasko Testing.

> > First, Should ALL Genetic Dr's be able to help with this protocol

> > after learning from Amy's website??

> > My son goes to his genetics Dr. for a re-check & he hasn't seen

her

> > in 2 yrs. He just turned 5 & was sent to her from his neurologist

to

> > check for mitochondrial problems, due to him showing autistic

> > tendencies, but something not being right (extemely affectionate

w/

> > people,good eye contact, but stimming (w/ hands, vocally &

visually)

> > covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!).

His 2

> > MRI's both came back showing low myelin in the brain but not

> > deteriorating, just low/normal.

> > Nothing came back from the blood work showing mitochondrial

issues at

> > all. We haven't seen either his neurologist or Genetics since

> > learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST,

Metals

> > (he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in

MARCH

> > of THIS yr.The earlies his gentics Dr. can work him in is April

2nd.

> >

> > DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC

> > MEDICAID, WHO " KNOWS " THIS PROTOCOL??

> > We live between Asheville, NC & Spartanburg/Greenville SC.

> >

> > I have read several times that after getting this test results,

that

> > there were kids that couldn't tolerate the B-12. My son had

> > practically NO cobalt on his hair test, & he getting shots now,

just

> > curious if there is a way to KNOW they can't tolerate it, before

> > getting the tests....

> >

> > Is there ANYTHING else anyone would like to share about this??

> > We are waiting on a french urine test so we can do this next.

> >

> > Thanks so much for any help anyone can give me!!!

> > Michele

> >

>

[Guest guest]

> >

> > I've had people the Yasko testing said should have lots of B-12 do

> very poorly on it.

> >

> > I think any real genetics doctor would realize that what is on the

> Yasko website mostly

> > does not make sense and can't be so. However most genetic doctors

> would be too

> > prejudiced by the mainstream medical religion to really look into

> it and form a reasoned

> > opinion - and thus might miss some things that would actually help.

> >

> I APPOLOGIZE IF I MISUNDERSTOOD THIS, BUT IS THIS TO MEAN THAT THE

> YASKO'S PROTOCOL... " CAN'T BE SO " ???

That is correct, my personal opinion, based on reading some of her books, a few

client

reports for cases I was familiar with, and knowing a lot about kinetics, mass

balance, and

the relevant physiology and metabolism is that at least most of her protocol is

incorrect in

terms of its explanation and also not helpful for a lot of people.

> I AM VERY INTERESTED TO KNOW

> ANYONES OPINION ON THIS, BEFORE WE SPEND A LOT OF $ THAT WE DON'T

> HAVE.

I suggest not spending the money.

> IT WAS MY UNDERSTANDING, IT WILL TELL WHAT SUPPS, ETC. THAT

> EACH CHILD CAN/CAN NOT TOLERATE & NEEDS/DOESN'T NEED. I

That is certainly what it CLAIMS to do.

The explanation of how this is determined is not technically accurate, and in

most cases I

have seen the predictions were not true.

> > Recall that all heavy metal intoxications are mitochondrial

> disorders - they impair

> > mitochondrial ATP production - and that doctors usually tell you

> tests are normal when

> > the tests come back abnormal in a way the doctor doesn't

> understand. The only way to

> > have real information is to get actual photoicopies of the test

> results from the lab yourself

> > and go over them.

>

> > I WISH I COULD DO THIS....I TOOK MY SON IN & THEY DREW 5 LITTLE

> TUBES OF BLOOD FROM HIM, THAT TOOK 4 OF US TO HOLD HIM & 8 STRAIGHT

> MINUTES OF h***!! TO GET THAT BLOOD, THEN I WAS CONTACTED & SAID THEY

> LOST IT..I WAS REALLY UPSET & THE GENETICS DOC TOLD ME THAT IF HE

> HAD'VE HAD ANY MITOCHONDRIAL ISSUES THEY WOULD ALL COME FROM ME (MOM)

> SO THEY SAID FOR ME TO COME UP & GIVE MY BLOOD & IT WAS TESTED... SO

> I WOULDN'T HAVE ANY TESTS LIKE THIS, ON HIM. SO, IF IT WAS CAUSED BY

> METAL POISONING, THAT WOULDN'T SHOW UP ON ME ANYWAY,HUH.

> THANKS FOR YOUR REPLY, ANDY. I AM STILL VERY NEW & TRYING TO LEARN

> EVERYDAY TO HELP MY SON. THANKS FOR ANY MORE ADVICE OR SUGGESTIONS!

> MICHELE

> >

> Andy

> >

> > > Hello Everyone!

> > > I am hoping that someone can help answer a few questions for me

> about

> > > Yasko Testing.

> > > First, Should ALL Genetic Dr's be able to help with this protocol

> > > after learning from Amy's website??

> > > My son goes to his genetics Dr. for a re-check & he hasn't seen

> her

> > > in 2 yrs. He just turned 5 & was sent to her from his neurologist

> to

> > > check for mitochondrial problems, due to him showing autistic

> > > tendencies, but something not being right (extemely affectionate

> w/

> > > people,good eye contact, but stimming (w/ hands, vocally &

> visually)

> > > covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!).

> His 2

> > > MRI's both came back showing low myelin in the brain but not

> > > deteriorating, just low/normal.

> > > Nothing came back from the blood work showing mitochondrial

> issues at

> > > all. We haven't seen either his neurologist or Genetics since

> > > learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST,

> Metals

> > > (he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in

> MARCH

> > > of THIS yr.The earlies his gentics Dr. can work him in is April

> 2nd.

> > >

> > > DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC

> > > MEDICAID, WHO " KNOWS " THIS PROTOCOL??

> > > We live between Asheville, NC & Spartanburg/Greenville SC.

> > >

> > > I have read several times that after getting this test results,

> that

> > > there were kids that couldn't tolerate the B-12. My son had

> > > practically NO cobalt on his hair test, & he getting shots now,

> just

> > > curious if there is a way to KNOW they can't tolerate it, before

> > > getting the tests....

> > >

> > > Is there ANYTHING else anyone would like to share about this??

> > > We are waiting on a french urine test so we can do this next.

> > >

> > > Thanks so much for any help anyone can give me!!!

> > > Michele

> > >

> >

>

[Guest guest]

All I know regarding the Yasko appraoch and her RNAs is that 2 individuals I

know claim that while chelating using the AC protocal, they also used RNAs and

the amount of metal that was chelating, increased by 10X.

One of the individuals is a DAN Dr. and the other a person from this site who

I talk with very often. For this reason, I beleive it is worth investigating.

Also, a thorough genetic profile is supposed to help explain why some respond

to MB12 and others do not.

andrewhallcutler <AndyCutler@...> wrote:

> >

> > I've had people the Yasko testing said should have lots of B-12 do

> very poorly on it.

> >

> > I think any real genetics doctor would realize that what is on the

> Yasko website mostly

> > does not make sense and can't be so. However most genetic doctors

> would be too

> > prejudiced by the mainstream medical religion to really look into

> it and form a reasoned

> > opinion - and thus might miss some things that would actually help.

> >

> I APPOLOGIZE IF I MISUNDERSTOOD THIS, BUT IS THIS TO MEAN THAT THE

> YASKO'S PROTOCOL... " CAN'T BE SO " ???

That is correct, my personal opinion, based on reading some of her books, a few

client

reports for cases I was familiar with, and knowing a lot about kinetics, mass

balance, and

the relevant physiology and metabolism is that at least most of her protocol is

incorrect in

terms of its explanation and also not helpful for a lot of people.

> I AM VERY INTERESTED TO KNOW

> ANYONES OPINION ON THIS, BEFORE WE SPEND A LOT OF $ THAT WE DON'T

> HAVE.

I suggest not spending the money.

> IT WAS MY UNDERSTANDING, IT WILL TELL WHAT SUPPS, ETC. THAT

> EACH CHILD CAN/CAN NOT TOLERATE & NEEDS/DOESN'T NEED. I

That is certainly what it CLAIMS to do.

The explanation of how this is determined is not technically accurate, and in

most cases I

have seen the predictions were not true.

> > Recall that all heavy metal intoxications are mitochondrial

> disorders - they impair

> > mitochondrial ATP production - and that doctors usually tell you

> tests are normal when

> > the tests come back abnormal in a way the doctor doesn't

> understand. The only way to

> > have real information is to get actual photoicopies of the test

> results from the lab yourself

> > and go over them.

>

> > I WISH I COULD DO THIS....I TOOK MY SON IN & THEY DREW 5 LITTLE

> TUBES OF BLOOD FROM HIM, THAT TOOK 4 OF US TO HOLD HIM & 8 STRAIGHT

> MINUTES OF h***!! TO GET THAT BLOOD, THEN I WAS CONTACTED & SAID THEY

> LOST IT..I WAS REALLY UPSET & THE GENETICS DOC TOLD ME THAT IF HE

> HAD'VE HAD ANY MITOCHONDRIAL ISSUES THEY WOULD ALL COME FROM ME (MOM)

> SO THEY SAID FOR ME TO COME UP & GIVE MY BLOOD & IT WAS TESTED... SO

> I WOULDN'T HAVE ANY TESTS LIKE THIS, ON HIM. SO, IF IT WAS CAUSED BY

> METAL POISONING, THAT WOULDN'T SHOW UP ON ME ANYWAY,HUH.

> THANKS FOR YOUR REPLY, ANDY. I AM STILL VERY NEW & TRYING TO LEARN

> EVERYDAY TO HELP MY SON. THANKS FOR ANY MORE ADVICE OR SUGGESTIONS!

> MICHELE

> >

> Andy

> >

> > > Hello Everyone!

> > > I am hoping that someone can help answer a few questions for me

> about

> > > Yasko Testing.

> > > First, Should ALL Genetic Dr's be able to help with this protocol

> > > after learning from Amy's website??

> > > My son goes to his genetics Dr. for a re-check & he hasn't seen

> her

> > > in 2 yrs. He just turned 5 & was sent to her from his neurologist

> to

> > > check for mitochondrial problems, due to him showing autistic

> > > tendencies, but something not being right (extemely affectionate

> w/

> > > people,good eye contact, but stimming (w/ hands, vocally &

> visually)

> > > covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!).

> His 2

> > > MRI's both came back showing low myelin in the brain but not

> > > deteriorating, just low/normal.

> > > Nothing came back from the blood work showing mitochondrial

> issues at

> > > all. We haven't seen either his neurologist or Genetics since

> > > learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST,

> Metals

> > > (he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in

> MARCH

> > > of THIS yr.The earlies his gentics Dr. can work him in is April

> 2nd.

> > >

> > > DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC

> > > MEDICAID, WHO " KNOWS " THIS PROTOCOL??

> > > We live between Asheville, NC & Spartanburg/Greenville SC.

> > >

> > > I have read several times that after getting this test results,

> that

> > > there were kids that couldn't tolerate the B-12. My son had

> > > practically NO cobalt on his hair test, & he getting shots now,

> just

> > > curious if there is a way to KNOW they can't tolerate it, before

> > > getting the tests....

> > >

> > > Is there ANYTHING else anyone would like to share about this??

> > > We are waiting on a french urine test so we can do this next.

> > >

> > > Thanks so much for any help anyone can give me!!!

> > > Michele

> > >

> >

>

__________________________________________________

[Guest guest]

I would be very currious to see this data. These are not particularly easy

measurements to

make. If they took 2 spot urine samples it means nothing, those vary by that

much

randomly. Also there is the " roller coaster ride " phenonmenon to account for in

exactly

when each sample was taken.

Andy

> All I know regarding the Yasko appraoch and her RNAs is that 2 individuals I

know claim

that while chelating using the AC protocal, they also used RNAs and the amount

of metal

that was chelating, increased by 10X.

>

> One of the individuals is a DAN Dr. and the other a person from this site

who I talk

with very often. For this reason, I beleive it is worth investigating.

>

> Also, a thorough genetic profile is supposed to help explain why some

respond to

MB12 and others do not.

>

> andrewhallcutler <AndyCutler@...> wrote:

>

> > >

> > > I've had people the Yasko testing said should have lots of B-12 do

> > very poorly on it.

> > >

> > > I think any real genetics doctor would realize that what is on the

> > Yasko website mostly

> > > does not make sense and can't be so. However most genetic doctors

> > would be too

> > > prejudiced by the mainstream medical religion to really look into

> > it and form a reasoned

> > > opinion - and thus might miss some things that would actually help.

> > >

> > I APPOLOGIZE IF I MISUNDERSTOOD THIS, BUT IS THIS TO MEAN THAT THE

> > YASKO'S PROTOCOL... " CAN'T BE SO " ???

>

> That is correct, my personal opinion, based on reading some of her books, a

few client

> reports for cases I was familiar with, and knowing a lot about kinetics, mass

balance,

and

> the relevant physiology and metabolism is that at least most of her protocol

is incorrect

in

> terms of its explanation and also not helpful for a lot of people.

>

> > I AM VERY INTERESTED TO KNOW

> > ANYONES OPINION ON THIS, BEFORE WE SPEND A LOT OF $ THAT WE DON'T

> > HAVE.

>

> I suggest not spending the money.

>

> > IT WAS MY UNDERSTANDING, IT WILL TELL WHAT SUPPS, ETC. THAT

> > EACH CHILD CAN/CAN NOT TOLERATE & NEEDS/DOESN'T NEED. I

>

> That is certainly what it CLAIMS to do.

>

> The explanation of how this is determined is not technically accurate, and in

most cases

I

> have seen the predictions were not true.

>

> > > Recall that all heavy metal intoxications are mitochondrial

> > disorders - they impair

> > > mitochondrial ATP production - and that doctors usually tell you

> > tests are normal when

> > > the tests come back abnormal in a way the doctor doesn't

> > understand. The only way to

> > > have real information is to get actual photoicopies of the test

> > results from the lab yourself

> > > and go over them.

> >

> > > I WISH I COULD DO THIS....I TOOK MY SON IN & THEY DREW 5 LITTLE

> > TUBES OF BLOOD FROM HIM, THAT TOOK 4 OF US TO HOLD HIM & 8 STRAIGHT

> > MINUTES OF h***!! TO GET THAT BLOOD, THEN I WAS CONTACTED & SAID THEY

> > LOST IT..I WAS REALLY UPSET & THE GENETICS DOC TOLD ME THAT IF HE

> > HAD'VE HAD ANY MITOCHONDRIAL ISSUES THEY WOULD ALL COME FROM ME (MOM)

> > SO THEY SAID FOR ME TO COME UP & GIVE MY BLOOD & IT WAS TESTED... SO

> > I WOULDN'T HAVE ANY TESTS LIKE THIS, ON HIM. SO, IF IT WAS CAUSED BY

> > METAL POISONING, THAT WOULDN'T SHOW UP ON ME ANYWAY,HUH.

> > THANKS FOR YOUR REPLY, ANDY. I AM STILL VERY NEW & TRYING TO LEARN

> > EVERYDAY TO HELP MY SON. THANKS FOR ANY MORE ADVICE OR SUGGESTIONS!

> > MICHELE

> > >

> > Andy

> > >

> > > > Hello Everyone!

> > > > I am hoping that someone can help answer a few questions for me

> > about

> > > > Yasko Testing.

> > > > First, Should ALL Genetic Dr's be able to help with this protocol

> > > > after learning from Amy's website??

> > > > My son goes to his genetics Dr. for a re-check & he hasn't seen

> > her

> > > > in 2 yrs. He just turned 5 & was sent to her from his neurologist

> > to

> > > > check for mitochondrial problems, due to him showing autistic

> > > > tendencies, but something not being right (extemely affectionate

> > w/

> > > > people,good eye contact, but stimming (w/ hands, vocally &

> > visually)

> > > > covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!).

> > His 2

> > > > MRI's both came back showing low myelin in the brain but not

> > > > deteriorating, just low/normal.

> > > > Nothing came back from the blood work showing mitochondrial

> > issues at

> > > > all. We haven't seen either his neurologist or Genetics since

> > > > learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST,

> > Metals

> > > > (he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in

> > MARCH

> > > > of THIS yr.The earlies his gentics Dr. can work him in is April

> > 2nd.

> > > >

> > > > DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC

> > > > MEDICAID, WHO " KNOWS " THIS PROTOCOL??

> > > > We live between Asheville, NC & Spartanburg/Greenville SC.

> > > >

> > > > I have read several times that after getting this test results,

> > that

> > > > there were kids that couldn't tolerate the B-12. My son had

> > > > practically NO cobalt on his hair test, & he getting shots now,

> > just

> > > > curious if there is a way to KNOW they can't tolerate it, before

> > > > getting the tests....

> > > >

> > > > Is there ANYTHING else anyone would like to share about this??

> > > > We are waiting on a french urine test so we can do this next.

> > > >

> > > > Thanks so much for any help anyone can give me!!!

> > > > Michele

> > > >

> > >

> >

>

>

>

>

>

> __________________________________________________

>

[Guest guest]

>

> Also, a thorough genetic profile is supposed to help explain why

some respond to MB12 and others do not.

But would this matter, if all you have to do to find out whether B12

will work is give a small amount and see the result? If the result is

bad, then I know there's a blockage in the cycle, right?

Unless the expensive testing leads to some ironclad treatment

decisions, I don't get it. But maybe I got put off by her book that

seemed wacky to me and not like she understood supplements at all (the

RNA stuff I don't know enough to evaluate). Also the emphasis on

genetics -- if my son and I hadn't gotten slammed by a bunch of Hg,

our genetics would be working just fine.

Nell

[Guest guest]

I don't know. Once you do the genetic profiling, you are supposd to find out

how to avoid a blocked path. FOr example, you may be asked to take folapro.

I am reading this now and I paid for and waiting for genetic test results.

I'll keep all posted.

lanellici <lanellici@...> wrote:

>

> Also, a thorough genetic profile is supposed to help explain why

some respond to MB12 and others do not.

But would this matter, if all you have to do to find out whether B12

will work is give a small amount and see the result? If the result is

bad, then I know there's a blockage in the cycle, right?

Unless the expensive testing leads to some ironclad treatment

decisions, I don't get it. But maybe I got put off by her book that

seemed wacky to me and not like she understood supplements at all (the

RNA stuff I don't know enough to evaluate). Also the emphasis on

genetics -- if my son and I hadn't gotten slammed by a bunch of Hg,

our genetics would be working just fine.

Nell

__________________________________________________