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I agree with everything Channa says and also want to add that for us, when we

treated for and passed tapeworms, our light stools and breath issues went away.

We haven't seen them since. This has been several months now.

>

> > when i see light colored stool in my son my first thought is

liver/gallbladder....usually a food infraction causes the inflamation which

seems to effect the bile output....this is my own theory in my own son...

> > also bacteria overgrowth......to get my son back on track i put him on a

real bland diet of cooked veggie soup something easy to digest for a couple

days....i added each food in carefully....i added iodine mixed with ACV at the

end of his biggest meal of day with selenium and (copper in my case)

> > but the iodine seemed to kill infection in the stomach and got his bile

flowing again better...

> > plastic breath im thinkin acidosis? caused by the body becoming acidic from

all the back up of toxins...

> > (bakin soda non aluminum kind) helped with extreme cases of acidosis in my

child.

> > channa

> >

> > To: mb12valtrex

> > Sent: Sunday, January 8, 2012 2:15 PM

> > Subject: His stools are white and breath smells like plastic!

> >

> >

> > These are some strange things I see pretty regularly lately in my 12 yr. old

boy.Does anyone have a clue what they might be a sign of??? Thanks for any

ideas,Tammy F.

> >

> >

> >

> >

>

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,

You may have mentioned this on your prior posts but just wanted to know that did

you treat tapeworms with the help of your dan or you did it on your own. I

brought up tapeworms to my dan and he said that he actually doesn't mind those

as they help in certain ways. I don't agree with him as I had a tapeworm myself

as a kid. Nobody ever got that formally treated and I feel that I developed

fatigue and dark circles after that. I do want to treat the worms but just

wanted to check if any of you have done it without informing the dan?

Thanks

is

>

> I agree with everything Channa says and also want to add that for us, when we

treated for and passed tapeworms, our light stools and breath issues went away.

We haven't seen them since. This has been several months now.

>

>

>

> >

> > > when i see light colored stool in my son my first thought is

liver/gallbladder....usually a food infraction causes the inflamation which

seems to effect the bile output....this is my own theory in my own son...

> > > also bacteria overgrowth......to get my son back on track i put him on a

real bland diet of cooked veggie soup something easy to digest for a couple

days....i added each food in carefully....i added iodine mixed with ACV at the

end of his biggest meal of day with selenium and (copper in my case)

> > > but the iodine seemed to kill infection in the stomach and got his bile

flowing again better...

> > > plastic breath im thinkin acidosis? caused by the body becoming acidic

from all the back up of toxins...

> > > (bakin soda non aluminum kind) helped with extreme cases of acidosis in

my child.

> > > channa

> > > From: Tamara <stoplyme@>

> > > To: mb12valtrex

> > > Sent: Sunday, January 8, 2012 2:15 PM

> > > Subject: His stools are white and breath smells like

plastic!

> > >

> > >

> > > These are some strange things I see pretty regularly lately in my 12 yr.

old boy.Does anyone have a clue what they might be a sign of??? Thanks for any

ideas,Tammy F.

> > >

> > >

> > >

> > >

> >

>

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Thanks ,Channa ,,Sophie,And is.I am trying and

researching everything you all have generously given to me.I had

liver levels checked but no news yet.Had an an appt..With his DAN

doc. he found in his hair test that his mercury levels where high

and also said his liver test he did last year was high but he is not

concerned.He insist I just need to push through the olive leaf die

off (he has suggested that in the past but disregaurds my sons

severe reaction to things).He tells me to do more cleansing and it

would be better.But I have doing this for 6yrs to no avail..Don't

the docs think maybe there is something more they can do.Why does he

tell me to do the same thing everytime.I always think he may learn

something new that would pertain to my son.So I continue to do the

coffee enemas(3 a month when hes at his worst).I tried the NAC he

got a rash on the back of his neck,but I am trying more because he

has actually not freaked out on it like he usually does on naturals.

I have been getting him cranial sacral and he really freaks out

after those.So when I don't respond to your responses please know

that I reallyyyyyy appreciate your help I just have not found the

words or time to respond .Tammy F.

I agree with everything Channa says and also want to add

that for us, when we treated for and passed tapeworms, our

light stools and breath issues went away. We haven't seen

them since. This has been several months now.

>

> > when i see light colored stool in my son my

first thought is liver/gallbladder....usually a food

infraction causes the inflamation which seems to effect

the bile output....this is my own theory in my own son...

> > also bacteria overgrowth......to get my son back

on track i put him on a real bland diet of cooked veggie

soup something easy to digest for a couple days....i added

each food in carefully....i added iodine mixed with ACV at

the end of his biggest meal of day with selenium and

(copper in my case)

> > but the iodine seemed to kill infection in the

stomach and got his bile flowing again better...

> > plastic breath im thinkin acidosis? caused by

the body becoming acidic from all the back up of toxins...

> > (bakin soda non aluminum kind) helped with

extreme cases of acidosis in my child.

> > channa

> >

> > To: mb12valtrex

> > Sent: Sunday, January 8, 2012 2:15 PM

> > Subject: His stools are white and

breath smells like plastic!

> >

> >

> > These are some strange things I see pretty

regularly lately in my 12 yr. old boy.Does anyone have a

clue what they might be a sign of??? Thanks for any

ideas,Tammy F.

> >

> >

> >

> >

>

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Tammy,

I feel your frustration. Is it possible for you to give us a list of supps,

herbs and meds your son is on? If your child had abnormal LFTs last time, did

your dan stop the possible culprit? Were the liver enzymes elevated last time or

he also had low albumin or low platelets? Elevated liver enzymes show that liver

has some inflammation or it shows some liver distress. But if you also see low

albumin, low platelets and increased INR(coagulation test), that could be

serious as it indicates that liver is not doing the job it is supposed to do. If

you want and if you get some time, you can send me an email with details as I

don't want you to take the liver issue lightly.

Good Luck

is

>

> Thanks ,Channa ,,Sophie,And is.I am trying and

> researching everything you all have generously given to me.I had liver

> levels checked but no news yet.Had an an appt..With his DAN doc. he

> found in his hair test that his mercury levels where high and also said

> his liver test he did last year was high but he is not concerned.He

> insist I just need to push through the olive leaf die off (he has

> suggested that in the past but disregaurds my sons severe reaction to

> things).He tells me to do more cleansing and it would be better.But I

> have doing this for 6yrs to no avail..Don't the docs think maybe there

> is something more they can do.Why does he tell me to do the same thing

> everytime.I always think he may learn something new that would pertain

> to my son.So I continue to do the coffee enemas(3 a month when hes at

> his worst).I tried the NAC he got a rash on the back of his neck,but I

> am trying more because he has actually not freaked out on it like he

> usually does on naturals. I have been getting him cranial sacral and he

> really freaks out after those.So when I don't respond to your responses

> please know that I reallyyyyyy appreciate your help I just have not

> found the words or time to respond .Tammy F.

>

>

> > I agree with everything Channa says and also want to add that for us,

> > when we treated for and passed tapeworms, our light stools and breath

> > issues went away. We haven't seen them since. This has been several

> > months now.

> >

> >

> >

> > >

> > > > when i see light colored stool in my son my first thought is

> > liver/gallbladder....usually a food infraction causes the inflamation

> > which seems to effect the bile output....this is my own theory in my

> > own son...

> > > > also bacteria overgrowth......to get my son back on track i put

> > him on a real bland diet of cooked veggie soup something easy to

> > digest for a couple days....i added each food in carefully....i added

> > iodine mixed with ACV at the end of his biggest meal of day with

> > selenium and (copper in my case)

> > > > but the iodine seemed to kill infection in the stomach and got his

> > bile flowing again better...

> > > > plastic breath im thinkin acidosis? caused by the body becoming

> > acidic from all the back up of toxins...

> > > > (bakin soda non aluminum kind) helped with extreme cases of

> > acidosis in my child.

> > > > channa

> > > > From: Tamara <stoplyme@>

> > > > To: mb12valtrex

> > <mailto:mb12valtrex%40yahoogroups.com>

> > > > Sent: Sunday, January 8, 2012 2:15 PM

> > > > Subject: His stools are white and breath smells like

> > plastic!

> > > >

> > > >

> > > > These are some strange things I see pretty regularly lately in my

> > 12 yr. old boy.Does anyone have a clue what they might be a sign of???

> > Thanks for any ideas,Tammy F.

> > > >

> > > >

> > > >

> > > >

> > >

> >

> >

>

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Wow is this is a loaded question as you will see.Sorry I know it

will be long.My son has Hashimotos ,Hypothyroid,Congenitil

Lyme,Babesia,Pandas ,Strep(He had tonsils out last year but strep

levals are still high,when checked this month ,all sorts of vit.

defficiencies,oxidative stress is the highest Dr.usemans office has

ever seen,expressive receptive disorder,uses the same simple

sentences daily to get by, brain injuries shown on spec probably

from the lyme,no sleep,eye balls and cheeks get puffy.The only med

he has responded well to is valtrex but now after 1 and half years

he seems to be doing bad.He has white sploches that come and go on

his cheaks,and he has to have a light shining in his face at night

to sleep.He is 12 and just last most he was able to move out of my

bedroom.He slept on the floor .He says the floor is better and hes

too afraid to be in his own room.He started acyclover for a few

months because I thought the corn in the valtrex is the cause of him

not doing well.The acyclovir broke the fear in him,but he went a

little wacky in other areas so I had to stop it so now I am trying

one third a capsol of the virastop.Thats been for about a week

now.So I am very currious about the viral hepatitus,it seems viral.

I almost died of pancreatitus when I was 16.But they never figured

out why.I am currently filling out paperwork to see if my son might

be a good candidate for stem cells with Dr.Bradstreet,because all

treatments have made my son sicker (even after waiting years

thinking it is "Die Off Reaction", naturals, homeopathic and

meds.He currently sees Dr.,but have not had good results

except with the valtrex.My son doesn't have fevers (thats pretty

rare though because his temp always runs 96.He complains of tummy

aches always,but is on strict allergin diet with lots of different

allergy testings.

Oh,I see here he had that test you spoke of last month it was high

(100-300 and my son was at 307),thats the test the dan doc. was not

worried about.I am sure that the doc tested for it yesterday also so

it will be good to compare hopefully tomarrow.I will write again

tomarrow.Thank you for your concern is , Sincerely,Tammy F.

Get his Liver function test done right away. How is his

complexion and the color of the white of the eye(sclera)?

Does he have any other symptoms like nausea or abdominal

pain? Any fevers etc. I am not aware of any of the

protocols that your son is on so please provide some

details. A milder form of viral hepatitis can sometimes do

that. I recommend seeing a pediatrician and getting liver

function test especially alkaline phosphatase levels. How

is he feeling otherwise. Please provide more detail

regarding his symptoms and the treatments he is on.

is

>

> These are some strange things I see pretty regularly

lately in my 12 yr. old boy.Does anyone have a clue what

they might be a sign of??? Thanks for any ideas,Tammy F.

>

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every one is diffrent....but for me if die off lasts more then two weeks and im not seeing improvement...then i stop whatever i am doin.....other people may disagree...as far as docs are concerned i have a rule that i give a doc 6 months. if he dont help my kid in 6 months...im done or he is done..

that was back when i saw docters and other practitioners of health...(hiissss)....just take deep breaths....try one thing at a time....write everything down you give to your son food or supp wise...write down all behaviors and times....write down all bowel movements.....you will get to the answers you are looking for....you will find a pattern....

when i first got into all this biomed i had so many moments of feeling like i was looking for a needle in a haystack....( I still get those moments but less often)

and then i realized if its a million straws then you need to go thru and pick out every last straw until you get to the needle that your lookin for........keep writing to the group..we will help you troubleshoot for more answers.....

To: mb12valtrex Sent: Tuesday, January 10, 2012 11:34 PMSubject: Re: His stools are white and breath smells like plastic!

Thanks ,Channa ,,Sophie,And is.I am trying and researching everything you all have generously given to me.I had liver levels checked but no news yet.Had an an appt..With his DAN doc. he found in his hair test that his mercury levels where high and also said his liver test he did last year was high but he is not concerned.He insist I just need to push through the olive leaf die off (he has suggested that in the past but disregaurds my sons severe reaction to things).He tells me to do more cleansing and it would be better.But I have doing this for 6yrs to no avail..Don't the docs think maybe there is something more they can do.Why does he tell me to do the same thing everytime.I always think he may learn something new that would pertain to my son.So I continue to do the coffee enemas(3 a month when hes at his worst).I tried the NAC he got a rash on the back of his neck,but I am trying more because he has actually not

freaked out on it like he usually does on naturals. I have been getting him cranial sacral and he really freaks out after those.So when I don't respond to your responses please know that I reallyyyyyy appreciate your help I just have not found the words or time to respond .Tammy F.

I agree with everything Channa says and also want to add that for us, when we treated for and passed tapeworms, our light stools and breath issues went away. We haven't seen them since. This has been several months now. > > > when i see light colored stool in my son my first thought is liver/gallbladder....usually a food infraction causes the inflamation which seems to effect the bile output....this is my own theory in my own son...> > also bacteria overgrowth......to get my son back on track i put him on a real bland diet of cooked veggie soup something easy to digest for a couple days....i added each food in carefully....i added iodine mixed with ACV at the end of his biggest meal of day with selenium and (copper in my case)> > but the iodine seemed to kill infection in the stomach and got his bile flowing again better...> > plastic breath im thinkin acidosis? caused by the body

becoming acidic from all the back up of toxins...> > (bakin soda non aluminum kind) helped with extreme cases of acidosis in my child.> > channa> > > > To: mb12valtrex > > Sent: Sunday, January 8, 2012 2:15 PM> > Subject: His stools are white and breath smells like plastic!> > > > > > These are some strange things I see pretty regularly lately in my 12 yr. old boy.Does anyone have a clue what they might be a sign of??? Thanks for any ideas,Tammy F. > > > > > > >

>>

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tammy if i say things you already heard then just ignore,, have you looked into andy cutler chelation...if your sons hair test is showing high in mercury...AC chelation could help him...mercury messes with the liver digestive system brain....ect

what kind of digestive enzymes is your son on? that is one of the most important things for gut kids ..

with his system so messed up supps may not be too much of an option...in the begginning my son couldnt tolerate almost anything....i started slow with digestive enzymes....strict diet.....cut out all grains for a while..all friut....lots of easy to digest veggies and farm organic meat....now i give my son only fish and eggs....but if i was to give him other meat it would be wild game....fed no GMO grains....

how about a couple days of a potassium rich soup with root veggies greens kelp.....i would be givin his gut a rest if he was showing such signs of digestive problems like you mention...

also the homeopathic remedy stramonium is used a lot with ASD kids....i used it for my son with a lot of success in the begginnig.....needing light on face and not wanting to be alone...is strong signs for stramonium....its action is helping with brain inflammation....

just some more ideas...

channa

To: mb12valtrex Sent: Wednesday, January 11, 2012 12:11 AMSubject: Re: Re: His stools are white and breath smells like plastic!

Wow is this is a loaded question as you will see.Sorry I know it will be long.My son has Hashimotos ,Hypothyroid,Congenitil Lyme,Babesia,Pandas ,Strep(He had tonsils out last year but strep levals are still high,when checked this month ,all sorts of vit. defficiencies,oxidative stress is the highest Dr.usemans office has ever seen,expressive receptive disorder,uses the same simple sentences daily to get by, brain injuries shown on spec probably from the lyme,no sleep,eye balls and cheeks get puffy.The only med he has responded well to is valtrex but now after 1 and half years he seems to be doing bad.He has white sploches that come and go on his cheaks,and he has to have a light shining in his face at night to sleep.He is 12 and just last most he was able to move out of my bedroom.He slept on the floor .He says the floor is better and hes too afraid to be in his own room.He started acyclover for a few months because I thought the corn in the

valtrex is the cause of him not doing well.The acyclovir broke the fear in him,but he went a little wacky in other areas so I had to stop it so now I am trying one third a capsol of the virastop.Thats been for about a week now.So I am very currious about the viral hepatitus,it seems viral. I almost died of pancreatitus when I was 16.But they never figured out why.I am currently filling out paperwork to see if my son might be a good candidate for stem cells with Dr.Bradstreet,because all treatments have made my son sicker (even after waiting years thinking it is "Die Off Reaction", naturals, homeopathic and meds.He currently sees Dr.,but have not had good results except with the valtrex.My son doesn't have fevers (thats pretty rare though because his temp always runs 96.He complains of tummy aches always,but is on strict allergin diet with lots of different allergy testings.Oh,I see here he had that test you spoke of last month

it was high (100-300 and my son was at 307),thats the test the dan doc. was not worried about.I am sure that the doc tested for it yesterday also so it will be good to compare hopefully tomarrow.I will write again tomarrow.Thank you for your concern is , Sincerely,Tammy F.

Get his Liver function test done right away. How is his complexion and the color of the white of the eye(sclera)? Does he have any other symptoms like nausea or abdominal pain? Any fevers etc. I am not aware of any of the protocols that your son is on so please provide some details. A milder form of viral hepatitis can sometimes do that. I recommend seeing a pediatrician and getting liver function test especially alkaline phosphatase levels. How is he feeling otherwise. Please provide more detail regarding his symptoms and the treatments he is on. is>> These are some strange things I see pretty

regularly lately in my 12 yr. old boy.Does anyone have a clue what they might be a sign of??? Thanks for any ideas,Tammy F.>

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Tammy, we are all here to help you. Details help give the right advice. I think

it is a good idea to talk to Dr Bradstreet. He has some treatment options even

before stem cell transplant like GCMAF etc. If your kid is a viral one, you can

get some testing done including nagalase test and Anne Connelly IGM and IGG test

and that would help determine the treatments. God has given you your instincts

and follow them. If you are tired of trying the same treatments over and over

again, it is time to switch the dan. I know there are many parents who love

naturals but not everyone can tolerate those just like antibiotics are not for

everyone. Dr Dan Rossignol has experience treating PANDAS but Dr Bradstreet is

trying a lot of new things with kids especially the ones with the immune

dysfunction. Email me and let me know if you would like to talk. My son is still

dealing with a lot of misery but improved in certain areas after I discontinued

the crazy homeotoxicology protocols he was on last year when he was just

regressing and developing more and more allergies. Let me know if I can be of

any help.

is

> > >

> > > These are some strange things I see pretty regularly lately in my 12

> > yr. old boy.Does anyone have a clue what they might be a sign of???

> > Thanks for any ideas,Tammy F.

> > >

> >

> >

>

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Tammy, Whew! Loaded question is right!I'm keeping you and your son in my prayers. I pray you are able to find the answers you need. -Tammy To: mb12valtrex Sent: Wednesday, January 11, 2012 12:11 AM Subject: Re: Re: His stools are white and breath smells like plastic!

Wow is this is a loaded question as you will see.Sorry I know it

will be long.My son has Hashimotos ,Hypothyroid,Congenitil

Lyme,Babesia,Pandas ,Strep(He had tonsils out last year but strep

levals are still high,when checked this month ,all sorts of vit.

defficiencies,oxidative stress is the highest Dr.usemans office has

ever seen,expressive receptive disorder,uses the same simple

sentences daily to get by, brain injuries shown on spec probably

from the lyme,no sleep,eye balls and cheeks get puffy.The only med

he has responded well to is valtrex but now after 1 and half years

he seems to be doing bad.He has white sploches that come and go on

his cheaks,and he has to have a light shining in his face at night

to sleep.He is 12 and just last most he was able to move out of my

bedroom.He slept on the floor .He says the floor is better and hes

too afraid to be in his own room.He started acyclover for a few

months because I thought the corn in the valtrex is the cause of him

not doing well.The acyclovir broke the fear in him,but he went a

little wacky in other areas so I had to stop it so now I am trying

one third a capsol of the virastop.Thats been for about a week

now.So I am very currious about the viral hepatitus,it seems viral.

I almost died of pancreatitus when I was 16.But they never figured

out why.I am currently filling out paperwork to see if my son might

be a good candidate for stem cells with Dr.Bradstreet,because all

treatments have made my son sicker (even after waiting years

thinking it is "Die Off Reaction", naturals, homeopathic and

meds.He currently sees Dr.,but have not had good results

except with the valtrex.My son doesn't have fevers (thats pretty

rare though because his temp always runs 96.He complains of tummy

aches always,but is on strict allergin diet with lots of different

allergy testings.

Oh,I see here he had that test you spoke of last month it was high

(100-300 and my son was at 307),thats the test the dan doc. was not

worried about.I am sure that the doc tested for it yesterday also so

it will be good to compare hopefully tomarrow.I will write again

tomarrow.Thank you for your concern is , Sincerely,Tammy F.

Get his Liver function test done right away. How is his

complexion and the color of the white of the eye(sclera)?

Does he have any other symptoms like nausea or abdominal

pain? Any fevers etc. I am not aware of any of the

protocols that your son is on so please provide some

details. A milder form of viral hepatitis can sometimes do

that. I recommend seeing a pediatrician and getting liver

function test especially alkaline phosphatase levels. How

is he feeling otherwise. Please provide more detail

regarding his symptoms and the treatments he is on.

is

>

> These are some strange things I see pretty regularly

lately in my 12 yr. old boy.Does anyone have a clue what

they might be a sign of??? Thanks for any ideas,Tammy F.

>

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Tammy,I think your prayers are working.I received my sons test

results back from the 23 and me gentics testing and the 2 things he

shows as high health risks are   Hypothyroid and Primary Biliary

Cirrhosis.I am not sure what to do with that  imfo. yet but this is

making a little bit of sense.(Maybe) Thank you for your prayers.I

have to go now,

 Best Regards Tammy F.

 

Tammy,

 

Whew!  Loaded question is right!

I'm keeping you and your son in my prayers.  I

pray you are able to find the answers you need.

 

 

-Tammy

From:

Tammy

To:

mb12valtrex

Sent:

Wednesday, January 11, 2012 12:11 AM

Subject:

Re: Re: His stools are white and

breath smells like plastic!

 

Wow is this is a loaded question as

you will see.Sorry I know it will be long.My

son has Hashimotos ,Hypothyroid,Congenitil

Lyme,Babesia,Pandas ,Strep(He had tonsils out

last year but strep levals are still high,when

checked this month ,all sorts of vit.

defficiencies,oxidative stress is the highest

Dr.usemans office has ever seen,expressive

receptive disorder,uses the same simple

sentences daily to get by, brain injuries

shown on spec probably from the lyme,no

sleep,eye balls and cheeks get puffy.The only

med he has responded well to is valtrex but

now after 1 and half years he seems to be

doing bad.He has white sploches that come and

go on his cheaks,and he has to have a light

shining in his face at night to sleep.He is 12

and just last most he was able to move out of

my bedroom.He slept on the floor .He says the

floor is better and hes too afraid to be in

his own room.He started acyclover for a few

months because I thought the corn in the

valtrex is the cause of him not doing well.The

acyclovir broke the fear in him,but he went a

little wacky in other areas so I had to stop

it so now I am trying one third a capsol of

the virastop.Thats been for about a week

now.So I  am very currious about the viral

hepatitus,it seems viral. I almost died of

pancreatitus when I was 16.But they never

figured out why.I am currently filling out

paperwork to see if my son might be a good

candidate for stem cells with

Dr.Bradstreet,because all treatments have made

my son sicker (even after waiting years

thinking it is  "Die Off Reaction", naturals,

homeopathic and meds.He currently sees

Dr.,but have not had good results

except with the valtrex.My son doesn't have

fevers (thats pretty rare though because his

temp always runs 96.He complains of tummy

aches always,but is on strict allergin diet

with lots of different allergy testings.

Oh,I see here he had that test you spoke of

last month it was high (100-300 and my son was

at 307),thats the test the dan doc. was not

worried about.I am sure that the doc tested

for it yesterday also so it will be good to

compare hopefully tomarrow.I will write again

tomarrow.Thank you for your concern is ,

Sincerely,Tammy F.

 

Get his Liver function test done

right away. How is his complexion and

the color of the white of the

eye(sclera)? Does he have any other

symptoms like nausea or abdominal pain?

Any fevers etc. I am not aware of any of

the protocols that your son is on so

please provide some details. A milder

form of viral hepatitis can sometimes do

that. I recommend seeing a pediatrician

and getting liver function test

especially alkaline phosphatase levels.

How is he feeling otherwise. Please

provide more detail regarding his

symptoms and the treatments he is on.

is

>

> These are some strange things I see

pretty regularly lately in my 12 yr. old

boy.Does anyone have a clue what they

might be a sign of??? Thanks for any

ideas,Tammy F.

>

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Share on other sites

Tammy,

May be you are already working on this and you don't need my input but just

wanted to add that your son needs to be evaluated by

gastroenterologist/hepatologist right away. If you are getting any more blood

work done, check antimitochondrial antibodies also. Stop all the supps and meds

that can affect liver in any way. I am praying for you and your son also and

hope that even if he is at risk, he doesn't really get Primary biliary

cirrhosis. Early diagnosis is the key and it is manageable. Good luck with all

the workup and I hope that your little one feels better. Let me know if you need

any clarification on any medical jargon that your doctor confuses you with.

is

> >> >

> >> > These are some strange things I see pretty regularly lately in my

> >> 12 yr. old boy.Does anyone have a clue what they might be a sign

> >> of??? Thanks for any ideas,Tammy F.

> >> >

> >>

> >

> >

> >

> >

>

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sounds like his gall blatter is shutting down

From: Tammy

Sent: Wednesday, January 11, 2012 10:57 AM

To: mb12valtrex

Subject: Re: Re: His stools are white and breath smells like plastic!

Tammy,I think your prayers are working.I received my sons test results back from the 23 and me gentics testing and the 2 things he shows as high health risks are Hypothyroid and Primary Biliary Cirrhosis.I am not sure what to do with that imfo. yet but this is making a little bit of sense.(Maybe) Thank you for your prayers.I have to go now, Best Regards Tammy F.

Tammy,

Whew! Loaded question is right!

I'm keeping you and your son in my prayers. I pray you are able to find the answers you need.

-Tammy

To: mb12valtrex Sent: Wednesday, January 11, 2012 12:11 AMSubject: Re: Re: His stools are white and breath smells like plastic!

Wow is this is a loaded question as you will see.Sorry I know it will be long.My son has Hashimotos ,Hypothyroid,Congenitil Lyme,Babesia,Pandas ,Strep(He had tonsils out last year but strep levals are still high,when checked this month ,all sorts of vit. defficiencies,oxidative stress is the highest Dr.usemans office has ever seen,expressive receptive disorder,uses the same simple sentences daily to get by, brain injuries shown on spec probably from the lyme,no sleep,eye balls and cheeks get puffy.The only med he has responded well to is valtrex but now after 1 and half years he seems to be doing bad.He has white sploches that come and go on his cheaks,and he has to have a light shining in his face at night to sleep.He is 12 and just last most he was able to move out of my bedroom.He slept on the floor .He says the floor is better and hes too afraid to be in his own room.He started acyclover for a few months because I thought the corn in the valtrex is the cause of him not doing well.The acyclovir broke the fear in him,but he went a little wacky in other areas so I had to stop it so now I am trying one third a capsol of the virastop.Thats been for about a week now.So I am very currious about the viral hepatitus,it seems viral. I almost died of pancreatitus when I was 16.But they never figured out why.I am currently filling out paperwork to see if my son might be a good candidate for stem cells with Dr.Bradstreet,because all treatments have made my son sicker (even after waiting years thinking it is "Die Off Reaction", naturals, homeopathic and meds.He currently sees Dr.,but have not had good results except with the valtrex.My son doesn't have fevers (thats pretty rare though because his temp always runs 96.He complains of tummy aches always,but is on strict allergin diet with lots of different allergy testings.Oh,I see here he had that test you spoke of last month it was high (100-300 and my son was at 307),thats the test the dan doc. was not worried about.I am sure that the doc tested for it yesterday also so it will be good to compare hopefully tomarrow.I will write again tomarrow.Thank you for your concern is , Sincerely,Tammy F.

Get his Liver function test done right away. How is his complexion and the color of the white of the eye(sclera)? Does he have any other symptoms like nausea or abdominal pain? Any fevers etc. I am not aware of any of the protocols that your son is on so please provide some details. A milder form of viral hepatitis can sometimes do that. I recommend seeing a pediatrician and getting liver function test especially alkaline phosphatase levels. How is he feeling otherwise. Please provide more detail regarding his symptoms and the treatments he is on. is>> These are some strange things I see pretty regularly lately in my 12 yr. old boy.Does anyone have a clue what they might be a sign of??? Thanks for any ideas,Tammy F.>

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Thank you for your reply Christel,I am going to ask the doc. about

that.I am waiting in k.c. doc. office,at his primary care.This doc.

has not been much help with other things but maybe he knows about

this. .He will have this months lab work,hopefully showing

something. Best Regards,Tammy F.

 

sounds like his gall blatter is

shutting down

 

From: Tammy

Sent: Wednesday, January 11, 2012 10:57 AM

To: mb12valtrex

Subject: Re: Re: His stools

are white and breath smells like plastic!

 

Tammy,I think your prayers are working.I received my

sons test results back from the 23 and me gentics

testing and the 2 things he shows as high health risks

are   Hypothyroid and Primary Biliary Cirrhosis.I am not

sure what to do with that  imfo. yet but this is making

a little bit of sense.(Maybe) Thank you for your

prayers.I have to go now,

 Best Regards Tammy F.

 

Tammy,

 

Whew!  Loaded question is right!

I'm keeping you and your son in my

prayers.  I pray you are able to find the

answers you need.

 

 

-Tammy

From:

Tammy

To:

mb12valtrex

Sent:

Wednesday, January 11, 2012 12:11 AM

Subject:

Re: Re: His stools are white

and breath smells like plastic!

 

Wow is this is a loaded question

as you will see.Sorry I know it will be

long.My son has Hashimotos

,Hypothyroid,Congenitil

Lyme,Babesia,Pandas ,Strep(He had

tonsils out last year but strep levals

are still high,when checked this month

,all sorts of vit.

defficiencies,oxidative stress is the

highest Dr.usemans office has ever

seen,expressive receptive disorder,uses

the same simple sentences daily to get

by, brain injuries shown on spec

probably from the lyme,no sleep,eye

balls and cheeks get puffy.The only med

he has responded well to is valtrex but

now after 1 and half years he seems to

be doing bad.He has white sploches that

come and go on his cheaks,and he has to

have a light shining in his face at

night to sleep.He is 12 and just last

most he was able to move out of my

bedroom.He slept on the floor .He says

the floor is better and hes too afraid

to be in his own room.He started

acyclover for a few months because I

thought the corn in the valtrex is the

cause of him not doing well.The

acyclovir broke the fear in him,but he

went a little wacky in other areas so I

had to stop it so now I am trying one

third a capsol of the virastop.Thats

been for about a week now.So I  am very

currious about the viral hepatitus,it

seems viral. I almost died of

pancreatitus when I was 16.But they

never figured out why.I am currently

filling out paperwork to see if my son

might be a good candidate for stem cells

with Dr.Bradstreet,because all

treatments have made my son sicker (even

after waiting years thinking it is  "Die

Off Reaction", naturals, homeopathic and

meds.He currently sees Dr.,but

have not had good results except with

the valtrex.My son doesn't have fevers

(thats pretty rare though because his

temp always runs 96.He complains of

tummy aches always,but is on strict

allergin diet with lots of different

allergy testings.

Oh,I see here he had that test you spoke

of last month it was high (100-300 and

my son was at 307),thats the test the

dan doc. was not worried about.I am sure

that the doc tested for it yesterday

also so it will be good to compare

hopefully tomarrow.I will write again

tomarrow.Thank you for your concern

is , Sincerely,Tammy F.

 

Get his Liver function test

done right away. How is his

complexion and the color of the

white of the eye(sclera)? Does he

have any other symptoms like

nausea or abdominal pain? Any

fevers etc. I am not aware of any

of the protocols that your son is

on so please provide some details.

A milder form of viral hepatitis

can sometimes do that. I recommend

seeing a pediatrician and getting

liver function test especially

alkaline phosphatase levels. How

is he feeling otherwise. Please

provide more detail regarding his

symptoms and the treatments he is

on.

is

>

> These are some strange things

I see pretty regularly lately in

my 12 yr. old boy.Does anyone have

a clue what they might be a sign

of??? Thanks for any ideas,Tammy

F.

>

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Hi is,O.K. this is whats going on,his level was high last month

but normal now.Of course my son didn't have that smell by the time

the doc. got the lab order.He said it all looks normal.I told of my

past with pancreatitis,and my sons genetics test.I asked him for a

cat scan to be preventative,he said there is no such test.So back to

the drawing board.What kind of doc. would check for mito antibodies?

This was a primary care I also asked his dan doc. but he just checks

the oats,hair metals,allergies,and vitamin defficiencies.My sons

anger is over the top.His entire room is ripped up,and he feels

terrible.The liver diagnosis made so much sense to me.My son reacts

to absolutely everything.I buy distilled water now because I found

he reacts more to the filtered water.With him reacting to everything

doesn't that make sense that it has to be an organ or liver issue.He

reacts to all topicals vit.s. also.So its not the leaky gut so

much.Thank you for all your ideas,Tammy F.

Tammy,

May be you are already working on this and you don't need

my input but just wanted to add that your son needs to be

evaluated by gastroenterologist/hepatologist right away.

If you are getting any more blood work done, check

antimitochondrial antibodies also. Stop all the supps and

meds that can affect liver in any way. I am praying for

you and your son also and hope that even if he is at risk,

he doesn't really get Primary biliary cirrhosis. Early

diagnosis is the key and it is manageable. Good luck with

all the workup and I hope that your little one feels

better. Let me know if you need any clarification on any

medical jargon that your doctor confuses you with.

is

> >> >

> >> > These are some strange things I see

pretty regularly lately in my

> >> 12 yr. old boy.Does anyone have a clue what

they might be a sign

> >> of??? Thanks for any ideas,Tammy F.

> >> >

> >>

> >

> >

> >

> >

>

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Hi Tammy,

I am so sorry that your son is going through all this. The antibodies I

suggested are called AMA or antimitochondrial antibodies that indicate the

primary biliary cirrhosis. Even your primary medical doctor can order that to be

done along with other blood work. If you want you can email me the liver

enzymes, albumin, platelets, ammonia and coagulation results and I might be able

to suggest whether he needs to see a specialist right away. If you are not

comfortable with that then I would suggest you get him evaluated by a pediatric

hepatologist/gastroenterologist especially if he is still having light stools.

Light or clay colored stool indicate blockage of biliary duct or blockage in the

tiny ducts in the liver. It could even be caused by some parasites. The fact

that your son reacts to everything indicates a dysregulated immune system. In

our children there are several causes of that including chronic viral

infections, vitamin D deficiency, chronic inflammation etc. A CAT scan is not

needed to see liver pathology and a liver and GB ultrasound is better but the

blood work is first step. I know how difficult your situation is right now but

if you get a chance, give me a brief history of your son, the treatments that

you have tried and what supps or meds cause worse reactions.

is

> > > >> >

> > > >> > These are some strange things I see pretty regularly lately in my

> > > >> 12 yr. old boy.Does anyone have a clue what they might be a sign

> > > >> of??? Thanks for any ideas,Tammy F.

> > > >> >

> > > >>

> > > >

> > > >

> > > >

> > > >

> > >

> >

> >

>

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Hi is, Heres my sons labs.Dec.-Album-4.9 (3.2-5.5)

Jan.-Album-4.1(3.5-4.8)

Dec.-Plattlets-355(150-450) Jan.-No test done.

Dec.-Ammonia No test done either month.

Dec.-Coagulation-No test done either months.

I am very surprised that neither doc checked for those.Thats imfo

from his dan doctor Dr.Baptist and Primary care and they will not do

more tests.They have done tests in the past but I think everyone has

given up.Well too bad that I don't have that luxery as they have .I

am not sure how they sleep at night.They just say "there is no

explination".I am so fed up with doctors.I have been to a gastro.

specialist 4 months ago he said it must be something structurally in

his stomach and ordered a colon oscopy and a throat scope and put

him under.I do not believe in that I know all this is from infection

or similar.He would not listen to me to check my son for the same

stomach infections that I had.That didn't make sense to him.Of

course I dropped him immedietly.Hes supposed to be the best also.I

have done Homeopathics couple different ,couple

naturalpaths,naet,LLMD that does naturals homeopathics and

conventienal,NIDS (Dr.),2 cranial sacrals,massage therapy,5

chiropractic,physical therapy,Dr.Useman,100's of conventional and 5

osteopaths.I have not tried Homeotoxicology you said you had

done,and haven't tried stem cells or Dr.Bradstreet.Those seem to be

the only things left that seem to fit,but not if they can't figure

out why he can't take things.Its gotten way worse as the years go

by.It should be the other way around,he should be getting better

now. I have always been open to moving to anywhere that I find a

doc that thinks they know whats up,but they only say,he can't react

like that the ,medicine has to be out of his system by now.Boy are

they wrong but they don't check why the things linger in

him. Thank you for listening,Tammy F.

Hi Tammy,

I am so sorry that your son is going through all this. The

antibodies I suggested are called AMA or antimitochondrial

antibodies that indicate the primary biliary cirrhosis.

Even your primary medical doctor can order that to be done

along with other blood work. If you want you can email me

the liver enzymes, albumin, platelets, ammonia and

coagulation results and I might be able to suggest whether

he needs to see a specialist right away. If you are not

comfortable with that then I would suggest you get him

evaluated by a pediatric hepatologist/gastroenterologist

especially if he is still having light stools. Light or

clay colored stool indicate blockage of biliary duct or

blockage in the tiny ducts in the liver. It could even be

caused by some parasites. The fact that your son reacts to

everything indicates a dysregulated immune system. In our

children there are several causes of that including

chronic viral infections, vitamin D deficiency, chronic

inflammation etc. A CAT scan is not needed to see liver

pathology and a liver and GB ultrasound is better but the

blood work is first step. I know how difficult your

situation is right now but if you get a chance, give me a

brief history of your son, the treatments that you have

tried and what supps or meds cause worse reactions.

is

> > > >> >

> > > >> > These are some strange things

I see pretty regularly lately in my

> > > >> 12 yr. old boy.Does anyone have a

clue what they might be a sign

> > > >> of??? Thanks for any ideas,Tammy

F.

> > > >> >

> > > >>

> > > >

> > > >

> > > >

> > > >

> > >

> >

> >

>

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Have you ever looked into Amy Yasko's genetic testing?

Cathy

>Thats imfo from

> his dan doctor Dr.Baptist and Primary care and they will not do more

> tests.They have done tests in the past but I think everyone has given

> up.Well too bad that I don't have that luxery as they have .I am not

> sure how they sleep at night.They just say " there is no explination " .I

> am so fed up with doctors.

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Share on other sites

Unfortunately I spent 800.00 on a Detoxi Profile from Genova

Diagnostics And 23 And Me testing,but do not know what to do with

the info. I have taken the Genova test to all those doctors on my

last e-mail but no one knows how to use it.So I went to Yaskos

website and how I understand it she doesn't see patients anymore.I

have asked a couple of his Primary care Doc.s to send him to a local

Genetisist but they don't believe there is anything you can do,so

they wont refer.I feel stuck.I am not sure which way to go.I will

scrap that 800.00 and get yaskos,if she can't use mine,but she can't

see my son anyway.Thank you Cathy,Tammy F.

Have you ever looked into Amy Yasko's genetic testing?

Cathy

>Thats imfo from

> his dan doctor Dr.Baptist and Primary care and they

will not do more

> tests.They have done tests in the past but I think

everyone has given

> up.Well too bad that I don't have that luxery as they

have .I am not

> sure how they sleep at night.They just say "there is

no explination".I

> am so fed up with doctors.

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Share on other sites

Tammy, this might seem way out there and it might be a long shot, but $800 is alot of money. How about contacting a local college or university? You might have a doctor/professor who can help you out or at the very least be able to point you in the right direction? -Tammy H. From: Tammy

To: mb12valtrex Sent: Monday, January 16, 2012 11:08 AM Subject: Re: Re: His stools are white and breath smells like plastic!

Unfortunately I spent 800.00 on a Detoxi Profile from Genova

Diagnostics And 23 And Me testing,but do not know what to do with

the info. I have taken the Genova test to all those doctors on my

last e-mail but no one knows how to use it.So I went to Yaskos

website and how I understand it she doesn't see patients anymore.I

have asked a couple of his Primary care Doc.s to send him to a local

Genetisist but they don't believe there is anything you can do,so

they wont refer.I feel stuck.I am not sure which way to go.I will

scrap that 800.00 and get yaskos,if she can't use mine,but she can't

see my son anyway.Thank you Cathy,Tammy F.

Have you ever looked into Amy Yasko's genetic testing?

Cathy

>Thats imfo from

> his dan doctor Dr.Baptist and Primary care and they

will not do more

> tests.They have done tests in the past but I think

everyone has given

> up.Well too bad that I don't have that luxery as they

have .I am not

> sure how they sleep at night.They just say "there is

no explination".I

> am so fed up with doctors.

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Share on other sites

Hi Tammy H,Kansas University is in my town.What are you

thinking?Going to the Biology Dept.?       Thank You,Tammy F.

 

Tammy, this might seem way out there and it

might be a long shot, but $800 is alot of money.  How

about contacting a local college or university?  You

might have a doctor/professor who can help you out or

at the very least be able to point you in the right

direction?

 

-Tammy H.

From:

Tammy

To:

mb12valtrex

Sent:

Monday, January 16, 2012 11:08 AM

Subject:

Re: Re: His stools are white and

breath smells like plastic!

 

Unfortunately I spent 800.00 on a Detoxi

Profile from Genova Diagnostics And 23 And Me

testing,but do not know what to do with the

info. I have taken the Genova test to all

those doctors on my last e-mail but no one

knows how to use it.So I went to Yaskos

website and how I understand it she doesn't

see patients anymore.I have asked a couple of

his Primary care Doc.s to send him to a local

Genetisist but they don't believe there is

anything you can do,so they wont refer.I feel

stuck.I am not sure which way to go.I will

scrap that 800.00 and get yaskos,if she can't

use mine,but she can't see my son anyway.Thank

you Cathy,Tammy F.

 

Have you ever looked into Amy Yasko's

genetic testing?

Cathy

>Thats imfo from

> his dan doctor Dr.Baptist and

Primary care and they will not do more

> tests.They have done tests in the

past but I think everyone has given

> up.Well too bad that I don't have

that luxery as they have .I am not

> sure how they sleep at night.They

just say "there is no explination".I

> am so fed up with doctors.

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Share on other sites

You betcha. Biology/Microbiology...Genetics would be even better. "Autism" is a hot topic, it might catch someone's attention.I'd check out their website, take a look at their departments and see if anything might look helpful. Good luck! -Tammy H. From: Tammy

To: mb12valtrex Sent: Monday, January 16, 2012 11:29 AM Subject: Re: Re: His stools are white and breath smells like plastic!

Hi Tammy H,Kansas University is in my town.What are you

thinking?Going to the Biology Dept.? Thank You,Tammy F.

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Well, I am new to Dr. Amy Yasko, so I don't know a lot. What I do know is that

even though she doesn't personally see patients one-on-one, she is still

involved and puts a lot of information out there for free. When you order her

genetic testing, she will send a CD of the results and give personalized advice.

Additionally, she has an online community group of parents. Experienced parents

will answer your questions and she will too. She also does monthly webinars

where she fields live questions that have been gleaned from the community

boards. She then posts those online for free listening. There is a lending

library on the group and all you have to do is pay shipping in order to borrow

books or DVDs. A parent runs that, not Dr. Amy herself.

Dr. Amy has included all the protocols based on the different mutations online

for free. Her overall protocol is basically divided into three steps. The

first is basic organ and body support to prepare for detox that will come when

you start specific methylation support (although you can go through detox even

in this step.) Next is basic methylation support to target your areas of

genetic mutations, and third (if necessary at that point) is specifically

dealing with metals and pathogens.

She does recommend a lot of testing to see where you are at as you go through

the protocol, but honestly, you can only do what you can do. I would not be

able to afford to test constantly, but I totally agree with her philosophy on

it. You can't really know if you are not tolerating a supplement or if it has

caused detox of some sort, so she recommends testing to try to determine what is

going on in the body. But all these tests (other than the genetic ones) are

done through Doctor's Data or whoever. You could have them run by your doctor

if you prefer. The benefit to running them through her as that when she gets

the results, she will give handwritten advice to you right on the test results

for no extra charge. Her website does sell all the different supplements she

recommends and some of them are her formulations, but some are basic supps you

could buy elsewhere and she doesn't charge more for them than what you would pay

anywhere else from what I can see. Her philosophy seems to be to use small

amounts of a variety of things, rather than high doses of one thing, so it can

be helpful to get her supplements if you agree with that because she has

formulations that include a lot of different little things to target a specific

need. When you look at a supplement list for a specific mutation or whatever,

it can be overwhelming to think, " I have to give all that?? " But you don't have

to give it all. She says each person is individual and one person may need very

little from the list while another needs more. You are given many choices.

If you can afford it, I would highly recommend buying her book/dvd/workbook

package " Autism: Pathways to Recovery " . I have learned SO much and I'm not even

done reading it all. Her information makes so much sense! I watched the DVD

through once, then rewatched the first two hours a second time and took notes

which I am going to type up. I am reading the book and will need to read it

again when I am done. I have been at biomed for four years and I still have to

watch and re-watch to get it all stuck in my brain. If you can't afford the $55

for the package, I would recommend joining the community and seeing if you can

borrow the material. You might want to join the community anyway to try to

learn more if you are interested.

She always recommends working with a doctor, but the truth is, everything she

recommends can be done on your own. You can order the tests through her site,

if you choose. All of the supports are supplements and not prescriptions.

I have mentioned this before, but my great (mean that seriously, not

sarcastically) DAN ran the MTHFR test for three of my children. My ASD son has

both types of mutations, which the doc said is the worst scenario to have (one

of each type.) But the only supports he advised were mb12 which we are already

doing and testing homocysteine every five years. This is all well and fine,

except I recently learned through Yasko's information that one of those

mutations also affects seratonin, dopamine, and histamine! This explains a lot

for my son and targeted supplements are making a HUGE difference in his daily

quality of life. HUGE! If ONLY I had know that two years ago when the testing

was done, how much better would my son be now and how much happier could he have

been through those important developmental years???

I ordered the Yasko genetic testing for this son and one of my NT daughters who

is having some health issues right now. I can't wait for the results to help me

target the supports I give them! It will be nice to reduce some of the

guesswork. Eventually I am going to test my other two children also (have to

scrounge up the cash. Haha.)

I know her information is confusing because there is a LOT of it out there, but

I really think it could be helpful, espcially for a " tough nut " case like your

child. I don't know anything about the test you had done, but if it tested some

of the same genetic pathways that she tests, you might be able to look at her

recommended protocols and find some helpful information.

She basically tests all along what she calls the methylation cycle. It includes

the methionine cycle, the folate cycle, the BH4 cycle, and the urea cycle.

Sorry this is so long, espcially if you aren't really interested...haha.

Blessings,

Cathy

>

> Unfortunately I spent 800.00 on a Detoxi Profile from Genova Diagnostics

> And 23 And Me testing,but do not know what to do with the info. I have

> taken the Genova test to all those doctors on my last e-mail but no one

> knows how to use it.So I went to Yaskos website and how I understand it

> she doesn't see patients anymore.I have asked a couple of his Primary

> care Doc.s to send him to a local Genetisist but they don't believe

> there is anything you can do,so they wont refer.I feel stuck.I am not

> sure which way to go.I will scrap that 800.00 and get yaskos,if she

> can't use mine,but she can't see my son anyway.Thank you Cathy,Tammy F.

>

>

> > Have you ever looked into Amy Yasko's genetic testing?

> >

> > Cathy

> >

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Hi Tammy,

Your son's albumin and platelets are in good range which indicates that liver

function itself is good. This doesn't rule out any obstruction in biliary duct.

If there is an obstruction then alkaline phosphatase will be elevated. I

suggested gastroenterologist since you mentioned that one of the pediatricians

suspected primary biliary cirrhosis. Ammonia and coagulation is not routinely

tested unless liver failure is suspected. Since your son's albumin and platelet

count is normal, I don't think we need to see ammonia and coags as platelets and

albumin indicate the liver function too. I agree with Cathy that you may need

some metabolic/genetic workup. There are so many metabolic diseases in which a

child's symptoms mimic autistic symptoms. I am trying to figure out myself also

as my son has not shown a lot of improvement and he also has lost a lot of his

acquired skills. Alyssa Davi posted few days ago about mito analysis and I am

hoping that she will come back to the forum so we could ask her more questions.

I will gather some info and share with you asap. Don't worry about the

Gastroenterologist at this point. A metabolic disease workup and genetic

analysis is more important. Hang in there. We will all try to help as much as we

can. You and your family are in my prayers.

is

> > > > > >> >

> > > > > >> > These are some strange things I see pretty regularly lately

> > in my

> > > > > >> 12 yr. old boy.Does anyone have a clue what they might be a sign

> > > > > >> of??? Thanks for any ideas,Tammy F.

> > > > > >> >

> > > > > >>

> > > > > >

> > > > > >

> > > > > >

> > > > > >

> > > > >

> > > >

> > > >

> > >

> >

> >

>

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Cathy,

Thank you so much for the detailed post. It is really informative and I will

definitely look into Dr Yasko's work.

is

> >

> > Unfortunately I spent 800.00 on a Detoxi Profile from Genova Diagnostics

> > And 23 And Me testing,but do not know what to do with the info. I have

> > taken the Genova test to all those doctors on my last e-mail but no one

> > knows how to use it.So I went to Yaskos website and how I understand it

> > she doesn't see patients anymore.I have asked a couple of his Primary

> > care Doc.s to send him to a local Genetisist but they don't believe

> > there is anything you can do,so they wont refer.I feel stuck.I am not

> > sure which way to go.I will scrap that 800.00 and get yaskos,if she

> > can't use mine,but she can't see my son anyway.Thank you Cathy,Tammy F.

> >

> >

> > > Have you ever looked into Amy Yasko's genetic testing?

> > >

> > > Cathy

> > >

>

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