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Re: Looking for a Miracle result for PST Defiecency!

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> What is the proper term for my childs diagnosis as I don't think " PST

deficiency " is accurate. :)

The body's inability to convert phenol/salicylate foods into antioxidants.

> We would like to not have to be so restrictive of his diet if possible as you

know that can be very difficult. Do you think that using options 2-4 would ever

allow him to safely eat more like all his friends?

No-Fenol helped my son eat all phenol/salicylate foods, except those containing

carotenes. See my previous reply on what was needed for that.

My son lost his phenol/salicylate problem after 10 rounds of ALA chelation. I

lost my own phenol/salicylate problem after 50 rounds.

> If there was one remedy that gave you miracle results to the PST deficiency

what would it be?

No-Fenol enzyme and ALA chelation.

Dana

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Dana - Thank you for your response.

Thank you very much for your response.

We have been experimenting with the Epsom Salt baths along with cranberry juice.

The first night we did both of these the very next morning was the VERY first

time he got up by himself, dressed himself, brushed his teeth without us having

to prod him.

Because we gave him the Salt bath along with the Cranberry juice - we are not

sure what made such a drastic change in him.

Last night he was having a Phenol Episode (aggressive behavior) and we gave him

about 5 ounces of Cranberry juice and then a Epsom Salt bath.

30 minutes later his aggression went away and he spent the rest of the night

playing with his brother without fighting. The fighting is the norm when they

play. We were amazed! It's like a different kid.

We are going to experiment with his next Phenol Episode and only administer one

remedy. Cranberry or Epsom Salt bath...

Anyway - we understand that No-Fenol should help to prevent the Phenol Episodes

in the first place and would like recommendations on how to start him out. We

bought the chewables and they were delivered yesterday and want to start him out

on it ASAP.

Suggestions on time, quantity, and how often would be greatly appreciated...

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Suplementing Molybdenum helped my son a lot with phenol issues.

HTH,

.

Looking for a Miracle result for PST Defiecency!

My wife and I have been struggling with our 5 year old... We first noticed his

aggression problems when he was around 1 after eating an apple. As the years

have progressed we have found more and more things that cause his behavior to

change. Orange juice causes him to have downright tourettes type symptoms, it's

scary. Sodium Benzoate and Yellow #5 turn him into a monster for a day or two

depending on his total intake.

We have learned through our own trial and error what he can eat. The problem

now is that he is in Kindergarten and we have little control over what his

little friends might be sharing with him in the lunchroom. Also, there is an

occasion when we go out to to eat we make a mistake because we can't read all

the ingredients like we do at home before giving it to him.

We really had no idea what was wrong with our child until we recently stumbled

upon this article. http://www.enzymestuff.com/epsomsalts.htm

This leads us to believe that our son definitely has a PST deficiency. At this

point we don't even know if that is what we should call it.

Anyway after researching tons of articles online we have found many

suggestions.

1. Feingold diet - we have derived our own version of this with trial and

error. We have been buying lots of All-Natural foods lately.

2. Epsom salt baths: we have not tried this yet

3. No-Feno: I ordered already

4. Cranberry juice: We read that it is possible that cranberry juice might be

able to help reverse and episode if we accidentally give him something we

shouldn't have.

FYI - We did read the entire very lengthy Sulfur and PST document in the FILES

folder. I also did extensive reading on Rosemary Warings's Epson salt studies,

Dana's View website, No-Fenols website, etc... :)

So to our questions...

What is the proper term for my childs diagnosis as I don't think " PST

deficiency " is accurate. :)

We would like to not have to be so restrictive of his diet if possible as you

know that can be very difficult. Do you think that using options 2-4 would ever

allow him to safely eat more like all his friends?

If there was one remedy that gave you miracle results to the PST deficiency

what would it be?

Has anyone done the MHPG Test as mentioned in this website below?

http://www.feingold.org/Research/sinaiko.html

Are there any other suggestion and/or remedies that I am missing?

Thanks in advance!!!

The Brinsons

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> Because we gave him the Salt bath along with the Cranberry juice - we are not

sure what made such a drastic change in him.

Try just the bath, not the juice, see what happens.

> Anyway - we understand that No-Fenol should help to prevent the Phenol

Episodes in the first place and would like recommendations on how to start him

out. We bought the chewables and they were delivered yesterday and want to

start him out on it ASAP.

> Suggestions on time, quantity, and how often would be greatly appreciated...

I would try 1/2 tablet just before a meal.

Dana

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may i ask how much moly you used? do you still use the same amt?

________________________________

From: Augusto Federighi <luis.federighi@...>

Sent: Tue, November 17, 2009 9:50:11 PM

Subject: Re: Looking for a Miracle result for PST Defiecency!

Suplementing Molybdenum helped my son a lot with phenol issues.

HTH,

.

Looking for a Miracle result for PST Defiecency!

My wife and I have been struggling with our 5 year old... We first noticed his

aggression problems when he was around 1 after eating an apple. As the years

have progressed we have found more and more things that cause his behavior to

change. Orange juice causes him to have downright tourettes type symptoms, it's

scary. Sodium Benzoate and Yellow #5 turn him into a monster for a day or two

depending on his total intake.

We have learned through our own trial and error what he can eat. The problem now

is that he is in Kindergarten and we have little control over what his little

friends might be sharing with him in the lunchroom. Also, there is an occasion

when we go out to to eat we make a mistake because we can't read all the

ingredients like we do at home before giving it to him.

We really had no idea what was wrong with our child until we recently stumbled

upon this article. http://www.enzymestuff.com/epsomsalts.htm

This leads us to believe that our son definitely has a PST deficiency. At this

point we don't even know if that is what we should call it.

Anyway after researching tons of articles online we have found many suggestions.

1. Feingold diet - we have derived our own version of this with trial and error.

We have been buying lots of All-Natural foods lately.

2. Epsom salt baths: we have not tried this yet

3. No-Feno: I ordered already

4. Cranberry juice: We read that it is possible that cranberry juice might be

able to help reverse and episode if we accidentally give him something we

shouldn't have.

FYI - We did read the entire very lengthy Sulfur and PST document in the FILES

folder. I also did extensive reading on Rosemary Warings's Epson salt studies,

Dana's View website, No-Fenols website, etc... :)

So to our questions...

What is the proper term for my childs diagnosis as I don't think " PST

deficiency " is accurate. :)

We would like to not have to be so restrictive of his diet if possible as you

know that can be very difficult. Do you think that using options 2-4 would ever

allow him to safely eat more like all his friends?

If there was one remedy that gave you miracle results to the PST deficiency what

would it be?

Has anyone done the MHPG Test as mentioned in this website below?

http://www.feingold.org/Research/sinaiko.html

Are there any other suggestion and/or remedies that I am missing?

Thanks in advance!!!

The Brinsons

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I use E-Lyte (Body Bio) Liquid Moly - 14 drops/day. I can't remember now how

much miligrams.

HTH,

.

Looking for a Miracle result for PST Defiecency!

My wife and I have been struggling with our 5 year old... We first noticed his

aggression problems when he was around 1 after eating an apple. As the years

have progressed we have found more and more things that cause his behavior to

change. Orange juice causes him to have downright tourettes type symptoms, it's

scary. Sodium Benzoate and Yellow #5 turn him into a monster for a day or two

depending on his total intake.

We have learned through our own trial and error what he can eat. The problem

now is that he is in Kindergarten and we have little control over what his

little friends might be sharing with him in the lunchroom. Also, there is an

occasion when we go out to to eat we make a mistake because we can't read all

the ingredients like we do at home before giving it to him.

We really had no idea what was wrong with our child until we recently stumbled

upon this article. http://www.enzymestuff.com/epsomsalts.htm

This leads us to believe that our son definitely has a PST deficiency. At this

point we don't even know if that is what we should call it.

Anyway after researching tons of articles online we have found many

suggestions.

1. Feingold diet - we have derived our own version of this with trial and

error. We have been buying lots of All-Natural foods lately.

2. Epsom salt baths: we have not tried this yet

3. No-Feno: I ordered already

4. Cranberry juice: We read that it is possible that cranberry juice might be

able to help reverse and episode if we accidentally give him something we

shouldn't have.

FYI - We did read the entire very lengthy Sulfur and PST document in the FILES

folder. I also did extensive reading on Rosemary Warings's Epson salt studies,

Dana's View website, No-Fenols website, etc... :)

So to our questions...

What is the proper term for my childs diagnosis as I don't think " PST

deficiency " is accurate. :)

We would like to not have to be so restrictive of his diet if possible as you

know that can be very difficult. Do you think that using options 2-4 would ever

allow him to safely eat more like all his friends?

If there was one remedy that gave you miracle results to the PST deficiency

what would it be?

Has anyone done the MHPG Test as mentioned in this website below?

http://www.feingold.org/Research/sinaiko.html

Are there any other suggestion and/or remedies that I am missing?

Thanks in advance!!!

The Brinsons

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My son also had trouble processing phenols/salycitates. Epsom salt baths and

Feindgold diet worked wonders for him, and once we chelated his toxic metals, he

improved. He was unable to eat apple or drink the juice without having urine

accidents, meltdowns, and extreme stims. We did 8 months of IV CaEDTA chelation

with glutathione and NAC. His metals are within normal range except the mercury

so we are using OSR now. But once we addressed the metal, his PST issues and gut

bacteria improved. And molybdenum helps him too.

Joanne

> > Because we gave him the Salt bath along with the Cranberry juice - we are

not sure what made such a drastic change in him.

>

>

> Try just the bath, not the juice, see what happens.

>

>

> > Anyway - we understand that No-Fenol should help to prevent the Phenol

Episodes in the first place and would like recommendations on how to start him

out. We bought the chewables and they were delivered yesterday and want to

start him out on it ASAP.

> > Suggestions on time, quantity, and how often would be greatly appreciated...

>

>

> I would try 1/2 tablet just before a meal.

>

> Dana

>

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