Re: Re: Article on ... HBOT warning/Rhona

[Guest guest]

A warning about HBOT -- it kicks up a nasty yeast problem. Dr. Rossignol says

it's likely because at ATAs as low as 1.3-1.75, clostridia and other bacteria

are killed, but yeast is not killed below 2.4 ATA. The yeast moves in when the

bacteria is killed. Most of the kids with autism end up with a mega yeast

flare. I would still do HBOT (it did great things for my child), but do a

preHBOT OAT and postHBOT OAT and pretreat with Diflucan -- even if you normally

don't need a prescription anti-fungal (even if your DAN doctor has not heard

this about HBOT!).

-

Rhona Silverbush wrote:

Dear Antoinette --

Please forgive the delay in writing to thank you -- I

haven't been able to log on in a couple of days.

THANK YOU VERY MUCH for this information -- all

evidence from what tests we have done (as well as his

particular profile -- hypotonia, dyspraxia, apraxia)

points to it.

I will most certainly go to the website you suggested

I look at, and I would LOVE to get more info from you

about this, so thank you for your kind offer of that,

too.

We are relatively new to the whole biomedical approach

-- I'd been giving my son fish oil, carnosine, DMG,

and a bunch of other supplements for a year, but only

started with a DAN! doctor in November. My son is

3-1/2, gets daily MB12 shots, a slew of supplements

tailored to him (and we are now upping the amounts of

most of the " mito cocktail " stuff), we're treating

yeast/bad gut bugs (and will be taking him to Arthur

Krigsman, because we're not getting on top of the

dysbiosis), and, since my little one has tested

positive for lead and mercury toxicity (plus some

aluminum and arsenic) we're about to begin

chelation/glutathione IVs in August. Oh, yes, plus

HBOT!

I want to leave no stone unturned. I am VERY keen to

learn more about the mitochondria piece of Jack's

puzzle and to do whatever I can to help him with it.

How do I follow up with you on this? And again, I

can't thank you enough for your kindness in being

willing to help.

Warmest, best regards,

Rhona

--- Bunce wrote:

> Dear Rhonda,

>

> If this fits your son to a T, please go to

> www.umdf.org<http://www.umdf.org/> and find out what

> to do next. Your journey is not going to be an easy

> one. I will be there to support you off serve if

> you need it.

>

> I sent this to Pecan bread, because the AUTISM

> SOCIETY of America is realizing that MANY PDD/NOS

> and " High functioning " forms of " atypical " autism

> are mitochondrial disease (MtD) in origin. Plan

> FACT...We ARE BEING MISSED by ignorant doctors who

> do not know. This can be very " mild " to

> " fetal " ....the mild cases....are the worse to

> detect. Blood work is not always indicative of

> having it either. BEWARE of this. The specialist

> know it...but your doctors might not.

>

> The thing is, VERY few doctors realize what this is

> about...and you will have to go to mitochondria

> specialist either in Atlanta Georgia or Cleveland

> Ohio.. THE BEST in the COUNTRY. United WAY should

> be able to help you with the cost of the trip! Well

> worth it to get answers now. Children with

> diagnosis...will be first in line for new therapies

> (like stem cell etc...) that might be able to " cure "

> this when they find a cure. It is worth it to have

> your confirmed diagnosis! MILLIONS of dollars are

> being spent to find a cure for MtD. You never know

> when it will happen.

>

> Antoinette

>

> " The important thing is never to stop questioning. "

> -Albert Einstein

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________________

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

---------------------------------

Fussy? Opinionated? Impossible to please? Perfect. Join Yahoo!'s user panel and

lay it on us.

[Guest guest]

,

This is very interesting to me because we did HBOT in February for iel.

He had been SCD for nine months with no yeast issues, but we have been battling

yeast ever since we did a Genova Diagnostics metabolic analysis in March. We

tried all of the natural antifungal stuff, and have now been using Diflucan for

a month along with all of the natural antifungals. We still can't get rid of

the yeast. Now, what about using high pressure HBOT? Would this yeast thing

still be an issue? We used a mild chamber in February, but will more than

likely be using a hard chamber this fall when a clinic opens near us.

Meleah

Re: Re: Article on ... HBOT warning/Rhona

A warning about HBOT -- it kicks up a nasty yeast problem. Dr. Rossignol says

it's likely because at ATAs as low as 1.3-1.75, clostridia and other bacteria

are killed, but yeast is not killed below 2.4 ATA. The yeast moves in when the

bacteria is killed. Most of the kids with autism end up with a mega yeast flare.

I would still do HBOT (it did great things for my child), but do a preHBOT OAT

and postHBOT OAT and pretreat with Diflucan -- even if you normally don't need a

prescription anti-fungal (even if your DAN doctor has not heard this about

HBOT!).

-

Rhona Silverbush wrote:

Dear Antoinette --

Please forgive the delay in writing to thank you -- I

haven't been able to log on in a couple of days.

THANK YOU VERY MUCH for this information -- all

evidence from what tests we have done (as well as his

particular profile -- hypotonia, dyspraxia, apraxia)

points to it.

I will most certainly go to the website you suggested

I look at, and I would LOVE to get more info from you

about this, so thank you for your kind offer of that,

too.

We are relatively new to the whole biomedical approach

-- I'd been giving my son fish oil, carnosine, DMG,

and a bunch of other supplements for a year, but only

started with a DAN! doctor in November. My son is

3-1/2, gets daily MB12 shots, a slew of supplements

tailored to him (and we are now upping the amounts of

most of the " mito cocktail " stuff), we're treating

yeast/bad gut bugs (and will be taking him to Arthur

Krigsman, because we're not getting on top of the

dysbiosis), and, since my little one has tested

positive for lead and mercury toxicity (plus some

aluminum and arsenic) we're about to begin

chelation/glutathione IVs in August. Oh, yes, plus

HBOT!

I want to leave no stone unturned. I am VERY keen to

learn more about the mitochondria piece of Jack's

puzzle and to do whatever I can to help him with it.

How do I follow up with you on this? And again, I

can't thank you enough for your kindness in being

willing to help.

Warmest, best regards,

Rhona

--- Bunce wrote:

> Dear Rhonda,

>

> If this fits your son to a T, please go to

> www.umdf.org<http://www.umdf.org/> and find out what

> to do next. Your journey is not going to be an easy

> one. I will be there to support you off serve if

> you need it.

>

> I sent this to Pecan bread, because the AUTISM

> SOCIETY of America is realizing that MANY PDD/NOS

> and " High functioning " forms of " atypical " autism

> are mitochondrial disease (MtD) in origin. Plan

> FACT...We ARE BEING MISSED by ignorant doctors who

> do not know. This can be very " mild " to

> " fetal " ....the mild cases....are the worse to

> detect. Blood work is not always indicative of

> having it either. BEWARE of this. The specialist

> know it...but your doctors might not.

>

> The thing is, VERY few doctors realize what this is

> about...and you will have to go to mitochondria

> specialist either in Atlanta Georgia or Cleveland

> Ohio.. THE BEST in the COUNTRY. United WAY should

> be able to help you with the cost of the trip! Well

> worth it to get answers now. Children with

> diagnosis...will be first in line for new therapies

> (like stem cell etc...) that might be able to " cure "

> this when they find a cure. It is worth it to have

> your confirmed diagnosis! MILLIONS of dollars are

> being spent to find a cure for MtD. You never know

> when it will happen.

>

> Antoinette

>

> " The important thing is never to stop questioning. "

> -Albert Einstein

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________________

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

---------------------------------

Fussy? Opinionated? Impossible to please? Perfect. Join Yahoo!'s user panel

and lay it on us.

[Guest guest]

Dear --

Thank you VERY much for that information!!! We're

about to begin treating with Diflucan (and are doing

more HBOT in August), so it was great to read that

this is just what we should be doing! And I'll be

absolutely sure to do pre-HBOT and post-HBOT OATs.

Plus, we're going to be bringing our little guy to see

Dr. Krigsman to really figure out what to do to get on

top of the whole gut thing -- I have a gazillion tests

to do for him before we can get the appointment, but

I'm working on it as we speak and am hopeful that with

his help we can make good strides in that area.

Meanwhile, your message is invaluable!!! I had no

idea!

I'm so glad HBOT was helpful for your child! :-)

Again, many, many thanks!

Warmest,

-Rhona

--- Rob or Sunseri

wrote:

> A warning about HBOT -- it kicks up a nasty yeast

> problem. Dr. Rossignol says it's likely because at

> ATAs as low as 1.3-1.75, clostridia and other

> bacteria are killed, but yeast is not killed below

> 2.4 ATA. The yeast moves in when the bacteria is

> killed. Most of the kids with autism end up with a

> mega yeast flare. I would still do HBOT (it did

> great things for my child), but do a preHBOT OAT and

> postHBOT OAT and pretreat with Diflucan -- even if

> you normally don't need a prescription anti-fungal

> (even if your DAN doctor has not heard this about

> HBOT!).

>

> -

>

> Rhona Silverbush wrote:

> Dear Antoinette --

>

> Please forgive the delay in writing to thank you --

> I

> haven't been able to log on in a couple of days.

> THANK YOU VERY MUCH for this information -- all

> evidence from what tests we have done (as well as

> his

> particular profile -- hypotonia, dyspraxia, apraxia)

> points to it.

>

> I will most certainly go to the website you

> suggested

> I look at, and I would LOVE to get more info from

> you

> about this, so thank you for your kind offer of

> that,

> too.

>

> We are relatively new to the whole biomedical

> approach

> -- I'd been giving my son fish oil, carnosine, DMG,

> and a bunch of other supplements for a year, but

> only

> started with a DAN! doctor in November. My son is

> 3-1/2, gets daily MB12 shots, a slew of supplements

> tailored to him (and we are now upping the amounts

> of

> most of the " mito cocktail " stuff), we're treating

> yeast/bad gut bugs (and will be taking him to Arthur

> Krigsman, because we're not getting on top of the

> dysbiosis), and, since my little one has tested

> positive for lead and mercury toxicity (plus some

> aluminum and arsenic) we're about to begin

> chelation/glutathione IVs in August. Oh, yes, plus

> HBOT!

>

> I want to leave no stone unturned. I am VERY keen to

> learn more about the mitochondria piece of Jack's

> puzzle and to do whatever I can to help him with it.

>

> How do I follow up with you on this? And again, I

> can't thank you enough for your kindness in being

> willing to help.

>

> Warmest, best regards,

> Rhona

>

> --- Bunce wrote:

>

> > Dear Rhonda,

> >

> > If this fits your son to a T, please go to

> > www.umdf.org<http://www.umdf.org/> and find out

> what

> > to do next. Your journey is not going to be an

> easy

> > one. I will be there to support you off serve if

> > you need it.

> >

> > I sent this to Pecan bread, because the AUTISM

> > SOCIETY of America is realizing that MANY PDD/NOS

> > and " High functioning " forms of " atypical " autism

> > are mitochondrial disease (MtD) in origin. Plan

> > FACT...We ARE BEING MISSED by ignorant doctors who

> > do not know. This can be very " mild " to

> > " fetal " ....the mild cases....are the worse to

> > detect. Blood work is not always indicative of

> > having it either. BEWARE of this. The specialist

> > know it...but your doctors might not.

> >

> > The thing is, VERY few doctors realize what this

> is

> > about...and you will have to go to mitochondria

> > specialist either in Atlanta Georgia or Cleveland

> > Ohio.. THE BEST in the COUNTRY. United WAY should

> > be able to help you with the cost of the trip!

> Well

> > worth it to get answers now. Children with

> > diagnosis...will be first in line for new

> therapies

> > (like stem cell etc...) that might be able to

> " cure "

> > this when they find a cure. It is worth it to have

> > your confirmed diagnosis! MILLIONS of dollars are

> > being spent to find a cure for MtD. You never know

> > when it will happen.

> >

> > Antoinette

> >

> > " The important thing is never to stop

> questioning. "

> > -Albert Einstein

> >

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

>

__________________________________________________________

> Boardwalk for $500? In 2007? Ha! Play Monopoly Here

> and Now (it's updated for today's economy) at Yahoo!

> Games.

>

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

>

>

>

>

>

>

>

> ---------------------------------

> Fussy? Opinionated? Impossible to please? Perfect.

> Join Yahoo!'s user panel and lay it on us.

>

> [Non-text portions of this message have been

> removed]

>

>

________________________________________________________________________________\

____

Be a better Globetrotter. Get better travel answers from someone who knows.

Yahoo! Answers - Check it out.

http://answers.yahoo.com/dir/?link=list&sid=396545469

[Guest guest]

Good luck! Please post a follow up to your appointment with Krigsman.

-

Rhona Silverbush wrote:

Dear --

Thank you VERY much for that information!!! We're

about to begin treating with Diflucan (and are doing

more HBOT in August), so it was great to read that

this is just what we should be doing! And I'll be

absolutely sure to do pre-HBOT and post-HBOT OATs.

Plus, we're going to be bringing our little guy to see

Dr. Krigsman to really figure out what to do to get on

top of the whole gut thing -- I have a gazillion tests

to do for him before we can get the appointment, but

I'm working on it as we speak and am hopeful that with

his help we can make good strides in that area.

Meanwhile, your message is invaluable!!! I had no

idea!

I'm so glad HBOT was helpful for your child! :-)

Again, many, many thanks!

Warmest,

-Rhona

--- Rob or Sunseri

wrote:

> A warning about HBOT -- it kicks up a nasty yeast

> problem. Dr. Rossignol says it's likely because at

> ATAs as low as 1.3-1.75, clostridia and other

> bacteria are killed, but yeast is not killed below

> 2.4 ATA. The yeast moves in when the bacteria is

> killed. Most of the kids with autism end up with a

> mega yeast flare. I would still do HBOT (it did

> great things for my child), but do a preHBOT OAT and

> postHBOT OAT and pretreat with Diflucan -- even if

> you normally don't need a prescription anti-fungal

> (even if your DAN doctor has not heard this about

> HBOT!).

>

> -

>

> Rhona Silverbush wrote:

> Dear Antoinette --

>

> Please forgive the delay in writing to thank you --

> I

> haven't been able to log on in a couple of days.

> THANK YOU VERY MUCH for this information -- all

> evidence from what tests we have done (as well as

> his

> particular profile -- hypotonia, dyspraxia, apraxia)

> points to it.

>

> I will most certainly go to the website you

> suggested

> I look at, and I would LOVE to get more info from

> you

> about this, so thank you for your kind offer of

> that,

> too.

>

> We are relatively new to the whole biomedical

> approach

> -- I'd been giving my son fish oil, carnosine, DMG,

> and a bunch of other supplements for a year, but

> only

> started with a DAN! doctor in November. My son is

> 3-1/2, gets daily MB12 shots, a slew of supplements

> tailored to him (and we are now upping the amounts

> of

> most of the " mito cocktail " stuff), we're treating

> yeast/bad gut bugs (and will be taking him to Arthur

> Krigsman, because we're not getting on top of the

> dysbiosis), and, since my little one has tested

> positive for lead and mercury toxicity (plus some

> aluminum and arsenic) we're about to begin

> chelation/glutathione IVs in August. Oh, yes, plus

> HBOT!

>

> I want to leave no stone unturned. I am VERY keen to

> learn more about the mitochondria piece of Jack's

> puzzle and to do whatever I can to help him with it.

>

> How do I follow up with you on this? And again, I

> can't thank you enough for your kindness in being

> willing to help.

>

> Warmest, best regards,

> Rhona

>

> --- Bunce wrote:

>

> > Dear Rhonda,

> >

> > If this fits your son to a T, please go to

> > www.umdf.org<http://www.umdf.org/> and find out

> what

> > to do next. Your journey is not going to be an

> easy

> > one. I will be there to support you off serve if

> > you need it.

> >

> > I sent this to Pecan bread, because the AUTISM

> > SOCIETY of America is realizing that MANY PDD/NOS

> > and " High functioning " forms of " atypical " autism

> > are mitochondrial disease (MtD) in origin. Plan

> > FACT...We ARE BEING MISSED by ignorant doctors who

> > do not know. This can be very " mild " to

> > " fetal " ....the mild cases....are the worse to

> > detect. Blood work is not always indicative of

> > having it either. BEWARE of this. The specialist

> > know it...but your doctors might not.

> >

> > The thing is, VERY few doctors realize what this

> is

> > about...and you will have to go to mitochondria

> > specialist either in Atlanta Georgia or Cleveland

> > Ohio.. THE BEST in the COUNTRY. United WAY should

> > be able to help you with the cost of the trip!

> Well

> > worth it to get answers now. Children with

> > diagnosis...will be first in line for new

> therapies

> > (like stem cell etc...) that might be able to

> " cure "

> > this when they find a cure. It is worth it to have

> > your confirmed diagnosis! MILLIONS of dollars are

> > being spent to find a cure for MtD. You never know

> > when it will happen.

> >

> > Antoinette

> >

> > " The important thing is never to stop

> questioning. "

> > -Albert Einstein

> >

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

>

__________________________________________________________

> Boardwalk for $500? In 2007? Ha! Play Monopoly Here

> and Now (it's updated for today's economy) at Yahoo!

> Games.

>

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

>

>

>

>

>

>

>

> ---------------------------------

> Fussy? Opinionated? Impossible to please? Perfect.

> Join Yahoo!'s user panel and lay it on us.

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________________

Be a better Globetrotter. Get better travel answers from someone who knows.

Yahoo! Answers - Check it out.

http://answers.yahoo.com/dir/?link=list&sid=396545469

---------------------------------

Looking for a deal? Find great prices on flights and hotels with Yahoo!

FareChase.

[Guest guest]

You would have to use a hard chamber with a pressure that kills yeast (similar

to a Lymes protocol 2.2-2.4). No doctor would write a script for that as

avoiding yeast is not justification for literally " diving " into the unknown with

such a deep ATA. Some doctors also report regression in neurological patients

with such deep pressures.

It's frustrating to have to deal with the yeast, but then again HBOT has been

the first intervention that made me believe that recovery is even possible for

my son (with about 300 dives maybe!) I've just never seen such a quick response

to anything. It is possible that you may kick the yeast if you go into your

next session already on anti-fungals because the HBOT causes the anti-fungals to

be more effective (same thing with antibiotics).

-

robin wrote:

,

This is very interesting to me because we did HBOT in February for iel. He

had been SCD for nine months with no yeast issues, but we have been battling

yeast ever since we did a Genova Diagnostics metabolic analysis in March. We

tried all of the natural antifungal stuff, and have now been using Diflucan for

a month along with all of the natural antifungals. We still can't get rid of the

yeast. Now, what about using high pressure HBOT? Would this yeast thing still be

an issue? We used a mild chamber in February, but will more than likely be using

a hard chamber this fall when a clinic opens near us.

Meleah

Re: Re: Article on ... HBOT warning/Rhona

A warning about HBOT -- it kicks up a nasty yeast problem. Dr. Rossignol says

it's likely because at ATAs as low as 1.3-1.75, clostridia and other bacteria

are killed, but yeast is not killed below 2.4 ATA. The yeast moves in when the

bacteria is killed. Most of the kids with autism end up with a mega yeast flare.

I would still do HBOT (it did great things for my child), but do a preHBOT OAT

and postHBOT OAT and pretreat with Diflucan -- even if you normally don't need a

prescription anti-fungal (even if your DAN doctor has not heard this about

HBOT!).

-

Rhona Silverbush wrote:

Dear Antoinette --

Please forgive the delay in writing to thank you -- I

haven't been able to log on in a couple of days.

THANK YOU VERY MUCH for this information -- all

evidence from what tests we have done (as well as his

particular profile -- hypotonia, dyspraxia, apraxia)

points to it.

I will most certainly go to the website you suggested

I look at, and I would LOVE to get more info from you

about this, so thank you for your kind offer of that,

too.

We are relatively new to the whole biomedical approach

-- I'd been giving my son fish oil, carnosine, DMG,

and a bunch of other supplements for a year, but only

started with a DAN! doctor in November. My son is

3-1/2, gets daily MB12 shots, a slew of supplements

tailored to him (and we are now upping the amounts of

most of the " mito cocktail " stuff), we're treating

yeast/bad gut bugs (and will be taking him to Arthur

Krigsman, because we're not getting on top of the

dysbiosis), and, since my little one has tested

positive for lead and mercury toxicity (plus some

aluminum and arsenic) we're about to begin

chelation/glutathione IVs in August. Oh, yes, plus

HBOT!

I want to leave no stone unturned. I am VERY keen to

learn more about the mitochondria piece of Jack's

puzzle and to do whatever I can to help him with it.

How do I follow up with you on this? And again, I

can't thank you enough for your kindness in being

willing to help.

Warmest, best regards,

Rhona

--- Bunce wrote:

> Dear Rhonda,

>

> If this fits your son to a T, please go to

> www.umdf.org<http://www.umdf.org/> and find out what

> to do next. Your journey is not going to be an easy

> one. I will be there to support you off serve if

> you need it.

>

> I sent this to Pecan bread, because the AUTISM

> SOCIETY of America is realizing that MANY PDD/NOS

> and " High functioning " forms of " atypical " autism

> are mitochondrial disease (MtD) in origin. Plan

> FACT...We ARE BEING MISSED by ignorant doctors who

> do not know. This can be very " mild " to

> " fetal " ....the mild cases....are the worse to

> detect. Blood work is not always indicative of

> having it either. BEWARE of this. The specialist

> know it...but your doctors might not.

>

> The thing is, VERY few doctors realize what this is

> about...and you will have to go to mitochondria

> specialist either in Atlanta Georgia or Cleveland

> Ohio.. THE BEST in the COUNTRY. United WAY should

> be able to help you with the cost of the trip! Well

> worth it to get answers now. Children with

> diagnosis...will be first in line for new therapies

> (like stem cell etc...) that might be able to " cure "

> this when they find a cure. It is worth it to have

> your confirmed diagnosis! MILLIONS of dollars are

> being spent to find a cure for MtD. You never know

> when it will happen.

>

> Antoinette

>

> " The important thing is never to stop questioning. "

> -Albert Einstein

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________________

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

---------------------------------

Fussy? Opinionated? Impossible to please? Perfect. Join Yahoo!'s user panel and

lay it on us.

[Guest guest]

I absolutely will.

Again, thanks.

-Rhona

--- Rob or Sunseri

wrote:

> Good luck! Please post a follow up to your

> appointment with Krigsman.

>

> -

>

> Rhona Silverbush wrote:

> Dear --

>

> Thank you VERY much for that information!!! We're

> about to begin treating with Diflucan (and are doing

> more HBOT in August), so it was great to read that

> this is just what we should be doing! And I'll be

> absolutely sure to do pre-HBOT and post-HBOT OATs.

> Plus, we're going to be bringing our little guy to

> see

> Dr. Krigsman to really figure out what to do to get

> on

> top of the whole gut thing -- I have a gazillion

> tests

> to do for him before we can get the appointment, but

> I'm working on it as we speak and am hopeful that

> with

> his help we can make good strides in that area.

> Meanwhile, your message is invaluable!!! I had no

> idea!

>

> I'm so glad HBOT was helpful for your child! :-)

>

> Again, many, many thanks!

> Warmest,

> -Rhona

>

> --- Rob or Sunseri

> wrote:

>

> > A warning about HBOT -- it kicks up a nasty yeast

> > problem. Dr. Rossignol says it's likely because at

> > ATAs as low as 1.3-1.75, clostridia and other

> > bacteria are killed, but yeast is not killed below

> > 2.4 ATA. The yeast moves in when the bacteria is

> > killed. Most of the kids with autism end up with a

> > mega yeast flare. I would still do HBOT (it did

> > great things for my child), but do a preHBOT OAT

> and

> > postHBOT OAT and pretreat with Diflucan -- even if

> > you normally don't need a prescription anti-fungal

> > (even if your DAN doctor has not heard this about

> > HBOT!).

> >

> > -

> >

> > Rhona Silverbush wrote:

> > Dear Antoinette --

> >

> > Please forgive the delay in writing to thank you

> --

> > I

> > haven't been able to log on in a couple of days.

> > THANK YOU VERY MUCH for this information -- all

> > evidence from what tests we have done (as well as

> > his

> > particular profile -- hypotonia, dyspraxia,

> apraxia)

> > points to it.

> >

> > I will most certainly go to the website you

> > suggested

> > I look at, and I would LOVE to get more info from

> > you

> > about this, so thank you for your kind offer of

> > that,

> > too.

> >

> > We are relatively new to the whole biomedical

> > approach

> > -- I'd been giving my son fish oil, carnosine,

> DMG,

> > and a bunch of other supplements for a year, but

> > only

> > started with a DAN! doctor in November. My son is

> > 3-1/2, gets daily MB12 shots, a slew of

> supplements

> > tailored to him (and we are now upping the amounts

> > of

> > most of the " mito cocktail " stuff), we're treating

> > yeast/bad gut bugs (and will be taking him to

> Arthur

> > Krigsman, because we're not getting on top of the

> > dysbiosis), and, since my little one has tested

> > positive for lead and mercury toxicity (plus some

> > aluminum and arsenic) we're about to begin

> > chelation/glutathione IVs in August. Oh, yes, plus

> > HBOT!

> >

> > I want to leave no stone unturned. I am VERY keen

> to

> > learn more about the mitochondria piece of Jack's

> > puzzle and to do whatever I can to help him with

> it.

> >

> > How do I follow up with you on this? And again, I

> > can't thank you enough for your kindness in being

> > willing to help.

> >

> > Warmest, best regards,

> > Rhona

> >

> > --- Bunce wrote:

> >

> > > Dear Rhonda,

> > >

> > > If this fits your son to a T, please go to

> > > www.umdf.org<http://www.umdf.org/> and find out

> > what

> > > to do next. Your journey is not going to be an

> > easy

> > > one. I will be there to support you off serve if

> > > you need it.

> > >

> > > I sent this to Pecan bread, because the AUTISM

> > > SOCIETY of America is realizing that MANY

> PDD/NOS

> > > and " High functioning " forms of " atypical "

> autism

> > > are mitochondrial disease (MtD) in origin. Plan

> > > FACT...We ARE BEING MISSED by ignorant doctors

> who

> > > do not know. This can be very " mild " to

> > > " fetal " ....the mild cases....are the worse to

> > > detect. Blood work is not always indicative of

> > > having it either. BEWARE of this. The specialist

> > > know it...but your doctors might not.

> > >

> > > The thing is, VERY few doctors realize what this

> > is

> > > about...and you will have to go to mitochondria

> > > specialist either in Atlanta Georgia or

> Cleveland

> > > Ohio.. THE BEST in the COUNTRY. United WAY

> should

> > > be able to help you with the cost of the trip!

> > Well

> > > worth it to get answers now. Children with

> > > diagnosis...will be first in line for new

> > therapies

> > > (like stem cell etc...) that might be able to

> > " cure "

> > > this when they find a cure. It is worth it to

> have

> > > your confirmed diagnosis! MILLIONS of dollars

> are

> > > being spent to find a cure for MtD. You never

> know

> > > when it will happen.

> > >

> > > Antoinette

> > >

> > > " The important thing is never to stop

> > questioning. "

> > > -Albert Einstein

> > >

> > >

> > > [Non-text portions of this message have been

> > > removed]

> > >

> > >

> >

> >

>

__________________________________________________________

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> >

>

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> >

> >

> >

> >

> >

> >

> >

> > ---------------------------------

> > Fussy? Opinionated? Impossible to please? Perfect.

>

> > Join Yahoo!'s user panel and lay it on us.

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

>

__________________________________________________________

> Be a better Globetrotter. Get better travel answers

> from someone who knows. Yahoo! Answers - Check it

> out.

>

http://answers.yahoo.com/dir/?link=list&sid=396545469

>

>

>

>

=== message truncated ===

________________________________________________________________________________\

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