HBOT

[Guest guest]

Hi!, we've taking hbot every 3 months, we started the program since 1 year, first 20 sessions during 90 minutes, rest 3 months and the rest of the steps 10 sessions by 90 min. The atmosphere is 1,74 ATA, this detail is very important if you decide to take hbot by renting a chamber at home that used to be low presure ( 1,24 ATA).Look on google Dr Rossignol's protocol he has a clininc in California, but he has many researchs abot hbot with autistic children.It was useful for my son for his health in general. Specially in motricity after hbot he eat by himself and take-put his clothesGreets!Enviado desde mi dispositivo BlackBerry® de Orange.Sender: mb12valtrex Date: Mon, 23 Jul 2012 03:18:12 -0000To: <mb12valtrex >ReplyTo: mb12valtrex Subject: HBOT Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We arecurrently going after a virus with Valtrex and soon, HBOT. We are thinking of renting one to try to get in 40 hour long sessions in a month or so. Just wanted tohear any of your experiences with the chamber. Thanks!

[Guest guest]

my son did very well with hbot. at first I wasn't sure, its a bit scary at

first, and the literature is mixed.

after 12 hours he started playing tag with the other kids at school.

his stools looked better as well.

we went right on up to 50 hours, 1 hour at pressure (1.4atm) at a time with the

oxygen mask.

no electronics in the chamber but we did take food (chicken and veggies), water,

books, and games. go to the bathroom before you go in.

we felt a bit tired after each one but invariably the next day was " a good one "

for him.

we could only manage 3 per week and then tapered to 1 per week.

we supplemented with some vitamins but didn't go overboard.

we were extremely careful with his ears. if they did not pop or there was any

pain I terminated the session. This happended a couple times I think due to

heavy allergies that come and go.

overall very beneficial but be careful.

we did the whole thing on our own in the spare bedroom. if you can put the

compressor and concentrator in the hallway and run the hoses under the door it

makes for a quieter and more enjoyable experience.

a couple pillows are good too.

I hope this helps you and your son

>

> Hi!, we've taking hbot every 3 months, we started the program since 1 year,

first 20 sessions during 90 minutes, rest 3 months and the rest of the steps 10

sessions by 90 min. The atmosphere is 1,74 ATA, this detail is very important if

you decide to take hbot by renting a chamber at home that used to be low presure

( 1,24 ATA).

> Look on google Dr Rossignol's protocol he has a clininc in California, but he

has many researchs abot hbot with autistic children.

>

> It was useful for my son for his health in general. Specially in motricity

after hbot he eat by himself and take-put his clothes

>

> Greets!

> Enviado desde mi dispositivo BlackBerry® de Orange.

>

> HBOT

>

> Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We are

> currently going after a virus with Valtrex and soon, HBOT. We are thinking of

> renting one to try to get in 40 hour long sessions in a month or so. Just

wanted to

> hear any of your experiences with the chamber. Thanks!

>

[Guest guest]

My 8yr old daughter is also starting HBOT next month and i am excited and very nervous at the same time. We are doing the hard chamber at 100%. She wont be able to tell me if she gets ear pain /discomfort and this worries me. I guess the trick is to keep giving her sips of water inside the chamber, is that right? Jenjitta From: drymeadow06

To: mb12valtrex Sent: Monday, 23 July 2012, 11:35 Subject: Re: HBOT

my son did very well with hbot. at first I wasn't sure, its a bit scary at first, and the literature is mixed.

after 12 hours he started playing tag with the other kids at school.

his stools looked better as well.

we went right on up to 50 hours, 1 hour at pressure (1.4atm) at a time with the oxygen mask.

no electronics in the chamber but we did take food (chicken and veggies), water, books, and games. go to the bathroom before you go in.

we felt a bit tired after each one but invariably the next day was "a good one" for him.

we could only manage 3 per week and then tapered to 1 per week.

we supplemented with some vitamins but didn't go overboard.

we were extremely careful with his ears. if they did not pop or there was any pain I terminated the session. This happended a couple times I think due to heavy allergies that come and go.

overall very beneficial but be careful.

we did the whole thing on our own in the spare bedroom. if you can put the compressor and concentrator in the hallway and run the hoses under the door it makes for a quieter and more enjoyable experience.

a couple pillows are good too.

I hope this helps you and your son

>

> Hi!, we've taking hbot every 3 months, we started the program since 1 year, first 20 sessions during 90 minutes, rest 3 months and the rest of the steps 10 sessions by 90 min. The atmosphere is 1,74 ATA, this detail is very important if you decide to take hbot by renting a chamber at home that used to be low presure ( 1,24 ATA).

> Look on google Dr Rossignol's protocol he has a clininc in California, but he has many researchs abot hbot with autistic children.

>

> It was useful for my son for his health in general. Specially in motricity after hbot he eat by himself and take-put his clothes

>

> Greets!

> Enviado desde mi dispositivo BlackBerry® de Orange.

>

> HBOT

>

> Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We are

> currently going after a virus with Valtrex and soon, HBOT. We are thinking of

> renting one to try to get in 40 hour long sessions in a month or so. Just wanted to

> hear any of your experiences with the chamber. Thanks!

>

[Guest guest]

chewing and drinking help.

it was the hold your nose and blow gently that did the trick though...like

you're on an airplane. it took him a while to learn it effectively.

if there's a mountain nearby I would take her up there a few times and see if

you can teach it to her thru signs. when yours pop try to get her to do it.

100% oxygen scared me too much so we just did the mask @ 90%.

right or wrong, thats how we did it. my very best to you and your daughter

> >

> > Hi!, we've taking hbot every 3 months, we started the program since 1 year,

first 20 sessions during 90 minutes, rest 3 months and the rest of the steps 10

sessions by 90 min. The atmosphere is 1,74 ATA, this detail is very important if

you decide to take hbot by renting a chamber at home that used to be low presure

( 1,24 ATA).

> > Look on google Dr Rossignol's protocol he has a clininc in California, but

he has many researchs abot hbot with autistic children.

> >

> > It was useful for my son for his health in general. Specially in motricity

after hbot he eat by himself and take-put his clothes

> >

> > Greets!

> > Enviado desde mi dispositivo BlackBerry® de Orange.

> >

> > HBOT

> >

> > Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We are

> > currently going after a virus with Valtrex and soon, HBOT. We are thinking

of

> > renting one to try to get in 40 hour long sessions in a month or so. Just

wanted to

> > hear any of your experiences with the chamber. Thanks!

> >

>

[Guest guest]

HBOT brought back my son's speech at around 60 dives, but even after the third

dive his migraine was already gone. We used 100% oxygen at 1.5 ATA in a hard

chamber. Some DAN docs recommended lower pressure and oxygen concentration for

maintenance but we continued on with what we started.

Sheila

>

> Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We are

> currently going after a virus with Valtrex and soon, HBOT. We are thinking of

> renting one to try to get in 40 hour long sessions in a month or so. Just

wanted to

> hear any of your experiences with the chamber. Thanks!

>

[Guest guest]

Thanks for sharing. We're renting a soft chamber for a month to see if it's

something we want to invest in furtherer. We'll be using 100% oxygen at 1.3

ATA. I'd love to do the hard chamber, but it's $190/dive!

> >

> > Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We are

> > currently going after a virus with Valtrex and soon, HBOT. We are thinking

of

> > renting one to try to get in 40 hour long sessions in a month or so. Just

wanted to

> > hear any of your experiences with the chamber. Thanks!

> >

>

[Guest guest]

We are interested in renting a chamber for a month too. Where are you going to

rent from and do they rent the oxygen concentrator too? Anyone that has

purchased one, which one is best? Where do you buy the oxygen concentrator? I

see you can buy the soft chamber with the compressor, but I never see anyone

advertising the OC. Isn't is necessary to use the OC? Also, is there a book

anyone recommends on HBOT or a specific study they have found to be useful?

On another note, I have seen great improvements in speech and understanding with

a sublingual methylcobalamin and L-methylfolate or metafolin. My Dr. gets it

from Labs and puts on her on label, but it is the same from Dr. Ben's

(MTHFR web site) www.seekinghealth.com called Sublingual Active B12 with

Metafolin. I saw Dr. Rossingal's research on cerebral folate and he said to use

high doses of folinic acid (NOT FOLIC ACID...this is snythetic form and those

with MTHFR mutations can't use it and it gets stored in the liver and can cause

a lot of disease and problems...snythetic forms can feed cancer in those with

MTHFR mutations) There are great youtubes on MTHFR from Dr. and Dr.

Rawlings explaining the gene mutation. Some research says as many as 95-98% of

those on the spectrum have MTHFR.

My dd is heter MTHFR C776T so she methylates less, meaning toxins are methlated

less and neurotransmitters, thyroid hormones, and HGH are less because of the

gene. We have been giving her one tablet a day and then increased to two

tablets. They melt in her mouth. Each one contains 1,000 methylcobalamin and

800 metafolin or L-methylfolate. Also, I used one pump of cream of

www.neurobiologix.com neuro-immune stabilizer with methylated B's and vitamin D.

Dr. Kendall sees autistic children too. I found youtubes of him and his

products to be helpful. Many with ASD try Methyl-B12 ,but forgot that

L-methylfolate is just as important.

From watching the study given by Dr. Rossignal at an Autism One Conference, he

said to give 2 mg per 1 kg....I have worked up to giving her 12 tablets a day

and it has been amazing. She takes 4 under the tongue, 3 times a day right now.

When I first started the supplement back in Feb. with only one tablet, she did

not speak real words. She made up her own language and had a few one word

vocabulary. Then she started to do two words and when she tried to put

sentences together, but they were not in the correct order. Quickly, she began

copying our correct sentences, which she also had never done before and then

started to make her own. Now, she answers questions and asks questions plus

follows commands, which she never did before.

I was going to try the methyl B12 shots that my Dr. ordered, but when the

compounding pharmacy mixed up my order, I tried the sublingual I already had on

hand for my other 3 children who are NT, but have either heter A1298C or

compound heter C667T/A1298C. I have seen miracles in my other children using

the sublingual's and also P5P. They have clearer thinking, more energy and can

handle stress better. The boy with A1298C and my husband with A1298C, both had

ADD, but now that is gone taking the supplements. I started taking them too in

October, because I have heter C667T like PDD-NOS dd. I had taken out all my

amalgams and didn't know that mercury would be released into my breast milk. My

dd regressed after nursing and started arm flapping and not responding to her

own name, and lost all language. She have never been vacinnated. Here

regression was clearly from the mercury.

I, too, developed several illnesses from the removal. I grew 5 nodules on my

thyroid, developed allergies(never had them before), CFS, Fibermyalgia starting

in one finger and then moving into all fingers, extreme pain in my hips, extreme

foggy thinking, no energy, withdrew from friends and became anti-social....and

extreme depression. This lasted a year, until last October when the oncologist

told me to take L-methylfolate 4000 mcg, Methylcobalamin 2,000 mcg and P5P 50

mg, and my MD told me to add milk thistle and NAC. The oncologist tested my

homocysteine and it was a 4, which is too low.

Dr. in the youtubes who treat autism, said that his patients tested in

the 4 range as well. He thinks this shows their neuro-immune system is not

well. 6.3 is healthy. Over 7 is too high. I retested my homocysteine after 9

months of methylated b's and was a 6.3! All my illnesses have disappeared. No

allergies, no depression, no pain, no brain fog! I have energy and feel

healthy! If you haven't tried these supplements, it is worth a try. I also use

Garden of Life, Vitamin Code multi-vitamin because they all contain natural

forms, not snythetic forms of B's in them. They are capsules and I open them in

protein shakes for my kids who can't swallow pills.

Thanks in advance for any answers on HBOT.

> > >

> > > Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We are

> > > currently going after a virus with Valtrex and soon, HBOT. We are thinking

of

> > > renting one to try to get in 40 hour long sessions in a month or so. Just

wanted to

> > > hear any of your experiences with the chamber. Thanks!

> > >

> >

>

[Guest guest]

Hi Tami,

Thanks for the great info, just what I was looking for. If you don't mind

sharing could you please let me know what are the exact MB12/Methylfolate

supplements your dd takes and how much? What other supplements does she take to

complement the sublinguals? What about children who don't know hoe to melt the

tabs under tongue and chew it instead of melting it? Can we still use it? We

have been on MB12 shots for almost 2.5 years but looking in to more research, I

thinks my dd needs something more than just MB12 shots.

Thanks much in advance

Pratima

> > > >

> > > > Has anyone tried Hyperbaric Oxygen Chamber Therapy with their kids? We

are

> > > > currently going after a virus with Valtrex and soon, HBOT. We are

thinking of

> > > > renting one to try to get in 40 hour long sessions in a month or so.

Just wanted to

> > > > hear any of your experiences with the chamber. Thanks!

> > > >

> > >

> >

>

[Guest guest]

We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4

days off...Tues-Thursday. She is completely recovered. She was tested at 3 yrs

old at our school district. She tested only 1% in cognition. She was NEVER

vaccinated, but got mercury poisoned through nursing her while I took out a

mouth full of amalgams. The mercury went straight through my breast milk. She

nursed until a little over 3 yrs, when I was told by my MD that mercury crosses

into breast milk. She regressed around 2.6 mths old. She stopped talking,

stopped eye contact, started lining up toys, hand flapping and then her flapping

went into seizure looking panting episodes. Meanwhile, I too was affected by

the mercury released into my body. I developed 5 nodules on my thyroid,

fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear

infections, and severe depression. My oncologist said that because I had MTHFR

C667T, (MTHFR.net) that I should be taking L-methylfolate, methylcobalamin and

P5P. My MD had me start on these supplements. I was already taking nattokinase

to prevent blood clots and high dose VIt. D (5,000). She then added in NAC. I

couldn't believe how great I felt. My depression lifted, my nodules disappeared

over 9 months, and all my pain went away. I did have methylcobalamin shots in

my hips twice a week for a few months. My homocysteine was low..4.8 and went to

a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started

giving her those three methylated B's, took epson salt baths. She started

talking. At first it was not in the correct order but over a few months words

came in the correct order. She started repeating words and then I started HBOT

and on the 12th dive, I added in TMG and her language took off that night.

Before she only spoke demands. After, she talked non-stop with adjectives and

imagination. We did 40 dives. It took us from late August-Nov last year. We

used neurobiologix immune stablizer cream before we went into HBOT. It has B's

for her mutation and Vit. D. Also, I started studying NAC, because it had

worked for myself. I found a Standford University study used on ASD kids and it

helped with hand flapping and OCD. After 5 days on NAC (Now brand with

cofactors), she stopped ALL OCD behavior and her seizure looking panting hand

flapping. She did twirl her fingers occasionally when she was really excited.

But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and

lipsomal glutathione. Now all finger twirling is gone. She has lost her

diagnosis. She also started taking Get Smart (1 capsule) www.smartnutrition.com

and nattokinase. I was interested in studying nattokinase because I used it

while recovering. I found articles on biofilms and how nattokinase can break

them down and more mercury was dumped while taking it. She has lost her

diagnosis and has learned after 1 yr doing biomedical stuff, she is completely

recovered. She just turned 4. She knows her ABC's and numbers and plays with

her toys and friends appropriately. She has 4 older brothers ages 18-8. I

believe every child on the spectrum should do genetic testing for MTHFR.

23andme.com now has their genetic test for only $99 for all methylation genes.

4 out of 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child

was 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem

cells. I liked we did 3 days on and 4 days off for neuron growth. Look up

facebook page of Rapid Recovery Hyerbarics. They have great articles on HBOT

and they own a center in San Diego. They just posted they lowered their prices

for children.

Here is an article on HBOT. This is an excellent overview of HBOT and its

history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the

US only 16. Sad...

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%\

20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

[Guest guest]

That is amazing, Tami.  Thanks for sharing this story.  I am in Utah too - would you mind sharing who your physician is?

We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4 days off...Tues-Thursday.  She is completely recovered.  She was tested at 3 yrs old at our school district.  She tested only 1% in cognition.  She was NEVER vaccinated, but got mercury poisoned through nursing her while I took out a mouth full of amalgams.  The mercury went straight through my breast milk.  She nursed until a little over 3 yrs, when I was told by my MD that mercury crosses into breast milk.  She regressed around 2.6 mths old.  She stopped talking, stopped eye contact, started lining up toys, hand flapping and then her flapping went into seizure looking panting episodes.  Meanwhile, I too was affected by the mercury released into my body.  I developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear infections, and severe depression.  My oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should be taking L-methylfolate, methylcobalamin and P5P.  My MD had me start on these supplements.  I was already taking nattokinase to prevent blood clots and high dose VIt. D (5,000).  She then added in NAC.  I couldn't believe how great I felt.  My depression lifted, my nodules disappeared over 9 months, and all my pain went away.  I did have methylcobalamin shots in my hips twice a week for a few months.  My homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started giving her those three methylated B's, took epson salt baths.  She started talking.  At first it was not in the correct order but over a few months words came in the correct order.  She started repeating words and then I started HBOT and on the 12th dive, I added in TMG and her language took off that night.  Before she only spoke demands.  After, she talked non-stop with adjectives and imagination.  We did 40 dives.  It took us from late August-Nov last year.  We used neurobiologix immune stablizer cream before we went into HBOT. It has B's for her mutation and Vit. D.  Also, I started studying NAC, because it had worked for myself.  I found a Standford University study used on ASD kids and it helped with hand flapping and OCD.  After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior and her seizure looking panting hand flapping.  She did twirl her fingers occasionally when she was really excited.  But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all finger twirling is gone.  She has lost her diagnosis.  She also started taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase.  I was interested in studying nattokinase because I used it while recovering.  I found articles on biofilms and how nattokinase can break them down and more mercury was dumped while taking it.  She has lost her diagnosis and has learned after 1 yr doing biomedical stuff, she is completely recovered. She just turned 4.   She knows her ABC's and numbers and plays with her toys and friends appropriately.  She has 4 older brothers ages 18-8.  I believe every child on the spectrum should do genetic testing for MTHFR.  23andme.com now has their genetic test for only $99 for all methylation genes.  4 out of 5 kids have the gene.  Luckily, I stopped immunizing after my 2nd child was 8 mths old.  Anyway, I believe in HBOT.  It grows back neurons and stem cells.  I liked we did 3 days on and 4 days off for neuron growth.  Look up facebook page of Rapid Recovery Hyerbarics.  They have great articles on HBOT and they own a center in San Diego.  They just posted they lowered their prices for children.

Here is an article on  HBOT.  This is an excellent overview of HBOT and its history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the US only 16. Sad...

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

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

[Guest guest]

So which kit do i order again to find out about MTHFR defects.Can I order without Dr and are the results easy to interpret? thanks for sharing by the way.it was very helpful for me To: mb12valtrex Sent: Monday, February 25, 2013 5:26 PM Subject: HBOT

We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4 days off...Tues-Thursday. She is completely recovered. She was tested at 3 yrs old at our school district. She tested only 1% in cognition. She was NEVER vaccinated, but got mercury poisoned through nursing her while I took out a mouth full of amalgams. The mercury went straight through my breast milk. She nursed until a little over 3 yrs, when I was told by my MD that mercury crosses into breast milk. She regressed around 2.6 mths old. She stopped talking, stopped eye contact, started lining up toys, hand flapping and then her flapping went into seizure looking panting episodes. Meanwhile, I too was affected by the mercury released into my body. I developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear infections, and severe depression. My oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should be taking L-methylfolate, methylcobalamin and P5P. My MD had me start on these supplements. I was already taking nattokinase to prevent blood clots and high dose VIt. D (5,000). She then added in NAC. I couldn't believe how great I felt. My depression lifted, my nodules disappeared over 9 months, and all my pain went away. I did have methylcobalamin shots in my hips twice a week for a few months. My homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started giving her those three methylated B's, took epson salt baths. She started talking. At first it was not in the correct order but over a few months words came in the correct order. She started repeating words and then I started HBOT and on the 12th dive, I added in TMG and her language took off that night. Before she only spoke demands. After, she talked non-stop

with adjectives and imagination. We did 40 dives. It took us from late August-Nov last year. We used neurobiologix immune stablizer cream before we went into HBOT. It has B's for her mutation and Vit. D. Also, I started studying NAC, because it had worked for myself. I found a Standford University study used on ASD kids and it helped with hand flapping and OCD. After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior and her seizure looking panting hand flapping. She did twirl her fingers occasionally when she was really excited. But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all finger twirling is gone. She has lost her diagnosis. She also started taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase. I was interested in studying

nattokinase because I used it while recovering. I found articles on biofilms and how nattokinase can break them down and more mercury was dumped while taking it. She has lost her diagnosis and has learned after 1 yr doing biomedical stuff, she is completely recovered. She just turned 4. She knows her ABC's and numbers and plays with her toys and friends appropriately. She has 4 older brothers ages 18-8. I believe every child on the spectrum should do genetic testing for MTHFR. 23andme.com now has their genetic test for only $99 for all methylation genes. 4 out of 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem cells. I liked we did 3 days on and 4 days off for neuron growth. Look up facebook page of Rapid Recovery Hyerbarics. They have great articles on HBOT and they own a center in San Diego. They just posted they lowered their prices for children.

Here is an article on HBOT. This is an excellent overview of HBOT and its history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the US only 16. Sad...

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

[Guest guest]

One more question can you do HBOT without Dr? Can anyone do it? I also have a daughter whos is 5 and has issues due to being premature.Shes an identical twin.So Im curious for her also.I also have a 3 year old w/ASD.From what ive read its expensive.Thanks again!!!! To: "mb12valtrex " <mb12valtrex > Sent: Monday, February 25, 2013 9:06

PM Subject: Re: HBOT

So which kit do i order again to find out about MTHFR defects.Can I order without Dr and are the results easy to interpret? thanks for sharing by the way.it was very helpful for me To: mb12valtrex Sent: Monday, February 25, 2013 5:26 PM Subject: HBOT

We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4 days off...Tues-Thursday. She is completely recovered. She was tested at 3 yrs old at our school district. She tested only 1% in cognition. She was NEVER vaccinated, but got mercury poisoned through nursing her while I took out a mouth full of amalgams. The mercury went straight through my breast milk. She nursed until a little over 3 yrs, when I was told by my MD that mercury crosses into breast milk. She regressed around 2.6 mths old. She stopped talking, stopped eye contact, started lining up toys, hand flapping and then her flapping went into seizure looking panting episodes. Meanwhile, I too was affected by the mercury released into my body. I developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear infections, and severe depression. My oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should be taking L-methylfolate, methylcobalamin and P5P. My MD had me start on these supplements. I was already taking nattokinase to prevent blood clots and high dose VIt. D (5,000). She then added in NAC. I couldn't believe how great I felt. My depression lifted, my nodules disappeared over 9 months, and all my pain went away. I did have methylcobalamin shots in my hips twice a week for a few months. My homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started giving her those three methylated B's, took epson salt baths. She started talking. At first it was not in the correct order but over a few months words came in the correct order. She started repeating words and then I started HBOT and on the 12th dive, I added in TMG and her language took off that night. Before she only spoke demands. After, she

talked non-stop

with adjectives and imagination. We did 40 dives. It took us from late August-Nov last year. We used neurobiologix immune stablizer cream before we went into HBOT. It has B's for her mutation and Vit. D. Also, I started studying NAC, because it had worked for myself. I found a Standford University study used on ASD kids and it helped with hand flapping and OCD. After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior and her seizure looking panting hand flapping. She did twirl her fingers occasionally when she was really excited. But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all finger twirling is gone. She has lost her diagnosis. She also started taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase. I was

interested in studying

nattokinase because I used it while recovering. I found articles on biofilms and how nattokinase can break them down and more mercury was dumped while taking it. She has lost her diagnosis and has learned after 1 yr doing biomedical stuff, she is completely recovered. She just turned 4. She knows her ABC's and numbers and plays with her toys and friends appropriately. She has 4 older brothers ages 18-8. I believe every child on the spectrum should do genetic testing for MTHFR. 23andme.com now has their genetic test for only $99 for all methylation genes. 4 out of 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem cells. I liked we did 3 days on and 4 days off for neuron growth. Look up facebook page of Rapid Recovery Hyerbarics. They have great articles on HBOT and they own a center

in San Diego. They just posted they lowered their prices for children.

Here is an article on HBOT. This is an excellent overview of HBOT and its history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the US only 16. Sad...

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

[Guest guest]

Thanks for sharing!OCD and Flapping is something I must address too, so can you tell the dosage of the liposomal vit c and glutathione? My son is 2/11 mo.CristinaEnviado via iPadEm 25/02/2013, às 19:26, "Tami" escreveu:

We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4 days off...Tues-Thursday. She is completely recovered. She was tested at 3 yrs old at our school district. She tested only 1% in cognition. She was NEVER vaccinated, but got mercury poisoned through nursing her while I took out a mouth full of amalgams. The mercury went straight through my breast milk. She nursed until a little over 3 yrs, when I was told by my MD that mercury crosses into breast milk. She regressed around 2.6 mths old. She stopped talking, stopped eye contact, started lining up toys, hand flapping and then her flapping went into seizure looking panting episodes. Meanwhile, I too was affected by the mercury released into my body. I developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear infections, and severe depression. My oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should be taking L-methylfolate, methylcobalamin and P5P. My MD had me start on these supplements. I was already taking nattokinase to prevent blood clots and high dose VIt. D (5,000). She then added in NAC. I couldn't believe how great I felt. My depression lifted, my nodules disappeared over 9 months, and all my pain went away. I did have methylcobalamin shots in my hips twice a week for a few months. My homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started giving her those three methylated B's, took epson salt baths. She started talking. At first it was not in the correct order but over a few months words came in the correct order. She started repeating words and then I started HBOT and on the 12th dive, I added in TMG and her language took off that night. Before she only spoke demands. After, she talked non-stop with adjectives and imagination. We did 40 dives. It took us from late August-Nov last year. We used neurobiologix immune stablizer cream before we went into HBOT. It has B's for her mutation and Vit. D. Also, I started studying NAC, because it had worked for myself. I found a Standford University study used on ASD kids and it helped with hand flapping and OCD. After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior and her seizure looking panting hand flapping. She did twirl her fingers occasionally when she was really excited. But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all finger twirling is gone. She has lost her diagnosis. She also started taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase. I was interested in studying nattokinase because I used it while recovering. I found articles on biofilms and how nattokinase can break them down and more mercury was dumped while taking it. She has lost her diagnosis and has learned after 1 yr doing biomedical stuff, she is completely recovered. She just turned 4. She knows her ABC's and numbers and plays with her toys and friends appropriately. She has 4 older brothers ages 18-8. I believe every child on the spectrum should do genetic testing for MTHFR. 23andme.com now has their genetic test for only $99 for all methylation genes. 4 out of 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem cells. I liked we did 3 days on and 4 days off for neuron growth. Look up facebook page of Rapid Recovery Hyerbarics. They have great articles on HBOT and they own a center in San Diego. They just posted they lowered their prices for children.

Here is an article on HBOT. This is an excellent overview of HBOT and its history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the US only 16. Sad...

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

[Guest guest]

That is amazing I'm so happy for you, actually my son (just turned 4) made 80 sessions HBOT but still non-verbal.. but it wasn't 1.75 ata, it was less than that.. I think next time will make it same as you did..congratulations... To:

mb12valtrex Sent: Tuesday, February 26, 2013 1:26 AM Subject: HBOT

We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4 days off...Tues-Thursday. She is completely recovered. She was tested at 3 yrs old at our school district. She tested only 1% in cognition. She was NEVER vaccinated, but got mercury poisoned through nursing her while I took out a mouth full of amalgams. The mercury went straight through my breast milk. She nursed until a little over 3 yrs, when I was told by my MD that mercury crosses into breast milk. She regressed around 2.6 mths old. She stopped talking, stopped eye contact, started lining up toys, hand flapping and then her flapping went into seizure looking panting episodes. Meanwhile, I too was affected by the mercury released into my body. I developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear infections, and severe depression. My oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should be taking L-methylfolate, methylcobalamin and P5P. My MD had me start on these supplements. I was already taking nattokinase to prevent blood clots and high dose VIt. D (5,000). She then added in NAC. I couldn't believe how great I felt. My depression lifted, my nodules disappeared over 9 months, and all my pain went away. I did have methylcobalamin shots in my hips twice a week for a few months. My homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started giving her those three methylated B's, took epson salt baths. She started talking. At first it was not in the correct order but over a few months words came in the correct order. She started repeating words and then I started HBOT and on the 12th dive, I added in TMG and her language took off that night. Before she only spoke demands. After, she talked non-stop

with adjectives and imagination. We did 40 dives. It took us from late August-Nov last year. We used neurobiologix immune stablizer cream before we went into HBOT. It has B's for her mutation and Vit. D. Also, I started studying NAC, because it had worked for myself. I found a Standford University study used on ASD kids and it helped with hand flapping and OCD. After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior and her seizure looking panting hand flapping. She did twirl her fingers occasionally when she was really excited. But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all finger twirling is gone. She has lost her diagnosis. She also started taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase. I was interested in studying

nattokinase because I used it while recovering. I found articles on biofilms and how nattokinase can break them down and more mercury was dumped while taking it. She has lost her diagnosis and has learned after 1 yr doing biomedical stuff, she is completely recovered. She just turned 4. She knows her ABC's and numbers and plays with her toys and friends appropriately. She has 4 older brothers ages 18-8. I believe every child on the spectrum should do genetic testing for MTHFR. 23andme.com now has their genetic test for only $99 for all methylation genes. 4 out of 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem cells. I liked we did 3 days on and 4 days off for neuron growth. Look up facebook page of Rapid Recovery Hyerbarics. They have great articles on HBOT and they own a center in San Diego. They just posted they lowered their prices for children.

Here is an article on HBOT. This is an excellent overview of HBOT and its history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the US only 16. Sad...

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

[Guest guest]

Is there anyone in this group that has had success with HBOT with

older children? My son turned 17 this month and I have tried so many

different treatments for him without real lasting results. I don't

want to throw away money that I don't have if this is just going to be

another failure.

Thanks for your input

> That is amazing I'm so happy for you, actually my son (just turned 4) made

> 80 sessions HBOT but still non-verbal.. but it wasn't 1.75 ata, it was less

> than that.. I think next time will make it same as you did..

> congratulations...

>

>

>

> ________________________________

>

> To: mb12valtrex

> Sent: Tuesday, February 26, 2013 1:26 AM

> Subject: HBOT

>

>

>

> We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4

> days off...Tues-Thursday. She is completely recovered. She was tested at 3

> yrs old at our school district. She tested only 1% in cognition. She was

> NEVER vaccinated, but got mercury poisoned through nursing her while I took

> out a mouth full of amalgams. The mercury went straight through my breast

> milk. She nursed until a little over 3 yrs, when I was told by my MD that

> mercury crosses into breast milk. She regressed around 2.6 mths old. She

> stopped talking, stopped eye contact, started lining up toys, hand flapping

> and then her flapping went into seizure looking panting episodes.

> Meanwhile, I too was affected by the mercury released into my body. I

> developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis

> in my hips, allergies, eye and ear infections, and severe depression. My

> oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should

> be taking L-methylfolate, methylcobalamin and P5P. My MD had me start on

> these supplements. I was already taking nattokinase to prevent blood clots

> and high dose VIt. D (5,000). She then added in NAC. I couldn't believe

> how great I felt. My depression lifted, my nodules disappeared over 9

> months, and all my pain went away. I did have methylcobalamin shots in my

> hips twice a week for a few months. My homocysteine was low..4.8 and went

> to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I

> started giving her those three methylated B's, took epson salt baths. She

> started talking. At first it was not in the correct order but over a few

> months words came in the correct order. She started repeating words and

> then I started HBOT and on the 12th dive, I added in TMG and her language

> took off that night. Before she only spoke demands. After, she talked

> non-stop with adjectives and imagination. We did 40 dives. It took us from

> late

> August-Nov last year. We used neurobiologix immune stablizer cream before

> we went into HBOT. It has B's for her mutation and Vit. D. Also, I started

> studying NAC, because it had worked for myself. I found a Standford

> University study used on ASD kids and it helped with hand flapping and OCD.

> After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior

> and her seizure looking panting hand flapping. She did twirl her fingers

> occasionally when she was really excited. But, in Jan., I switched her NAC

> to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all

> finger twirling is gone. She has lost her diagnosis. She also started

> taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase. I was

> interested in studying nattokinase because I used it while recovering. I

> found articles on biofilms and how nattokinase can break them down and more

> mercury was dumped while taking it. She has lost her diagnosis and

> has learned after 1 yr doing biomedical stuff, she is completely recovered.

> She just turned 4. She knows her ABC's and numbers and plays with her toys

> and friends appropriately. She has 4 older brothers ages 18-8. I believe

> every child on the spectrum should do genetic testing for MTHFR. 23andme.com

> now has their genetic test for only $99 for all methylation genes. 4 out of

> 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child was

> 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem

> cells. I liked we did 3 days on and 4 days off for neuron growth. Look up

> facebook page of Rapid Recovery Hyerbarics. They have great articles on

> HBOT and they own a center in San Diego. They just posted they lowered

> their prices for children.

> Here is an article on HBOT. This is an excellent overview of HBOT and its

> history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in

> the US only 16. Sad...

>

http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%\

20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

>

>

>

[Guest guest]

For those interested in HBOT for their children, there is a great program especially designed to provide HBOT treatments for special needs children. The program is offered at a convenient HBOT clinic offering a group rate for families with special needs children. The rates are $50 per treatment which is the lowest in the USA and group rate includes lodging at a nice Comfort Inn and Suites for $47 per night. More information is available at http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_cooperative-1-2-2013.pdfwww.myhbot.orgHBOT CO-OP program for special needs children and adults O2 Clinics still has a couple of seats left in our April, May and June 2013 special needs Group Hyperbaric ative sessions. We are also offering Co-op Group rate programs from July to November. See complete schedule at http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_cooperative-1-2-2013.pdf This ative program brings affordable hard chamber HBOT to families and individuals. This program offers the lowest cost, hard chamber Hyperbaric Oxygen Treatments in North America. The chamber is operated by well trained and experienced CHT and staff. FLAT RATECOST STRUCTURE $2575 or$3085 includes 40 HBOT treatments and 23 nights lodging at Comfort Inn and Suites. (The$2575 rate is for double occupancy ((two families) (1 parent and 1 child each)– $3085 for private room) -$50 per 1 hr HBOT treatment-$47 per night at Comfort Inn and Suites ($23.50 double occupancy) HBOT Chamber features: • 72 inch(6 foot) diameter walk in chamber •Rectangular walk in door • 100%medical grade oxygen via hood or mask • Theater style seating Comfort Inn and Suites is a new facility featuring: • Large rooms with two queen beds • Couch with hideaway bed •Microwave and refrigerator •Elevators • Hot continental breakfast • Indoor heated swimming pool More information available at: O2 Clinics HBOT Co-op - http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_cooperative-1-2-2013.pdf O2Clinicsweb site - www.myhbot.org ComfortInn - http://www.comfortsuites.com/hotel-johnson_creek-wisconsin-WI127?source O2Clinics phone - or after hours>> That is amazing I'm so happy for you, actually my son (just turned 4) made 80 sessions HBOT but still non-verbal.. but it wasn't 1.75 ata, it was less than that.. I think next time will make it same as you did..> congratulations...> > > > ________________________________> To: mb12valtrex > Sent: Tuesday, February 26, 2013 1:26 AM> Subject: HBOT> > > Â > We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on and 4 days off...Tues-Thursday. She is completely recovered. She was tested at 3 yrs old at our school district. She tested only 1% in cognition. She was NEVER vaccinated, but got mercury poisoned through nursing her while I took out a mouth full of amalgams. The mercury went straight through my breast milk. She nursed until a little over 3 yrs, when I was told by my MD that mercury crosses into breast milk. She regressed around 2.6 mths old. She stopped talking, stopped eye contact, started lining up toys, hand flapping and then her flapping went into seizure looking panting episodes. Meanwhile, I too was affected by the mercury released into my body. I developed 5 nodules on my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips, allergies, eye and ear infections, and severe depression. My oncologist said that because I had MTHFR C667T, (MTHFR.net) that I should> be taking L-methylfolate, methylcobalamin and P5P. My MD had me start on these supplements. I was already taking nattokinase to prevent blood clots and high dose VIt. D (5,000). She then added in NAC. I couldn't believe how great I felt. My depression lifted, my nodules disappeared over 9 months, and all my pain went away. I did have methylcobalamin shots in my hips twice a week for a few months. My homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So, when they gave me my dd diagnosis I started giving her those three methylated B's, took epson salt baths. She started talking. At first it was not in the correct order but over a few months words came in the correct order. She started repeating words and then I started HBOT and on the 12th dive, I added in TMG and her language took off that night. Before she only spoke demands. After, she talked non-stop with adjectives and imagination. We did 40 dives. It took us from late> August-Nov last year. We used neurobiologix immune stablizer cream before we went into HBOT. It has B's for her mutation and Vit. D. Also, I started studying NAC, because it had worked for myself. I found a Standford University study used on ASD kids and it helped with hand flapping and OCD. After 5 days on NAC (Now brand with cofactors), she stopped ALL OCD behavior and her seizure looking panting hand flapping. She did twirl her fingers occasionally when she was really excited. But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin C and lipsomal glutathione. Now all finger twirling is gone. She has lost her diagnosis. She also started taking Get Smart (1 capsule) www.smartnutrition.com and nattokinase. I was interested in studying nattokinase because I used it while recovering. I found articles on biofilms and how nattokinase can break them down and more mercury was dumped while taking it. She has lost her diagnosis and> has learned after 1 yr doing biomedical stuff, she is completely recovered. She just turned 4. She knows her ABC's and numbers and plays with her toys and friends appropriately. She has 4 older brothers ages 18-8. I believe every child on the spectrum should do genetic testing for MTHFR. 23andme.com now has their genetic test for only $99 for all methylation genes. 4 out of 5 kids have the gene. Luckily, I stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe in HBOT. It grows back neurons and stem cells. I liked we did 3 days on and 4 days off for neuron growth. Look up facebook page of Rapid Recovery Hyerbarics. They have great articles on HBOT and they own a center in San Diego. They just posted they lowered their prices for children. > Here is an article on HBOT. This is an excellent overview of HBOT and its history and uses. In Russia, HBOT is approved for 73 diagnosis, but here in the US only 16. Sad...> http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyperbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf>

[Guest guest]

Do these clinics help older children? What is your percentage rates of

helping and recovering 17 year olds? That is an awful lot of money to

through away when you are already in bad debt. If it actually helps

recover older teenagers it is worth every penny.

> For those interested in HBOT for their children, there is a great

> program especially designed to provide HBOT treatments for special needs

> children. The program is offered at a convenient HBOT clinic offering a

> group rate for families with special needs children.

> The rates are $50 per treatment which is the lowest in the USA and group

> rate includes lodging at a nice Comfort Inn and Suites for $47 per

> night.

> More information is available at

> http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_coope\

> rative-1-2-2013.pdf

> <http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_coop\

> erative-1-2-2013.pdf>

> www.myhbot.org <http://www.myhbot.org/>

>

> HBOT CO-OP program for special needs children and adults

>

>

>

> O2 Clinics still has a couple of seats left in our April, May and June

> 2013 special needs Group Hyperbaric ative sessions. We are also

> offering Co-op Group rate programs from July to November. See complete

> schedule at

> http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_coope\

> rative-1-2-2013.pdf

> <http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_coop\

> erative-1-2-2013.pdf>

>

>

>

> This ative program brings affordable hard chamber HBOT to families

> and individuals. This program offers the lowest cost, hard chamber

> Hyperbaric Oxygen Treatments in North America. The chamber is operated

> by well trained and experienced CHT and staff.

>

>

>

> FLAT RATECOST STRUCTURE

>

>

>

> $2575 or$3085 includes 40 HBOT treatments and 23 nights lodging at

> Comfort Inn and Suites.

>

> (The$2575 rate is for double occupancy ((two families) (1 parent and 1

> child each)– $3085 for private room)

>

> -$50 per 1 hr HBOT treatment

>

> -$47 per night at Comfort Inn and Suites ($23.50 double occupancy)

>

>

>

> HBOT Chamber features:

>

> • 72 inch(6 foot) diameter walk in chamber

>

> •Rectangular walk in door

>

> • 100%medical grade oxygen via hood or mask

>

> • Theater style seating

>

>

>

> Comfort Inn and Suites is a new facility featuring:

>

> • Large rooms with two queen beds

>

> • Couch with hideaway bed

>

> •Microwave and refrigerator

>

> •Elevators

>

> • Hot continental breakfast

>

> • Indoor heated swimming pool

>

>

>

> More information available at:

>

>

>

> O2 Clinics HBOT Co-op -

> http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_coope\

> rative-1-2-2013.pdf

> <http://www.o2clinics.com/uploads/1/0/7/4/10744868/group_hyperbaric_coop\

> erative-1-2-2013.pdf>

>

>

>

> O2Clinicsweb site - www.myhbot.org <http://www.myhbot.org/>

>

>

>

> ComfortInn -

> http://www.comfortsuites.com/hotel-johnson_creek-wisconsin-WI127?source

> <http://www.comfortsuites.com/hotel-johnson_creek-wisconsin-WI127?source\

>>

>

>

>

> O2Clinics phone - or after hours

>

>

>

>

>>

>> That is amazing I'm so happy for you, actually my son (just turned 4)

> made 80 sessions HBOT but still non-verbal.. but it wasn't 1.75 ata, it

> was less than that.. I think next time will make it same as you did..

>> congratulations...

>>

>>

>>

>> ________________________________

>> From: Tami hirschome@...

>> To: mb12valtrex

>> Sent: Tuesday, February 26, 2013 1:26 AM

>> Subject: HBOT

>>

>>

>> Â

>> We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on

> and 4 days off...Tues-Thursday. She is completely recovered. She was

> tested at 3 yrs old at our school district. She tested only 1% in

> cognition. She was NEVER vaccinated, but got mercury poisoned through

> nursing her while I took out a mouth full of amalgams. The mercury went

> straight through my breast milk. She nursed until a little over 3 yrs,

> when I was told by my MD that mercury crosses into breast milk. She

> regressed around 2.6 mths old. She stopped talking, stopped eye

> contact, started lining up toys, hand flapping and then her flapping

> went into seizure looking panting episodes. Meanwhile, I too was

> affected by the mercury released into my body. I developed 5 nodules on

> my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips,

> allergies, eye and ear infections, and severe depression. My oncologist

> said that because I had MTHFR C667T, (MTHFR.net) that I should

>> be taking L-methylfolate, methylcobalamin and P5P. My MD had me

> start on these supplements. I was already taking nattokinase to prevent

> blood clots and high dose VIt. D (5,000). She then added in NAC. I

> couldn't believe how great I felt. My depression lifted, my nodules

> disappeared over 9 months, and all my pain went away. I did have

> methylcobalamin shots in my hips twice a week for a few months. My

> homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So,

> when they gave me my dd diagnosis I started giving her those three

> methylated B's, took epson salt baths. She started talking. At first

> it was not in the correct order but over a few months words came in the

> correct order. She started repeating words and then I started HBOT and

> on the 12th dive, I added in TMG and her language took off that night.

> Before she only spoke demands. After, she talked non-stop with

> adjectives and imagination. We did 40 dives. It took us from late

>> August-Nov last year. We used neurobiologix immune stablizer cream

> before we went into HBOT. It has B's for her mutation and Vit. D. Also,

> I started studying NAC, because it had worked for myself. I found a

> Standford University study used on ASD kids and it helped with hand

> flapping and OCD. After 5 days on NAC (Now brand with cofactors), she

> stopped ALL OCD behavior and her seizure looking panting hand flapping.

> She did twirl her fingers occasionally when she was really excited.

> But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin

> C and lipsomal glutathione. Now all finger twirling is gone. She has

> lost her diagnosis. She also started taking Get Smart (1 capsule)

> www.smartnutrition.com and nattokinase. I was interested in studying

> nattokinase because I used it while recovering. I found articles on

> biofilms and how nattokinase can break them down and more mercury was

> dumped while taking it. She has lost her diagnosis and

>> has learned after 1 yr doing biomedical stuff, she is completely

> recovered. She just turned 4. She knows her ABC's and numbers and

> plays with her toys and friends appropriately. She has 4 older brothers

> ages 18-8. I believe every child on the spectrum should do genetic

> testing for MTHFR. 23andme.com now has their genetic test for only $99

> for all methylation genes. 4 out of 5 kids have the gene. Luckily, I

> stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe

> in HBOT. It grows back neurons and stem cells. I liked we did 3 days

> on and 4 days off for neuron growth. Look up facebook page of Rapid

> Recovery Hyerbarics. They have great articles on HBOT and they own a

> center in San Diego. They just posted they lowered their prices for

> children.

>> Here is an article on HBOT. This is an excellent overview of HBOT

> and its history and uses. In Russia, HBOT is approved for 73 diagnosis,

> but here in the US only 16. Sad...

>>

> http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyp\

> erbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf

>>

>

>

[Guest guest]

The age of the child does not matter. HBOT can help any child at any age. What must be understood is how HBOT works and then a decision made if HBOT can help with the childs condition(s).Here are some links to studies at the Federal Gov't Pub Med web site:Hyperbaric treatment for children with autism: a multicenter, randomized, double-blind, controlled trialHyperbaric oxygen therapy in Thai autistic childrenHyperbaric oxygen therapy might improve certain pathophysiological findings in autismHyperbaric oxygen therapy may improve symptoms in autistic children You can call me at or email me at info@... if you would like to discuss this further.K MacLaughlin> >>> >> That is amazing I'm so happy for you, actually my son (just turned 4)> > made 80 sessions HBOT but still non-verbal.. but it wasn't 1.75 ata, it> > was less than that.. I think next time will make it same as you did..> >> congratulations...> >>> >>> >>> >> ________________________________> >> From: Tami hirschome@> >> To: mb12valtrex > >> Sent: Tuesday, February 26, 2013 1:26 AM> >> Subject: HBOT> >>> >>> >> Â> >> We are in Utah and did HBOT 1.75 ata for my PDD-NOS daughter 3 days on> > and 4 days off...Tues-Thursday. She is completely recovered. She was> > tested at 3 yrs old at our school district. She tested only 1% in> > cognition. She was NEVER vaccinated, but got mercury poisoned through> > nursing her while I took out a mouth full of amalgams. The mercury went> > straight through my breast milk. She nursed until a little over 3 yrs,> > when I was told by my MD that mercury crosses into breast milk. She> > regressed around 2.6 mths old. She stopped talking, stopped eye> > contact, started lining up toys, hand flapping and then her flapping> > went into seizure looking panting episodes. Meanwhile, I too was> > affected by the mercury released into my body. I developed 5 nodules on> > my thyroid, fibrolmyalgia, chronic fatigue, bursitis in my hips,> > allergies, eye and ear infections, and severe depression. My oncologist> > said that because I had MTHFR C667T, (MTHFR.net) that I should> >> be taking L-methylfolate, methylcobalamin and P5P. My MD had me> > start on these supplements. I was already taking nattokinase to prevent> > blood clots and high dose VIt. D (5,000). She then added in NAC. I> > couldn't believe how great I felt. My depression lifted, my nodules> > disappeared over 9 months, and all my pain went away. I did have> > methylcobalamin shots in my hips twice a week for a few months. My> > homocysteine was low..4.8 and went to a healthy 6.3 within 9 mths. So,> > when they gave me my dd diagnosis I started giving her those three> > methylated B's, took epson salt baths. She started talking. At first> > it was not in the correct order but over a few months words came in the> > correct order. She started repeating words and then I started HBOT and> > on the 12th dive, I added in TMG and her language took off that night.> > Before she only spoke demands. After, she talked non-stop with> > adjectives and imagination. We did 40 dives. It took us from late> >> August-Nov last year. We used neurobiologix immune stablizer cream> > before we went into HBOT. It has B's for her mutation and Vit. D. Also,> > I started studying NAC, because it had worked for myself. I found a> > Standford University study used on ASD kids and it helped with hand> > flapping and OCD. After 5 days on NAC (Now brand with cofactors), she> > stopped ALL OCD behavior and her seizure looking panting hand flapping.> > She did twirl her fingers occasionally when she was really excited.> > But, in Jan., I switched her NAC to seekinghealth.com's lipsomal Vitamin> > C and lipsomal glutathione. Now all finger twirling is gone. She has> > lost her diagnosis. She also started taking Get Smart (1 capsule)> > www.smartnutrition.com and nattokinase. I was interested in studying> > nattokinase because I used it while recovering. I found articles on> > biofilms and how nattokinase can break them down and more mercury was> > dumped while taking it. She has lost her diagnosis and> >> has learned after 1 yr doing biomedical stuff, she is completely> > recovered. She just turned 4. She knows her ABC's and numbers and> > plays with her toys and friends appropriately. She has 4 older brothers> > ages 18-8. I believe every child on the spectrum should do genetic> > testing for MTHFR. 23andme.com now has their genetic test for only $99> > for all methylation genes. 4 out of 5 kids have the gene. Luckily, I> > stopped immunizing after my 2nd child was 8 mths old. Anyway, I believe> > in HBOT. It grows back neurons and stem cells. I liked we did 3 days> > on and 4 days off for neuron growth. Look up facebook page of Rapid> > Recovery Hyerbarics. They have great articles on HBOT and they own a> > center in San Diego. They just posted they lowered their prices for> > children.> >> Here is an article on HBOT. This is an excellent overview of HBOT> > and its history and uses. In Russia, HBOT is approved for 73 diagnosis,> > but here in the US only 16. Sad...> >>> > http://nirvanahbo.com/images/uploads/Presentation%20-%20Value%20of%20Hyp\> > erbaric%20Oxygen%20Therapy%20(HBOT)%20Cancer%20Care_Maxfield_2010.pdf> >>> >> >>

[Guest guest]

We do Budwig mixture to flood the cells with oxygen every morning. Only organic home made food. After experimenting with multiple restrictive diets that made her worse we eat everything now and don't take any chemicals or supplements or treatments. She is 3.2 stimming greatly decreased, knows alphabet, numbers, started making requests recently and potty trained in several weeks. Hope she'll outgrow by 4-5 years of age like 70% of kids with PDD.

[Guest guest]

What is a Budwig mixture?

Thx,

Patty

>

> We do Budwig mixture to flood the cells with oxygen every morning. Only

organic home made food. After experimenting with multiple restrictive diets that

made her worse we eat everything now and don't take any chemicals or supplements

or treatments. She is 3.2 stimming greatly decreased, knows alphabet, numbers,

started making requests recently and potty trained in several weeks. Hope she'll

outgrow by 4-5 years of age like 70% of kids with PDD.

>

[Guest guest]

2 tbsp cottage cheese to 1 tbsp barlean flaxseed oil stored in fridge mixed in

blender. Add 1-2 tbsp milk if cheese is thick.

http://www.budwigcenter.com/anti-cancer-diet.php

if you are interested, ask them for free guide, they provide explanation behind

the theory why it works and free recipes. They also don't recommend any other

sources of oxygen besides their mixture. We follow it loosely and give eggs and

meat occasionally, fish almost every day. Budwig mixture we do every morning.

> >

> > We do Budwig mixture to flood the cells with oxygen every morning. Only

organic home made food. After experimenting with multiple restrictive diets that

made her worse we eat everything now and don't take any chemicals or supplements

or treatments. She is 3.2 stimming greatly decreased, knows alphabet, numbers,

started making requests recently and potty trained in several weeks. Hope she'll

outgrow by 4-5 years of age like 70% of kids with PDD.

> >

>

[Guest guest]

thank you for this info Marina!!!!!!

To: mb12valtrex Sent: Friday, March 1, 2013 6:43 AMSubject: Re: HBOT

2 tbsp cottage cheese to 1 tbsp barlean flaxseed oil stored in fridge mixed in blender. Add 1-2 tbsp milk if cheese is thick.

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..

[Guest guest]

Glad to be of help:)

I take it myself every morning, I know it works. Very cheap, very effective.

>

> thank you for this info Marina!!!!!!

>

>

>

> ________________________________

>

> To: mb12valtrex

> Sent: Friday, March 1, 2013 6:43 AM

> Subject: Re: HBOT

>

>  

> 2 tbsp cottage cheese to 1 tbsp barlean flaxseed oil stored in fridge mixed in

blender. Add 1-2 tbsp milk if cheese is thick.

>  

> Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use • Send

us Feedback

> .

>

[Guest guest]

Angelika - how does the cottage cheese and barlean flaxseed oil oxygenate the

body?

> >

> > thank you for this info Marina!!!!!!

> >

> >

> >

> > ________________________________

> > From: angelika99_00 <angelika99_00@>

> > To: mb12valtrex

> > Sent: Friday, March 1, 2013 6:43 AM

> > Subject: Re: HBOT

> >

> >  

> > 2 tbsp cottage cheese to 1 tbsp barlean flaxseed oil stored in fridge mixed

in blender. Add 1-2 tbsp milk if cheese is thick.

> >  

> > Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use • Send

us Feedback

> > .

> >

>

[Guest guest]

http://www.whale.to/cancer/Flax%20Oil%20as%20a%20true%20aid.pdf

Here is the link why it works

I figured if people successfully use for autism Gerson therapy which is

nutritional protocol for cancer, why not something less painful and as

effective?

Yes, all this DAN protocols you read about " borrowed " from Gerson therapy. B12

shots B3 pill, juicing, iodine, enzymes and many others. Highly recommend to

read the Gerson therapy book. Only $10 and wealth of information.

> > >

> > > thank you for this info Marina!!!!!!

> > >

> > >

> > >

> > > ________________________________

> > > From: angelika99_00 <angelika99_00@>

> > > To: mb12valtrex

> > > Sent: Friday, March 1, 2013 6:43 AM

> > > Subject: Re: HBOT

> > >

> > >  

> > > 2 tbsp cottage cheese to 1 tbsp barlean flaxseed oil stored in fridge

mixed in blender. Add 1-2 tbsp milk if cheese is thick.

> > >  

> > > Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use •

Send us Feedback

> > > .

> > >

> >

>