Re: Anyone else living as 2 people?

[Guest guest]

My heart goes out to you!!! I was where you are. I wish there were

guarantees. I wish there was a panacea, but here on this site is where you

shall find the best chance of your child recovering.

When my son first regressed, this was the ONLY site I could find, and they

put me on the right road. You did not say how old your child was.

I regret that I did not listen to ANDY at first. We did follow a lot of

advice except the AC Protocol for chelation. I really feel that if we had

followed it then, our son would be one that is fully recovered. But I took

away casein when my son was two. then six months later I took away gluten.

Then several months after that I took away soy, and four days later he said

his first sentence! We did other biomed things too. We looked for

nutritional deficiencies. We put him on ALC very early on.

I also did an ABA/Floor-time program with him all by myself. His dad spent

all his time with him once he came home so I had a break, and he took the

weekends too so I could rejuvenate.

Every child different,and I don't know all you've done or how old your child

is. I know how easy it is to get lost --to lose yourself.

Four years ago I also had to start taking care of my mother. My passion is

horses and has been all my life, and it just dawned on me the other day that

I have ridden about four times in four years! This is unheard of for me.

You have got to take time for yourself, too.

I felt many times as you do -- I was so afraid he would never come back, I

mean, after all, the mainstream doctors had told me he would never talk,

make a friend, go to college, be potty trained. Often I had trouble being

around people with normal kids --I had to get away or I knew I would cry in

front of them.

But everyday I just kept plugging along --one step at a time. Then I fought

the battle with the school, and now I have to home-school him if he has a

chance to become what he wants to become. He wants to be an architect!

Come hell or high water, I aim to see he gets his chance.

Maybe my son won't get there. But I will do whatever I have to do , to see

he gets his chance.

What all have you done so far? This is a long road, and my son still has

immune issues, but his " autism " is sooo much better. He is high functioning

and has regained all types of speech (receptive, expressive, reciprocal). He

lost all speech after vaccination and was moderate/severe with episodes of

what looked like catatonia.

Our journey --each parent's journey is going to be different. My son was

given broad spectrum antibiotics during his first (he's had eight since

regression) bout of pneumonia. On the fourth day of his treatment, he said

every word he had known before regression. this moment proved to me that

there was something biomedical going on. I researched and found that a

study showed children with autism improved with vancomycin, but when they

went off, they regressed. When I read this, I cried. But my son did not

regress all the way, so I built on what he retained.

You must find some balance between biomed and " You. " You cannot give up.

You must find solace in doing the best you can for as long as you can.

When we tried something new, we took notes. Andy told me in the beginning

that if something is going to work then it works, and if something doesn't

you'll know. Now things like diet and chelation take time.

We are not done with our journey yet. We did IV chelation, and I am just

happy my son survived. It caused him to have asthma attacks. I am studying

now to get ready to do chelation with ALA alone.

I am to the point that I love the child my son is. There are parts of his

autism I wish he would not lose. He is a very genuine human being. He

doesn't hold the cruelty other ten and a half year old boys often display.

In fact, this summer my son was playing --actually playing with another boy,

and this NT boy was taught to play rough. My goddaughter was supposed to be

watching them. Well, the other boy got rough with Ethan, and I am outside

working and a police car pulls up! When the boy got rough with Ethan, Ethan

called 911 because he has not been taught that it is okay to play rough! I

explained the situation to the officer, and everything was okay, but BOTH

boys got a talking to, and then I had a talk with my goddaughter, too.

Try not to think of the end of the race. Think of the next step in the race

and get there first.

There were so many things that went into my son's getting better, and I

cannot discount prayer.

What all have you tried so far? How old is your son? I hope you feel

better soon, and know that all of us here on this list are here for you. We

cannot wave a magic wand -- we would if we could -- What I would give if

this tragedy had not happened to all our children!

Take care of yourself. Please hang in there. Your child needs you.

[Guest guest]

My son is 8. He's diagnosed at severe. Diets didn't work, ivig didn't work, iv

chelation didn't work, supplements don't work, oral dmsa killed his gut.... So

that takes out ac .....unless I can do AC with dmps.

We have a hyperbaric chamber, got it a couple of days ago so don't know if it'll

work yet. We did hard chamber dives and he really responded. here's hoping!

 

________________________________

From: Haven DeLay <hdelay@...>

Sent: Fri, September 10, 2010 10:09:15 PM

Subject: Re: [ ] Anyone else living as 2 people?

 

My heart goes out to you!!! I was where you are. I wish there were

guarantees. I wish there was a panacea, but here on this site is where you

shall find the best chance of your child recovering.

When my son first regressed, this was the ONLY site I could find, and they

put me on the right road. You did not say how old your child was.

I regret that I did not listen to ANDY at first. We did follow a lot of

advice except the AC Protocol for chelation. I really feel that if we had

followed it then, our son would be one that is fully recovered. But I took

away casein when my son was two. then six months later I took away gluten.

Then several months after that I took away soy, and four days later he said

his first sentence! We did other biomed things too. We looked for

nutritional deficiencies. We put him on ALC very early on.

I also did an ABA/Floor-time program with him all by myself. His dad spent

all his time with him once he came home so I had a break, and he took the

weekends too so I could rejuvenate.

Every child different,and I don't know all you've done or how old your child

is. I know how easy it is to get lost --to lose yourself.

Four years ago I also had to start taking care of my mother. My passion is

horses and has been all my life, and it just dawned on me the other day that

I have ridden about four times in four years! This is unheard of for me.

You have got to take time for yourself, too.

I felt many times as you do -- I was so afraid he would never come back, I

mean, after all, the mainstream doctors had told me he would never talk,

make a friend, go to college, be potty trained. Often I had trouble being

around people with normal kids --I had to get away or I knew I would cry in

front of them.

But everyday I just kept plugging along --one step at a time. Then I fought

the battle with the school, and now I have to home-school him if he has a

chance to become what he wants to become. He wants to be an architect!

Come hell or high water, I aim to see he gets his chance.

Maybe my son won't get there. But I will do whatever I have to do , to see

he gets his chance.

What all have you done so far? This is a long road, and my son still has

immune issues, but his " autism " is sooo much better. He is high functioning

and has regained all types of speech (receptive, expressive, reciprocal). He

lost all speech after vaccination and was moderate/severe with episodes of

what looked like catatonia.

Our journey --each parent's journey is going to be different. My son was

given broad spectrum antibiotics during his first (he's had eight since

regression) bout of pneumonia. On the fourth day of his treatment, he said

every word he had known before regression. this moment proved to me that

there was something biomedical going on. I researched and found that a

study showed children with autism improved with vancomycin, but when they

went off, they regressed. When I read this, I cried. But my son did not

regress all the way, so I built on what he retained.

You must find some balance between biomed and " You. " You cannot give up.

You must find solace in doing the best you can for as long as you can.

When we tried something new, we took notes. Andy told me in the beginning

that if something is going to work then it works, and if something doesn't

you'll know. Now things like diet and chelation take time.

We are not done with our journey yet. We did IV chelation, and I am just

happy my son survived. It caused him to have asthma attacks. I am studying

now to get ready to do chelation with ALA alone.

I am to the point that I love the child my son is. There are parts of his

autism I wish he would not lose. He is a very genuine human being. He

doesn't hold the cruelty other ten and a half year old boys often display.

In fact, this summer my son was playing --actually playing with another boy,

and this NT boy was taught to play rough. My goddaughter was supposed to be

watching them. Well, the other boy got rough with Ethan, and I am outside

working and a police car pulls up! When the boy got rough with Ethan, Ethan

called 911 because he has not been taught that it is okay to play rough! I

explained the situation to the officer, and everything was okay, but BOTH

boys got a talking to, and then I had a talk with my goddaughter, too.

Try not to think of the end of the race. Think of the next step in the race

and get there first.

There were so many things that went into my son's getting better, and I

cannot discount prayer.

What all have you tried so far? How old is your son? I hope you feel

better soon, and know that all of us here on this list are here for you. We

cannot wave a magic wand -- we would if we could -- What I would give if

this tragedy had not happened to all our children!

Take care of yourself. Please hang in there. Your child needs you.

[Guest guest]

Hi Kate,

We all feel that way sometimes.  It takes time for our kids to heal.  Waiting

is the most difficult part of this whole thing, and it doesn't help when you

have a shi$$y day and your kid is bouncing off the wall or stimming like crazy

or doing something you haven't seen for two years and thought he had

outgrown......ugh.  It will get better, it takes time and patience and

sometimes we all cry ourselves to sleep or have one too many cocktails to make

us sleep or eat too much or.......pick your drug of choice (mine is gin and

buttered popcorn).  However then the good days make is easier to see the

light.  Hang in there, we are here to hold you up on the bad days and celebrate

with you on the good ones.  We're just moms and grandmoms trying to be Super

Women and sometimes we crash, but only temporarily.

nancy j

a child is diagnosed with

asd every 20 seconds

From: Kate Grayce <kategrayce11@...>

Subject: [ ] Anyone else living as 2 people?

mb12 valtrex , autism treatment

Date: Friday, September 10, 2010, 7:39 PM

 

I feel like I have 2 different lives. The mom that cooks and cleans and

runs the

kids to school and pretends to her husband, friends and family that everything

is ok, and the real me scared sh*tless that I'm never going to get him

recovered.

  I am so scared...night and day..all the time. What if I never do it?

 I've never excepted that he's not coming back. Every time I think of that

thought I immediately start go weak, can't breath and in a panic run to my list

on the fridge  and read everything I'm doing for him just to reassure myself

.......he's coming back.  I have a couple memories of him before autism and I'm

losing those too. It's like it's been so long I can't remember that well

anymore.

 I''ve lived this biomed life with such passion and intensity I've lost myself,

and i've been around the biomed block a couple times now that I don't know where

I'm even going now. I've done everything.

i'll stop writing .......one of those nights ......

[Guest guest]

Dear Kate:

We all have nights and days like you are having tonight-you

are definitely not alone.

My son is severe too and I can hardly remember the boy he once was, but I

know he is in there somewhere.

I'm not to sure, but I don't think DMSA is what hurts their stomach. Am I

wrong, anyone?

Z

On Fri, Sep 10, 2010 at 7:39 PM, Kate Grayce <kategrayce11@...> wrote:

>

>

> I feel like I have 2 different lives. The mom that cooks and cleans and

> runs the

> kids to school and pretends to her husband, friends and family that

> everything

> is ok, and the real me scared sh*tless that I'm never going to get him

> recovered.

> I am so scared...night and day..all the time. What if I never do it?

> I've never excepted that he's not coming back. Every time I think of that

> thought I immediately start go weak, can't breath and in a panic run to my

> list

> on the fridge and read everything I'm doing for him just to reassure

> myself

> ......he's coming back. I have a couple memories of him before autism and

> I'm

> losing those too. It's like it's been so long I can't remember that well

> anymore.

>

> I''ve lived this biomed life with such passion and intensity I've lost

> myself,

> and i've been around the biomed block a couple times now that I don't know

> where

> I'm even going now. I've done everything.

>

> i'll stop writing .......one of those nights ......

>

>

[Guest guest]

Dear Kate, Your not alone....if this is any consolation to you. We've all gone

or are going through many of the same things with our kids. The hardest thing

for me is when my son would say , " Mommy I just want Jesus to take me home " . And

I know I should have elated over the fact he is verbal. But my son developed

" leaky gut " syndrome. This often caused years of pain until we found Dr.Mercola

and visited his clinic. But there is light at the end of the tunnel. Keep the

faith and make sure you find ppl to support you while juggling a dozen plates by

yourself. That is the analogy I often used. I didn't have a lot of support and

so much ridicule which made my situation difficult also. I turned to prayer and

that helped me through so much. Im holding you up there Kate. Never never give

up the fight! Laurie

________________________________

From: Zurama <autismtookmickie@...>

Sent: Sat, September 11, 2010 1:41:37 AM

Subject: Re: [ ] Anyone else living as 2 people?

Dear Kate:

We all have nights and days like you are having tonight-you

are definitely not alone.

My son is severe too and I can hardly remember the boy he once was, but I

know he is in there somewhere.

I'm not to sure, but I don't think DMSA is what hurts their stomach. Am I

wrong, anyone?

Z

On Fri, Sep 10, 2010 at 7:39 PM, Kate Grayce <kategrayce11@...> wrote:

>

>

> I feel like I have 2 different lives. The mom that cooks and cleans and

> runs the

> kids to school and pretends to her husband, friends and family that

> everything

> is ok, and the real me scared sh*tless that I'm never going to get him

> recovered.

> I am so scared...night and day..all the time. What if I never do it?

> I've never excepted that he's not coming back. Every time I think of that

> thought I immediately start go weak, can't breath and in a panic run to my

> list

> on the fridge and read everything I'm doing for him just to reassure

> myself

> ......he's coming back. I have a couple memories of him before autism and

> I'm

> losing those too. It's like it's been so long I can't remember that well

> anymore.

>

> I''ve lived this biomed life with such passion and intensity I've lost

> myself,

> and i've been around the biomed block a couple times now that I don't know

> where

> I'm even going now. I've done everything.

>

> i'll stop writing .......one of those nights ......

>

>

[Guest guest]

Kate,

What diet were you doing? Is your son on Acetyl-L-Carnitine? Have you

considered chelating with ALA alone, transdermal per Andy's instructions?

We IV chelated and saw gains, but our son had frightening reactions to it on

three occasions, so we won't do that again. I am studying and preparing to

chelate him with ALA alone, transdermal every three hours. We have been

gf/cf since he was two and sf since he was three, and for our son, it

helped, but even now I am looking at Body Ecology Diet.

You are about to try HBOT. that is great. We have never tried that, but I

have heard good things about it.

I am praying that you find the answer for your son.

I know when we started everything was bleak, and all the doctors were

fatalistic. My husband and I talked and I said we may do all these things

and he still not get better, but then I decided that twenty years from that

day, if he were no better, I would know that at least I had tried everything

I knew to make him better. i wanted my son fully recovered by age six. It

didn't happen. He is so much better. He got back speech but we never

really had a conversation until he was ten. I know if things had not worked

for my son, I would feel exactly as you do, but you just can't give up

hope. I believe in my heart there is an answer for each child. It may be a

different key from child to child. You are doing the right thing: you are

trying something you haven't tried before.

If he is not taking Acetyl-L-carnitine, I suggest you try it. consider the

AC protocol for ALA only, and given your child's tummy issues, considering

doing it transdermal. You are to be commended for not giving up!

[Guest guest]

Where do you find the instructions for transdermal ALA.

From: Haven DeLay <hdelay@...>

Subject: Re: [ ] Anyone else living as 2 people?

Date: Saturday, September 11, 2010, 10:48 AM

 

Kate,

What diet were you doing? Is your son on Acetyl-L-Carnitine? Have you

considered chelating with ALA alone, transdermal per Andy's instructions?

We IV chelated and saw gains, but our son had frightening reactions to it on

three occasions, so we won't do that again. I am studying and preparing to

chelate him with ALA alone, transdermal every three hours. We have been

gf/cf since he was two and sf since he was three, and for our son, it

helped, but even now I am looking at Body Ecology Diet.

You are about to try HBOT. that is great. We have never tried that, but I

have heard good things about it.

I am praying that you find the answer for your son.

I know when we started everything was bleak, and all the doctors were

fatalistic. My husband and I talked and I said we may do all these things

and he still not get better, but then I decided that twenty years from that

day, if he were no better, I would know that at least I had tried everything

I knew to make him better. i wanted my son fully recovered by age six. It

didn't happen. He is so much better. He got back speech but we never

really had a conversation until he was ten. I know if things had not worked

for my son, I would feel exactly as you do, but you just can't give up

hope. I believe in my heart there is an answer for each child. It may be a

different key from child to child. You are doing the right thing: you are

trying something you haven't tried before.

If he is not taking Acetyl-L-carnitine, I suggest you try it. consider the

AC protocol for ALA only, and given your child's tummy issues, considering

doing it transdermal. You are to be commended for not giving up!

[Guest guest]

We've done them all!  gfcf, sf, cf, scd, bed..... We are doing Acetyl l

carnitine. We are thinking now of doing oral dmps.

________________________________

From: Haven DeLay <hdelay@...>

Sent: Sat, September 11, 2010 9:48:48 AM

Subject: Re: [ ] Anyone else living as 2 people?

 

Kate,

What diet were you doing? Is your son on Acetyl-L-Carnitine? Have you

considered chelating with ALA alone, transdermal per Andy's instructions?

We IV chelated and saw gains, but our son had frightening reactions to it on

three occasions, so we won't do that again. I am studying and preparing to

chelate him with ALA alone, transdermal every three hours. We have been

gf/cf since he was two and sf since he was three, and for our son, it

helped, but even now I am looking at Body Ecology Diet.

You are about to try HBOT. that is great. We have never tried that, but I

have heard good things about it.

I am praying that you find the answer for your son.

I know when we started everything was bleak, and all the doctors were

fatalistic. My husband and I talked and I said we may do all these things

and he still not get better, but then I decided that twenty years from that

day, if he were no better, I would know that at least I had tried everything

I knew to make him better. i wanted my son fully recovered by age six. It

didn't happen. He is so much better. He got back speech but we never

really had a conversation until he was ten. I know if things had not worked

for my son, I would feel exactly as you do, but you just can't give up

hope. I believe in my heart there is an answer for each child. It may be a

different key from child to child. You are doing the right thing: you are

trying something you haven't tried before.

If he is not taking Acetyl-L-carnitine, I suggest you try it. consider the

AC protocol for ALA only, and given your child's tummy issues, considering

doing it transdermal. You are to be commended for not giving up!

[Guest guest]

I think you can find the protocol for the ALA only in the archives. i am

reading Andy's book again and then will ask a lot of questions and then

forge ahead.

[Guest guest]

Hi Kate. Everyone has those days. We are approaching 100 rounds with my son -

recently he turned a corner and made some amazing gains. Then this past couple

of weeks he has had the runs, bowel disturbance and some yeast resurfaced. He

was foggy, acting out, stimming, non verbal all of a sudden - it was like we

were back at round 1. I just wanted to cry. And like you at night, I thought,

is this what we are doomed to do - get gains, and then have none? Is he beyond

repair? Has Pharma damaged my boy for good?

This is human nature. However, we got my son's bowels under control, beat back

the yeast. Took a week or two break from chelation. Now my boy is back. No

more dark circles, bad behaviors. This is a long, slow road. It is true we

have to lead double lives - the public one - the face you show to family and the

school, and then the private biomed drudgery. But always remember AC chelation

is soooo slow, tedious, takes what seems like forever, but it does work. I can

attest to this. I am chelating myself as well. It does work for kids and

adults. Tell yourself, there will be an end. Kind of like when I was a

doubting teenager and asked my parents about God - how do I know He really

exists, how do I know I can trust in this? I was told to have " faith " - and in

a sense you have to have faith through this journey and listen to those who have

recovered themselves and their kids this way.

Even as Andy has said on occasion, if 100% recovery is not possible, your child

can become much, much better. As long as they can get well enough to be in a

regular class, to live independently some day, be healthy, and happy, earn a

living, have a family. That is what I wish for my son. It may not be exactly

as we would have wished, and their childhood's may have been stolen from us, but

not their futures, if we have anything to say about it. This is so much more

than most kids on the spectrum can hope for for their kids who do not do biomed.

Be thankful that you have found a safe way to make your child better that is

within your own control.

Take heart, recovery is possible, you just have to persevere long enough and

seek support here and wherever else you can find it, in times of distress when

you need it. Just like you did.

Hang in there.

Irene

5 year old, 98 rounds

57 rounds, Me

>

> I feel like I have 2 different lives. The mom that cooks and cleans and runs

the

> kids to school and pretends to her husband, friends and family that everything

> is ok, and the real me scared sh*tless that I'm never going to get him

> recovered.

>   I am so scared...night and day..all the time. What if I never do it?

>  I've never excepted that he's not coming back. Every time I think of that

> thought I immediately start go weak, can't breath and in a panic run to my

list

> on the fridge  and read everything I'm doing for him just to reassure myself

> ......he's coming back.  I have a couple memories of him before autism and I'm

> losing those too. It's like it's been so long I can't remember that well

> anymore.

>

>  I''ve lived this biomed life with such passion and intensity I've lost

myself,

> and i've been around the biomed block a couple times now that I don't know

where

> I'm even going now. I've done everything.

>

>

> i'll stop writing .......one of those nights ......

>

>

>

>

>

[Guest guest]

Hi Kate,

I will be honest: There are days when I feel suicidal, and days when I feel his

only presence, even if he is not 100% there, keeps me going because I do see he

has improved, because those moments when he does look at me, open my soul to an

universe of love and hope. On those terrible days, cry if you must, but don't

let him see u, even when we think they don't realize, oh madam, they do......

Everything, they sense everything. So it's better if you give yourself an hour

or two on your own, then breathe deeply, hAve a cup of coffee or a glass of

wine, and smile again from the bottom of your heart.... Sounds easy, uh? I have

even been on anti-depressants for a long time, on and off, on and off. Our kids

need healthy, positive moms, with faith and strength to win this fight, they

deserve it and so do we. I often feel that my kid is suffering due to his

incapacity to communicate and that he is frustrated about not being " ok " ? My

husband says he doesn't suffer, I differ. His soul needs to heal too, his

childhood has been stolen from us, the only medicine to compensate for this is

LOVE, the elixir of all existence...

We all love our kids and that's why we are fighting so hard, I realize I

sometimes feel so stressed, isolated and busy that I don't remember to show him

my love intense as it is. He reacts so well to it, and I feel happy to manage

my negative emotions and be what he needs: a loving, loving mom. This is the

way I pick up myself easily. Others might think or see me from a different

point of view, I have learned NOT to care about what they think of me: my

in-laws, when they see me ok, say: oh, you manage things so well! When I am

unstable, stressed or introspective, I am and that's it. I don't try to please

anybody and be " picture perfect- smiling and happy wife and person " if they can

cope w me being quiet, it's fine, otherwise they should keep their opinion to

themselves. I already have enough on my plate, I allow myself to live my moment

and I feel free to forgive myself for falling when I do.

You are not alone, thank you for your post because it gave me the chance to let

go on my sadness today, so thank you for bringing up the topic.

With blessings,

Isa

(Mom to , 6yo

Mexico city)

Enviado desde mi oficina móvil BlackBerry® de Telcel

Re: [ ] Anyone else living as 2 people?

 

Kate,

What diet were you doing? Is your son on Acetyl-L-Carnitine? Have you

considered chelating with ALA alone, transdermal per Andy's instructions?

We IV chelated and saw gains, but our son had frightening reactions to it on

three occasions, so we won't do that again. I am studying and preparing to

chelate him with ALA alone, transdermal every three hours. We have been

gf/cf since he was two and sf since he was three, and for our son, it

helped, but even now I am looking at Body Ecology Diet.

You are about to try HBOT. that is great. We have never tried that, but I

have heard good things about it.

I am praying that you find the answer for your son.

I know when we started everything was bleak, and all the doctors were

fatalistic. My husband and I talked and I said we may do all these things

and he still not get better, but then I decided that twenty years from that

day, if he were no better, I would know that at least I had tried everything

I knew to make him better. i wanted my son fully recovered by age six. It

didn't happen. He is so much better. He got back speech but we never

really had a conversation until he was ten. I know if things had not worked

for my son, I would feel exactly as you do, but you just can't give up

hope. I believe in my heart there is an answer for each child. It may be a

different key from child to child. You are doing the right thing: you are

trying something you haven't tried before.

If he is not taking Acetyl-L-carnitine, I suggest you try it. consider the

AC protocol for ALA only, and given your child's tummy issues, considering

doing it transdermal. You are to be commended for not giving up!

[Guest guest]

>

> I feel like I have 2 different lives. The mom that cooks and cleans and runs

the

> kids to school and pretends to her husband, friends and family that everything

> is ok, and the real me scared sh*tless that I'm never going to get him

> recovered.

>   I am so scared...night and day..all the time. What if I never do it?

>  I've never excepted that he's not coming back.

When I was extremely ill and doctors were telling me " people like you don't get

well " and I was getting divorced while too sick to get job and people around me

telling me (in essence) " You can't get divorced, you need his money " , I was

horribly, horribly terrified. I put blinders and dealt with only what I had to

do to get through the immediate future -- today or this week or whatever (short)

time frame made sense. I just didn't spend a lot of time dwelling on how dire

my situation was because I knew if I did that, I wouldn't be able to function at

all. I had to be able to keep putting one foot in front of the other and being

frozen with terror was not going to help anything.

But, having said all that, one thing that kept me holding the course was the

realization that doing nothing was the worst possible thing I could do. There

was nothing but upside to trying to get better. Accepting the normal course of

my condition was far worse. If I did nothing, it was an automatic fail. That

course had zero hope for a better future. The odds were long against me getting

well but it was my *only* hope. So I concluded that I couldn't really fail as I

was already damned, if that makes sense. In other words, if I didn't get

better, that was already thing the entire world was telling me I should expect.

Anything better than that would be glorious, no matter how unlikely.

Peace.

Michele

http://www.healthgazelle.com

http://www.kidslikemine.com

http://www.solanorail.com

[Guest guest]

Hi Kate,

I presume your son has NO mercury amalgam dental fillings. What dose and dosing

frequency were you using when you did oral DMSA? What yeast protocol did you

use? What diets did you try? See if your local library has a copy of Son-Rise

by Barry Neil Kaufman. Please tell us the top three aspects of your son's

autism you find most problematic. We're glad you're here and willing to share

your experience with us.

S S

Re: Anyone else living as 2 people?

Posted by: " Kate Grayce " kategrayce11@... kategrayce11

Fri Sep 10, 2010 8:15 pm (PDT)

My son is 8. He's diagnosed at severe. Diets didn't work, ivig didn't work, iv

chelation didn't work, supplements don't work, oral dmsa killed his gut.... So

that takes out ac .....unless I can do AC with dmps.

We have a hyperbaric chamber, got it a couple of days ago so don't know if it'll

work yet. We did hard chamber dives and he really responded. here's hoping!