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Re: [MedicaidforHDOT] Facts and more facts.

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Lucinda,

Thanks so much for taking the time to tell all of us what you encountered in

Montana in your effort to get some sort of an HBOT capability in your home

where it is so needed.

I had the same experience in Virginia when I was opening a hyperbaric clinic

and the local Lion's Club refused ; me 5 minutes to tell them what the clinic

was all about and how it was meant to help seniors with strokes such as my

wife.

So the challenge is nationwide. Surely something can be done with your

experience. I am hoping that Dr. Bill Duncan and his wife Anita. Will hear

about

it. Anita is Exec. Dir. of the new organization IHMA. which is currently in

the process of getting started.

Meanwhile those suffering brain injuries cannot wait, and the mystery is how

the few opponents of pressurized oxygen therapy can hold back the hundreds

o;f thousands needing the therapy.

I thought the fact that some 30 portable chambers were sent to Afghanistan

recently to deal with high altitude sickness and the 60 which were sent to Iraq

would be made public but so far not a peep. We are keeping secrets fro;m

ourselves and for whose benefit the world wonders. Certainly I remain mystified

by the blocking efforts to this miracle therapy.

Lucinda I suggest you e-mail copies of your letter to Montana's state and

national political leaders,, And send a copy to Gov. Arnold Schwartzneggar. He

may have some inside knowledge on hyperbaric miracles. Manson Capt. USN

Ret.

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I go to all the Greater Cincinnati Autism Meetings for new cases. I get

looked at like I'm crazy. In addition, every time I show up they make a big

speech about how some people (me) just want everyone to do what they are

doing because then they (I) will feel better about it. (hun?) I just keep

going so I can live with myself. But make no mistake, they know about it.

Every time I go they act surprised like I'm way out there, but don't believe

them, they know. These poor people who run our Society have older children

and it has become their life, God forbid there be a cure, What would they

do? Yes, I know what I am accusing them of. And I accuse the doctors of

the same thing. They would have to find new careers, think of the money

they would lose.

However, I no longer get personally involved. I have spent too many hours

with people trying to convince them. It is all for nothing. When I have

gotten someone to try it, it seems their heart isn't in it. They miss too

much, are late, and don't take it seriously. With autism it takes a build up

of at least 30 treatments and sometimes more we have found with no breaks to

see a difference. We will keep putting the information out there but that

is all I have the energy for.

Love to all,

Rose

Re: [MedicaidforHDOT] Facts and more facts.

>

>

> rhartsoe wrote:

>

> " If you go out and begin asking every victim

> of brain injury including stroke, cp, ms, tbi, etc. you would find that

less

> than 5% have ever heard of hbot treatments. Go out and try it yourself,

> everyone. See how many victims know about hbot. Of stroke victims it

is

> probably 1% or less. Of CP it may be as high as 7%. If you are around

an

> area where a center is located, it could go as high as 10 or 12% "

>

>

> I have done this . I attended the local Brain Injury meeting's

> here in Montana this summer, the state BI Conference was coming up and

> was held right here in my town about two weeks ago. They had the

> conference here, because we have a BI Rehab Center that is supposedly

> cutting edge...... just about a mile from my house. I am sure you all

> know where this is going. Everyone I talked to looked at me like I had

> green cheese coming out of me ears. These experts claimed to have never

> heard of hbot for treating brain injury. I am not sure if I believed

> them, or if they just wanted me to go away, but clearly they did not

> want to even HEAR about HBOT. To add insult to injury, I am merely a

> Mom, so health professionals really do not want to hear from me about a

> possible therapy. I have less than zero credibility, because my

> emotions are invested, therefore my opinions and experiences are totally

> discounted. This is the reality, I am just offering the facts of my

> personal experience's here. (no offense intended to those professionals

> on the list. I do realize there are exceptions, but very few.)

>

>

> So long story short: the entire experience for me was extremely

> discouraging. My motives for this effort were entirely selfish, I want a

> chamber in my state for my family, or to find people interested in the

> co-op idea, but in this climate of thinking, forget about it. One very

> sweet elderly woman who has both toxic enceph. and is a stroke victim,

> took pity on me and said, " Whatever you do don't talk to the doctor's in

> charge of the Rehab Center, I am a patient there and they will really

> shoot you down. " She handed me a card for a chiropractor and said,

> " This doctor is helping me more than the rehab center. " A chiropractor!

>

>

> Well, I am now a patient of the chiropractor. He is great, but it ain't

> HBOT. This is the best my entire state has to offer....one lone

> chiropractor?!* I would laugh if it were not so sad.

>

>

> So PLEASE, educate these BI Centers and hospitals! They will not hear

> it or accept it from the patients or the mother's of patients. I would

> hand out brochures all day if I thought it would make a difference. I

> wanted to become involved with the local BI chapter. They even have the

> state office here, but it is too depressing to see so many injuries and

> no one wants to even think about something new, except the patients who

> have no money and no ability to do this on their own.

>

>

> I was not even going to post my recent experiences, but 's post

> today gave me the umph to share this.

>

>

> For some reason, I really hate to buy a home chamber and give up on

> medically supervised treatment, even though I know the home chamber

> would work out great for my family, and it is clearly the most cost

> effective way to go when your whole family is brain injured, as mine is,

> and we have great insurance but they aren't going to pay. So, I guess a

> home chamber is the way to go, because I can not afford to continually

> travel and disrupt my family for HBOT. It makes no sense, and to wait

> for the local's to catch on could take several life times. But, after

> the reactions I received from the professional's I feel like I would

> hide the chamber and what we were doing except from close friends. That

> is pathetic isn't it? I live in a town that advertise's world class,

> cutting edge, brain injury rehab and I am hiding from them. There is

> definitely something wrong with this picture.

>

>

> Lucinda

>

>

>

>

>

>

>

>

>

> _._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._.

> Join the International Hyperbaric Medical Association

http://www.hyperbaricmedicalassociation.org/forms/Friends_of_IHMA_Join.pdf

>

> Unrestricted downloads of 50+ pdf files on HBOT efficacy

medicaid/files/ ,

HDO-documentation/files/ and

http://www.drneubauerhbo.com/papers.htm

>

> Download your state EPSDT program

http://www.hcfa.gov/medicaid/stateplan/Map.asp by doing a search on the word

" ameliorate " . State Medicaid websites

http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver

programs: http://www.geocities.com/HotSprings/Villa/1029/medicaid.html

>

> Find a hyperbaric clinic http://www.netnet.net/mums/hbolist.htm

>

> HBOT can save billions of dollars and millions of heartaches. Subscribe to

by sending a blank email to

mailto:medicaid-subscribe

>

> Unsubscribe? Click here mailto:medicaid-unsubscribe

..

>

>

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Guest guest

rhartsoe wrote:

" If you go out and begin asking every victim

of brain injury including stroke, cp, ms, tbi, etc. you would find that less

than 5% have ever heard of hbot treatments. Go out and try it yourself,

everyone. See how many victims know about hbot. Of stroke victims it is

probably 1% or less. Of CP it may be as high as 7%. If you are around an

area where a center is located, it could go as high as 10 or 12% "

I have done this . I attended the local Brain Injury meeting's

here in Montana this summer, the state BI Conference was coming up and

was held right here in my town about two weeks ago. They had the

conference here, because we have a BI Rehab Center that is supposedly

cutting edge...... just about a mile from my house. I am sure you all

know where this is going. Everyone I talked to looked at me like I had

green cheese coming out of me ears. These experts claimed to have never

heard of hbot for treating brain injury. I am not sure if I believed

them, or if they just wanted me to go away, but clearly they did not

want to even HEAR about HBOT. To add insult to injury, I am merely a

Mom, so health professionals really do not want to hear from me about a

possible therapy. I have less than zero credibility, because my

emotions are invested, therefore my opinions and experiences are totally

discounted. This is the reality, I am just offering the facts of my

personal experience's here. (no offense intended to those professionals

on the list. I do realize there are exceptions, but very few.)

So long story short: the entire experience for me was extremely

discouraging. My motives for this effort were entirely selfish, I want a

chamber in my state for my family, or to find people interested in the

co-op idea, but in this climate of thinking, forget about it. One very

sweet elderly woman who has both toxic enceph. and is a stroke victim,

took pity on me and said, " Whatever you do don't talk to the doctor's in

charge of the Rehab Center, I am a patient there and they will really

shoot you down. " She handed me a card for a chiropractor and said,

" This doctor is helping me more than the rehab center. " A chiropractor!

Well, I am now a patient of the chiropractor. He is great, but it ain't

HBOT. This is the best my entire state has to offer....one lone

chiropractor?!* I would laugh if it were not so sad.

So PLEASE, educate these BI Centers and hospitals! They will not hear

it or accept it from the patients or the mother's of patients. I would

hand out brochures all day if I thought it would make a difference. I

wanted to become involved with the local BI chapter. They even have the

state office here, but it is too depressing to see so many injuries and

no one wants to even think about something new, except the patients who

have no money and no ability to do this on their own.

I was not even going to post my recent experiences, but 's post

today gave me the umph to share this.

For some reason, I really hate to buy a home chamber and give up on

medically supervised treatment, even though I know the home chamber

would work out great for my family, and it is clearly the most cost

effective way to go when your whole family is brain injured, as mine is,

and we have great insurance but they aren't going to pay. So, I guess a

home chamber is the way to go, because I can not afford to continually

travel and disrupt my family for HBOT. It makes no sense, and to wait

for the local's to catch on could take several life times. But, after

the reactions I received from the professional's I feel like I would

hide the chamber and what we were doing except from close friends. That

is pathetic isn't it? I live in a town that advertise's world class,

cutting edge, brain injury rehab and I am hiding from them. There is

definitely something wrong with this picture.

Lucinda

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Guest guest

Have you consider handing out medical, or other, literature about HBOT?

Marie

Re: [MedicaidforHDOT] Facts and more facts.

>

>

> >

> >

> > rhartsoe wrote:

> >

> > " If you go out and begin asking every victim

> > of brain injury including stroke, cp, ms, tbi, etc. you would find that

> less

> > than 5% have ever heard of hbot treatments. Go out and try it

yourself,

> > everyone. See how many victims know about hbot. Of stroke victims it

> is

> > probably 1% or less. Of CP it may be as high as 7%. If you are around

> an

> > area where a center is located, it could go as high as 10 or 12% "

> >

> >

> > I have done this . I attended the local Brain Injury meeting's

> > here in Montana this summer, the state BI Conference was coming up and

> > was held right here in my town about two weeks ago. They had the

> > conference here, because we have a BI Rehab Center that is supposedly

> > cutting edge...... just about a mile from my house. I am sure you all

> > know where this is going. Everyone I talked to looked at me like I had

> > green cheese coming out of me ears. These experts claimed to have never

> > heard of hbot for treating brain injury. I am not sure if I believed

> > them, or if they just wanted me to go away, but clearly they did not

> > want to even HEAR about HBOT. To add insult to injury, I am merely a

> > Mom, so health professionals really do not want to hear from me about a

> > possible therapy. I have less than zero credibility, because my

> > emotions are invested, therefore my opinions and experiences are totally

> > discounted. This is the reality, I am just offering the facts of my

> > personal experience's here. (no offense intended to those professionals

> > on the list. I do realize there are exceptions, but very few.)

> >

> >

> > So long story short: the entire experience for me was extremely

> > discouraging. My motives for this effort were entirely selfish, I want a

> > chamber in my state for my family, or to find people interested in the

> > co-op idea, but in this climate of thinking, forget about it. One very

> > sweet elderly woman who has both toxic enceph. and is a stroke victim,

> > took pity on me and said, " Whatever you do don't talk to the doctor's in

> > charge of the Rehab Center, I am a patient there and they will really

> > shoot you down. " She handed me a card for a chiropractor and said,

> > " This doctor is helping me more than the rehab center. " A chiropractor!

> >

> >

> > Well, I am now a patient of the chiropractor. He is great, but it ain't

> > HBOT. This is the best my entire state has to offer....one lone

> > chiropractor?!* I would laugh if it were not so sad.

> >

> >

> > So PLEASE, educate these BI Centers and hospitals! They will not hear

> > it or accept it from the patients or the mother's of patients. I would

> > hand out brochures all day if I thought it would make a difference. I

> > wanted to become involved with the local BI chapter. They even have the

> > state office here, but it is too depressing to see so many injuries and

> > no one wants to even think about something new, except the patients who

> > have no money and no ability to do this on their own.

> >

> >

> > I was not even going to post my recent experiences, but 's post

> > today gave me the umph to share this.

> >

> >

> > For some reason, I really hate to buy a home chamber and give up on

> > medically supervised treatment, even though I know the home chamber

> > would work out great for my family, and it is clearly the most cost

> > effective way to go when your whole family is brain injured, as mine is,

> > and we have great insurance but they aren't going to pay. So, I guess a

> > home chamber is the way to go, because I can not afford to continually

> > travel and disrupt my family for HBOT. It makes no sense, and to wait

> > for the local's to catch on could take several life times. But, after

> > the reactions I received from the professional's I feel like I would

> > hide the chamber and what we were doing except from close friends. That

> > is pathetic isn't it? I live in a town that advertise's world class,

> > cutting edge, brain injury rehab and I am hiding from them. There is

> > definitely something wrong with this picture.

> >

> >

> > Lucinda

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

_._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._.

> > Join the International Hyperbaric Medical Association

> http://www.hyperbaricmedicalassociation.org/forms/Friends_of_IHMA_Join.pdf

> >

> > Unrestricted downloads of 50+ pdf files on HBOT efficacy

> medicaid/files/ ,

> HDO-documentation/files/ and

> http://www.drneubauerhbo.com/papers.htm

> >

> > Download your state EPSDT program

> http://www.hcfa.gov/medicaid/stateplan/Map.asp by doing a search on the

word

> " ameliorate " . State Medicaid websites

> http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver

> programs: http://www.geocities.com/HotSprings/Villa/1029/medicaid.html

> >

> > Find a hyperbaric clinic http://www.netnet.net/mums/hbolist.htm

> >

> > HBOT can save billions of dollars and millions of heartaches. Subscribe

to

> by sending a blank email to

> mailto:medicaid-subscribe

> >

> > Unsubscribe? Click here

mailto:medicaid-unsubscribe

> .

> >

> >

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Guest guest

Another interesting message!

Best wishes and much love, Ken

Ken Gullan

Institute for Research Integration (IRI)

San Diego, CA 92106-2424

IRI is a 501C(3) non-profit corporation established to help children with

developmental difficulties.

To contact me off-list use kengullan@... or call 619-222-1104

Re: [MedicaidforHDOT] Facts and more facts.

>

>

> >

> >

> > rhartsoe wrote:

> >

> > " If you go out and begin asking every victim

> > of brain injury including stroke, cp, ms, tbi, etc. you would find that

> less

> > than 5% have ever heard of hbot treatments. Go out and try it

yourself,

> > everyone. See how many victims know about hbot. Of stroke victims it

> is

> > probably 1% or less. Of CP it may be as high as 7%. If you are around

> an

> > area where a center is located, it could go as high as 10 or 12% "

> >

> >

> > I have done this . I attended the local Brain Injury meeting's

> > here in Montana this summer, the state BI Conference was coming up and

> > was held right here in my town about two weeks ago. They had the

> > conference here, because we have a BI Rehab Center that is supposedly

> > cutting edge...... just about a mile from my house. I am sure you all

> > know where this is going. Everyone I talked to looked at me like I had

> > green cheese coming out of me ears. These experts claimed to have never

> > heard of hbot for treating brain injury. I am not sure if I believed

> > them, or if they just wanted me to go away, but clearly they did not

> > want to even HEAR about HBOT. To add insult to injury, I am merely a

> > Mom, so health professionals really do not want to hear from me about a

> > possible therapy. I have less than zero credibility, because my

> > emotions are invested, therefore my opinions and experiences are totally

> > discounted. This is the reality, I am just offering the facts of my

> > personal experience's here. (no offense intended to those professionals

> > on the list. I do realize there are exceptions, but very few.)

> >

> >

> > So long story short: the entire experience for me was extremely

> > discouraging. My motives for this effort were entirely selfish, I want a

> > chamber in my state for my family, or to find people interested in the

> > co-op idea, but in this climate of thinking, forget about it. One very

> > sweet elderly woman who has both toxic enceph. and is a stroke victim,

> > took pity on me and said, " Whatever you do don't talk to the doctor's in

> > charge of the Rehab Center, I am a patient there and they will really

> > shoot you down. " She handed me a card for a chiropractor and said,

> > " This doctor is helping me more than the rehab center. " A chiropractor!

> >

> >

> > Well, I am now a patient of the chiropractor. He is great, but it ain't

> > HBOT. This is the best my entire state has to offer....one lone

> > chiropractor?!* I would laugh if it were not so sad.

> >

> >

> > So PLEASE, educate these BI Centers and hospitals! They will not hear

> > it or accept it from the patients or the mother's of patients. I would

> > hand out brochures all day if I thought it would make a difference. I

> > wanted to become involved with the local BI chapter. They even have the

> > state office here, but it is too depressing to see so many injuries and

> > no one wants to even think about something new, except the patients who

> > have no money and no ability to do this on their own.

> >

> >

> > I was not even going to post my recent experiences, but 's post

> > today gave me the umph to share this.

> >

> >

> > For some reason, I really hate to buy a home chamber and give up on

> > medically supervised treatment, even though I know the home chamber

> > would work out great for my family, and it is clearly the most cost

> > effective way to go when your whole family is brain injured, as mine is,

> > and we have great insurance but they aren't going to pay. So, I guess a

> > home chamber is the way to go, because I can not afford to continually

> > travel and disrupt my family for HBOT. It makes no sense, and to wait

> > for the local's to catch on could take several life times. But, after

> > the reactions I received from the professional's I feel like I would

> > hide the chamber and what we were doing except from close friends. That

> > is pathetic isn't it? I live in a town that advertise's world class,

> > cutting edge, brain injury rehab and I am hiding from them. There is

> > definitely something wrong with this picture.

> >

> >

> > Lucinda

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

_._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._.

> > Join the International Hyperbaric Medical Association

> http://www.hyperbaricmedicalassociation.org/forms/Friends_of_IHMA_Join.pdf

> >

> > Unrestricted downloads of 50+ pdf files on HBOT efficacy

> medicaid/files/ ,

> HDO-documentation/files/ and

> http://www.drneubauerhbo.com/papers.htm

> >

> > Download your state EPSDT program

> http://www.hcfa.gov/medicaid/stateplan/Map.asp by doing a search on the

word

> " ameliorate " . State Medicaid websites

> http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver

> programs: http://www.geocities.com/HotSprings/Villa/1029/medicaid.html

> >

> > Find a hyperbaric clinic http://www.netnet.net/mums/hbolist.htm

> >

> > HBOT can save billions of dollars and millions of heartaches. Subscribe

to

> by sending a blank email to

> mailto:medicaid-subscribe

> >

> > Unsubscribe? Click here

mailto:medicaid-unsubscribe

> .

> >

> >

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Guest guest

My apologies, I meant that to go to my wife who I am trying to convince to

support my daughter in doing HBOT more. Sorry! ;-)

Best wishes and much love, Ken

Ken Gullan

Institute for Research Integration (IRI)

San Diego, CA 92106-2424

IRI is a 501C(3) non-profit corporation established to help children with

developmental difficulties.

To contact me off-list use kengullan@... or call 619-222-1104

Re: [MedicaidforHDOT] Facts and more facts.

Have you consider handing out medical, or other, literature about HBOT?

Marie

Share this post


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Guest guest

I always give a letter with what we have seen with our son and my nephew.

And also some web sites address and facts about no side effects and general

info on HDOT. I change it every time hoping to make it better. It just

doesn't seem to matter. It just makes me sad for all the kids that could

get help.

Love to all

Rose

Re: [MedicaidforHDOT] Facts and more facts.

> >

> >

> > >

> > >

> > > rhartsoe wrote:

> > >

> > > " If you go out and begin asking every victim

> > > of brain injury including stroke, cp, ms, tbi, etc. you would find

that

> > less

> > > than 5% have ever heard of hbot treatments. Go out and try it

> yourself,

> > > everyone. See how many victims know about hbot. Of stroke victims

it

> > is

> > > probably 1% or less. Of CP it may be as high as 7%. If you are

around

> > an

> > > area where a center is located, it could go as high as 10 or 12% "

> > >

> > >

> > > I have done this . I attended the local Brain Injury meeting's

> > > here in Montana this summer, the state BI Conference was coming up

and

> > > was held right here in my town about two weeks ago. They had the

> > > conference here, because we have a BI Rehab Center that is supposedly

> > > cutting edge...... just about a mile from my house. I am sure you

all

> > > know where this is going. Everyone I talked to looked at me like I

had

> > > green cheese coming out of me ears. These experts claimed to have

never

> > > heard of hbot for treating brain injury. I am not sure if I believed

> > > them, or if they just wanted me to go away, but clearly they did not

> > > want to even HEAR about HBOT. To add insult to injury, I am merely a

> > > Mom, so health professionals really do not want to hear from me about

a

> > > possible therapy. I have less than zero credibility, because my

> > > emotions are invested, therefore my opinions and experiences are

totally

> > > discounted. This is the reality, I am just offering the facts of my

> > > personal experience's here. (no offense intended to those

professionals

> > > on the list. I do realize there are exceptions, but very few.)

> > >

> > >

> > > So long story short: the entire experience for me was extremely

> > > discouraging. My motives for this effort were entirely selfish, I want

a

> > > chamber in my state for my family, or to find people interested in the

> > > co-op idea, but in this climate of thinking, forget about it. One

very

> > > sweet elderly woman who has both toxic enceph. and is a stroke victim,

> > > took pity on me and said, " Whatever you do don't talk to the doctor's

in

> > > charge of the Rehab Center, I am a patient there and they will really

> > > shoot you down. " She handed me a card for a chiropractor and said,

> > > " This doctor is helping me more than the rehab center. " A

chiropractor!

> > >

> > >

> > > Well, I am now a patient of the chiropractor. He is great, but it

ain't

> > > HBOT. This is the best my entire state has to offer....one lone

> > > chiropractor?!* I would laugh if it were not so sad.

> > >

> > >

> > > So PLEASE, educate these BI Centers and hospitals! They will not hear

> > > it or accept it from the patients or the mother's of patients. I

would

> > > hand out brochures all day if I thought it would make a difference. I

> > > wanted to become involved with the local BI chapter. They even have

the

> > > state office here, but it is too depressing to see so many injuries

and

> > > no one wants to even think about something new, except the patients

who

> > > have no money and no ability to do this on their own.

> > >

> > >

> > > I was not even going to post my recent experiences, but 's post

> > > today gave me the umph to share this.

> > >

> > >

> > > For some reason, I really hate to buy a home chamber and give up on

> > > medically supervised treatment, even though I know the home chamber

> > > would work out great for my family, and it is clearly the most cost

> > > effective way to go when your whole family is brain injured, as mine

is,

> > > and we have great insurance but they aren't going to pay. So, I guess

a

> > > home chamber is the way to go, because I can not afford to continually

> > > travel and disrupt my family for HBOT. It makes no sense, and to wait

> > > for the local's to catch on could take several life times. But, after

> > > the reactions I received from the professional's I feel like I would

> > > hide the chamber and what we were doing except from close friends.

That

> > > is pathetic isn't it? I live in a town that advertise's world class,

> > > cutting edge, brain injury rehab and I am hiding from them. There is

> > > definitely something wrong with this picture.

> > >

> > >

> > > Lucinda

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> _._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._.

> > > Join the International Hyperbaric Medical Association

> >

http://www.hyperbaricmedicalassociation.org/forms/Friends_of_IHMA_Join.pdf

> > >

> > > Unrestricted downloads of 50+ pdf files on HBOT efficacy

> > medicaid/files/ ,

> > HDO-documentation/files/ and

> > http://www.drneubauerhbo.com/papers.htm

> > >

> > > Download your state EPSDT program

> > http://www.hcfa.gov/medicaid/stateplan/Map.asp by doing a search on the

> word

> > " ameliorate " . State Medicaid websites

> > http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver

> > programs: http://www.geocities.com/HotSprings/Villa/1029/medicaid.html

> > >

> > > Find a hyperbaric clinic http://www.netnet.net/mums/hbolist.htm

> > >

> > > HBOT can save billions of dollars and millions of heartaches.

Subscribe

> to

> > by sending a blank email to

> > mailto:medicaid-subscribe

> > >

> > > Unsubscribe? Click here

> mailto:medicaid-unsubscribe

> > .

> > >

> > >

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Guest guest

Would you like for me to forward it to her, Ken? :-)

Re: [MedicaidforHDOT] Facts and more facts.

>

>

> Have you consider handing out medical, or other, literature about

HBOT?

> Marie

>

>

>

>

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Guest guest

Y'know, has an interesting point here and it goes hand-in-hand

with Ed Nemeth's post of a bit ago. What would happen if one or a

group of us drafted a brief but succinct form letter that explained

the benefits of HBOT for neurological (and other) conditions, as well

as the difficulty BI individuals have in accessing this form of

treatment? Then each member of this list and the NeuroHBOT list

would be responsible for printing said letter, along with an

assortment of perhaps 5 articles/studies/testimonials/whatever

(probably all already posted in the Files on this site) and

forwarding the entire packet to their local, state and federal

representatives. This would take a minimum of time, effort and

expense from each of us and, who knows, perhaps we might find someone

who listens. It just takes one person. I think now is the time,

particularly with the upcoming hearing in Washington. The goal is to

give these individuals our perspective in advance rather than have

their opinions formed by others who are less....positive about HBOT

for BI. You can bet those who oppose this treatment will be

contacting every single representative. Also, I regularly see

postings in my local paper saying that my state representatives are

holding open office hours in my area. My guess is that this happens

in most states. Has anyone actually taken it upon themselves to make

an appointment to discuss this issue? Perhaps I am naive so feel

free to blast away but it seems we cannot complain about not being

listened to if we haven't knocked on every door and bent every ear.

Lynn

> Lucinda,

>

> Thanks so much for taking the time to tell all of us what you

encountered in

> Montana in your effort to get some sort of an HBOT capability in

your home

> where it is so needed.

>

> I had the same experience in Virginia when I was opening a

hyperbaric clinic

> and the local Lion's Club refused ; me 5 minutes to tell them what

the clinic

> was all about and how it was meant to help seniors with strokes

such as my

> wife.

>

> So the challenge is nationwide. Surely something can be done with

your

> experience. I am hoping that Dr. Bill Duncan and his wife Anita.

Will hear about

> it. Anita is Exec. Dir. of the new organization IHMA. which is

currently in

> the process of getting started.

>

> Meanwhile those suffering brain injuries cannot wait, and the

mystery is how

> the few opponents of pressurized oxygen therapy can hold back the

hundreds

> o;f thousands needing the therapy.

> I thought the fact that some 30 portable chambers were sent to

Afghanistan

> recently to deal with high altitude sickness and the 60 which were

sent to Iraq

> would be made public but so far not a peep. We are keeping secrets

fro;m

> ourselves and for whose benefit the world wonders. Certainly I

remain mystified

> by the blocking efforts to this miracle therapy.

>

> Lucinda I suggest you e-mail copies of your letter to Montana's

state and

> national political leaders,, And send a copy to Gov. Arnold

Schwartzneggar. He

> may have some inside knowledge on hyperbaric miracles.

Manson Capt. USN

> Ret.

>

>

>

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Guest guest

Good Morning and the list,

Thank you for your supportive words . Once I started typing the

past few months/years of frustration came gushing out. Until I wrote it

down, I did not realize how much the whole situation was bothering me,

and I do realize most people on this list are grappling with a similar

set of circumstances so I don't mean to burden others that are carrying

a similar weight.

In my case, I do not think it is the right time to approach the

political leaders in my state. The way that my family was injured was

very public and the state leadership is well aware of our injuries. If

I started to push them to support hyperbarics it would be a tremendous

task and would take a great deal of energy. Energy I am willing to

expend, but only when I think there is a chance of gaining ground. I

need local allies, which is another reason why I reached out to test the

waters in the brain injury community here. I do think it would be

fairly easy to get patient support, but the experts are another story,

and that is who the political leaders listen to when the sympathetic

brain injured family walks out the door -- they listen to the government

experts.

With that said, I do think the upcoming IHMA Washington conference is

an opportunity for all of us to educate our state political and brain

injury leaders. I am assuming/hoping that the IHMA will provide,

written support/packets for anyone attending the conference, in order

to invite their political and brain injury leaders to the conference. I

believe the conference could showcase hyperbarics as a viable

mainstream medical treatment, and with an organized effort, in a

political year, and some good press, we could gain some ground.

Especially, if we have some government doctors on our side, since as

correctly points out, that is who the senators and congressman

will turn to when the day is done. So, do we have some government

experts, doctors, on our side?

I have not joined the IHMA yet, but I intend to, if this conference

becomes a reality. I want to go to DC in March and personally drag

Montana Senator's Baucus and Burn's right along with me. Hyperbaric's

is that important to my family. As I stated in the earlier e-mail my

whole family suffers from brain injury, toxic enceph, so the money and

the means to follow through can be a real challenge, but we are making

every effort to support the most viable medical treatment we know of--hobt.

Blessings,

Lucinda

FAMANSON@... wrote:

> Lucinda,

>

> Thanks so much for taking the time to tell all of us what you

> encountered in

> Montana in your effort to get some sort of an HBOT capability in your

> home

> where it is so needed.

>

> I had the same experience in Virginia when I was opening a hyperbaric

> clinic

> and the local Lion's Club refused ; me 5 minutes to tell them what the

> clinic

> was all about and how it was meant to help seniors with strokes such

> as my

> wife.

>

> So the challenge is nationwide. Surely something can be done with your

> experience. I am hoping that Dr. Bill Duncan and his wife Anita. Will

> hear about

> it. Anita is Exec. Dir. of the new organization IHMA. which is

> currently in

> the process of getting started.

>

> Meanwhile those suffering brain injuries cannot wait, and the mystery

> is how

> the few opponents of pressurized oxygen therapy can hold back the

> hundreds

> o;f thousands needing the therapy.

> I thought the fact that some 30 portable chambers were sent to

> Afghanistan

> recently to deal with high altitude sickness and the 60 which were

> sent to Iraq

> would be made public but so far not a peep. We are keeping secrets fro;m

> ourselves and for whose benefit the world wonders. Certainly I remain

> mystified

> by the blocking efforts to this miracle therapy.

>

> Lucinda I suggest you e-mail copies of your letter to Montana's state and

> national political leaders,, And send a copy to Gov. Arnold

> Schwartzneggar. He

> may have some inside knowledge on hyperbaric miracles. Manson

> Capt. USN

> Ret.

>

>

>

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