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I just called and was told the AHI was purchased by VanGuard. They will resume

CCSVI in January and they have a new program that focuses more on CCSVI for MS.

Lifeguard does not know yet what insurance they will take. The girl that I

talked with said that the stories of bankruptcy were falsely reported.

>

> OMG! I just got the application. We're going to see more of these situations

in the future. I think the clinic who does this does it at the AHI and they

might still be doing this somewhere else. I'm going to call today.

>

>

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I just called and was told the AHI was purchased by VanGuard. They will resume

CCSVI in January and they have a new program that focuses more on CCSVI for MS.

Lifeguard does not know yet what insurance they will take. The girl that I

talked with said that the stories of bankruptcy were falsely reported.

>

> OMG! I just got the application. We're going to see more of these situations

in the future. I think the clinic who does this does it at the AHI and they

might still be doing this somewhere else. I'm going to call today.

>

>

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Share on other sites

I just called and was told the AHI was purchased by VanGuard. They will resume

CCSVI in January and they have a new program that focuses more on CCSVI for MS.

Lifeguard does not know yet what insurance they will take. The girl that I

talked with said that the stories of bankruptcy were falsely reported.

>

> OMG! I just got the application. We're going to see more of these situations

in the future. I think the clinic who does this does it at the AHI and they

might still be doing this somewhere else. I'm going to call today.

>

>

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Thank goodness! I hope they notify the people who are upset not only by

their procedure being halted but also reimburse them their money if they

choose to go elsewhere. What attracted me to the AHI was the drs being

cardios.

Cait

>

>

> I just called and was told the AHI was purchased by VanGuard. They will

> resume CCSVI in January and they have a new program that focuses more on

> CCSVI for MS. Lifeguard does not know yet what insurance they will take. The

> girl that I talked with said that the stories of bankruptcy were falsely

> reported.

>

>

>

> >

> > OMG! I just got the application. We're going to see more of these

> situations in the future. I think the clinic who does this does it at the

> AHI and they might still be doing this somewhere else. I'm going to call

> today.

> >

> >

>

>

>

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Thank goodness! I hope they notify the people who are upset not only by

their procedure being halted but also reimburse them their money if they

choose to go elsewhere. What attracted me to the AHI was the drs being

cardios.

Cait

>

>

> I just called and was told the AHI was purchased by VanGuard. They will

> resume CCSVI in January and they have a new program that focuses more on

> CCSVI for MS. Lifeguard does not know yet what insurance they will take. The

> girl that I talked with said that the stories of bankruptcy were falsely

> reported.

>

>

>

> >

> > OMG! I just got the application. We're going to see more of these

> situations in the future. I think the clinic who does this does it at the

> AHI and they might still be doing this somewhere else. I'm going to call

> today.

> >

> >

>

>

>

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Share on other sites

Thank goodness! I hope they notify the people who are upset not only by

their procedure being halted but also reimburse them their money if they

choose to go elsewhere. What attracted me to the AHI was the drs being

cardios.

Cait

>

>

> I just called and was told the AHI was purchased by VanGuard. They will

> resume CCSVI in January and they have a new program that focuses more on

> CCSVI for MS. Lifeguard does not know yet what insurance they will take. The

> girl that I talked with said that the stories of bankruptcy were falsely

> reported.

>

>

>

> >

> > OMG! I just got the application. We're going to see more of these

> situations in the future. I think the clinic who does this does it at the

> AHI and they might still be doing this somewhere else. I'm going to call

> today.

> >

> >

>

>

>

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They may have the same staff. It is LifeGaurd clinic who does the CCSVI at the

AHI. Call them for more information.

>

> Thank goodness! I hope they notify the people who are upset not only by

> their procedure being halted but also reimburse them their money if they

> choose to go elsewhere. What attracted me to the AHI was the drs being

> cardios.

>

> Cait

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They may have the same staff. It is LifeGaurd clinic who does the CCSVI at the

AHI. Call them for more information.

>

> Thank goodness! I hope they notify the people who are upset not only by

> their procedure being halted but also reimburse them their money if they

> choose to go elsewhere. What attracted me to the AHI was the drs being

> cardios.

>

> Cait

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They may have the same staff. It is LifeGaurd clinic who does the CCSVI at the

AHI. Call them for more information.

>

> Thank goodness! I hope they notify the people who are upset not only by

> their procedure being halted but also reimburse them their money if they

> choose to go elsewhere. What attracted me to the AHI was the drs being

> cardios.

>

> Cait

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even though lifeguard said that they did not go bankrupt, the newspaper in

phoenix (the arizona republic) said that they did file chapter 11 as part of

their agreement with the new buyers so that they did not incur the debt of the

AZHI.

Re: Re: CCSVI

Thank goodness! I hope they notify the people who are upset not only by

their procedure being halted but also reimburse them their money if they

choose to go elsewhere. What attracted me to the AHI was the drs being

cardios.

Cait

>

>

> I just called and was told the AHI was purchased by VanGuard. They will

> resume CCSVI in January and they have a new program that focuses more on

> CCSVI for MS. Lifeguard does not know yet what insurance they will take. The

> girl that I talked with said that the stories of bankruptcy were falsely

> reported.

>

>

>

> >

> > OMG! I just got the application. We're going to see more of these

> situations in the future. I think the clinic who does this does it at the

> AHI and they might still be doing this somewhere else. I'm going to call

> today.

> >

> >

>

>

>

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Share on other sites

even though lifeguard said that they did not go bankrupt, the newspaper in

phoenix (the arizona republic) said that they did file chapter 11 as part of

their agreement with the new buyers so that they did not incur the debt of the

AZHI.

Re: Re: CCSVI

Thank goodness! I hope they notify the people who are upset not only by

their procedure being halted but also reimburse them their money if they

choose to go elsewhere. What attracted me to the AHI was the drs being

cardios.

Cait

>

>

> I just called and was told the AHI was purchased by VanGuard. They will

> resume CCSVI in January and they have a new program that focuses more on

> CCSVI for MS. Lifeguard does not know yet what insurance they will take. The

> girl that I talked with said that the stories of bankruptcy were falsely

> reported.

>

>

>

> >

> > OMG! I just got the application. We're going to see more of these

> situations in the future. I think the clinic who does this does it at the

> AHI and they might still be doing this somewhere else. I'm going to call

> today.

> >

> >

>

>

>

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Share on other sites

even though lifeguard said that they did not go bankrupt, the newspaper in

phoenix (the arizona republic) said that they did file chapter 11 as part of

their agreement with the new buyers so that they did not incur the debt of the

AZHI.

Re: Re: CCSVI

Thank goodness! I hope they notify the people who are upset not only by

their procedure being halted but also reimburse them their money if they

choose to go elsewhere. What attracted me to the AHI was the drs being

cardios.

Cait

>

>

> I just called and was told the AHI was purchased by VanGuard. They will

> resume CCSVI in January and they have a new program that focuses more on

> CCSVI for MS. Lifeguard does not know yet what insurance they will take. The

> girl that I talked with said that the stories of bankruptcy were falsely

> reported.

>

>

>

> >

> > OMG! I just got the application. We're going to see more of these

> situations in the future. I think the clinic who does this does it at the

> AHI and they might still be doing this somewhere else. I'm going to call

> today.

> >

> >

>

>

>

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Share on other sites

I talked to live person who said they're still in business. Newspapers don't

always have the facts. It doesn't matter to me what the deal was as long as

CCSVI is still performed there.

> > >

> > > OMG! I just got the application. We're going to see more of these

> > situations in the future. I think the clinic who does this does it at the

> > AHI and they might still be doing this somewhere else. I'm going to call

> > today.

> > >

> > >

> >

> >

> >

>

>

Link to comment
Share on other sites

I talked to live person who said they're still in business. Newspapers don't

always have the facts. It doesn't matter to me what the deal was as long as

CCSVI is still performed there.

> > >

> > > OMG! I just got the application. We're going to see more of these

> > situations in the future. I think the clinic who does this does it at the

> > AHI and they might still be doing this somewhere else. I'm going to call

> > today.

> > >

> > >

> >

> >

> >

>

>

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Share on other sites

I talked to live person who said they're still in business. Newspapers don't

always have the facts. It doesn't matter to me what the deal was as long as

CCSVI is still performed there.

> > >

> > > OMG! I just got the application. We're going to see more of these

> > situations in the future. I think the clinic who does this does it at the

> > AHI and they might still be doing this somewhere else. I'm going to call

> > today.

> > >

> > >

> >

> >

> >

>

>

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i received an email from dr. edward diethrich yesterday explaining what had

happened and how he was attempting to re-establish ccsvi. it will be up to

vanguard as they will have the final word.

Re: CCSVI

I talked to live person who said they're still in business. Newspapers don't

always have the facts. It doesn't matter to me what the deal was as long as

CCSVI is still performed there.

> > >

> > > OMG! I just got the application. We're going to see more of these

> > situations in the future. I think the clinic who does this does it at the

> > AHI and they might still be doing this somewhere else. I'm going to call

> > today.

> > >

> > >

> >

> >

> >

>

>

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A while back someone posted a specific thread within the This is MS CCSVI forum

where there were lists of people's experiences pre and post CCSVI procedure,

including how long they had MS and what they experienced after the procedure,

etc. I cannot find that thread now. Can anyone link me to it? Thanks.

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OK, never mind I found it.

________________________________

To: mscured

Sent: Wed, November 17, 2010 7:00:51 PM

Subject: CCSVI

A while back someone posted a specific thread within the This is MS CCSVI forum

where there were lists of people's experiences pre and post CCSVI procedure,

including how long they had MS and what they experienced after the procedure,

etc. I cannot find that thread now. Can anyone link me to it? Thanks.

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Share on other sites

OK, never mind I found it.

________________________________

To: mscured

Sent: Wed, November 17, 2010 7:00:51 PM

Subject: CCSVI

A while back someone posted a specific thread within the This is MS CCSVI forum

where there were lists of people's experiences pre and post CCSVI procedure,

including how long they had MS and what they experienced after the procedure,

etc. I cannot find that thread now. Can anyone link me to it? Thanks.

Link to comment
Share on other sites

OK, never mind I found it.

________________________________

To: mscured

Sent: Wed, November 17, 2010 7:00:51 PM

Subject: CCSVI

A while back someone posted a specific thread within the This is MS CCSVI forum

where there were lists of people's experiences pre and post CCSVI procedure,

including how long they had MS and what they experienced after the procedure,

etc. I cannot find that thread now. Can anyone link me to it? Thanks.

Link to comment
Share on other sites

It is hard, isn't it, when everything you read is about CCSVI. It used to drive

me mad especially as I was so against any invasive treatment and it was still

turning up in alternative groups although it is mainstream. In the end I

thought if you can't beat 'em, join 'em.

Quite by chance I feel I have done things in the right order.

Attacked diet and my allergies/food intolerances.

Started daily routined exercise.

Had my amalgams removed.

Took vitamin D and all the other suggested supplements.

Changed my lifestyle to get rid of stress.

Added medicinal marijuana (I am in one of the places it is OK).

Checked into heavy metal toxicity and am doing an on-going detox programme.

Got tested for Lyme Disease, Syndrome and a bunch of others that mimic

MS.

I did all these things that we already knew about with the exception of LDN

which I had on the back-burner.

THEN did CCSVI testing and treatment. I chose Poland as they had good surgeons

and track record.

If that doesn't sort you out I am at a loss as to know what else will.

People who aren't improved after CCSVI treatment or who indeed don't have CCSVI,

maybe don't have MS? Just a thought.

Janet

To: mscured

From: alansamston@...

It is still very hard for me to get a grasp on this. At first I was not

interested as I am into the natural things and it seemed invasive and hard to

find in the U.S., etc.

But now it seems every post is about CCSVI, to the point nobody is even talking

about Vitamin D, BBD, Ldn, Amalgam removal, etc.

I have read (skimmed) through many of the testimonials and there seems to be

quite a varied response. Some people report great improvement, others report

little improvement, and others report some complications such as shoulder pain

for months after the procedure. It is still a bit daunting to me and hard to put

together that all the things we have been writing about for years (Vitamin D,

Detox, Diet, etc) were not the answer? And yet there are people who remain in

complete remission without CCSVI.

It is also tough not to know which doctor has the most skill with this

procedure. As we all know, the skill of the doctor can make much of the

difference in outcome.

Link to comment
Share on other sites

It is hard, isn't it, when everything you read is about CCSVI. It used to drive

me mad especially as I was so against any invasive treatment and it was still

turning up in alternative groups although it is mainstream. In the end I

thought if you can't beat 'em, join 'em.

Quite by chance I feel I have done things in the right order.

Attacked diet and my allergies/food intolerances.

Started daily routined exercise.

Had my amalgams removed.

Took vitamin D and all the other suggested supplements.

Changed my lifestyle to get rid of stress.

Added medicinal marijuana (I am in one of the places it is OK).

Checked into heavy metal toxicity and am doing an on-going detox programme.

Got tested for Lyme Disease, Syndrome and a bunch of others that mimic

MS.

I did all these things that we already knew about with the exception of LDN

which I had on the back-burner.

THEN did CCSVI testing and treatment. I chose Poland as they had good surgeons

and track record.

If that doesn't sort you out I am at a loss as to know what else will.

People who aren't improved after CCSVI treatment or who indeed don't have CCSVI,

maybe don't have MS? Just a thought.

Janet

To: mscured

From: alansamston@...

It is still very hard for me to get a grasp on this. At first I was not

interested as I am into the natural things and it seemed invasive and hard to

find in the U.S., etc.

But now it seems every post is about CCSVI, to the point nobody is even talking

about Vitamin D, BBD, Ldn, Amalgam removal, etc.

I have read (skimmed) through many of the testimonials and there seems to be

quite a varied response. Some people report great improvement, others report

little improvement, and others report some complications such as shoulder pain

for months after the procedure. It is still a bit daunting to me and hard to put

together that all the things we have been writing about for years (Vitamin D,

Detox, Diet, etc) were not the answer? And yet there are people who remain in

complete remission without CCSVI.

It is also tough not to know which doctor has the most skill with this

procedure. As we all know, the skill of the doctor can make much of the

difference in outcome.

Link to comment
Share on other sites

It is hard, isn't it, when everything you read is about CCSVI. It used to drive

me mad especially as I was so against any invasive treatment and it was still

turning up in alternative groups although it is mainstream. In the end I

thought if you can't beat 'em, join 'em.

Quite by chance I feel I have done things in the right order.

Attacked diet and my allergies/food intolerances.

Started daily routined exercise.

Had my amalgams removed.

Took vitamin D and all the other suggested supplements.

Changed my lifestyle to get rid of stress.

Added medicinal marijuana (I am in one of the places it is OK).

Checked into heavy metal toxicity and am doing an on-going detox programme.

Got tested for Lyme Disease, Syndrome and a bunch of others that mimic

MS.

I did all these things that we already knew about with the exception of LDN

which I had on the back-burner.

THEN did CCSVI testing and treatment. I chose Poland as they had good surgeons

and track record.

If that doesn't sort you out I am at a loss as to know what else will.

People who aren't improved after CCSVI treatment or who indeed don't have CCSVI,

maybe don't have MS? Just a thought.

Janet

To: mscured

From: alansamston@...

It is still very hard for me to get a grasp on this. At first I was not

interested as I am into the natural things and it seemed invasive and hard to

find in the U.S., etc.

But now it seems every post is about CCSVI, to the point nobody is even talking

about Vitamin D, BBD, Ldn, Amalgam removal, etc.

I have read (skimmed) through many of the testimonials and there seems to be

quite a varied response. Some people report great improvement, others report

little improvement, and others report some complications such as shoulder pain

for months after the procedure. It is still a bit daunting to me and hard to put

together that all the things we have been writing about for years (Vitamin D,

Detox, Diet, etc) were not the answer? And yet there are people who remain in

complete remission without CCSVI.

It is also tough not to know which doctor has the most skill with this

procedure. As we all know, the skill of the doctor can make much of the

difference in outcome.

Link to comment
Share on other sites

I think we need to remember there are stories of healing through other methods

such as chelation, fasting, biodenitcal hormone therapy, calcium eap injections

3x per week, Klenner protocol, vegan diet, and for some BBD alone is enough.

________________________________

To: MS-Cured <mscured >

Sent: Thu, November 18, 2010 12:34:52 PM

Subject: RE: CCSVI

 

It is hard, isn't it, when everything you read is about CCSVI. It used to drive

me mad especially as I was so against any invasive treatment and it was still

turning up in alternative groups although it is mainstream. In the end I thought

if you can't beat 'em, join 'em.

Quite by chance I feel I have done things in the right order.

Attacked diet and my allergies/food intolerances.

Started daily routined exercise.

Had my amalgams removed.

Took vitamin D and all the other suggested supplements.

Changed my lifestyle to get rid of stress.

Added medicinal marijuana (I am in one of the places it is OK).

Checked into heavy metal toxicity and am doing an on-going detox programme.

Got tested for Lyme Disease, Syndrome and a bunch of others that mimic

MS.

I did all these things that we already knew about with the exception of LDN

which I had on the back-burner.

THEN did CCSVI testing and treatment. I chose Poland as they had good surgeons

and track record.

If that doesn't sort you out I am at a loss as to know what else will.

People who aren't improved after CCSVI treatment or who indeed don't have CCSVI,

maybe don't have MS? Just a thought.

Janet

To: mscured

From: alansamston@...

It is still very hard for me to get a grasp on this. At first I was not

interested as I am into the natural things and it seemed invasive and hard to

find in the U.S., etc.

But now it seems every post is about CCSVI, to the point nobody is even talking

about Vitamin D, BBD, Ldn, Amalgam removal, etc.

I have read (skimmed) through many of the testimonials and there seems to be

quite a varied response. Some people report great improvement, others report

little improvement, and others report some complications such as shoulder pain

for months after the procedure. It is still a bit daunting to me and hard to put

together that all the things we have been writing about for years (Vitamin D,

Detox, Diet, etc) were not the answer? And yet there are people who remain in

complete remission without CCSVI.

It is also tough not to know which doctor has the most skill with this

procedure. As we all know, the skill of the doctor can make much of the

difference in outcome.

Link to comment
Share on other sites

I think we need to remember there are stories of healing through other methods

such as chelation, fasting, biodenitcal hormone therapy, calcium eap injections

3x per week, Klenner protocol, vegan diet, and for some BBD alone is enough.

________________________________

To: MS-Cured <mscured >

Sent: Thu, November 18, 2010 12:34:52 PM

Subject: RE: CCSVI

 

It is hard, isn't it, when everything you read is about CCSVI. It used to drive

me mad especially as I was so against any invasive treatment and it was still

turning up in alternative groups although it is mainstream. In the end I thought

if you can't beat 'em, join 'em.

Quite by chance I feel I have done things in the right order.

Attacked diet and my allergies/food intolerances.

Started daily routined exercise.

Had my amalgams removed.

Took vitamin D and all the other suggested supplements.

Changed my lifestyle to get rid of stress.

Added medicinal marijuana (I am in one of the places it is OK).

Checked into heavy metal toxicity and am doing an on-going detox programme.

Got tested for Lyme Disease, Syndrome and a bunch of others that mimic

MS.

I did all these things that we already knew about with the exception of LDN

which I had on the back-burner.

THEN did CCSVI testing and treatment. I chose Poland as they had good surgeons

and track record.

If that doesn't sort you out I am at a loss as to know what else will.

People who aren't improved after CCSVI treatment or who indeed don't have CCSVI,

maybe don't have MS? Just a thought.

Janet

To: mscured

From: alansamston@...

It is still very hard for me to get a grasp on this. At first I was not

interested as I am into the natural things and it seemed invasive and hard to

find in the U.S., etc.

But now it seems every post is about CCSVI, to the point nobody is even talking

about Vitamin D, BBD, Ldn, Amalgam removal, etc.

I have read (skimmed) through many of the testimonials and there seems to be

quite a varied response. Some people report great improvement, others report

little improvement, and others report some complications such as shoulder pain

for months after the procedure. It is still a bit daunting to me and hard to put

together that all the things we have been writing about for years (Vitamin D,

Detox, Diet, etc) were not the answer? And yet there are people who remain in

complete remission without CCSVI.

It is also tough not to know which doctor has the most skill with this

procedure. As we all know, the skill of the doctor can make much of the

difference in outcome.

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