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I would like to say a big `thank you' to those responsible

for the group. I can say categorically that I have gained more

understanding of the condition from using this site than from the

most of the consultants I have seen.

All, bar one, have seemed totally unaware of the many idiosyncrasies

of the condition; many of these are commonly discussed by the group.

I agree with a previous contributor who felt that resources such as

these go largely untapped by the medical profession. I presume that

they are probably more interested in `academic' issues than

exploring human-interest stories.

In this respect, I have found the AF database interesting and

helpful. On a personal note, I have recently seen a cardiologist who

specialises in arryrthmias (although not an out-and-out EP) and, at

least, we were `talking' the same language. A sad indictment

of the situation in Britain is that I waited nine months to see him.

In this time I suffered two further episodes!

Has anyone else met the same blank stares in the consulting room?

in Wales

40M-flec 100mg per day-warfarin 3mg per day-magnesium and omega-3

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I could not agree with you more with this one. I am

surprised that

as you life in Wales they know what AF is, I am serious on

this and not taking the Micky. I live in London and went

through a series of Drs both NHS and private and only the web

saved me after making

contact with A Dr in the USA, I able to make contact with

an Ep In London. Up to that Point I did not know what an EP

was or there were such Dr.

It was so insane in the end that I was complaining of Pain in

my chest, shortness of breath extreme tiredness and was

Categorically informed in no uncertain terms this was

nothing to

do with AF. YEA and pigs Fly Honest.

I have leaned to my great cost,what ever is wrong with you go

to a Dr who

works in that area, not somebody who dabbles.

C Uk

Ps I ended up in France for my treatment.

>

>I would like to say a big `thank you' to those responsible

>for the group. I can say categorically that I have gained

more

>understanding of the condition from using this site than

from the

>most of the consultants I have seen.

>

>All, bar one, have seemed totally unaware of the many

idiosyncrasies

>of the condition; many of these are commonly discussed by

the group.

>I agree with a previous contributor who felt that resources

such as

>these go largely untapped by the medical profession. I

presume that

>they are probably more interested in `academic' issues than

>exploring human-interest stories.

>

>In this respect, I have found the AF database interesting

and

>helpful. On a personal note, I have recently seen a

cardiologist who

>specializes in arryrthmias (although not an out-and-out EP)

and, at

>least, we were `talking' the same language. A sad indictment

>of the situation in Britain is that I waited nine months to

see him.

>In this time I suffered two further episodes!

>

>Has anyone else met the same blank stares in the consulting

room?

>

> in Wales

>40M-flec 100mg per day-warfarin 3mg per day-magnesium and

omega-3

>

>

>

>

>>

Codling

Hornchurch Essex England

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Guest guest

I could not agree with you more with this one. I am

surprised that

as you life in Wales they know what AF is, I am serious on

this and not taking the Micky. I live in London and went

through a series of Drs both NHS and private and only the web

saved me after making

contact with A Dr in the USA, I able to make contact with

an Ep In London. Up to that Point I did not know what an EP

was or there were such Dr.

It was so insane in the end that I was complaining of Pain in

my chest, shortness of breath extreme tiredness and was

Categorically informed in no uncertain terms this was

nothing to

do with AF. YEA and pigs Fly Honest.

I have leaned to my great cost,what ever is wrong with you go

to a Dr who

works in that area, not somebody who dabbles.

C Uk

Ps I ended up in France for my treatment.

>

>I would like to say a big `thank you' to those responsible

>for the group. I can say categorically that I have gained

more

>understanding of the condition from using this site than

from the

>most of the consultants I have seen.

>

>All, bar one, have seemed totally unaware of the many

idiosyncrasies

>of the condition; many of these are commonly discussed by

the group.

>I agree with a previous contributor who felt that resources

such as

>these go largely untapped by the medical profession. I

presume that

>they are probably more interested in `academic' issues than

>exploring human-interest stories.

>

>In this respect, I have found the AF database interesting

and

>helpful. On a personal note, I have recently seen a

cardiologist who

>specializes in arryrthmias (although not an out-and-out EP)

and, at

>least, we were `talking' the same language. A sad indictment

>of the situation in Britain is that I waited nine months to

see him.

>In this time I suffered two further episodes!

>

>Has anyone else met the same blank stares in the consulting

room?

>

> in Wales

>40M-flec 100mg per day-warfarin 3mg per day-magnesium and

omega-3

>

>

>

>

>>

Codling

Hornchurch Essex England

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Guest guest

I could not agree with you more with this one. I am

surprised that

as you life in Wales they know what AF is, I am serious on

this and not taking the Micky. I live in London and went

through a series of Drs both NHS and private and only the web

saved me after making

contact with A Dr in the USA, I able to make contact with

an Ep In London. Up to that Point I did not know what an EP

was or there were such Dr.

It was so insane in the end that I was complaining of Pain in

my chest, shortness of breath extreme tiredness and was

Categorically informed in no uncertain terms this was

nothing to

do with AF. YEA and pigs Fly Honest.

I have leaned to my great cost,what ever is wrong with you go

to a Dr who

works in that area, not somebody who dabbles.

C Uk

Ps I ended up in France for my treatment.

>

>I would like to say a big `thank you' to those responsible

>for the group. I can say categorically that I have gained

more

>understanding of the condition from using this site than

from the

>most of the consultants I have seen.

>

>All, bar one, have seemed totally unaware of the many

idiosyncrasies

>of the condition; many of these are commonly discussed by

the group.

>I agree with a previous contributor who felt that resources

such as

>these go largely untapped by the medical profession. I

presume that

>they are probably more interested in `academic' issues than

>exploring human-interest stories.

>

>In this respect, I have found the AF database interesting

and

>helpful. On a personal note, I have recently seen a

cardiologist who

>specializes in arryrthmias (although not an out-and-out EP)

and, at

>least, we were `talking' the same language. A sad indictment

>of the situation in Britain is that I waited nine months to

see him.

>In this time I suffered two further episodes!

>

>Has anyone else met the same blank stares in the consulting

room?

>

> in Wales

>40M-flec 100mg per day-warfarin 3mg per day-magnesium and

omega-3

>

>

>

>

>>

Codling

Hornchurch Essex England

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Guest guest

My AF episodes were diagnosed quickly at our local General hospital

in Cheshire. When it was decided that I might need an ablation by

the cardiologists there, I was referred to Wythenshawe Hospital, a

South Manchester University Hospital. It took less than two months to

see a real EP, but then had to be referred to a cardio-thoracic

surgeon because a defect was found. Now I am going to be operated on

by Steve Hunter in the Cook University Hospital, Middlesbro.

Apart from knowing about my defect, he has also been trained recently

in microwave abalation by Adam Saltman of Massachusetts. Seems I may

have struck lucky - except that I have been waiting since mid-March

for the op for a condition which can be fatal.

Best wishes

Sue

>

> I could not agree with you more with this one. I am

> surprised that

> as you life in Wales they know what AF is, I am serious on

> this and not taking the Micky. I live in London and went

> through a series of Drs both NHS and private and only the web

> saved me after making

> contact with A Dr in the USA, I able to make contact with

> an Ep In London. Up to that Point I did not know what an EP

> was or there were such Dr.

>

> It was so insane in the end that I was complaining of Pain in

> my chest, shortness of breath extreme tiredness and was

> Categorically informed in no uncertain terms this was

> nothing to

> do with AF. YEA and pigs Fly Honest.

>

>

> I have leaned to my great cost,what ever is wrong with you go

> to a Dr who

> works in that area, not somebody who dabbles.

>

> C Uk

> Ps I ended up in France for my treatment.

>

>

> >

> >I would like to say a big `thank you' to those responsible

> >for the group. I can say categorically that I have gained

> more

> >understanding of the condition from using this site than

> from the

> >most of the consultants I have seen.

> >

> >All, bar one, have seemed totally unaware of the many

> idiosyncrasies

> >of the condition; many of these are commonly discussed by

> the group.

> >I agree with a previous contributor who felt that resources

> such as

> >these go largely untapped by the medical profession. I

> presume that

> >they are probably more interested in `academic' issues than

> >exploring human-interest stories.

> >

> >In this respect, I have found the AF database interesting

> and

> >helpful. On a personal note, I have recently seen a

> cardiologist who

> >specializes in arryrthmias (although not an out-and-out EP)

> and, at

> >least, we were `talking' the same language. A sad indictment

> >of the situation in Britain is that I waited nine months to

> see him.

> >In this time I suffered two further episodes!

> >

> >Has anyone else met the same blank stares in the consulting

> room?

> >

> > in Wales

> >40M-flec 100mg per day-warfarin 3mg per day-magnesium and

> omega-3

> >

> >

> >

> >

> >>

> Codling

> Hornchurch Essex England

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