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Why would a hitherto healthy muscle will suddenly stop working?

The nerves... Why would the nerves work?\

Maybe someone messed them up. But who... No one messed with my nerves...Hang on. I had three root canals at the dentist in the past five years... They kill the nerve....and when I get the so called spasm, it goes from chest to jaw!

Just wondering if there is a thread...Had any of you undergone root treatments in the years before the onset of A?

Dorian Wolfson, London.

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Questions about the possible causes come up here frequently and most

of us would like to understand better, where their " A " is coming from.

The most recent examples in this group are the root treatment and

Amalgan. However it seems to be unlikely, since 1. there are much more

people with Amalgan and/or a root treatment than with " A " . On the

other hand each poll in this group that asked for possible causes

showed that there are many people without the possible cause.

There are even web-pages discussing " A " of pets. Pets usually don't

have Amalgan or root treatments. They also don't take anti-depressiva

or drugs or things like that.

And it is even unclear if there is only one reason. Since the symptoms

differ between the people with " A " it is also possible that there is

more than one reason.

In short, I fear with polls like this we cannot find the reason. This

would require a systematic study with high statistics, e.g. a high

number of people with " A " .

Lars.

>

>

> Why would a hitherto healthy muscle will suddenly stop working?

>

> The nerves... Why would the nerves work?\

>

> Maybe someone messed them up. But who... No one messed with my

nerves...Hang on. I had three root canals at the dentist in the past

five years... They kill the nerve....and when I get the so called

spasm, it goes from chest to jaw!

>

>

>

> Just wondering if there is a thread...Had any of you undergone root

treatments in the years before the onset of A?

>

> Dorian Wolfson, London.

>

>

>

>

>

>

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I agree with Lars' reasoning.

Some of us have asthma, some don't.

Some have allergies, some don't.

Some have had Chicken Pox (varicella), some haven't.

Some have had recurrent infection problems (tonsillitis, etc.), some haven't.

Some have autoimmune disorders, some don't.

Some are old, some are young.

Some are overweight, some are normal, some are thin.

You get the idea.

Personally, I've never had a root canal and I doubt I'll ever need one. I did, however, have over a decade of constant tonsillitis / strep infections and ear infections. I do have allergies, but I don't have asthma, I haven't had Chicken Pox, and I was in my mid-20's when my symptoms first showed up.

Debbi in Michigan

Questions about the possible causes come up here frequently and mostof us would like to understand better, where their "A" is coming from.The most recent examples in this group are the root treatment andAmalgan. However it seems to be unlikely, since 1. there are much morepeople with Amalgan and/or a root treatment than with "A". On theother hand each poll in this group that asked for possible causesshowed that there are many people without the possible cause.There are even web-pages discussing "A" of pets. Pets usually don'thave Amalgan or root treatments. They also don't take anti-depressivaor drugs or things like that.And it is even unclear if there is only one reason. Since the symptomsdiffer between the people with "A" it is also possible that there ismore than one reason.In short, I fear with polls like this we cannot find the reason. Thiswould require a systematic study with high statistics, e.g. a highnumber of people with "A".Lars.

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And if everybody with " A " had chickenpox, or allergies or something

else (which seems not to be the case),then there would be still the

question " Why only we? Why is " A " so rare? " , since all of this

possible causes are much, much more common than " A " .

Lars.

> I agree with Lars' reasoning.

>

> Some of us have asthma, some don't.

> Some have allergies, some don't.

> Some have had Chicken Pox (varicella), some haven't.

> Some have had recurrent infection problems (tonsillitis, etc.), some

haven't.

> Some have autoimmune disorders, some don't.

> Some are old, some are young.

> Some are overweight, some are normal, some are thin.

> You get the idea.

>

> Personally, I've never had a root canal and I doubt I'll ever need

one. I did, however, have over a decade of constant tonsillitis /

strep infections and ear infections. I do have allergies, but I don't

have asthma, I haven't had Chicken Pox, and I was in my mid-20's when

my symptoms first showed up.

>

> Debbi in Michigan

> Questions about the possible causes come up here frequently and

most

> of us would like to understand better, where their " A " is coming

from.

>

> The most recent examples in this group are the root treatment and

> Amalgan. However it seems to be unlikely, since 1. there are much

more

> people with Amalgan and/or a root treatment than with " A " . On the

> other hand each poll in this group that asked for possible causes

> showed that there are many people without the possible cause.

>

> There are even web-pages discussing " A " of pets. Pets usually

don't

> have Amalgan or root treatments. They also don't take

anti-depressiva

> or drugs or things like that.

>

> And it is even unclear if there is only one reason. Since the

symptoms

> differ between the people with " A " it is also possible that there

is

> more than one reason.

>

> In short, I fear with polls like this we cannot find the reason.

This

> would require a systematic study with high statistics, e.g. a high

> number of people with " A " .

>

> Lars.

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--- Hi,

I have never had any root treatments.

Jenifer

In achalasia , dennis matt <iopt182@y...> wrote:

>

>

> Why would a hitherto healthy muscle will suddenly stop working?

>

> The nerves... Why would the nerves work?\

>

> Maybe someone messed them up. But who... No one messed with my

nerves...Hang on. I had three root canals at the dentist in the past

five years... They kill the nerve....and when I get the so called

spasm, it goes from chest to jaw!

>

>

>

> Just wondering if there is a thread...Had any of you undergone root

treatments in the years before the onset of A?

>

> Dorian Wolfson, London.

>

>

>

>

>

>

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--

Hi,

Debbi said something that made me think. In the beginning

of my problem I swore it came from an ear infection. I

was getting dizzy and was wheezing went to the doctors and

he said I had a double ear infection that spread to my

and put me on antibiotics and an inhaler, only used

inhaler a couple times. I hadn't had an ear infection since

I was a kid. A couple of months after this was when my

first symptoms developed.

Jenifer

- In achalasia , " Debbi Heiser " <heiser@t...> wrote:

> I agree with Lars' reasoning.

>

> Some of us have asthma, some don't.

> Some have allergies, some don't.

> Some have had Chicken Pox (varicella), some haven't.

> Some have had recurrent infection problems (tonsillitis, etc.),

some haven't.

> Some have autoimmune disorders, some don't.

> Some are old, some are young.

> Some are overweight, some are normal, some are thin.

> You get the idea.

>

> Personally, I've never had a root canal and I doubt I'll ever need

one. I did, however, have over a decade of constant tonsillitis /

strep infections and ear infections. I do have allergies, but I

don't have asthma, I haven't had Chicken Pox, and I was in my mid-

20's when my symptoms first showed up.

>

> Debbi in Michigan

> Questions about the possible causes come up here frequently and

most

> of us would like to understand better, where their " A " is coming

from.

>

> The most recent examples in this group are the root treatment and

> Amalgan. However it seems to be unlikely, since 1. there are much

more

> people with Amalgan and/or a root treatment than with " A " . On the

> other hand each poll in this group that asked for possible causes

> showed that there are many people without the possible cause.

>

> There are even web-pages discussing " A " of pets. Pets usually

don't

> have Amalgan or root treatments. They also don't take anti-

depressiva

> or drugs or things like that.

>

> And it is even unclear if there is only one reason. Since the

symptoms

> differ between the people with " A " it is also possible that there

is

> more than one reason.

>

> In short, I fear with polls like this we cannot find the reason.

This

> would require a systematic study with high statistics, e.g. a high

> number of people with " A " .

>

> Lars.

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Lars wrote:

>... On the

>other hand each poll in this group that asked for possible causes

>showed that there are many people without the possible cause.

There are people that get lung cancer that have never been around cigarets.

It would be wrong to conclude from this that cigarets do not cause cancer.

>There are even web-pages discussing " A " of pets. Pets usually don't

>have Amalgan or root treatments. They also don't take anti-depressiva

>or drugs or things like that.

A problem can have different causes in different species.

>And it is even unclear if there is only one reason.

Right. There could easily be more than one cause. One should not be looking

for only 100% correlation. A correlation that is different from the norm

could be important, even if not 100%.

Putting all this together you could have something that 90% of the general

population is exposed to that causes, or predisposes to, achalasia,

resulting in only 0.0001% of the people that are exposed to it getting

achalasia, but only be a factor in a portion of the cases of achalasia. If

you took a poll about it, some with achalasia would never have been

exposed, most without achalasia would have been exposed, and some with

achalasia would have been exposed. The thing to look for would be that the

percent of those with achalasia that have been expose would not be 90%,

probably higher but less than 100%. Hard to see in a small poll.

For multiple sclerosis there is a correlation to cow milk that studies have

found. Populations with less cow milk consumption have less MS. Populations

without cow milk consumption are virtual MS free. Just think for a moment

how common drinking cow milk is.

And, a disease that has only one cause can effect different people

differently. So, even though we do not all have it the same, it could be

that 100% of us have something in common that we have never noticed.

>In short, I fear with polls like this we cannot find the reason. This

>would require a systematic study with high statistics, e.g. a high

>number of people with " A " .

You are probably right, but it is hard to prove a negative. That is, you

can not prove that polls like this will never produce something that could

lead to a better understanding of achalasia.

notan

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Lars wrote:

>And if everybody with " A " had chickenpox, or allergies or something

>else (which seems not to be the case),then there would be still the

>question " Why only we? Why is " A " so rare? " , since all of this

>possible causes are much, much more common than " A " .

It is possible that a number of things need to come into play for a disease

to take hold. Any one of the factors alone would to some degree predispose

you to the disease but would not mean you would get it. Again, think of MS

and cow milk. Something more than cow milk is probably part of the cause,

but cow milk seems to be a factor.

notan

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  • 1 year later...
Guest guest

Thanks guys for letting me know.....sometimes when you are at the

docs office you forget to ask things!!!!

> Hi Group,

> Here is a question I have never asked and didn't even think of

> until a few minutes ago....The doctors told me that a parent that

has

> BPES has a 50% chance of passing it on to their children. So I

> understand that part about how some of your children have gotten

it.

> My husbnad abd I took our daughter ( Rose) to a genetisist

and we

> were told she was a new mutation. I never thought to ask was

there

> something that during my pregnancy that I may have done wrong to

> affect that gene and cause the Bleph? Does anyone out there know

what

> casues it???

>

> love to all, amy hinchman

>

>

>

>

>

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  • 1 year later...

Does anyone know how I may have gotten this disease, and, can you ever

be CURED? I'm 48 years old and was diagnosed 4 months ago.I'm not sure

how long I've had it but when I noticed a major mental fog 5 months ago

I started looking on the Internet and found hypogonadism.I had all the

symptoms,some longer than others.When I was tested I was at 57.5.

Thanks for the help,

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>

> Does anyone know how I may have gotten this disease, and, can you ever

> be CURED? I'm 48 years old and was diagnosed 4 months ago.I'm not sure

> how long I've had it but when I noticed a major mental fog 5 months

ago

> I started looking on the Internet and found hypogonadism.I had all the

> symptoms,some longer than others.When I was tested I was at 57.5.

> Thanks for the help,

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

Hi ,

I think it would be impossible for anyone here to answer your

question any better than your own doctor can. Personally, I

believe that much of life is random, good and bad and inbetween,

and your now experiencing hypogonadism at 48 falls squarely into

the " stuff happens " bad category. Many here, and on other much

more serious life threatening public boards, have found their

own private ways to rationalize the " whys " of their condition,

and go about their lives just dealing with the symptoms.

Because you are recently diagnosed, I suspect you will have to

go through a period, hopefully not too long, of self pity or

attempts to assign " blame " . Personally, I think it helps one

to accept their lot in life by remembering literally billions

of other humans who spent their lives, however brief, suffering

horrible pain and death. A real wake up call is to go visit

a children's cancer hospital, and leave knowing many of these

innocent lives will die without ever experiencing anything good

at all about being alive. Hypogonadism, when viewed relative

to many other afflictions, is not so bad. My thoughts reflect

only how I personally from my own recognition, had to learn to

deal with this disease. I hope you find your own way.

Norton

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  • 1 month later...

Hi Tracey,

Of course, it is easy for me to blame procedures from my past for my cml. I

needed to be reminded that there are many others, like you, who have no

radiation or chemo in their past. Maybe my cml came from some of those

procedures and maybe it didn't. I guess it's just natural to wonder why I got

it.

Unfortunately, we have it, so does it really matter? I'm glad to know it is an

acquired disease and not an inherited one. There is some comfort in knowing

it doesn't get genetically passed on to our kids.

in NY

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