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Hi, Phil and . I'm new to the group as well and I think that I make the

third person

with this type of c-toma. Bilateral. Clean now for 5 years. Seven surgeries

later...and one

deaf ear.

PICK A GOOD SURGEON! Travel if you have to! The best advice I received was to

seek a

otolaringologist who also had some training in neurology. Yes, the disease, if

left

unchecked, can affect the brain. I did this and have had the most success to

date since

switching doctors.

Gretchen

>

> Hi

>

> As far as I know I'm the only other person on this list who has had to deal

> with " canal ctoma " . I've also had middle ear ctoma so I'm aware that there

> are a few differences between the two. As with any ctoma the surgeon has to

> do what is necessary to eliminate the disease otherwise it will keep on

> coming back. Since canal ctoma actively eats away the ear canal walls then a

> CWD would seem fairly inevitable. If the disease is caught early enough and

> still localized then treating it is less of problem. You should be OK if the

> only issue you have so far is mastoid invasion. Once it spreads, canal ctoma

> has a serious tendency to attack the facial nerve.

>

> There are a couple of things about this disease. One is that it is rare and

> therefore even the most experienced otologists don't know a great deal about

> it - and you can bet that there are no two cases which are identical. The

> other is that canal ctoma not only eats away ear canal but tends to embed

> itself inside the bone and from there it can spread throughout the temporal

> bone and resurface here and there even after the visible portions of it have

> been removed through surgery. At least that was my experience.

>

> I think you can also expect to have ear suctioning on regular basis to begin

> with. Not only to clean out debris from the mastoid and ear canal but also

> to watch for and combat any reappearance of the disease. One thing I should

> stress is that my experience with canal ctoma may not remotely resemble

> yours. I have the disease bilaterally. On one side it was pretty mild and

> unthreatening and on the other it was very advanced. So far I've a long

> struggle and several surgeries but I am winning.

>

> Good Luck

> Phil

>

>

> The ear specialist looked at my ear and said I have a very unusual

> type of cholesteatoma. My eardrum is not punctured, instead the

> cholesteatoma is growing into the mastoid from the outer ear canal.

> He thinks that it may be a byproduct of ear surgery I had about 20

> years ago to repair a perforated eardrum that I had at the time.

>

> I guess I'm lucky, because it was caught and I haven't experienced

> any hearing loss or other problems. If it weren't for the infection,

> it may not have been discovered for a long time. The ENT is

> recommending surgery and says it will likely be the " canal wall down "

> type of surgery.

>

> Can you share with me what to expect from this surgery, recovery

> time, etc.? I have to admit the " canal wall down " option scares me a

> little. Is there any change in the appearance of the ear? Do you have

> to go to the ENT frequently for cleaning after the surgery? Any info

> you can share would be greatly appreciated. I'm sure others have

> asked these questions before so I apologize in advance.

>

>

>

>

>

> --

> No virus found in this outgoing message.

> Checked by AVG Free Edition.

> Version: 7.1.408 / Virus Database: 268.13.17/505 - Release Date: 27/10/06

>

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Hi ,

Thanks for your support. Because of my husband's schedule, he can't

be with me all day the first couple of days after surgery - so I may

ask a friend to fill in during the times he's not available. Do you

think I should not be alone at all those first few days?

Also, I am wondering what your recovery was like. Why does it take

two weeks to recover? Were you laid up the whole time, or were you

able to do some light activity after a week or so? I'm a teaching

assistant in my grad program and I need to try to give my professor

an accurate estimate of when I can teach again after the surgery.

I'm in Phoenix, I see an otologist named Dr. Fucci. He was

recommended by my ENT and seems good, but I'm not sure how to

evaluate him. He does know and really likes the surgeon who did my

original ear surgery 20 years ago in Chicago (for perforated eardrums

and who was very good) so that carries some weight with me. But how

does one know if their dr. will be good for surgery? It always seems

like a hit or miss business with doctors.

Thanks again,

> >

> > Hi everyone,

> >

> > I just learned a few days ago that I have a cholesteatoma in my

right

> > ear. I had been having a stubborn external ear infection for

several

> > months, and one day while cleaning my ear my ENT noticed a cyst.

He

> > referred me to an ear specialist, but before I saw the ear

> > specialist, the cyst opened up due to the infection and the ENT

> > removed loads of keratin from my ear.

> >

> > The ear specialist looked at my ear and said I have a very

unusual

> > type of cholesteatoma. My eardrum is not punctured, instead the

> > cholesteatoma is growing into the mastoid from the outer ear

canal.

> > He thinks that it may be a byproduct of ear surgery I had about

20

> > years ago to repair a perforated eardrum that I had at the time.

> >

> > I guess I'm lucky, because it was caught and I haven't

experienced

> > any hearing loss or other problems. If it weren't for the

infection,

> > it may not have been discovered for a long time. The ENT is

> > recommending surgery and says it will likely be the " canal wall

down "

> > type of surgery.

> >

> > Can you share with me what to expect from this surgery, recovery

> > time, etc.? I have to admit the " canal wall down " option scares

me a

> > little. Is there any change in the appearance of the ear? Do you

have

> > to go to the ENT frequently for cleaning after the surgery? Any

info

> > you can share would be greatly appreciated. I'm sure others have

> > asked these questions before so I apologize in advance.

> >

> > Thanks,

> >

> >

>

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Best of luck to you! I recently had the surgery through the back of

the ear (whatever it is called!) and my Mom came over and stayed

with me for a few days. I would think that you should be ok without

anyone with you, as long as you have the majority of aeverything

that you possibly might need at your side (remote control, books,

water, phone, pain pills!, etc.). It was great having my Mom

around, but I don't think it was completely necessary. I was back

to my normal self after a few days, and back in the office after a

week and a half. I was working from home after 5 days. I hope this

helps!

> > >

> > > Hi everyone,

> > >

> > > I just learned a few days ago that I have a cholesteatoma in

my

> right

> > > ear. I had been having a stubborn external ear infection for

> several

> > > months, and one day while cleaning my ear my ENT noticed a

cyst.

> He

> > > referred me to an ear specialist, but before I saw the ear

> > > specialist, the cyst opened up due to the infection and the

ENT

> > > removed loads of keratin from my ear.

> > >

> > > The ear specialist looked at my ear and said I have a very

> unusual

> > > type of cholesteatoma. My eardrum is not punctured, instead

the

> > > cholesteatoma is growing into the mastoid from the outer ear

> canal.

> > > He thinks that it may be a byproduct of ear surgery I had

about

> 20

> > > years ago to repair a perforated eardrum that I had at the

time.

> > >

> > > I guess I'm lucky, because it was caught and I haven't

> experienced

> > > any hearing loss or other problems. If it weren't for the

> infection,

> > > it may not have been discovered for a long time. The ENT is

> > > recommending surgery and says it will likely be the " canal

wall

> down "

> > > type of surgery.

> > >

> > > Can you share with me what to expect from this surgery,

recovery

> > > time, etc.? I have to admit the " canal wall down " option

scares

> me a

> > > little. Is there any change in the appearance of the ear? Do

you

> have

> > > to go to the ENT frequently for cleaning after the surgery?

Any

> info

> > > you can share would be greatly appreciated. I'm sure others

have

> > > asked these questions before so I apologize in advance.

> > >

> > > Thanks,

> > >

> > >

> >

>

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I would think a person of normal health would be down 2 days at the most. I'm usually back in the gym 7 days after the surgery. The anesthesia is the worst part for me. It takes a while to clear your system of it.

Re: new member

Best of luck to you! I recently had the surgery through the back of the ear (whatever it is called!) and my Mom came over and stayed with me for a few days. I would think that you should be ok without anyone with you, as long as you have the majority of aeverything that you possibly might need at your side (remote control, books, water, phone, pain pills!, etc.). It was great having my Mom around, but I don't think it was completely necessary. I was back to my normal self after a few days, and back in the office after a week and a half. I was working from home after 5 days. I hope this helps!> > >> > > Hi everyone, > > > > > > I just learned a few days ago that I have a cholesteatoma in my > right > > > ear. I had been having a stubborn external ear infection for > several > > > months, and one day while cleaning my ear my ENT noticed a cyst. > He > > > referred me to an ear specialist, but before I saw the ear > > > specialist, the cyst opened up due to the infection and the ENT > > > removed loads of keratin from my ear. > > > > > > The ear specialist looked at my ear and said I have a very > unusual > > > type of cholesteatoma. My eardrum is not punctured, instead the > > > cholesteatoma is growing into the mastoid from the outer ear > canal. > > > He thinks that it may be a byproduct of ear surgery I had about > 20 > > > years ago to repair a perforated eardrum that I had at the time.> > > > > > I guess I'm lucky, because it was caught and I haven't > experienced > > > any hearing loss or other problems. If it weren't for the > infection, > > > it may not have been discovered for a long time. The ENT is > > > recommending surgery and says it will likely be the "canal wall > down" > > > type of surgery.> > > > > > Can you share with me what to expect from this surgery, recovery > > > time, etc.? I have to admit the "canal wall down" option scares > me a > > > little. Is there any change in the appearance of the ear? Do you > have > > > to go to the ENT frequently for cleaning after the surgery? Any > info > > > you can share would be greatly appreciated. I'm sure others have > > > asked these questions before so I apologize in advance.> > > > > > Thanks,> > > > > >> >>

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Wow - good for you! Of course, everyone is different and my problem

was the pain. Me - I won't go back to the gym for at least a couple

of weeks because I am afraid to mess up the work done. For example,

my following surgery instructions indicated to sneeze with your

mouth open for 7-10 days following, so no weight lifting for me, or

any physical exertion for that matter! I actually did not go back

to the office for 7 days because I was still taking pain medication

and I did not want to drive. Turns out, I was having an allergic

reaction to the antiobiotic drops and it caused a tremendous amount

of pain, so I was taking the meds to alleviate the pain from the

reaction (I did not learn it was an allergic reaction until I went

to my follow up visit a week following the surgery).

The point is, everyone is different. I have heard that some people

have vertigo following surgery, and I personally have never had that

problem. Some people have a higher threshold for pain and don't

require as much pain medicine. The very first time I had this

surgery (I have had it three times), I was laid up for a week, and I

think it had something to do with the type of anesthesia used, but

that's another story...

> > > >

> > > > Hi everyone,

> > > >

> > > > I just learned a few days ago that I have a cholesteatoma

in

> my

> > right

> > > > ear. I had been having a stubborn external ear infection

for

> > several

> > > > months, and one day while cleaning my ear my ENT noticed a

> cyst.

> > He

> > > > referred me to an ear specialist, but before I saw the ear

> > > > specialist, the cyst opened up due to the infection and

the

> ENT

> > > > removed loads of keratin from my ear.

> > > >

> > > > The ear specialist looked at my ear and said I have a very

> > unusual

> > > > type of cholesteatoma. My eardrum is not punctured,

instead

> the

> > > > cholesteatoma is growing into the mastoid from the outer

ear

> > canal.

> > > > He thinks that it may be a byproduct of ear surgery I had

> about

> > 20

> > > > years ago to repair a perforated eardrum that I had at the

> time.

> > > >

> > > > I guess I'm lucky, because it was caught and I haven't

> > experienced

> > > > any hearing loss or other problems. If it weren't for the

> > infection,

> > > > it may not have been discovered for a long time. The ENT

is

> > > > recommending surgery and says it will likely be the " canal

> wall

> > down "

> > > > type of surgery.

> > > >

> > > > Can you share with me what to expect from this surgery,

> recovery

> > > > time, etc.? I have to admit the " canal wall down " option

> scares

> > me a

> > > > little. Is there any change in the appearance of the ear?

Do

> you

> > have

> > > > to go to the ENT frequently for cleaning after the

surgery?

> Any

> > info

> > > > you can share would be greatly appreciated. I'm sure

others

> have

> > > > asked these questions before so I apologize in advance.

> > > >

> > > > Thanks,

> > > >

> > > >

> > >

> >

>

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I think it is a good idea to have someone around for a couple of days.

You may be a little off balance for a while and I needed help getting

from my bed to the bathroom.

> > > >

> > > > Hi everyone,

> > > >

> > > > I just learned a few days ago that I have a cholesteatoma in

> my

> > right

> > > > ear. I had been having a stubborn external ear infection for

> > several

> > > > months, and one day while cleaning my ear my ENT noticed a

> cyst.

> > He

> > > > referred me to an ear specialist, but before I saw the ear

> > > > specialist, the cyst opened up due to the infection and the

> ENT

> > > > removed loads of keratin from my ear.

> > > >

> > > > The ear specialist looked at my ear and said I have a very

> > unusual

> > > > type of cholesteatoma. My eardrum is not punctured, instead

> the

> > > > cholesteatoma is growing into the mastoid from the outer ear

> > canal.

> > > > He thinks that it may be a byproduct of ear surgery I had

> about

> > 20

> > > > years ago to repair a perforated eardrum that I had at the

> time.

> > > >

> > > > I guess I'm lucky, because it was caught and I haven't

> > experienced

> > > > any hearing loss or other problems. If it weren't for the

> > infection,

> > > > it may not have been discovered for a long time. The ENT is

> > > > recommending surgery and says it will likely be the " canal

> wall

> > down "

> > > > type of surgery.

> > > >

> > > > Can you share with me what to expect from this surgery,

> recovery

> > > > time, etc.? I have to admit the " canal wall down " option

> scares

> > me a

> > > > little. Is there any change in the appearance of the ear? Do

> you

> > have

> > > > to go to the ENT frequently for cleaning after the surgery?

> Any

> > info

> > > > you can share would be greatly appreciated. I'm sure others

> have

> > > > asked these questions before so I apologize in advance.

> > > >

> > > > Thanks,

> > > >

> > > >

> > >

> >

>

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Here is another point of view! It will depend greatly on how

extensive and invasive your surgery is. I was told NOT to do any

strenuous exercise for 4 weeks after surgery. It took me about 5 days

to feel half way decent the first time. It has taken me 4 weeks with

this surgery. I would feel good one day and completely exhausted the

next. I am 65 years old, but in excellent health otherwise. I just

have had a difficult time with this surgery. The point is, you won't

know until you experience it. Everyone is different. Best bet is

that you tell your prof that you will need two weeks. If you are

better before hand, you can surprise him!

> > > >

> > > > Hi everyone,

> > > >

> > > > I just learned a few days ago that I have a cholesteatoma in

> my

> > right

> > > > ear. I had been having a stubborn external ear infection for

> > several

> > > > months, and one day while cleaning my ear my ENT noticed a

> cyst.

> > He

> > > > referred me to an ear specialist, but before I saw the ear

> > > > specialist, the cyst opened up due to the infection and the

> ENT

> > > > removed loads of keratin from my ear.

> > > >

> > > > The ear specialist looked at my ear and said I have a very

> > unusual

> > > > type of cholesteatoma. My eardrum is not punctured, instead

> the

> > > > cholesteatoma is growing into the mastoid from the outer ear

> > canal.

> > > > He thinks that it may be a byproduct of ear surgery I had

> about

> > 20

> > > > years ago to repair a perforated eardrum that I had at the

> time.

> > > >

> > > > I guess I'm lucky, because it was caught and I haven't

> > experienced

> > > > any hearing loss or other problems. If it weren't for the

> > infection,

> > > > it may not have been discovered for a long time. The ENT is

> > > > recommending surgery and says it will likely be the " canal

> wall

> > down "

> > > > type of surgery.

> > > >

> > > > Can you share with me what to expect from this surgery,

> recovery

> > > > time, etc.? I have to admit the " canal wall down " option

> scares

> > me a

> > > > little. Is there any change in the appearance of the ear? Do

> you

> > have

> > > > to go to the ENT frequently for cleaning after the surgery?

> Any

> > info

> > > > you can share would be greatly appreciated. I'm sure others

> have

> > > > asked these questions before so I apologize in advance.

> > > >

> > > > Thanks,

> > > >

> > > >

> > >

> >

>

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Same for me Jen, the Dr. gave me specific written instructions to be off work for 7-10 days and no heavy lifting, sneezing with my mouth closed, blowing my nose or sexual intercourse until after my follow up visit with him 21 days after surgery. I wouldn't chance it, I would hate to ruin everything following what I had already gone through. jenvigli <jennifer.vigliano@...> wrote: Wow - good for you! Of course, everyone is different and my problem was the pain. Me - I won't go

back to the gym for at least a couple of weeks because I am afraid to mess up the work done. For example, my following surgery instructions indicated to sneeze with your mouth open for 7-10 days following, so no weight lifting for me, or any physical exertion for that matter! I actually did not go back to the office for 7 days because I was still taking pain medication and I did not want to drive. Turns out, I was having an allergic reaction to the antiobiotic drops and it caused a tremendous amount of pain, so I was taking the meds to alleviate the pain from the reaction (I did not learn it was an allergic reaction until I went to my follow up visit a week following the surgery).The point is, everyone is different. I have heard that some people have vertigo following surgery, and I personally have never had that problem. Some people have a higher threshold for pain and don't require as much pain medicine. The

very first time I had this surgery (I have had it three times), I was laid up for a week, and I think it had something to do with the type of anesthesia used, but that's another story...> > > >> > > > Hi everyone, > > > > > > > > I just learned a few days

ago that I have a cholesteatoma in > my > > right > > > > ear. I had been having a stubborn external ear infection for > > several > > > > months, and one day while cleaning my ear my ENT noticed a > cyst. > > He > > > > referred me to an ear specialist, but before I saw the ear > > > > specialist, the cyst opened up due to the infection and the > ENT > > > > removed loads of keratin from my ear. > > > > > > > > The ear specialist looked at my ear and said I have a very > > unusual > > > > type of cholesteatoma. My eardrum is not punctured, instead > the > > > > cholesteatoma is growing into the mastoid from the outer ear > > canal. > > > > He thinks that it may be a byproduct of ear surgery I had > about

> > 20 > > > > years ago to repair a perforated eardrum that I had at the > time.> > > > > > > > I guess I'm lucky, because it was caught and I haven't > > experienced > > > > any hearing loss or other problems. If it weren't for the > > infection, > > > > it may not have been discovered for a long time. The ENT is > > > > recommending surgery and says it will likely be the "canal > wall > > down" > > > > type of surgery.> > > > > > > > Can you share with me what to expect from this surgery, > recovery > > > > time, etc.? I have to admit the "canal wall down" option > scares > > me a > > > > little. Is there any change in the appearance of the ear? Do > you > > have > > > > to go to

the ENT frequently for cleaning after the surgery? > Any > > info > > > > you can share would be greatly appreciated. I'm sure others > have > > > > asked these questions before so I apologize in advance.> > > > > > > > Thanks,> > > > > > > >> > >> >>"Wherever you go, there you are!" Wagemanngeowags@...

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I'm curious ... did it start out bilateral, or develop that way

later? Mine's only one side, and fortunately has only grown a little

into the mastoid, as near as they can tell.

> >

> > Hi

> >

> > As far as I know I'm the only other person on this list who has

had to deal

> > with " canal ctoma " . I've also had middle ear ctoma so I'm aware

that there

> > are a few differences between the two. As with any ctoma the

surgeon has to

> > do what is necessary to eliminate the disease otherwise it will

keep on

> > coming back. Since canal ctoma actively eats away the ear canal

walls then a

> > CWD would seem fairly inevitable. If the disease is caught early

enough and

> > still localized then treating it is less of problem. You should

be OK if the

> > only issue you have so far is mastoid invasion. Once it spreads,

canal ctoma

> > has a serious tendency to attack the facial nerve.

> >

> > There are a couple of things about this disease. One is that it

is rare and

> > therefore even the most experienced otologists don't know a great

deal about

> > it - and you can bet that there are no two cases which are

identical. The

> > other is that canal ctoma not only eats away ear canal but tends

to embed

> > itself inside the bone and from there it can spread throughout

the temporal

> > bone and resurface here and there even after the visible portions

of it have

> > been removed through surgery. At least that was my experience.

> >

> > I think you can also expect to have ear suctioning on regular

basis to begin

> > with. Not only to clean out debris from the mastoid and ear canal

but also

> > to watch for and combat any reappearance of the disease. One

thing I should

> > stress is that my experience with canal ctoma may not remotely

resemble

> > yours. I have the disease bilaterally. On one side it was pretty

mild and

> > unthreatening and on the other it was very advanced. So far I've

a long

> > struggle and several surgeries but I am winning.

> >

> > Good Luck

> > Phil

> >

> >

> > The ear specialist looked at my ear and said I have a very unusual

> > type of cholesteatoma. My eardrum is not punctured, instead the

> > cholesteatoma is growing into the mastoid from the outer ear

canal.

> > He thinks that it may be a byproduct of ear surgery I had about 20

> > years ago to repair a perforated eardrum that I had at the time.

> >

> > I guess I'm lucky, because it was caught and I haven't experienced

> > any hearing loss or other problems. If it weren't for the

infection,

> > it may not have been discovered for a long time. The ENT is

> > recommending surgery and says it will likely be the " canal wall

down "

> > type of surgery.

> >

> > Can you share with me what to expect from this surgery, recovery

> > time, etc.? I have to admit the " canal wall down " option scares

me a

> > little. Is there any change in the appearance of the ear? Do you

have

> > to go to the ENT frequently for cleaning after the surgery? Any

info

> > you can share would be greatly appreciated. I'm sure others have

> > asked these questions before so I apologize in advance.

> >

> >

> >

> >

> >

> > --

> > No virus found in this outgoing message.

> > Checked by AVG Free Edition.

> > Version: 7.1.408 / Virus Database: 268.13.17/505 - Release Date:

27/10/06

> >

>

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No. I started in one ear and later occurred in the other. The only possible

reason I ever got

for their development, and this was a guess at best, was that oral surgery I had

as a child

stretched my eustation tubes and decreased the size of them, causing exceess

moisture in

the middle ear. But really, who knows.

Gretchen

> > >

> > > Hi

> > >

> > > As far as I know I'm the only other person on this list who has

> had to deal

> > > with " canal ctoma " . I've also had middle ear ctoma so I'm aware

> that there

> > > are a few differences between the two. As with any ctoma the

> surgeon has to

> > > do what is necessary to eliminate the disease otherwise it will

> keep on

> > > coming back. Since canal ctoma actively eats away the ear canal

> walls then a

> > > CWD would seem fairly inevitable. If the disease is caught early

> enough and

> > > still localized then treating it is less of problem. You should

> be OK if the

> > > only issue you have so far is mastoid invasion. Once it spreads,

> canal ctoma

> > > has a serious tendency to attack the facial nerve.

> > >

> > > There are a couple of things about this disease. One is that it

> is rare and

> > > therefore even the most experienced otologists don't know a great

> deal about

> > > it - and you can bet that there are no two cases which are

> identical. The

> > > other is that canal ctoma not only eats away ear canal but tends

> to embed

> > > itself inside the bone and from there it can spread throughout

> the temporal

> > > bone and resurface here and there even after the visible portions

> of it have

> > > been removed through surgery. At least that was my experience.

> > >

> > > I think you can also expect to have ear suctioning on regular

> basis to begin

> > > with. Not only to clean out debris from the mastoid and ear canal

> but also

> > > to watch for and combat any reappearance of the disease. One

> thing I should

> > > stress is that my experience with canal ctoma may not remotely

> resemble

> > > yours. I have the disease bilaterally. On one side it was pretty

> mild and

> > > unthreatening and on the other it was very advanced. So far I've

> a long

> > > struggle and several surgeries but I am winning.

> > >

> > > Good Luck

> > > Phil

> > >

> > >

> > > The ear specialist looked at my ear and said I have a very unusual

> > > type of cholesteatoma. My eardrum is not punctured, instead the

> > > cholesteatoma is growing into the mastoid from the outer ear

> canal.

> > > He thinks that it may be a byproduct of ear surgery I had about 20

> > > years ago to repair a perforated eardrum that I had at the time.

> > >

> > > I guess I'm lucky, because it was caught and I haven't experienced

> > > any hearing loss or other problems. If it weren't for the

> infection,

> > > it may not have been discovered for a long time. The ENT is

> > > recommending surgery and says it will likely be the " canal wall

> down "

> > > type of surgery.

> > >

> > > Can you share with me what to expect from this surgery, recovery

> > > time, etc.? I have to admit the " canal wall down " option scares

> me a

> > > little. Is there any change in the appearance of the ear? Do you

> have

> > > to go to the ENT frequently for cleaning after the surgery? Any

> info

> > > you can share would be greatly appreciated. I'm sure others have

> > > asked these questions before so I apologize in advance.

> > >

> > >

> > >

> > >

> > >

> > > --

> > > No virus found in this outgoing message.

> > > Checked by AVG Free Edition.

> > > Version: 7.1.408 / Virus Database: 268.13.17/505 - Release Date:

> 27/10/06

> > >

> >

>

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  • 1 month later...

Hi Diane. I don't know how to answer your question on how bad it is.

It was my first surgery ever and before hand I was so wrapped up in

loosing weight I never thought about recovery. So, much to my

surprise when I came out of surgery, I was like " Oh Hell No " . The

first day I was medicated so I slept through most of it. The second

day was worse for me. Hard to get comfortable, no sleeping on your

side, hard to sit up and get out of bed, coughing was brought to a

whole new level. But on day three, I got throught two airports and

car rides before I hit the safety of my own bed. Your belly is gonna

hurt for two days, then it starts to get better. By the end of the

first week I was sleeping on my side and doing much better. No pain

no gain. God, I hate that saying. On the other hand, when I went

back to get a fill, I met a girl who had surgery the day before. She

was dressed and up and walking and even did her hair. I'm pretty sure

she was some sort of robot or something, but I was very impressed. So

yeah, it's surgery and you're gonna need to recover and yup, you're

gonna be sore. Just part of the journey. But, I can tell you that

from where I stand, I wouldn't change a thing. My life is my own

again. I'm down 26 lbs and looking mighty fine. I didn't get to eat

much at Christmas, but I lost 2.5 lbs over the weekend. That's what

I'm talking about. You can do this and it's worth every pain and

every hunger pain. Every day I wake up thankful I heard about the lap

band and Dr. A and the crew.

>

> Hi, my name is Diane and I am having my surgery on 12/28. After

> reading some of the posts I am worried about the 2 week period after

> surgery. Is it really that bad?

>

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I haven't had my surgery yet. I'm set for the 10th of Jan and I'm

having the gastric by pass, but I believe they don't call it boot camp

for nothing. But remember it is only 2 weeks of your entire life. A

bump in a long road to a wonderful, healthy, and sexier body so go

with it and don't worry.

karne

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Hi Diane – I had surgery on 9/22/06

and I must have been one of the “lucky” ones – I had no pain

after the procedure. In fact, I was afraid when they took the I.V. out of

me and with it the pain medication. I thought I would be in “great”

pain, but was not. I could lie on my side after a day or two, had no

oozing or swelling out of the cuts and felt great when I went home.

I also did not feel hungry for the first 2

weeks, however, I was very happy to be able to go on yogurt in week three and

full liquids in week 4. I did begin to get hungry in week 3 – I think

because I was healing and also I was getting more active. I think the biggest

help to keep from feeling hungry is lots of water, popsicles, and keeping busy –

whether taking a walk, clean your house, read a book, or something. I

have just had my first fill and I can tell the difference from before. I

only eat a few bites and am full and not hungry for several hours.

Don’t worry about the first 2 weeks –

each day just think – just for today. Soon the 2 weeks will be

over, and you can have some variety in your diet. Congratulations on your

choice and I know you will do fine. Be sure to let us know how you are

doing.

Rhonda

DOB 9/22/06

292/259/150

From: [mailto: ] On Behalf Of dlurvina

Sent: Tuesday, December 26, 2006

9:28 PM

Subject: New

Member

Hi, my name is Diane and I am having my surgery on

12/28. After

reading some of the posts I am worried about the 2 week period after

surgery. Is it really that bad?

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It is for some people but it isn't difficult for everyone. Each person

is different. For me I just didn't let others eat around me and I have

to turn the channel on the TV when they start advertising pizza and

such.

I'm on week four as of today and I could have lots of things I'm not

having. I am basically on the 2 weeks of clear liquids with protein

shakes. But I'm not doing the yogurt and cream soups I could be having.

Just remember, the 14 days doesn't have to be horrible. Prevent

yourself from getting hungry by drinking something all the time. Look

at it this way, drink 3.3oz 20 times daily. Keep up your protein, that

will head off hunger.

>

> Hi, my name is Diane and I am having my surgery on 12/28. After

> reading some of the posts I am worried about the 2 week period after

> surgery. Is it really that bad?

>

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She must have been a Stepford Surgical Patient. All kidding aside

others do better and worse. I'm hoping I'm one of the good ones. I'm

prepared to jump out of that bed and get going walking the halls.

I just hope that everone gets a chance before their surgery to realize

that attitude is the most important.

so I hope when I hit the board and whine someone will remind me to get

my attitude in the right place.

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Diane, I am one of the oldies on this board. Many people think that you tend to forget those first two weeks and that we oldies try to gloss over that period. Well, I am here to tell you that all of us remember! There is really no way to forget those weeks! I hate to say it, but, it really is pure hell. HOWEVER, knowing that during those two weeks you are preparing for the journey of a lifetime makes it worth the frustration, hunger, sadness, and every other emotion you will feel during that time. It is a time for your body to regain a better level of health. I honestly think that if I had not gone through those two weeks of clear liquids that I may not be as healthy as I am now. I had been bombarding my body with toxins for so many years that had created my obesity that now my body was getting a much deserved break. Yeah, I was hungry. Yeah, I was missing my best friend

(food). And yeah, I was somewhat emotional due to all of the feelings I was having about surgery, a little discomfort, so many tv commercials about food, all those smells of food when you go anywhere. But, I did it and SO CAN YOU. 14 days from start to the next phase which is much, much easier. The key to survival is stay busy. I would take as little time off of work as possible so your mind stays busy and occupied. The down time is what kills you! When you get hungry, eat more popsicles and overload yourself with water. No, the first two weeks are horrible but tolerable because of the excitment just around the corner! Keep in touch on this board. That is what it is for....SUPPORT! We all have to help each other! Jenni Currie DOB 2/23/06 247/231/152/145dlurvina <dlurvina@...>

wrote: Hi, my name is Diane and I am having my surgery on 12/28. After reading some of the posts I am worried about the 2 week period after surgery. Is it really that bad? __________________________________________________

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thanks, I have been using the Medifast Shakes, and they are not real

good, and they are not clear.

> >

> > Hi, my name is Diane and I am having my surgery on 12/28. After

> > reading some of the posts I am worried about the 2 week period

after

> > surgery. Is it really that bad?

> >

>

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Thanks for responding, I have had my gall bladder removed so I know

about the pain. I am just worried about the foods we can and cannot

eat.-

-- In , " wendyelam81 " <welam@...>

wrote:

>

> Hi Diane. I don't know how to answer your question on how bad it

is.

> It was my first surgery ever and before hand I was so wrapped up

in

> loosing weight I never thought about recovery. So, much to my

> surprise when I came out of surgery, I was like " Oh Hell No " . The

> first day I was medicated so I slept through most of it. The

second

> day was worse for me. Hard to get comfortable, no sleeping on

your

> side, hard to sit up and get out of bed, coughing was brought to a

> whole new level. But on day three, I got throught two airports

and

> car rides before I hit the safety of my own bed. Your belly is

gonna

> hurt for two days, then it starts to get better. By the end of

the

> first week I was sleeping on my side and doing much better. No

pain

> no gain. God, I hate that saying. On the other hand, when I went

> back to get a fill, I met a girl who had surgery the day before.

She

> was dressed and up and walking and even did her hair. I'm pretty

sure

> she was some sort of robot or something, but I was very

impressed. So

> yeah, it's surgery and you're gonna need to recover and yup,

you're

> gonna be sore. Just part of the journey. But, I can tell you

that

> from where I stand, I wouldn't change a thing. My life is my own

> again. I'm down 26 lbs and looking mighty fine. I didn't get to

eat

> much at Christmas, but I lost 2.5 lbs over the weekend. That's

what

> I'm talking about. You can do this and it's worth every pain and

> every hunger pain. Every day I wake up thankful I heard about the

lap

> band and Dr. A and the crew.

>

> >

> > Hi, my name is Diane and I am having my surgery on 12/28. After

> > reading some of the posts I am worried about the 2 week period

after

> > surgery. Is it really that bad?

> >

>

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wow thats great, this post system is all new to me I just love how

everyone responded. thanks again.-

-- In , " Rhonda Olsen "

<olsenr@...> wrote:

>

> Hi Diane - I had surgery on 9/22/06 and I must have been one of

the " lucky "

> ones - I had no pain after the procedure. In fact, I was afraid

when they

> took the I.V. out of me and with it the pain medication. I

thought I would

> be in " great " pain, but was not. I could lie on my side after a

day or two,

> had no oozing or swelling out of the cuts and felt great when I

went home.

>

>

>

> I also did not feel hungry for the first 2 weeks, however, I was

very happy

> to be able to go on yogurt in week three and full liquids in week

4. I did

> begin to get hungry in week 3 - I think because I was healing and

also I was

> getting more active. I think the biggest help to keep from

feeling hungry

> is lots of water, popsicles, and keeping busy - whether taking a

walk, clean

> your house, read a book, or something. I have just had my first

fill and I

> can tell the difference from before. I only eat a few bites and

am full and

> not hungry for several hours.

>

>

>

> Don't worry about the first 2 weeks - each day just think - just

for today.

> Soon the 2 weeks will be over, and you can have some variety in

your diet.

> Congratulations on your choice and I know you will do fine. Be

sure to let

> us know how you are doing.

>

>

>

> Rhonda

>

> DOB 9/22/06

>

> 292/259/150

>

>

>

> _____

>

> From:

> [mailto: ] On Behalf Of dlurvina

> Sent: Tuesday, December 26, 2006 9:28 PM

>

> Subject: New Member

>

>

>

> Hi, my name is Diane and I am having my surgery on 12/28. After

> reading some of the posts I am worried about the 2 week period

after

> surgery. Is it really that bad?

>

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HAHA!!! I forgot about that already!!! Waking up, I mean. I was

exactly the same way. I was so focused on the band I didn't really

consider pain or recovery issues much.

I woke up and thought, WTH??? HOLY CRAP THIS HURTS! When I woke up

Dr. A was standing over the bed in recovery and I yelped that it HURT!

He said I was just given meds before I woke up and to give them time to

start working. The hell with that! I wanted something ELSE!! Within

moments the nurse was giving me something else.

That was the most pain of the entire ordeal. Just waking up and it was

resolved in moments. From then on it was just sore. Not a biggie. I

really think it was the shock of going to sleep and feeling fine and

waking up and something hurt. But again... it was short lived...

minutes at best. And I am a pain weenie, a big 'ol pain weenie.

So for anyone that hasn't had the surgery yet you don't get narcotics

because honestly, you don't need them. For a Lap Band it's just sore,

not absolute pain. There is a difference.

-- In , " wendyelam81 " <welam@>

wrote:

....I was so wrapped up in loosing weight I never thought about

recovery. So, much to my surprise when I came out of surgery, I was

like " Oh Hell No " . ...

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Oh my, well I guess you would know about pain then. I'm not sure I

will ever elect surgary again. Well, the food situation the first

two weeks pretty much sucks. No way to sugar coat it for you. I

actually didn't do too bad with it. It was ok. I sure was thankful

for cream soup though. I had popsicles at work and I had a thermos

of chicken broth with me at all times. It was just a matter of

getting through those two weeks so I could reclaim my life. I was

ready for it. I was in this for the long haul, so I think that's

what got me through those two weeks. You just have to go in there

ready and willing. I just had plain old chicken broth from a can

but I have since read some other suggestions. Lot's of people get

different kinds of clear soup and strain the solids out in order to

have a different taste. I wish you good luck and you will do just

fine. Remember this: I'm 3 months out, looking back it was by far

the best decision I've ever made and I wouldn't change a thing. I

can actually see myself again. I feel good when I walk into a

room. I don't look hideous in this years Christmas pictures. That

right there, is priceless. I am so thankful for this chance to live

again.

DOB

9/25/06

241/214.5/160

2 fills

> > >

> > > Hi, my name is Diane and I am having my surgery on 12/28.

After

> > > reading some of the posts I am worried about the 2 week period

> after

> > > surgery. Is it really that bad?

> > >

> >

>

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Yes!!!! Exactly. You're making me laugh right now. Boy, that just

brought me right back to the recovery room.

> ...I was so wrapped up in loosing weight I never thought about

> recovery. So, much to my surprise when I came out of surgery, I

was

> like " Oh Hell No " . ...

>

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Karne I agree with you. Just a bump in the road. When you have a baby you have a lot of pain but you don't dwell on it. When you see the baby you get on with life and take care of the baby and we have to take care of our bands like it is our baby because it is a very precious thing to most of us. Shirley magnoliamouth <karenostrom@...> wrote: I haven't had my surgery yet. I'm set for the 10th of Jan and

I'mhaving the gastric by pass, but I believe they don't call it boot campfor nothing. But remember it is only 2 weeks of your entire life. Abump in a long road to a wonderful, healthy, and sexier body so gowith it and don't worry.karne __________________________________________________

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Diane, One thing I found that helped me the 1st 2 weeks was...If at all possible...STAY OUT OF THE KITCHEN...If your married, ask your husband if he'll fend for himself and if he says no...Then make him :) ...I understand if you have kids especially small ones who can't fend for themselves then you may have too...But keep it simple...The temptation to eat will be very very strong and before you know it everything will look good even spinach...But remember it's only 2 weeks out of your life, you can do this...We're here to help you... J Currie <giftedtch@...> wrote: Diane, I am one of the oldies on this board. Many people think that you tend to forget those first two weeks and that we oldies try to gloss over that period. Well, I am here to tell you that all of us remember! There is really no way to forget those weeks! I hate to say it, but, it really is pure hell. HOWEVER, knowing that during those two weeks you are preparing for the journey of a lifetime makes it worth the frustration, hunger, sadness, and every other emotion you will feel during that time. It is a time for your body to regain a better level of health. I honestly think that if I had not gone through those two weeks of clear liquids that I may not be as healthy as I am now. I had been bombarding my body with toxins for so many years that had created my obesity that

now my body was getting a much deserved break. Yeah, I was hungry. Yeah, I was missing my best friend (food). And yeah, I was somewhat emotional due to all of the feelings I was having about surgery, a little discomfort, so many tv commercials about food, all those smells of food when you go anywhere. But, I did it and SO CAN YOU. 14 days from start to the next phase which is much, much easier. The key to survival is stay busy. I would take as little time off of work as possible so your mind stays busy and occupied. The down time is what kills you! When you get hungry, eat more popsicles and overload yourself with water. No, the first two weeks are horrible but tolerable because of the excitment just around the corner! Keep in touch on this board. That is what it is for....SUPPORT! We all have to help each other! Jenni

Currie DOB 2/23/06 247/231/152/145dlurvina <dlurvina > wrote: Hi, my name is Diane and I am having my surgery on 12/28. After reading some of the posts I am worried about the 2 week period after surgery. Is it really that bad? __________________________________________________

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Hi , and welcome to the group. I've been on Lexapro for over a month now

and I'm not having any side effects. I think it helps, as I don't cry all the

time anymore, and I'm easy to get along with. Crying for no reason and

hostility, anger, etc. are signs of depression. Lexapro is an SSRI, which means

more seratonin gets to the brain. Seratonin is important and if you don't have

enough, you feel bad. I'm glad my doctor put me on it.

Colleen

cathysim1017 <catherin_skinner@...> wrote:

I just signed up tonight & want to say Hello. I just sent the Cymbalta

vs Lexapro message. It is nice to find people to talk about this

subject. It seems the drs. use patients for guinee pigs. He tells

me " try this and see me in 4 weeks " . My friend at work believes the

pills are just a band-aid & don't really fix anything so she won't

take anything.My feeling is stuff happens in life you have no control

over.If meds help you get back on track, it seems worth it to try.

Thank you for listening,

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