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Wishing you a speedy recovery, in

Kentucky!

Sincerely, Tara

Re:

Surgery tomorrow

Good luck and have a speedy recovery ! -

Dee

-- In cholesteatoma ,

<travishoyt@y...> wrote:

> Well the blood work was done earlier

today. My surgery is bright

and early

> tomorrow morning at 7:30 a.m. Let's

hope all goes well. I'm

mostly hoping

> that I don't have to have the mastoidectomy

because that will

really put a

> damper on my water sports but if it needs to

be done it needs to be

done and

> I'll just live with it. I'll let you

all know how it works

out...thanks for

> the info thus far.

>

>

>

>

This Cholesteatoma

support group offers and provides information of a general nature about

cholesteatoma as well as members personal experiences with this disease. The

information provided is not intended to replace surgical or medical advice or

recommendations. Any information in the messages, postings or articles on the

web site should not be considered a substitute for consultation with a medical

professional to address individual medical needs. Individuals' particular facts

and circumstances will determine the treatment which is most appropriate.

This

Cholesteatoma support group offers and provides information of a general

nature about cholesteatoma as well as members personal experiences with this

disease. The information provided is not intended to replace surgical or

medical advice or recommendations. Any information in the messages, postings or

articles on the web site should not be considered a substitute for consultation

with a medical professional to address individual medical needs. Individuals'

particular facts and circumstances will determine the treatment which is most

appropriate.

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  • 5 months later...

From a fellow Alaskan - Good luck. Are you having the surgery in Soldotna or Anchorage? Are you having the CWU or CWD procedure? My son had a CWU mastoidectomy for chronic mastoiditis (no cholesteatoma) and he rebounded pretty quickly. His ear was sore to lay on for a few weeks and he got sick a few times (nauseated) but other than that he did really well.

Stay positive.

Barbara Misener - Anchorage, AKbryantsinalaska <bryantsinalaska@...> wrote:

Good morning all, (morning in Alaska anyway),I have posted a few times and met with quick responses. Thank you all for your input. I am a little concerned about this surgery as I have not had surgery for 30+ years. What should I prepare myself for? Post-op surgery care? Is it painful the next day? A week later? Is swallowing a problem? My surgery is scheduled for 9am alaska time. So if anyone could write back I would sure appreciate it.Thanks all and have a wonderful holiday season.Terrance

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Barbara,

I am having the surgery in Soldotna. The Dr. said he wasnt sure

until he got inside my head which one he would do. He is going to

try the CWU first, but if things are not good in there then he will

go to the CWD. I guess thats the thing that is disconcerning, not

knowing what the outcome will be. And if my nervousness is any

indication to the Dr then this will be a one surgery deal !!. I am

doing my best to stay positive, and appreciate your response. I do

really well, (like most men I would assume), comforting my wife or my

children when these life issues arise, but being the one in the bed

is not very easy. You all do a good job of easing a persons fears

and trust me I appreciate everyone that has posted here. Thanks

again Barbara and its about time we got enough snow to enjoy. I will

post as soon as I can after the surgery and maybe help someone else.

My wife passed along a good one to me. " The difference between

minor surgery and major surgery " Minor surgery is when someone else

is going in !!

Terrance

>

>

>

> Good morning all, (morning in Alaska anyway),

>

> I have posted a few times and met with quick responses. Thank you

> all for your input. I am a little concerned about this surgery as I

> have not had surgery for 30+ years. What should I prepare myself

> for? Post-op surgery care? Is it painful the next day? A week

> later? Is swallowing a problem?

> My surgery is scheduled for 9am alaska time. So if anyone could

> write back I would sure appreciate it.

>

> Thanks all and have a wonderful holiday season.

>

> Terrance

>

>

>

>

>

>

>

>

>

>

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Hi Terrance!

Good luck with your surgery tomorrow. I know how you're feeling, as

mine is coming up on Thursday and I too am a little nervous. But

like Barbara said, stay positive. I'll be anxious to hear how yours

went.

>

>

>

> Good morning all, (morning in Alaska anyway),

>

> I have posted a few times and met with quick responses. Thank you

> all for your input. I am a little concerned about this surgery as I

> have not had surgery for 30+ years. What should I prepare myself

> for? Post-op surgery care? Is it painful the next day? A week

> later? Is swallowing a problem?

> My surgery is scheduled for 9am alaska time. So if anyone could

> write back I would sure appreciate it.

>

> Thanks all and have a wonderful holiday season.

>

> Terrance

>

>

>

>

>

>

>

>

>

>

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Hi, Terrance -

I know how you feel. I had my first surgery in May and have the second next

Monday. Knowing what I am in for is good, but I am getting a little anxious

about going through it all again. WE can and will do it though!

You doctor or someone will give you some directions for post op care. The

big thing will be to not get water in your ear, so you will put a cotton

ball in your ear and then cover it with vaseline when you wash your hair.

The biggest thing I didn't expect was feeling so weird when I first went out

of the house. Just the whole ambiant air and sound thing was weird. I felt

all off - so plugged up on the c-toma side. That was so unexpected. I

suppose people have different experiences, but that was how it was for me.

Immediately after surgery I was just tired from the anesthesia, but did not

experience much pain. About four days after surgery I had horrible chest

pains, but it turned out they had bruised my chest wall in strapping me on

the table. That was it. I still have plenty of pain and nausea pills to get

me though this 'second look', so that should tell you it wasn't too bad. It

took a while to figure out how to sleep on my c-toma side comfortably now

and then, but that wasn't a big deal either.

One more thing - someone suggested we have a pillow in the car for the ride

home. That was a good idea. We will be thinking of you and hope it all goes

very well. Let us know how you are doing. We've had someone get on line in

the evening after their surgery, but I don't think that's true for most of

us!

le

P.S. , I know your surgery is in a couple of days too. Hang in there and

keep us posted.

----------

>From: bryantsinalaska <bryantsinalaska@...>

>cholesteatoma

>Subject: Surgery tomorrow

>Date: Tue, Dec 14, 2004, 12:26 PM

>

>

>

>

> Good morning all, (morning in Alaska anyway),

>

> I have posted a few times and met with quick responses. Thank you

> all for your input. I am a little concerned about this surgery as I

> have not had surgery for 30+ years. What should I prepare myself

> for? Post-op surgery care? Is it painful the next day? A week

> later? Is swallowing a problem?

> My surgery is scheduled for 9am alaska time. So if anyone could

> write back I would sure appreciate it.

>

> Thanks all and have a wonderful holiday season.

>

> Terrance

>

>

>

>

>

>

>

>

>

>

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le,

Thanks for the advice on a car pillow! We'll be heading home during

5:00 traffic, so that's a good idea.

> Hi, Terrance -

>

> I know how you feel. I had my first surgery in May and have the

second next

> Monday. Knowing what I am in for is good, but I am getting a little

anxious

> about going through it all again. WE can and will do it though!

>

> You doctor or someone will give you some directions for post op

care. The

> big thing will be to not get water in your ear, so you will put a

cotton

> ball in your ear and then cover it with vaseline when you wash your

hair.

> The biggest thing I didn't expect was feeling so weird when I first

went out

> of the house. Just the whole ambiant air and sound thing was weird.

I felt

> all off - so plugged up on the c-toma side. That was so unexpected.

I

> suppose people have different experiences, but that was how it was

for me.

>

> Immediately after surgery I was just tired from the anesthesia, but

did not

> experience much pain. About four days after surgery I had horrible

chest

> pains, but it turned out they had bruised my chest wall in

strapping me on

> the table. That was it. I still have plenty of pain and nausea

pills to get

> me though this 'second look', so that should tell you it wasn't too

bad. It

> took a while to figure out how to sleep on my c-toma side

comfortably now

> and then, but that wasn't a big deal either.

>

> One more thing - someone suggested we have a pillow in the car for

the ride

> home. That was a good idea. We will be thinking of you and hope it

all goes

> very well. Let us know how you are doing. We've had someone get on

line in

> the evening after their surgery, but I don't think that's true for

most of

> us!

>

> le

>

> P.S. , I know your surgery is in a couple of days too. Hang in

there and

> keep us posted.

>

>

>

> ----------

> >From: bryantsinalaska <bryantsinalaska@y...>

> >cholesteatoma

> >Subject: Surgery tomorrow

> >Date: Tue, Dec 14, 2004, 12:26 PM

> >

>

> >

> >

> >

> > Good morning all, (morning in Alaska anyway),

> >

> > I have posted a few times and met with quick responses. Thank you

> > all for your input. I am a little concerned about this surgery

as I

> > have not had surgery for 30+ years. What should I prepare myself

> > for? Post-op surgery care? Is it painful the next day? A week

> > later? Is swallowing a problem?

> > My surgery is scheduled for 9am alaska time. So if anyone could

> > write back I would sure appreciate it.

> >

> > Thanks all and have a wonderful holiday season.

> >

> > Terrance

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

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HELLO ALASKA. I AM HAVING MY FIRST SURGERY IN JAN TO BE EXACT. PLEASE FILL ME IN ON ALL THE DETAILS AFTER YOUR SURGERY PLEASE . WHAT WAS IT LIKE THE PAIN THE RIDE HOME DID YOU HAVE THE CWU OR CWD? PLEASE GET BACK IN TOUCH THANKS THANKSbryantsinalaska <bryantsinalaska@...> wrote:

Barbara, I am having the surgery in Soldotna. The Dr. said he wasnt sure until he got inside my head which one he would do. He is going to try the CWU first, but if things are not good in there then he will go to the CWD. I guess thats the thing that is disconcerning, not knowing what the outcome will be. And if my nervousness is any indication to the Dr then this will be a one surgery deal !!. I am doing my best to stay positive, and appreciate your response. I do really well, (like most men I would assume), comforting my wife or my children when these life issues arise, but being the one in the bed is not very easy. You all do a good job of easing a persons fears and trust me I appreciate everyone that has posted here. Thanks again Barbara and its about time we

got enough snow to enjoy. I will post as soon as I can after the surgery and maybe help someone else. My wife passed along a good one to me. " The difference between minor surgery and major surgery" Minor surgery is when someone else is going in !!Terrance> > > > Good morning all, (morning in Alaska anyway),> > I have posted a few times and met with quick responses. Thank you > all for your input. I am a little concerned about this surgery as I > have not had surgery for 30+ years. What should I prepare myself > for? Post-op surgery care? Is it painful the next day? A week > later? Is swallowing a problem? > My surgery is scheduled for 9am alaska time. So if anyone could > write back I would sure appreciate it.> > Thanks all and have a wonderful holiday season.> > Terrance> > > > > > > > > >

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  • 2 years later...
Guest guest

Peggy,

We will all be routing for you! Stay strong, and I know we'll be hearing great

things from

you soon.

Love,

Edie

>

> My big day is almost here. I'll be on my way to the hospital (Duke) in less

than 12

hours. My hubby doesn't want to stay in the hotel overnight so we will leave

here at 2 AM.

That makes it a little harder on me but I'm not the one driving. I have to be

there at 6 AM

and they will take me back for surgery about 8 AM.

>

> Seeing the ladies at the retreat earlier this week gave me the courage to go

through with

the surgery. I see how I can be in one year and it looks good! The girls said

I will be

cussing them out on Friday for talking me into surgery but I guess I'll get over

it as I heal!

I probably won't even remember it! I hope I don't remember a lot of things that

happen in

the hospital! I am taking my laptop with me and I'll try to get my hubby to

post a message

after a day or 2 after surgery. Please keep me in your prayers.

>

> Peggy

>

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Guest guest

Peggy,

If you are still up tonight and reading....good wishes for a safe and

good revision tomorrow and I look forward to hearing a great report

from your hubby!

Peace, Cam

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Guest guest

Best of luck Peggy! My thoughts and prayers are with you.

Does Dr. Hey have a web site?

Thanks, iewww.ieBush.comSee what's free at AOL.com.

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Guest guest

,

Thank you for sharing your story. It is really amazing to most of us

that the ortho/neuro doctors continue to act as if " flatback " (or the

new so called " transition syndrome " ) is not a readily identifiable

constellation of symptoms that arise following Harrington Rod

instrumentation and long fusion. I suspect that during most docs

training HR was still a procedure being done and sine they have gone

off to specialize in other areas they maybe are not as up to date as

they could be....but it seems inexcusable that we are shuttled around

the medical system with no clear direction, or are often exposed to

procedures that may make a real fix difficult in the hands of a

qualified expert...and even told we are hopeless and/or that our

problems are all in our head. Really....it brings tears to my eyes.

The experience of " coming home " when you find medical help that has a

clue is a good feeling. I wish you the best. My only fear for you now

is that all your previous procedures will create extra challenges for

DrHey. I do hope that is not true...and I know that experienced

surgeons in this field often wade in to spines that have had lots

of " work " ....and still get good outcomes. Geez, you would think that

the group of docs that deal with our malady would be standing on

the " medical rooftops " screaming about what needs to happen to our

population and help direct patients to appropriate care.

We look forward to hearing more from you and of course more about how

it all goes in just a few weeks.....yikes! It comes up fast but try

to stay centered and at peace and visualize a good outcome. You will

get there.

Take Care, Cam

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Guest guest

,

That's quite a story. I can relate to it in so many ways, as my first primary

care physician 3

years ago pulled the old " Your pain has nothing to do with your previous fusion,

I assure

you " routine, which led me to a series of epidural injections, pain killers,

crappy PT, etc.

But nothing to the extent of what you've experienced.

Doesn't it feel great to get that story off your chest to people who know what

you mean? I

hated feeling like I was crazy because I was in so much pain, and it was so

obviously

related to my previous fusion, but no one wanted to hear about it.

I feel the same way about my surgeon, Dr. Bendo, as you do about your

consultation with

Dr. Hey. Here is someone who is relatively young, but with lots of experience,

never once

questioned MY experience. All he had to do was look at my X-Rays, and he

immediately

identified my flatback, told me the cause of the pain, and was incredibly

sympathethic. He

urged me to get other opinions, but also told me that any ortho worth his salt

would look

at my X-Rays and understand that I needed revision surgery. (And of course, he

was right)

He is a confident doctor who takes tremendous pride in his work and does not

hide that

fact (But NOT pompous or arrogant). He has never once been condescending to me,

and

never made false promises. And so far as my correction goes according to my post

op X-

Rays, he had every reason in the world to be confident in his skills and instill

that

confidence in me as his patient. He visited me every day in the hospital, called

me when he

was going out of town to let me know if I had any questions or concerns, and

responds

within 24 hours to both my pre-op and post-op email queries.

So, even though he is not known in this circle, he is one of the better known

orthopedists

in NYC, and I couldn't have gone into this surgery in better hands...and I knew

that.

What a relief it is going into surgery with someone you absolutely 100% believe

you can

trust with your life. Literally.

Good luck with your upcoming visit. We'll all be anxious to hear how it goes. I

hope that

Dr. Hey can provide you with the relief you are seeking, and so deserve after

all these

years.

Love,

Edie

>

> Yes, Dr. Hey. My husband and I were so " blown away " when at my first

appointment

with him (April 4th, 2007). He offered to get us a softdrink, he took digital

photos of my

x-rays, films, etc. that were on the computer monitor. I've never met any

professional who

was so personable, compassionate, and confident in his skills (he's good and he

knows

that) - and I mean that in the most sincere, positive way. In about 3 minutes

he had my

situation summed up, and I could tell by what he was saying, the questions he

was asking

me, just everything in general, that he saw the reason for my pain and

limitations I've been

living with. Instead of asking " does it hurt for you to stand for a period of

time " he asked

" how long can you stand up " . I told him that on the average I could stand up

long enough

to fry an egg. Instead of asking " do you have any problems walking " he asked

" how far

can you walk " . I guess by using the term " blown away " entails a wide range of

things. As

he went into describing what he saw, both in my films and in how I walked,

stood, etc., he

directly connected it with scoliosis and the prior (1972) Harrington rod fusion.

Every

doctor I have seen, since 1999 when this set of issues with my back (lumbar),

would barely

acknowledge scoliosis, not even reference my prior spine fusion. The first MD I

saw clearly

stated that he was a sports doctor and knew nothing about scoliosis or back

problems (my

primary care physician's office set this visit up with a provider in my

insurance network).

The second MD was a little bit better than that but when he viewed the CT he had

ordered

(which was my first) and at this time there was just a bulging disk at L3-L4, he

said " this

can heal " . He ordered my first round of epidural injections, physical therapy

and very

freely prescribed Tylenol #3. At this point in my life I considered myself a

veteran to back

pain, having undergone T1 thru L1 fusion at age 17. My only concept of lower

back pain

was that of a pulled muscle (boy we surely learn by experience don't we!)...I

gave up

seeking help for about a year while hoping things would get better. Then

someone

recommended a neurosurgeon since the pain had long been radiating down my leg.

My

primary care doc. set up an appointment with a well known neuro at a well known

neuro &

spine clinic. He, as with the others, didn't see or indicate that they saw a

connection with

scolio & previous fusion and the lumbar problems. He did two surgeries, the

second to

re-do the first & to remove a cynovial cyst that was not previously detected,

and after the

removal of that, I did experience a broader range of motion but was only

minimal. After

my office visits I'd have to get the office notes for my employer and insurance

co. and it

continuously bewildered me what they said. According to the notes, I was

progressing

well and was released " full " to return to work. Nothing I had said was even

noted in the

files. After about two years I went back to him, in more distress than ever and

I'll never

forget that moment when he was holding my file in his hands, closed it like you

close a

book, and said " there's nothing else I can do " , " I'll send you to pain

management " . That

pain management turned out to be epidural injections AGAIN, and that doctor

asked " what

are you doing here? we usually send patients to them " . He really went on about

my

" crooked back " - not in a making fun way, but did see that my back was NOT

normal. I

had two of the three injections AGAIN, to no help, AGAIN. He then referred me

to physical

therapy. This particular program was to be in group form (about 12 people), to

be 4 hours

a day, 4 days a week, for 4 weeks - and was 1 1/2 hrs. commute time to get

there. I went

for the initial exam. The PT kept saying " Hmmm " . She also remarked about my

crooked

back. After the exam, she went through all of the exercises involved in the 4

week

program, and in EVERY instance she noted how the exercises would be modified for

me

because of my fusion, scoliosis, weird mobility range, etc. I wound up

canceling out of

this program because I figured if it didn't kill me, I'd kill myself - and

honestly couldn't

afford to take a month off work without pay - and this was not the treatment I

needed.

>

> All along, with each and every professional I saw, I made sure that I told

them that when

the lumbar pain started kicking in, that I also noticed that when I pulled my

pants up that

they were off center. Even my skirts would wind up out of center - it was like

the

scoliosis, or the rotation, had, after all of these years, kicked back in.

People that I knew

would even ask out of nowhere " is there something wrong with your back " - or

something

like that. The professionals never commented after I made this statement, which

I felt

HAD to have something to do with the newfound pain and never before experienced

corresponding pain going down my right leg.

>

> I spent two years with a pain D.O. who didn't prescribe meds - but did the

Medtronics

stimulator trial implant - that was a disaster - the leads came out 3 days

after, which is

unusual, but I attributed it to the abnormal motion going on in my back and I

think they

came out during my sleep.

>

> So, then, I saw another doctor (neuro) at the same practice as the other. Now

I felt like

something good was going to come out of this doctor. NOT. He fused L3-L4,

which left

L2-L3 there in between the old and new fusion. That was in 12/2005 and since

then, L2-

L3 literally sit on top of each other. There was another synovial cyst which he

removed

during the surgery.

>

> In one of my post op visits I point blank asked him if he felt that scoliosis

and the prior

fusion had anything to do with the lumbar problems I now had. His reply was

(after a

moment of pause) " well, they're all connected " . Did I get a warm and fuzzy

feeling about

being in his care? NO - though he did seem to listen more - but that was about

all.

>

> Since the Dec. 2005 surgery, and based on my calls to his office about

different things

going on, I've had 3 more MRIs, all of which he stated " of course they're not

normal,

because of your situation, but we just don't see anything that is causing the

pain you say

you're in " . So, forget the pain, why can I not sit, stand or walk, and why do I

look/feel 90

instead of 51-52? He phoned in a $400.00 prescription which my insurance did

not cover

and told me to call him back in two weeks if that didn't help and he would order

a CT, then

changed it to a Myleogram (not a stranger to that either). When I asked about

getting

documentation for my LTD and employer (they have already hired someone for my

position) - his reply was " it's fine by me if you go back to work " .

>

> It was that moment that I realized " he has no clue " -- he just has NO clue.

>

> It was within days of that phone conversation that I heard about Dr. Hey. At

first I was

thinking " yeah, another good doctor....until I visited his web site. I got so

emotional - like

I was being Saved - that same feeling came over me. In a few days I emailed

through their

website, the next day I got a response from both emails I had sent - scheduled

the April

4th appointment - going tomorrow for pre-op and May 15th is my surgery.

>

> I have been experiencing a LOT of anxiety about what I won't be able to do

after this

surgery continues the fusion from the Harrington rod to my sacrum but it hit me

that I was

concerned about being able to do things that I haven't been able to do for years

- so now I

am ready, ready to reclaim my life, and so grateful for good doctors like Dr.

Hey and the

rest of this small group of gifted surgeons.

>

> Sorry to have gone on so long, and, believe it or not, this is a condensed

version - and

though this wonderful group of people here share so much in common, and I

consider

myself fortunate because my situation is not nearly as complex as many, but we

all have

had our own set of nightmare diagnosis', personal letdowns, personal sacrifices

in our

individual bodies and worlds. So though we're a lot alike, we're still unique.

>

> Again, sorry about the rambling on....best of health to everyone,

>

> [ ] surgery tomorrow

>

>

>

> My big day is almost here. I'll be on my way to the hospital (Duke) in

less than 12

hours. My hubby doesn't want to stay in the hotel overnight so we will leave

here at 2 AM.

That makes it a little harder on me but I'm not the one driving. I have to be

there at 6 AM

and they will take me back for surgery about 8 AM.

>

> Seeing the ladies at the retreat earlier this week gave me the courage

to go through

with the surgery. I see how I can be in one year and it looks good! The girls

said I will be

cussing them out on Friday for talking me into surgery but I guess I'll get over

it as I heal!

I probably won't even remember it! I hope I don't remember a lot of things that

happen in

the hospital! I am taking my laptop with me and I'll try to get my hubby to

post a message

after a day or 2 after surgery. Please keep me in your prayers.

>

> Peggy

>

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Guest guest

Hi Cam,

Do you know the story behind the creation of the words "Transition Syndrome" to describe what is otherwise referred to as "Flatback Syndrome"? And what does Transition Syndrome really mean? Transition from what to what? So far, until I know more about it, the words "Transition Syndrome" have so little meaning.

Thanks,

Bonnie

[ ] Re: surgery tomorrow

,Thank you for sharing your story. It is really amazing to most of us that the ortho/neuro doctors continue to act as if "flatback" (or the new so called "transition syndrome") is not a readily identifiable constellation of symptoms that arise following Harrington Rod instrumentation and long fusion. I suspect that during most docs training HR was still a procedure being done and sine they have gone off to specialize in other areas they maybe are not as up to date as they could be....but it seems inexcusable that we are shuttled around the medical system with no clear direction, or are often exposed to procedures that may make a real fix difficult in the hands of a qualified expert...and even told we are hopeless and/or that our problems are all in our head. Really....it brings tears to my eyes.The experience of "coming home" when you find medical help that has a clue is a good feeling. I wish you the best. My only fear for you now is that all your previous procedures will create extra challenges for DrHey. I do hope that is not true...and I know that experienced surgeons in this field often wade in to spines that have had lots of "work"....and still get good outcomes. Geez, you would think that the group of docs that deal with our malady would be standing on the "medical rooftops" screaming about what needs to happen to our population and help direct patients to appropriate care.We look forward to hearing more from you and of course more about how it all goes in just a few weeks.....yikes! It comes up fast but try to stay centered and at peace and visualize a good outcome. You will get there.Take Care, Cam

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  • 5 months later...

Well, I can safely say I know how panicked you feel! My son had his

first surgery about 4 days before Halloween when he was 5 years old,

and it scared me and broke my heart. I turned to this Group

and learned so much. It didn't make me any less nervous, but it did

prepare me so I didn't feel so blind going into it. Did you check

out the " Files " link on the left of the page? After my first ordeal

I posted some tips I'd learned from other people. I hope you'll find

it helpful.

A word from one mom to another: For your son's sake, do your best

to be calm and in control, and loving but matter-of-fact about the

need for the surgery. When he goes into surgery, I would urge you

to keep control of your emotions while he is " falling asleep. " You

don't want your own emotions to scare him, but you WILL feel

emotional so just take a deep breath and put on a good act. After

he's asleep, you can fall apart. I did! Really, I can tell you

it's been very helpful for my son (who has had 4 of these surgeries,

soon to have his 5th) when I've just been normal, loving, helpful

mom up to and including the falling asleep part. I know he gets

anxious, but it helps him to believe that I'm in control and that

this isn't scaring me, too.

So for yourself, expect to be shaking and expect to cry your eyes

out while he's in surgery. Expect to cry again (from relief!) once

he's safely out of surgery, and then expect to feel exhausted from

all that emotion! Don't forget to eat something while he's in

surgery!!! Pack some food in your purse so you can sneak snacks in

the bathroom while he's waiting to go into the OR. Sometimes the

wait is VERY LONG, and you won't want to eat in front of him, so be

sure you have a strategy for keeping your blood sugar up.

At our hospital (Mass. Eye & Ear in Boston) the nurses will give you

a pager so you can go to the cafeteria while you're waiting out the

surgery. Maybe this will be the same at yours? We usually wait an

hour or so (in case the surgeon needs to call us from the OR, which

happened once), but then we know we have at least another hour

before we'll get a call because the surgeries aren't usually less

than 3 hours. We take that opportunity to eat as much as our

appetites can handle because once he comes out of the OR, there

really isn't an opportunity to go eat again. Buy chips, cookies or

other things you can take back to the room with you for later, in

case it gets to dinner time and you find yourself sagging from lack

of food.

Here's another tip: When you get called to the recovery room, go

use the bathroom quickly before you hurry to his side. You won't

want to leave him for something as silly as your bladder, but it

WILL catch up to you eventually, so you might as well do what you

can to stave off the inevitable. Again, I know this from

experience. :-)

Remember to pack an overnight bag for yourself so you can stay with

your son overnight if he's sick from the anesthesia. Yes, we've had

to do that several times, so take it from a pro! You'll want a

magazine (People is good because it's fairly shallow fare, not hard

to concentrate on), you'll want a full change of clothes, your

toothbrush, your hairbrush. Don't bother with makeup -- you'll just

cry it off. LOL

For your son, bring extra undies and a shirt that buttons down the

front if you can -- just much easier to get on him than a pull-over

shirt after surgery.

That's all I can think of. I'm writing it almost as much to remind

myself as to inform you ... my son goes in on November 7th for his

5th surgery. I'm unhappy about it but no longer crazy with

anxiety. I really feel for you and know what you're going through.

At this time tomorrow, it will all be over with and you can breathe

a sigh of relief.

Let us know how it goes. I'll be thinking of you.

Alice

>

> My 6 year old son is getting his surgery tomorrow. Me his mom is

a

> mess, so is Dad. This board has been helpful though, I think at

times

> we have learned to much though. So I am very hopeful that all

will go

> well . Just wanted to let people know that answered some questions

for

> me when we just found out about these damn c'tomas. Today I can't

seem

> to focus to much on anything and I had to take the week off just

to

> deal with all this and my little one is being such a champ about

it all

> he is just upset that he has to miss halloween. How I wish I

could

> have the innocense of not knowing like my child. Well thanks to

all

> here and I will let you all know how things went.

> Sincerely

>

>

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  • 5 months later...
Guest guest

Good luck... hope you're feeling right as rain soon.

Kazzy

xx

Surgery tomorrow

Well I am heading into the final stretch - My 2nd Ctoma surgery is tomorrow at 8:30. This is operation 14 - over 30 years. They are not certain if they will be able to reconstruct -but I have no complaints as I have had a great run and decent hearing for many years. I will post when I am all done. This site has helped even after all the operations it helps to read all the positive postings.Wish me luck!

No virus found in this incoming message.Checked by AVG. Version: 7.5.524 / Virus Database: 269.23.2/1388 - Release Date: 4/20/2008 3:01 PM

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Great attitude. After all those surgeries, you seem to have everything in perspective. Good luck!

Surgery tomorrow

Well I am heading into the final stretch - My 2nd Ctoma surgery is tomorrow at 8:30. This is operation 14 - over 30 years. They are not certain if they will be able to reconstruct -but I have no complaints as I have had a great run and decent hearing for many years. I will post when I am all done. This site has helped even after all the operations it helps to read all the positive postings.Wish me luck!

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I am sending all positive thoughts to you, as I am sure many others are. We'll be looking forward to hearing how it all has gone. Best of luck to you!leOn Apr 21, 2008, at 8:48 PM, nanctc wrote:Well I am heading into the final stretch - My 2nd Ctoma surgery is tomorrow at 8:30. This is operation 14 - over 30 years. They are not certain if they will be able to reconstruct -but I have no complaints as I have had a great run and decent hearing for many years. I will post when I am all done. This site has helped even after all the operations it helps to read all the positive postings.Wish me luck!

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Guest guest

>

> > Well I am heading into the final stretch - My 2nd Ctoma surgery

is

> > tomorrow at 8:30. This is operation 14 - over 30 years. They are

not

> > certain if they will be able to reconstruct -but I have no

complaints

> > as I have had a great run and decent hearing for many years. I

will

> > post when I am all done. This site has helped even after all the

> > operations it helps to read all the positive postings.

> > Wish me luck!

> >

> >

> >

>

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  • 2 weeks later...
Guest guest

I am not sure but I am going to say it thank you, and god bless you

too.

> >

> > > Well I am heading into the final stretch - My 2nd Ctoma surgery

> is

> > > tomorrow at 8:30. This is operation 14 - over 30 years. They

are

> not

> > > certain if they will be able to reconstruct -but I have no

> complaints

> > > as I have had a great run and decent hearing for many years. I

> will

> > > post when I am all done. This site has helped even after all the

> > > operations it helps to read all the positive postings.

> > > Wish me luck!

> > >

> > >

> > >

> >

>

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  • 3 weeks later...
Guest guest

I hope all goes well for you .

mark Hardin <gilachub@...> wrote: Hi all - my

surgery for Posterior fusion of C5-6 C6-7 is scheduled for

tomorrow (as well as decompression of the nerve root to my left arm) I

will keep you all informed when I can. I suspect I won't be posting

for at least a week. Thanks for all that have given me info and

support to this point.

mark

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  • 10 months later...
Guest guest

All the best, . I am really interested in how you go - almost

identical issues to mine. I also have had FM for more than a decade.

Jen

> From: Loest <boltzero@...>

> Reply-<spinal problems >

> Date: Mon, 30 Mar 2009 02:44:59 -0000

> <spinal problems >

> Subject: Surgery Tomorrow

>

> I'm going to the hospital tomorrow morning at 7:30am to hopefully correct 10

> years of misery.

>

> L5 is scheduled to be fused by Dr. Karl Swan & Dr. .

> Dr. Swan is the top neuro surgeon in my neck of the woods.

>

> He will be performing the clean out around L5, Dr will be installing

> the hardware which will consist of a Titanium plate and screws, some

> additional bone graft will also be performed.

>

> I'm curious how the pain amplification aspect of Fibromyalgia is going to play

> into the recovery, I suppose there is only one way to find out first hand.

>

> After the procedure I of course will be able to set off metal detectors, and I

> wonder if refrigerator magnets will stick to my lower back.

>

> Anywho I will be off the radar for awhile, hopefully everything will go as

> planned and I will get some of my life back afterwards.

>

>

>

> ------------------------------------

>

>

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Guest guest

I will be praying for u.

Dawn E.

(540) 247-1692

I would rather be hated for who I am

than to be like for who I am not ~Author Unknown

From: Loest <boltzero@...>

Subject: Surgery Tomorrow

spinal problems

Date: Monday, March 30, 2009, 2:44 AM

I'm going to the hospital tomorrow morning at 7:30am to hopefully correct 10

years of misery.

L5 is scheduled to be fused by Dr. Karl Swan & Dr. .

Dr. Swan is the top neuro surgeon in my neck of the woods.

He will be performing the clean out around L5, Dr will be installing the

hardware which will consist of a Titanium plate and screws, some additional bone

graft will also be performed.

I'm curious how the pain amplification aspect of Fibromyalgia is going to play

into the recovery, I suppose there is only one way to find out first hand.

After the procedure I of course will be able to set off metal detectors, and I

wonder if refrigerator magnets will stick to my lower back.

Anywho I will be off the radar for awhile, hopefully everything will go as

planned and I will get some of my life back afterwards.

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Guest guest

I will be praying for u.

Dawn E.

(540) 247-1692

I would rather be hated for who I am

than to be like for who I am not ~Author Unknown

From: Loest <boltzero@...>

Subject: Surgery Tomorrow

spinal problems

Date: Monday, March 30, 2009, 2:44 AM

I'm going to the hospital tomorrow morning at 7:30am to hopefully correct 10

years of misery.

L5 is scheduled to be fused by Dr. Karl Swan & Dr. .

Dr. Swan is the top neuro surgeon in my neck of the woods.

He will be performing the clean out around L5, Dr will be installing the

hardware which will consist of a Titanium plate and screws, some additional bone

graft will also be performed.

I'm curious how the pain amplification aspect of Fibromyalgia is going to play

into the recovery, I suppose there is only one way to find out first hand.

After the procedure I of course will be able to set off metal detectors, and I

wonder if refrigerator magnets will stick to my lower back.

Anywho I will be off the radar for awhile, hopefully everything will go as

planned and I will get some of my life back afterwards.

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