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Kate B:
Here is my own story about my experience with HEI. 

I think the *term* brain surgery can be frightening. It doesn't have to be.
I must admit that when reading the posts in the old format called a guestbook and on the
listserv, people were extremely satisfied with House. I believe that if you
go to an institution like House for surgery, you will get the best possible
outcome.

I had Middle Fossa Surgery for a 1.5 cm right sided AN on November 29, 2001 with Dr.
Brackmann and Dr. Hitselberger.  The staff there is very professional and
used to handling acoustic patients. As a matter of fact, House takes up the
whole sixth floor of St. Vincent's Hospital.

My surgery was 4-41/2 hours. You complete several tests the day before
surgery  including a hearing test, a meeting with the surgeons, bloodwork
etc..

The day of surgery is interesting.  They typically start the operations in
the late morning/early afternoon. You check into the hospital about 9 am and
you go to the sixth floor and wait in a private hospital room until surgery.
When it is time, you are wheeled down a corridor toward surgery. It seems
funny to remember this, but I remember the sunlight streaming in through all
of the windows. Then you are taken  to a room where you meet with the
anesthesiologist.  The doctor confirms the correct side of the AN and marks
your ear.  I remember the anesthesiologist asking me what I was most afraid
of prior to surgery.  I remember answering her and her reassuring me.  Then
I was out and before you know it they are waking you up and asking you to
wrinkle your nose and smile. These are actually informal observations that
they use to determine your facial nerve outcome.

You are kept in ICU 24 hours and then discharged to your own room. All of
the rooms are individual (private) by design. The first 24 hours were the
hardest for me because I was dizzy.  But before you know it, you are
returning to the sixth floor.    My surgery was Thursday, I was in ICU until
Friday night and discharged to Seton Hall on Monday. (Seton Hall is adjacent
to the hospital and is a facility where you recover). It is like a Holiday
Inn and the charge is a nominal $35.00 per night (2001) making the stay affordable.

By the following week,  I went to a restaurant in Hancock Park
and the waiter was in disbelief to learn that I had brain surgery the week
before. I must admit, I was tired afterward and that trip tired me out...I
set goals and stuck to them. I  just worked to get better.  I was 45 when
diagnosed and 46 when I had the surgery. I was *determined* to get back into
my routine ASAP without overdoing my recovery. I followed the doctor's
orders during my 5 week recovery time before my return to work.

The doctors  want you to stay in CA for two weeks.  I ran a low grade fever
for a few days about 5 days afterward.  Dr. Stephen (the internist that you
see out there) was not worried because of the low gradedness of it and no
headache associated with it. Fatigue was the biggest culprit the first few
weeks. I took daily naps. My facial nerve was preserved, my eye closed all
the way and I retained much hearing. (note: I had 100% hearing prior to the
surgery in that ear.  Now I have 50% low frequencies and ~80% high
frequencies and 84% word discrimination.)  Each day I grew stronger.  The
first day in my hospital room, I made a goal to walk around the floor once
per hour. The next day my goal was three times per hour.

We stayed at Seton Hall the
entire two weeks.  Some chose to move into a hotel after surgery.

The most important thing no matter which treatment you choose is to look at
the physicians and their experience.  On the listserv, people generally say
that the doctor should have more than 100 treatments under his/her belt.
Check out their statistics relative to patient outcomes for your specific type of treatment. 

Kindest Regards,
Kate

Becky:
I wish I could have gone to the House for mid fossa. 

Becky

David Wrubel:
I had almost no symptoms until I felt strange and dizzy going up and down a ladder. My Connecticutl Otologist (who ironically had been a fellow at House 30 years ago) sent me for an MRI to "eliminate" the possibility of a tumor, which I instantly knew I had. Thinking that the absence of symptoms correlated with the size of the tumor, within two days I was  ready to go down to Johns Hopkins or the Cleveland Clinic for radiosurgery. Then the MRI scans came back.

The AN was huge. Radiosurgery was out, he explained, because the tumor was so large that there was no room for swelling and that the pressure on my brain stem, already significant, would increase to the point where I could die. Thus began my quest for the best possible surgical outcome, starting locally, expanding to Mass. General, Yale, Sloane Kettering, Mt. Sinai, and House. All but House were relatively close, and all but Yale were out of network, according to my insurance company. But that's another story.

Discussions with doctors at these institutions revealed significant differences. Their personalities were a factor, their surgical approaches varied, and with the exception of House their prognoses were guarded and far less than I was looking for. Some estimated 14-16 hours under anesthesia, and a couple of the surgeons told me in no uncertain terms they would have to sever the facial nerve. One said I'd likely need two surgeries. I sent my scans to House, and the next day Drs. Rick Friedman and Bill Hitselberger called me. Basically, they said, I needed to have this thing out quickly, felt strongly that they could do it without severing the facial nerve, and expressed confidence that my outcome would be quite good. Surgery would take five to six hours, an entire floor of St. Vincent's hospital across the street for the Clinic was devoted to their surgical patients, and the medical staff - not just the surgeons -  had seen every complication and was accustomed to handling any situation.

Over the next two months, I submitted three formal appeals to my insurance company to allow me to go out of network and have the surgery performed at House. All three were rejected, this after extensive medical research and documented statistics, courtesy of access to the University of Connecticut Medical School Library via my good friend and cardiologist. The people at House were outstanding, sending letters on my behalf and agreeing to be reimbursed by my insurance comapny as if it were a California HMO. But the key was my wife, who out of frustration called the Medical Director of the insurance company and told him that she thought I was going to die. While that wasn't the case, it go his attetion and I got my approval. I had about four days to actually worry about the surgery.

My experience as a patient was outstanding. I believe that my absolute faith in Friedman and Hitselberger helped enormously. Not only did I never once think I might actually die, but I had no doubt that I would be able to resume my life with very few residual effects of the surgery, aside from losing the hearing on my right side. That, I figured, was a small price to pay.

There was very little pain, at least relative to what I expected. Because the tumor was so large and the surgery so long (6 hours, which for House is a long procedure), I was in ICU for three days, then in a room for another five days. I was released, but developed a very small CSF leak that only required that the incision (hole in my head!) be repacked and reclosed, which Hitselberger thought from the outset might have to be done. A few days later I was released, and my recovery began.

Rick Friedman told me when I left Calfornia that mine was the largest AN they had removed to that point where the outcome resulted in such a high degree of facial mobility, lack of headaches, almost no balance issues, and no eye problems. Hitselberger wanted to take me to a LA Dodgers game toward the end of my stay, but they were out of town!

The flight home was uneventful, and though I was much more tired than usual for the next three months or so, things were remarkably normal from the beginning. I started driving again two weeks after my return, and a month later attended my first business meeting in New York. That nobody present suspected anything unusual about me at this meeting was the result I was looking for.

It's now almost exactly five years since the surgery, and I can still tell you what I had for breakfast the day after I was released. As if it were yesterday, I remember my first post-hospital bath, certain things we bought in LA, and my wheelchair ride through LAX. There is some residual numbness in part of the right side of my face, sort of like permanent mild novocaine. I can't kayak (takes an amazing amount of coordination and balance), my basketball career is over (then again, at 50 yrs. old it was anyway), and I do shy away from concerts and really loud clubs, since I only have one ear left. Which brings me to the biggest problem I have....I miss hearing in stereo. Following conversations in noisy restaurants is difficult, and strategic seating in such places is a must. Again, a small price to pay for what might have been a far less satisfactory outcome.

If I had $10 million of spare change, I'd give a lot of it to House. They didn't just save my life...they preserved it. For those of you now facing all the decisions that are part of the AN process, this should be your goal: A Great Outcome. Let nothing, not distance, not cost, not even insurance companies, get in your way. Particularly if you have a large tumor, in my opinion 2 cm or larger, House is the best place to go. There is more individual and institutional experience in this very specialiozed form of brain surgery at House than there is anywnere else in the US.

Please, feel free to contact me with any questions or concerns. I have been in touch with lots of people over the past five years, including some other people on this forum. When I get an AN message on my machine, it's the first one I respond to. Same with emails. Talk to you soon.

Good luck....DW


Update 4/23/05: Recent MRI showed no tumor regrowth. Fourth year in a row. Radiologist who reads my scans can't get over the quality of the work. He calls the surgery a work of art every time he transmits the results to my internist.

sreda:
Hey, y'all (I'm from the southern US):
Replyling to Kate and Kristin aobut House. I had my tumor removed late last summer at House, by Drs. Hitselberger and Brackmann.
My experience before, during and after was as good as I could have hoped... better, actually. I have highest regard for the docs, House, St. Vincent's hospital, Seton Hall recovery/lodge, nursing staff, attending internist Dr. Stefan. They ALL "knew their stuff" thoroughly, and were compassionate, straightforward and thorough. I'd go back there for the same reason if I ever have to... but I hope I won't.

Sis

   

micbendz:
Has anyone had surgery  performed by Drs. Luxford or Schwartz at House?

Thanks, Mike

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