Author Topic: Informal Facial Paralysis survey  (Read 9882 times)

Zokess

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Informal Facial Paralysis survey
« on: June 30, 2006, 06:01:09 am »
Okay..I was doing good dealing with the facial paralysis that went along with the AN surgery.  I thought my surgeon said there wasn't much hope for any sort of recovery from the paralysis because those nerves were so inter-twined with the tumor that he could not save them.  My fiance on the other hand thought he said they were just very stretched and thinned. But anyway, after the initial denial, etc...I have accepted my "new" face as is and am learning to deal with it.  Then I read an article that someone else had posted a link to in another discussion, written by an eye specialist in the UK who had a AN removed.  The article mainly dealt with implications of the eye, but did mention that it could take as long as 18 months for damaged nerves (Like the ones responsible for facial paralysis) to regenerate/heal from the trauma of surgery.  So now here I am, almost 9 months post-op thinking that things could get better over the next 9 months.  I'm trying not to get to optamistic and set myself up for a dissapointment in 9 months when nothing has recovered.

So on to the informal survey........I know this has kinda-sorta-been covered in another discussion thread, so I apologize if this is s re-hash of that discussion....but of those of us who experienced facial paralysis post-op...how many of us have experienced a recovery to at least some voluntary muscle control, and how long post-op did this recovery occur.

Thanx in advance
Bruce E. Hamilton
5 CM Left Side Removed via Retrosigmoid/Sub-occipital Approach
11OCT05 Surgery date @
Wasahington Co Hosp. / Hagerstown, MD
Dr. David Caruso of Neurosurgical Specialists Llc

Joef

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Re: Informal Facial Paralysis survey
« Reply #1 on: June 30, 2006, 10:06:04 am »
    I'm in the same boat ... 11 months post-op .. face is feeling a little better (I think) .. but still no movement at first the Dr's said 6 months , then at the 3 month check up they said 1 year .. but I've read on different sites up to 18 months ..
   My eyes have been good. with all the wet weather we are having in the northeast has actually been helpful ! I'm using drops in the morning,  and before the drive home from work .. and at bed time I need the thick stuff still . and sometimes like last weekend I went fishing in the rain .. my eyes were as good a new .. I went ALL day without .... (I was soaking wet too by the time I came home).
  I have accepted the fact my face will always be a little "off" , but would like to be able to smile again for pictures and such .
4 cm AN/w BAHA Surgery @House Ear Clinic 08/09/05
Dr. Brackmann, Dr. Hitselberger, Dr. Stefan and Dr. Joni Doherty
1.7 Gram Gold Eye weight surgery on 6/8/07 Milford,CT Hospital

daylilly

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Re: Informal Facial Paralysis survey
« Reply #2 on: June 30, 2006, 01:05:01 pm »
I too am 11 months out. Facial paralysis is what led me to this site. I had some episodes of facial paralysis prior to finding the AN.
The Drs. left some tumor on the facial nerve to preserve it. The nerve was stretched and thin but they got a good reading
after surgery. At 6 mo. I had an EMG which showed electric potential in my lower lip and around my eye. At 11 mo. my lower lip
feels pretty strong. I have some slight movement in the corner of my brow by my nose and slight movement along the side of my
nose. My forehead wrinkles seem to be extending farther into the AN side. The bells palsy site indicates that there can be improvement
18 mos. and some beyond. My recent MRI was stable-yeah! I still have no eye blink and no smile. I think I have more tone. If
I sort of suck in the corner of my mouth on the AN side I sort of look symmetrical. My next appointment will be at 18 mo. Other
than dealing with the dry eye stuff, life is pretty much back to normal. I am hoping that there will be continued facial improvement.
3 cm AN
translab July 2005, Emory, Dr. Mattox, Dr. Olson
gold weight, Dr. Wojno
left-sided deaf
left-sided facial paralysis

amymeri

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Re: Informal Facial Paralysis survey
« Reply #3 on: June 30, 2006, 07:06:56 pm »
I am only 3 months out and had excellent nerve conduction after surgery and the paralysis took a couple days to set in.  Now it is total and I have no movement anywhere.  The eye dryness is the worst symptom.  Drs said 3-6 mos to get better, now I know it will be more like 18 mos...if it ever gets better.  I wish I had known the truth before the surgery. :-\
Amy

4 cm right AN removed restrosigmoid 4/13/06
Partial facial paralysis, SSD and trigeminal numbness for now

matti

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Re: Informal Facial Paralysis survey
« Reply #4 on: June 30, 2006, 07:46:50 pm »
I am 8 years post op and also had facial paralysis. The AN had wrapped itself around the nerve and severly splayed it. The nerve recovered to about 80% of normal within about a year after surgery and has stayed that way until last November. I started noticing the tightness in my face and head (AN side) slowly disapearing. My smile is not as crooked as it had been either. I can actually feel different muscles in my scalp move that I could not before.

 My doctors/surgeons were/are baffled and did an MRI, eveything was fine, no tumor.  Who knew I'd still be healing this far out....weird and amazing.

3.5 cm  - left side  Single sided deafness 
Middle Fossa Approach - California Ear Institute at Stanford - July 1998
Dr. Joseph Roberson and Dr. Gary Steinberg
Life is great at 50

Pembo

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Re: Informal Facial Paralysis survey
« Reply #5 on: July 01, 2006, 07:14:12 pm »
I started with a small, tiny movement at 4 months and have seen improvement on a regular basis since that point. (Now 2 years later). I've had a lot of recovery in the last 6 months, past the 18 month mark. Don't give up hope.
Surgery June 3, 2004, University Hospitals Cleveland, BAHA received in 2005, Facial Therapy at UPMC 2006

wadsy

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Re: Informal Facial Paralysis survey
« Reply #6 on: July 03, 2006, 12:37:36 am »
Hi all,

Good thread. I too have facial paralysis. I am 13mths out from surgery and even though I do not notice any change people that see me infrequently say that I look better (or are they just being nice? lol) I certainly seem to have more sensation developing as time goes on but no motor function on the AN side. Interestingly I emailed a surgeon about cross face grafting of the nerve from one side to the other and he told me that in his experience the facial nerve regenerates for up to FIVE YEARS!!!! My surgeon, who is apparently one of the best in his field (Professor Paul FAGAN is his name) is leaning towards a hypoglossal graft in a few months if there is no motor function evident because he said that is the most effective treatmnet for facial paralysis but I am resisting any further surgery. Good to know that there may be a chance in spontaneous recovery even though it is damn slow!!!!!!!!

Joef

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Re: Informal Facial Paralysis survey
« Reply #7 on: July 03, 2006, 06:14:30 am »
really!! thats his name  ;D .. because my full name is "Joe Paul Fagan" too !! LOL ...
4 cm AN/w BAHA Surgery @House Ear Clinic 08/09/05
Dr. Brackmann, Dr. Hitselberger, Dr. Stefan and Dr. Joni Doherty
1.7 Gram Gold Eye weight surgery on 6/8/07 Milford,CT Hospital

wadsy

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Re: Informal Facial Paralysis survey
« Reply #8 on: July 03, 2006, 07:13:03 pm »
Co-incidence eh? He is apparently the best acoustic neuroma surgeon in the southern hemisphere. Pioneered facial nerve monitoring in Australia etc.

Boppie

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Re: Informal Facial Paralysis survey
« Reply #9 on: July 03, 2006, 08:58:37 pm »
This might help some.  My tumor was very sticky.  Although it was 2cm, it took nine hours to get the bits unstuck from the facial nerve.  I had excellent conduction post op and for 9 days .  But then on day 10 I experienced "late onset paralysis", that is, the eyelid, forehead crease, eyebrow lift, nose wrinlkle, lip curl, pucker, smile curvature, and cheek lift ceased.  Numbness issues persisted for the next three weeks.  Then slowly the parts started moving.  By the end of two months most of the movement was back.       

But, then my tongue started to burn.  Actually it too had been numb on its side and I wasn't aware.  Today (at 6½ months out), I am still recovering from the tongue numbness and sore spots that come and go on my forehead and lip.  Mosts foods taste good but I try to keep my tongue still in there, not wanting it to explore my teeth too much, because that starts up the sore spots again on the tip of it.  My doctor predicts that 9 months will see the end of tongue problems too.  So far, he's been right.  So if you develop "late onset paralysis"  hang in there.  The only "cure" I used was eye lube, warm compresses, Biotene toothpaste, slow chewing, and very gentle massage with my palms.
« Last Edit: July 04, 2006, 12:42:31 am by Boppie »

ld_runner

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Re: Informal Facial Paralysis survey
« Reply #10 on: July 04, 2006, 12:08:37 pm »
3 years out from surgery at Hopkins.  Right side paralysis which the Doc at Hopkins assured me would get much better.  As a matter of fact, I remember him saying, "you'll be happy with the results."  Needless to say, I'm not.  No improvement in 3 years. Surgeons: Drs. Brem and Holliday at JHU.

Jeanlea

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Re: Informal Facial Paralysis survey
« Reply #11 on: July 04, 2006, 03:07:39 pm »
I'm nearly 10 months post-op.  I have paralysis and numbness on my left side.  After 3  months and a handful of days I had some tiny movement.  There continues to be more, but it's nowhere near back to normal.  At rest my face looks fine.  Still talk out of the side of my mouth.  I believe that the nerve was not cut, but I woke up from surgery with the paralysis and numbness.  At my six month check up my doctor told me my face would not come back.  Apparently he expected more progress by that time. 

It's good to hear that people continue to make progress long after surgery.  I have people that haven't seen me for long stretches of time that tell me my face has improved.  That is good to hear.  I also continually feel different sensations in my face.  Don't really know what it means.

Jean
translab on 3.5+ cm tumor
September 6, 2005
Drs. Friedland and Meyer
Milwaukee, WI
left-side facial paralysis and numbness
TransEar for SSD

Pembo

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Re: Informal Facial Paralysis survey
« Reply #12 on: July 05, 2006, 07:36:01 pm »
Oh Jean, I hate to hear when doctors say at 6 months out that you are recovered as much as you can. I believe my face will never be as it was before surgery but I have seen so much recovery in the last 6 months...18-24 months after surgery.

Keep the faith.....all those different sensations can only be the nerves trying to fire.
Surgery June 3, 2004, University Hospitals Cleveland, BAHA received in 2005, Facial Therapy at UPMC 2006

Jim Scott

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Re: Informal Facial Paralysis survey
« Reply #13 on: July 06, 2006, 01:13:43 pm »
I had some slight  facial numbness on my left side (where the AN tumor was located) pre-op, especially around my lips and tongue - and that didn't change (for better or worse) immediately following the tumor removal surgery - and that was a bit of a disappointment.  However, I had no facial paralysis post-op, so I was grateful for staying 'even' - and losing the tumor. 

Now, 4 + weeks post-surgery, normal feeling is returning to my left cheek area and both my lips and tongue are feeling less numb every day!  Time really does  help with AN post-op healing.

Jim
« Last Edit: July 06, 2006, 01:15:14 pm by Jim Scott »
4.5 cm AN diagnosed 5/06.  Retrosigmoid surgery 6/06.  Follow-up FSR completed 10/06.  Tumor shrinkage & necrosis noted on last MRI.  Life is good. 

Life is not the way it's supposed to be. It's the way it is.  The way we cope with it is what makes the difference.

DeniseSmith

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Re: Informal Facial Paralysis survey
« Reply #14 on: July 07, 2006, 06:49:47 am »
Jim,

Did they remove the whole tumor or did they leave some? Just curious.

DS