Acoustic Neuroma
Posted , 25 users are following.
Mine is a very positive story.
I had tinnitus for a year in my left ear. My doctor said there was nothing to be done and I just learned to live with it. No big deal.
Then on 25th August 2007, I woke up and couldn't hear anything out of my left ear. I had just moved to Dubai and thought it might be the flight.
An ENT specialist did some hearing tests and explained it was nothing to do with the flights as it was an inner ear problem and put me on steroids. They didn't make any difference so I had a gas therapy- I think it's called carbogen - a mixture of oxygen and carbon dioxide. I had this for twelve hours - half an hour on, half an hour off.
The next day I woke up and could hear a bit. I was delighted as had resigned myself to no hearing! I then went to the doctor for a repeat hearing test. He said it was good, but he wanted to send me for an MRI scan just in case.
I went and when it was nearly finished they injected a dye in. Slightly concerned but thought nothing of it really as knew some of my hearing had come back. I didn't really think much more about it until the doctor's secretary rang to ask that I come in for the results a few days later.
Anyway, he told me there was a tumour, 3.2cm by 2.2cm that was usually benign and I had an appointment to see a neuro-surgeon in two days time. It was a big shock, obviously, but I felt like it would be OK and trusted that it was usually benign.
The neuro surgeon told me it was an acoustic neuroma and that it was too big for gamma knife. He explained the surgery to me and assured me that he was 99.9% certain it wasn't cancerous. He said it was a fairly big but routine operation but that I would need lots of time to recuperate. I told him I was going to come home to UK and he recommended a surgeon at the Wellington hospital to me.
I met with the surgeon who was brilliant. Very calm and kind and told me the risks - 50% chance of facial paralysis, 100% no hearing and what the operation would entail. My tumour was just a bit too big for gamma knife and this surgery had only been carried out for twenty years. This meant any side effects after that time weren't known and as I was only 29, surgery was the way to go. He thought he may have to leave a few mm in because of it's position but that would be OK. He explained it brilliantly and my paretns and I felt calm about the whole thing.
On Monday 15th October 2007 I had the surgery. I think it lasted about eight hours as he was able to remove the whole thing. Another surgeon carried out the first part of the operation and the surgeon I'd been recommended did the removal. Both are brilliant and I felt completely at ease and trusted them implicitly.
I only vaguely remember coming round about ten hours later. The surgeon said something (I'm sure he said a lot but I can't really remember!) Then my parents came in and I smiled. Perfect smile with no facial paralysis at all. What a massive relief.
I remember a bit of the night I spent in ICU and a bit of the next two days in my room. I have never experienced thirst like it!! I had morphine drips and IV and spinal drain (to catch any brain leaks!) Was fairly out of it though.
Had a pretty bad night on Tuesday with extra pain injections. My head felt like, well, a bashed in cannon ball really, but once the spinal drain came out things started getting better. I didn't think I would ever feel better as I really did feel rubbish. The surgeon said once the drain was out it would get better and he was right! Wednesday I got out of bed (threw up a bit but felt better after, and was only sick once more through the whole thing), Thursday I walked down the corridor with physio. Was a bit wobbly but OK.
Once the catheter was out the walking got easier and by Saturday I was eating, watching TV and walking upstairs. I was taking oral pain medication every four hours and to be honest, I was ready for them, but it was not blinding pain. I had the odd anti-sickness injection or pain injection in between but Saturday was the last injection. Sunday I had a blinding headache again but by the afternoon I felt much better and went outside (my dad wheelchaired me round a park! I could walk, but was just easily tired.)
It wasn't the best week of my life but I got better every day and went home the following Monday, just one week later, and was told to take just paracetamol for the pain (I had been having paracetamol and tramadol). I couldn't believe it! A nurse took the stitches out and because my head was still numb it wasn't painful in the least. Just a tiny bit weird really. The scar is all along my hair line behind my ear. They shaved a little bit of my hair in the area but the rest of my hair falls over it and even when I tie my hair back, you can't see it. It's incredible really. (Everyone I've shown it to says how neat and small it is.)
At home, I was easily tired and my neck hurt from the position I lay in, my thigh needed penicillin as the scar got infected (they removed some fat from my thigh to put behind the ear where the bone had been! Yuk!)but other than that, my headaches were like the normal ones you sometimes get for no real reason and I could talk on the phone a little bit more each day and my freinds waited until I was ready for visitors. That was after about five days of being home and it was only a few more before I could manage whole days of visits and trips out for lunch!
Two weeks later was my 30th birthday and I had a fairly sedate tea party! But the following weekend I was out clubbing (fairly sober as promised myself I would not self induce a headache like the ones I had the first few days of hospital), and felt great the next day.
It is now five weeks since the operation and I haven't taken paracetamol for about ten days. I've gotten used to being deaf (bonus is that I get great night's sleep) and my tinnitus is still here. My thigh is numb where the scar is and I can't cry in my left eye (new party trick), but there's drops to help and I'm swimming, jogging, going to yoga, dinners out, drinking a bit of wine and generally thinking life is ace. It really wasn't that bad for me and I feel really lucky. Back to Dubai to carry on with my break dancing lessons in a week or two!
[color=red:73a7207470][size=9:73a7207470][b:73a7207470][i:73a7207470](Sorry but Patient Admin have removed a Doctor, Consultant and or Hospital name from this posting, as it is the policy of Patient UK not to publish these on this forum.) [/i:73a7207470][/b:73a7207470][/size:73a7207470][/color:73a7207470]
1 like, 38 replies
audrey02830 charis
Posted
Perhaps I should add that I am almost 80 years old and consider myself fortunate to have had the treatment and not been cast aside as too old.This was possible , my consultant told me that it was my general fitness and active life that made the decision for me.
Looking sensibly,the winter bug I might have had anyway and the labrynthitis could still turn out to be oif viral origin.
You see I am more cheerful this evening and realise that I will be better very soon .The best results come from a positive state of mind.
Keep active and I am certain everything will go well for you.
I still feel somewhat isolated by my deafness but I make it clear to people ( with a smile ) that I am "deaf not daft" and have found them understanding and helpful.
Take care and don't worry, I am sure that all will go well..Audrey
delphine85169 audrey02830
Posted
After being messed around with nhs appointments I finally got mri scan, was then called back for mri with contrast
Was then phoned to go to hospital while on holiday,so returned next day.
To my surprise I was told I had a acoustic neuroma BUT not inmy left ear,but on right side.since my hearing was already poor this made sense as I had dizzy spells, the beginning of last year.
So with my right ear hearing deteriorating and only 5% in my left ear I am facing a world of silence, either with or without treatment.
I have also found a large growth behind my right ear, it's boney and on occipital bone, painful now too. Awaiting ultrasound on that.
My general health is crap, type 2 diabetes, heart problems, cataracts,, arthritis..
I have tried to be positive about what will happen, and hope eventually I could have cochlear implant.
My question is how long did you wait for decision and were all the pro's and con's explained.
I already struggle with 2 hearing aids and do feel like wearing a 'deaf not daft' badge, such is the size of affliction.
I hope I haven't bored the pants off you, your input would be appreciated, cheers Del.
audrey02830 delphine85169
Posted
Like you I had ;watch and wait' for a couple of years until the neuroma had grown sufficiently to require intervention.Once referred my wait was very short and I had the choice of two hospitals that used the tecqnique I required.The worst part of the treatment was fixing the halo,that said everything was painless.
I researched on line and my consultants were verp good at explaining the pros and cons.I am aware that my age could have been a deterrent,thankfully in my case it wasn't.
Well Delphine,I feel that I haven't been very helpful as you can't have GK but it may help you to realise that even with treatment it is difficult to find a fairytale ending.
Meanwhile I remain determined to enjoy what ever is left of my life.
My love to you,chin up.Write again if you feel down, Audrey
delphine85169 audrey02830
Posted
I live in Wales. You?
Cheers del
audrey02830 delphine85169
Posted
It is natural that as we grow older we have other health problems too,mine is hypertension and is proving very difficult to control.
Keep smiling,sleep well and keep in touch ,Audrey
PS There is always something to be thankful for.My thanks go to you for listening to me as I am listening to you. x
kelly35712 charis
Posted
I am wondering if anybody had pain before they were diagnosed with AN ? Either ear or headaches? I have had constant ringing in my right ear for a good while now especially at night when I turn over it wakes me up and really hurts, then just over a week ago I woke with what feels like no hearing at all in my right ear , it feels full or like it needs to pop , for the passed 10 days I have either had severe ear ache or headaches. I've lost taste , I can taste things but nothing tastes right or smells right. I'm slightly dizzy on occasions but not too bad and slightly confused. I've been treated for 5 days for shingles although I never had a rash and now my doctors have said it's menieres so I'm being treated my more tablets for that. I also have numbness on my right side of my face. I had a CT scan 7 weeks ago as I had severe numbness on my right side and that was clear. Getting me down now. Any suggestions?
Michael_Knight kelly35712
Posted
kelly35712 Michael_Knight
Posted
Kelly
delphine85169 kelly35712
Posted
kelly35712 delphine85169
Posted
Rchurch544 charis
Posted
I suffered all the way to April 2015. The symptoms I had seemed to go in cycles and I could never figure out what caused them. I always had a headache, I did previous to gamma knife as well. I had poor balance, frequent nausea, vertigo, difficulties concentrating...those were the symptoms I had and they constantly cycled and showed up.
January 2015 during my scan, we discovered the tumor had begin growing again and we made the choice to have it removed. I had a skull base surgery, called Sigmoid Approach, on April 8,2015.
This was truly one of, if not the greatest, experience of my life. The surgery lasted nearly 10 hours and there was difficulties from the previous gamma knife. Lots of scar tissue and plus the location of tumor put it dangerously close to brain stem and jugular vein.
The surgery was on a Wednesday and because of the steroids I remained awake until Friday night. Upon waking the very first thing I noticed was that my headache was gone. Prior to this surgery, dating back to early 2010, I had a headache all day every day, ranging from 3 to 8 on pain scale.
I will say the nurses in ICU didn't like me too much because I was awake and had needs. Mostly water for my extremely dry mouth.
I took the morphine that first night and on the 2nd morning. At dinner and bed time I took oxycodone.
The next day I woke up and I still did not have the headache I had become accustomed to. I only took tylenol for the pain and it was sufficient. In fact that morning dose of tylenol was the last pain medicine I took for this surgery. I only mention all that because I am a recovering addict. I just celebrated 6 years clean.
I was released from the hospital on April 13th (5 days total, 3 of them was in ICU). I was in zero pain, in fact that same day as we got home we went to look at a house.
I returned to work after 6 weeks and we bought a house in July and renovated it and moved in on August 1.
I have never been so scared as i was going into that surgery. Fears of using pain medicine, that my face would be paralyzed, or that something more serious could occur...like a stroke or something. I just knew my life was going to be different, mostly projected bad stuff. I believe that is why I'm so grateful. My life did change, but for the better.
So, to get with why I'm even posting, it has been 6 months since the surgery and I am just now experiencing painful sensations. I realize it's probably just nerve cells healing, but for whatever reason, I am getting acute ear pain, and it hurts to lay down on that side. In fact it is hurting so much I can't sleep. Would like to get some experience, strength, and hope.
Thank you
jenk Rchurch544
Posted
audrey02830 charis
Posted
So ,a story of great hope for me and I hope for others with the same problem.
audrey02830
Posted
I can now walk in a straight line and circles are usually ok.I don't feel unbalanced when walking in spacious areas and best of all no pains in my head.Hopefully my autumn check up will say my ' an ' shows no further growth.It is 18 months since I had Gamma knife surgery.
My deafness continues to be something I find difficult to deal with as all my hobbies rely on sound and hearing.At 80 years old I had a degree of deafness in both ears BEFORE my neuroma was diagnosed
.In reality I have absolutely nothing to complain about.
Stay with it people,hopefully - wih patience - your outcomes will be successful too.
shakira02012 charis
Posted
Treatments for acoustic neuroma include regular monitoring, radiation and surgical removal.
audrey02830 shakira02012
Posted
2 years after gamma Knife surgery.My tumour has shrunk.
My balance issues are still a nuisance but bearable.
Deafness is my most unpleasant problem.
HOWEVER
I don't have tinnitus or any nerve involvement in my face .
I have no head pains.
I am as well as I think I shall ever be.
I would say that in spite of a few problems a long the way Gamma Knife surgery has been a success for me.
I think we must be positive on our journey and do our best to deal with problems that may arise.My thanks go to all the medical staff who have helped me on my way.
Harmon1961 audrey02830
Posted
I went thru Gamma Knife treatment 10 days ago.
My hearing seemed to improve for 5 days, then on the 6th, I woke up deaf in my right ear.
The headaches have subsided, but are not gone. The ringing has subsided, but not gone.
I am curious if this is just a stage of healing?
Naturally, I am seeking an optimal outcome, and I would Ike at least some hearing in my AN ear.
plus no pain, no ringing.....
I am grateful that I never suffered from dizziness, nor nausea...
Very disoriented when I first wake up....
Am I reacting too soon?
What was your experience?
Harmon
audrey02830 Harmon1961
Posted
Hello,I had Gamma knife surgery for AN almost three snd a half years ago.
For the first week I was just very tired.I began to get pain in my head on the affected side.My hearing in that ear was already poor.Five and a half months post surgery I suddenly developed rotary vertigo.For months I had no idea where my head was and had to cling on walls to feel safe.
The head pains and balance issues have slowly subsided although I am still not good in the dark. (amazing how much help eyes are with balance)
Sadly my hearing has deteriorated further.I now use a by cros hearing aid which I find useful but not everyone does.
I have only ever had mild tinnitus.
My good !! ear is not good so hearing is a problem,thankfully I lip read quite well.
I have asked myself if I regret having the surgery,Three years later I don't.Everyone doesn't lose so much hearing,sadly I did.Nevertheless the surgery was successfuk and I am fine.
Good luck .