My Successful Stapedectomy Experience
Nov 23, 2009
I am just in the recovery process a week after having the op.
On coming around from the operation i noticed an immediate volume change for the good, the sounds were very very loud for the first couple of days, but has settled a little know.
It feels like i have a shell over my ear so the sounds are not clear as yet, maybe to do with the dressing still in there, although there is no pain.
Family and friends say i am talking a lot quieter.
I believe this will open up a whole new world to me.
My operation was done on our NHS, only having to wait about 4 months.
I might sometime in the future be having the other ear done.
Good luck to anyone who is considering the operation it has taken me 3 years to reach a decision.
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After the usual IV insertion, walking to OR and walking up rather groggy, I must say the first few hours were strange. Having limited hearing in my right for the past 7 years ( and getting worse) I decided to go for the operation.
My mouth and throat were very dry (11am operation with no food or drink in 12 hours) and deep breathing was challenging. I was encouraged to take deep breaths to clear anything from my lungs. My OP ear was full of cotton and gauze so hearing from that side was nada. My good ear was very amplified like I had a microphone inside my mouth, I would scratch my head and it was LOUD. I was discharged after I could stand without aid and at home crashing on the couch.
I had a protein shake and a bowl of hot soup and felt very stable with no dizzy spells or balance issues, but still the amplification inside my head. I had ringing tones on my OP ear on and off but no pain. If I plugged my good ear I could hear nothing but the ringing.
Five hours now and I feel good but I can hear everything around me, the talking , the tv, things very far away are very clear. My dog barked right beside me and I nearly jumped off my chair, scared me. It was loud. I used to watch tv on 65 volume now it's at 40 volume.
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I am considering a stapedectomy in my left ear but worried that I may be getting too old for this type of surgery and will experience a much more difficult time with recovery.
I would like to hear from others close to my age with your experiences. My other option is a bone anchored hearing aid which I really do not want to do.
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I need help on all the things i need to know & what all i will need. I'm trying to have a successful breastfeeding process.
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I am 45, Male ,married with a daughter. active in profession. My hearing is facing problem as I am unable to hear soft voices in meetings & discussion. Doctor has suggested to go for Stapedotomy. Another option is Hearing Aid. I am very anxious to know how much risk is there to go for Stapedotomy? Can It worsen the hearing? Instead of 45, if I wait for another 5 years, will it be same effect of Stapedotomy or surgery at that stage will not bring any result?
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Now at day 41 and stapedectomy still not working. Hearing was no better when packing was removed at 2 weeks. Surgeon said it will still be fluid. Climbing the walls counting EVERY single day. Waiting for something to happen. Just had a weeks course of steroids, no difference. It feels as if i'm in a goldfish bowl and everybody around me is on the outside, i feel like i'm in a deep hole and can't get out. I'm sure there's still fluid there as i can feel it when i swallow, and also on several occasions each day when i swallow, mainly listening to music, i get a one split second burst of loudness which after reading the internet makes me thinks it's my tube blocked? But it doesn't hold open for longer than a swallow. I also get like a thumping on my eardrum when i belch, as if a blast hits it? This also wakes me in the night with the banging. Not that i sleep much as EVERY waking moment of my life at the moment is consumed by it. I've had 6 weeks off work until now, due to go back in tomorrow. My unsteadiness had cleared for about 10 days but came back with avengence a couple of days ago. Not vertigo dizziness, but like the quick movements dizziness. I do still get crackling and clicking in my ear. Spoke to surgeons secretary last thursday who is going to get a message to him this tuesday, as that's the first time she will see him apparently. Has anybody else had fluid for this amount of time, or can give any advice or anything to make me feel it'll still work and that i can get my life back?
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I was wondering how many people have had a successful pregnancy after having a tubal ligation? I was having early symptoms of pregnancy to continue to get negative results
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I've exhausted all other options. Everyone has told me not to get surgery, but I've tried every conceivable treatment and nothing has worked. Seven years of this and thousands and thousands later I'm still getting worse. Would love to hear someone out there felt better after surgery.
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I had surgery to remove 2 neuromas. I am now 9 weeks post op and still absolutely miserable. The pain and discomfort I have now are a thousand times worse than pre op. Has anyone had success with this surgery? If so how long did it take for full recovery?
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Has anyone had successful surgery for morton's neuroma? I've read all the negative please share some positive results.
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I've had bad hearing since a child. Am now 56. Had first hearing aids about ten years ago. Learnt to live with decreased hearing till then. Now got NHS aids. Six weeks (approx) ago, I noticed I'd lost 75% of what hearing I had in my left ear. No wax as had checked. Went to check aids. They were ok. Its my hearing that has deteriorated considerably in a very short space of time. Was offered stapedectomy 20yrs ago. Decided against it as success rate 50%! Now I think the time has come where I shall be offered stapedectomy and I need as much info as poss. Want to hear from people that have had this done and has it improved your hearing or made it worse (not that mine can get any worse!). Where you had it done? I would not be able to consider going abroad due to lack of funds.
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I am deciding whether or not to get a stapedectomy done, and my doctor told me that it is only a 0.1% chance (1 out of 1000) that i will go completely deaf. i think i am going to go through with it...since i have been partially deaf my whole life, and am excited to hear the difference.
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I'm 4 weeks in after a stapedectomy. Got advice to avoid lifting but also as much exercise as possible for the next month still (except for walking). Any ideas on what other mild exercise I could do? Anyone had difficulties with exercise after stapedectomy/ or want to tell how did it go with it afterwards and what kinds of exercise they did/do?
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I am 3 days out, having a stapedectomy. I feel like my head is full, and the bouts of dizziness is bad at times. Does anyone know about how long this may last the dizziness bout. Will it get better? I'm taking antivert every 12hrs, is there something better? I heard taking ibuprofen helps with the inflammation.
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I had a Stapedectomy in both my ears. My left ear I had done 4 yrs ago. Now I am getting vertigo, not full blown, but just enough to annoy me and make me feel light headed. My ear also feels sore. This has been going on for a few days. It's not like an ear infection sore, but just sore like something is not right. Now I am not sure what is causing this. I have been taking ibuprofen for the soreness and when I do, about 20 min later I don't feel as light headed. Could something be just swollen in my middle ear? About 2 months ago I had my ear flushed out with water by my regular doctor, but that didn't seem to bother anything. About 2 weeks ago I noticed like clicking in my ear and during that time I went to hear a band play. I don't know what is going on and I am getting kind of worried. I was going to wait a week and see if it all goes away. I do get this vertigo about once a year and it lasts about a week or so. Then I am fine. What do you all think? Any doctor's out there that could help? I don't want surgery again! I had a tough recovery and the thought of it terrifies me. Also am I not allowed to go scuba diving? We are going to turks and caicos next month and I wanted to scuba dive but I heard you can't.
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Can anyone tell me how long it took for the gel packing to "melt away" after the surgery? I don't have an appointment until a month after surgery-which seems unusual after reading other posts. I'm only 5 days post-surgery, but the packing is driving me crazy. I think it is causing a loud whooshing noise whenever I am sitting up. I think it is also making it painful if I lie on my non operated side-as if it is putting extra pressure on the ear drum?
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I had a stapedectomy in my right ear on 23-aug-2013 its 1-sep-2013 today but i really can't hear by my operated ear till now, The only thing that is worrying me is that I don't know if it worked or not. For those of you that have had the surgery, what was your hearing like afterward?
It just feels itchy and stuffed up (the gauze is still packed in there).
Has anyone had to wait until that was completely out to notice a significant difference?
can any one tell me is it ok to not still hearing by the operated ear if its ok then how long it'll take to hear normally by operated ear.
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I came across the following while doing research and had not heard of this treatment before:
" I have been able to treat patients effectively with kenalog injections. Usually on palpation the branch of the trigeminal nerve causing the pain can be identified. Its usually either supra orbital, supratrochlear or infraorbital. Then I inject 5mg of kenalog into the nerve itself using 30gauge needle with 0.5cc of Kenalog 10.It takes the pain away for about 3 months."
The guy was trained in otolaryngology at Yale before becoming a highly reputable plastic surgeon. It might be worth asking your doctor or neurologist about this proceedure.
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I have had BMS for several years. It has worsened to the point of being almost unbearable. I have taken an anti viral drug, tried vitamins and Alpha Lipoic Acid. I am now taking a medication for nerve pain. If anyone has BMS and have had successful treatment, please post this info.
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Go to your doctor or pharmacist and obtain a 20ml syringe. When you suffer an attack loosen the plunger in the syringe by moving it up and down the barrel several times. Put your lips to the spout at the end of the syringe and, blowing as hard as you can blow the plunger fully to the end of the barrel. If your eyes do not pop out you will find that your heart rate has returned to normal. When this treatment was first given to me in A&E I found it hard to believe. Now I use it successfully with every attack.
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I am a diabetic and take a background insulin and a quick acting insulin to cover my carbs. Has anyone else been on tablets and insulin and had a successful weight loss ?
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