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#1 (permalink) |
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Registered User
Join Date: Aug 2008
Location: Southeast England.
Posts: 87
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where do i start
I dont think it has been done, if it has they were guinea pigs...but i have been offered a double cochlear implant..........
I really dont know if im going through with this, ive been given 4 weeks to decide, but to me thats abit quick, i wont be rushed.... I WILL have complications, 1st i would have to have bone removal and also rebuilding before operation can start.. Yes it usual for CI'S to have dizzyness etc etc, but im told in my case the % is up to 60%, and it is possible that it might not work.... Then i think hey what have i to lose, im deaf anyway, have severe tinnitus both ears, headaches everyday, not all day but everyday none the less. severe dizzyness ive had everyday for past 7 or 8 years+. Is it worth the pain? I really am lost here, im open for anything that could help me...and advice. my history born deaf left ear. many many operations throughout the years averaging 2 ops a year right up til 12 weeks ago. i nearly dies with abcess on brain becasue of weeping ear, yes weeping travelled upwards. I was 1st person in Uk to have cavity built to stop weeping travelling upwards. 1 year later cavity broke down, i had rebuild. i had labrinthitis in left ear had labrinthectomy, made dizzyness worse. i had labrinthitis in right ear, had labrinthectomy, labrinthectomy leaves people deaf, so now im profoundly deaf..... in between all this im ops for this and that plyps, mastois, bone removals etc etc etc etc. 12 weeks or more ago i had HONG KONG flap a protection or something, anyway now ear doesnt stop weeping at all its 24/7. All i can now is OVER TO YOU LOT, IM OPEN TO ADVICE... My brain is saying NO at moment...... thansk people Stu |
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#4 (permalink) |
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Registered User
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Well medically it is possible to still have drainage from canal 12 weeks after having Hong Kong flap proceedure. The success of this operation is because the vasculature (blood supply) the flap provides. If you have had mastoidectomy, chronic abcesses with cholesteatoma and subsequent ear drainage of course, I would be willing to theorize the healing capacity is decreased in your case because of the longevity and degree of problems with cholesteatoma. I wonder why it take so long for physician to decide to do Hong Kong flap- it is not a seriously difficult surgery and has 90% success rates.
I would be very very cautious about bilateral implants with this dealio u have. Tell me this is only one side have the problem with cholesteatoma or both. Just by reading it sound like the disease process and subsequent proceedures cause you to be full deaf in your other ear. If the origianally deaf ear never had the infections, abcesses, surgeries, removal of bone, creation or drainage cavity etc, why not just do one, less chance for complication. But then again, if this is problem you have always have with the cholesteatoma and both eustachian tubes then I wouldn't do it if it were I. Either way good luck with healing and I do hope for the very best for you, it sounds like you have dealt with enough already. Get Well soon. |
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#6 (permalink) |
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Registered User
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I am not CI specialist. I was mostly thinking along lines of risk of serious medical complications cuz of preexisting problems outweighing the potential benifis. With having a labrynthectomy, I don't know how dizzyness improved with CI....never encounterd someone with both. Some patient I care for have had labrynthectomy and end up on vertigo meds forever. Yes I would be interested in the tinnitus and vertigo benefits, definately. It is so hard to guess on cases that are so individualized such as stuey, so I am just trying to objectively view the whole picture. Very good point though DD
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#7 (permalink) |
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Registered User
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I would be worried about the physical side of things. It has only been 12 weeks since you had surgery on your ear and they want you to make a life altering decision in 4 weeks? I am all for CI's, have just one more batch of testing before I am scheduled for mine (only one) and I was given loads of time to think things through and research, and come here asking questions.
Is there a doctor you trust? Not perhaps one that you have dealt with for ear trouble, but any knowledgeable doctor that can help guide you in making a healthy choice based on you and your history? As for the success rate, that is on a case by case basis and depends on a lot of factors.
__________________
E.T. Left Ear Implanted 11-07-08 (Nucleus Freedom) Activation 12-18-08 Right Ear Implanted 3-3-2010(N5) Activation 3-11-10 http://et-mybionicjourney.blogspot.com/ |
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#8 (permalink) |
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Registered User
Join Date: Jun 2008
Location: Great Britain
Posts: 2,028
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As he's based in UK i guess its South of England Cochlear implant centre (where i go) or the one in London Grays road... If it's SOECIC, who's your consulantant?
Sorry i can't help much as i don't suffer from problems prior to CI, However I do agree with Doug as Infection is worrying. PM me if you want. |
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#9 (permalink) | |
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Registered User
Join Date: Aug 2008
Location: Southeast England.
Posts: 87
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4 years on
Quote:
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#11 (permalink) |
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Registered User
Join Date: Apr 2007
Location: Jacksonville, Florida
Posts: 15,661
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Had Cholesteatoma surgery last Nov. (left ear) and still have drainage...or "weeping ear"....surgery on the right is forthcoming, I'm putting it off as long as possible, tho. I turned down the CI because of the problems I'm having. ...Sorry things didn't work out for you!..My way of thinking, Life is what you make it...so make it good!
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#12 (permalink) |
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Registered User
Join Date: Aug 2008
Location: Southeast England.
Posts: 87
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smiles
Hey no problem, Myself, Consultant everyone knew it was difficult and may not work, that why it took everyone concerned a year to decide if it was worth the amount of money involved, They decided I should have that chance after my history with ear and brain OpS. So it didn't work, Ive had both ear canals skin grafted over now, as no point looking in as there isnt anything there to look at, All completely Obliterated..
So I soldier on..Funny I say that my Tinnitus is soldiers marching non stop 24/7 both sides lol... Good luck to everyone else who has C.implants though
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#13 (permalink) | |
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Registered User
Join Date: Aug 2008
Location: Southeast England.
Posts: 87
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hope all works
Quote:
But we carry on forward, no point looking back we try to SMILE..and SOLDIER on Im always saying that, yet I have probs stepping outside my front door at minute lol.. |
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#14 (permalink) | |
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Registered User
Join Date: Aug 2008
Location: Southeast England.
Posts: 87
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reminded me
Quote:
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#15 (permalink) |
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Registered User
Join Date: Jun 2005
Location: Canada
Posts: 2,097
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Wirelessly posted (Blackberry Bold )
Based on what you've said - I'd wait on the CI ... Make sure that everything is medically and anatomicall stable for a year, then re assess. Yes there's a chance CI might help with the tinnitus, but considering the scope of your other ear issues, I'd think you might well end up with severe complications. By this I mean in terms of healing, infection and your body physically rejecting the implant. I'd wait til your ears are stable, infection and drainage free then get multiple opinions on if CI is a good option for you, then do a unilateral implantation first (with possible bilat implantation later)
__________________
Hoh/Deaf ~ +120db deaf right , mild/mod flux left & APD English & ASL ...PAH!! ![]() Ignorance is NOT Bliss |
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#16 (permalink) | |
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Registered User
Join Date: Apr 2007
Location: Jacksonville, Florida
Posts: 15,661
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Quote:
But there are sunny days ahead....hope you can manage to get outside and enjoy the weather when possible!...Keep in touch...rockin' |
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#17 (permalink) | |
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Registered User
Join Date: Aug 2008
Location: Southeast England.
Posts: 87
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yeah
Quote:
We soldier on Rockin and I will come on here twice a week so I keep in touch..
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