ETD, Deafness & me
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I cannot begin to tell you the misery I suffered following ETD, but hope that this may offer some sound advice to others with the same complaint.
Twelve weeks ago, exactly, what I thought was a head-cold, turned into a dreadfully sore throat for two days, and then, on the evening of day three, a terrific pain in my right ear, followed by almost complete deafness on that side. Not just deafness, but a full, `echoey` type of deafness, similar to what you might hear underwater.
Off to G.P. next day who prescribes anti-biotics and steam inhalation. Back to G.P. a week later - hearing still badly impared and popping and pain in ear. He prescribes FLIXONASE NASAL DROPS and says to continue with steam, and that hearing will return in about three days.
By now, I am going crazy with all this distorted sound in my ear, and am trying to keep working and driving with this awful condition. Hadn`t even heard of ETD until now, and start searching the internet in the hope of something positive.
Three days into Flixonase treatment, hearing improved - by about 30-40%, but still popping and cracking going on. Nightime is worse, by about 9pm, feels as if my ear is filling with fluid, and there is also a `worm-like` feeling going on. Back to G.P. - he is now getting a bit fed-up of me - and he says that my ear-drum is completely distorted, and that I have to keep going with the two-week Flixonase course, and that it may take several weeks for it to settle down. Seems like they only like giving you the bad news in small doses.
The nasal drops have made the lining of my nose swell-up, and on day 10, I start cutting down the dose to once a day in order to faze out.
Have started to find a lot of stuff on the Net about `negative pressure` in the ear, and how to equalise it. Send off for a kit called `Otovent` which uses a nasal baloon to try to right the pressure. Loads of cracking and popping going on, but it gives me an awful headache. At least my deafness is getting better in the morning, although I am sure this `Valsalva` menouvre, which the G.P. suggested I do all the time, (to enable air to get up my eustachian tube), has left me with this new problem of unequal pressure. Do I sound mad? At this point, I think I am going crazy - this problem is affecting my day to day living and I am very depressed.
I am slowly, very, very, slowly - getting my hearing back, although still have quite a bit of popping and cracking going on, especially when I lay down at night. The Deaf Society have a `ask a question` on their Website, and advised me that it can take up to three months to get back to normal, if the initial problem was a VIRUS and not an infection. This has given me hope - one more week before I reach that stage, (although of course, it may be a little longer). I propose to consult an ENT specialist (I will demand that my GP. gives me a letter of referal, if things do not clear up soon), and will take it from there.
I hope this will be of use to anyone suffering. I AM GETTING BETTER at long last, and I remember well, looking to find anything, positively anything, which offered some hope.
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Guest
Posted
Oh, my gosh, you are a godsend. I have been looking for the otovent for several years now. I used it several years ago and the doctor that gave it to me, left Houston and no one I talked to knew what I was talking about. I am in the process of trying to order a kit. I have over the last several years miss placed the device that connects to the balloon, so I will have to order a complete kit. I hope they sell them in an order of 1 kit. If not, I'll have to buy all six kits. When I used it several years ago, it WORKED and was the only thing that did work....I had had the condition for 6 months prior to using the device....it started to clear immediately with the otovent. Again, I was never so happy to read that you had used it lately. I could not find the website for the company several years ago, so I thought that the device no longer existed. Again, thank you so much.
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earmadness Guest
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