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![]() Sudden Hearing Loss (Page 5)
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| Author | Topic: Sudden Hearing Loss |
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Penny Member |
Tina, I am awaiting evaluation by the cochlear implant program here in Indianapolis and am very interested in corresponding with you directly about your experience with the implant. I am a nurse and up until 3 months ago I functioned well with hearing in one ear, although I wore an aid. Autoimmune Disease is also my diagnosis. My email address is pennypgage@aol.com. Please contact me, I have so many questions and it gives me hope to hear you are doing well inspite of your hearing loss. Penny IP: Logged |
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Patricia Member |
Rocco, I'm sure you have tried this, but since I don't see any mention of it in your postings, have you tried a tinnitus masker? It's worn like a hearing aid, and it puts out a steady constant masking noise that covers up the racket your ear is producing. Some people do well with them, some can't tolerate the masker noise any easier than they can tolerate their tinnitus, but it's something to try. Another thing to try is a noise generator that you put on your nighstand when you go to sleep. You can dial up any number of different sounds that are more pleasant than your tinnitus, like an ocean roar, babbling brook, rain, etc., and usually one of them will mask the tinnitus so you can sleep in peace. IP: Logged |
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Rosetta unregistered |
I am 42 year old female and lost my hearing suddenly 3 years ago. I wear hearing aids in both ears and my husband is very helpful. I guess you could say he is my humand hearing aid IP: Logged |
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ROCCO unregistered |
Patricia, I've tried the tinnitus masker at a therapy session. Did'nt care for it. I'd rather deal with it without the use of this device. It really was more annoying then the actual tinnitus. I also have an air cleaner, ionizer and radio in the bedroom which does help drown out the noise in my head. Afterall, tinnitus is at its loudest when all is quiet. I was also gonna move to Niagara Falls and sleep in a bag next to the cliff. This would rid the tinnitus for sure. With any luck, I'd roll over and die. Just kidding. I appreciate your advice. Thanks a million. The Rock IP: Logged |
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Compu_Girl Member |
I am a sufferer of progressive SNHL ( Sensori-neural Hearing Loss ) and Meniere's bilaterally. I did a research fellowship at Kresge Hearing Research Institute ( http://www.khri.med.umich.edu/ ) and was involved aith a study involving Sudden HL and antibodies found in those patients and results of various treatments. In short, a large percentage had a specific antibody. An impressively high number of with this antibody, showed remarkable recovery or a significant improvement when given immediate ( or close to onset of symptomology ) , very high-dose prednisone therapy for a period of 1-2 weeks.
Carey, TE, Nair, TS, Gray, JP, Zeitoun, H, Lansford, CD, Fisher, SG, Dolan, DF, Raphael, Y, Miller, JM, Ramakrishnan, A, Lee, DS, Denny, ED, Arts, HA, Telian, SA, El-Kashlan, H, Disher, MJ, Sataloff, RT, Yeom, K. The search for the inner ear antigen of autoimmune hearing loss. In: New Frontiers in Immunobiology. Veldman, JE, Passali, D, Lim, DJ. Eds., Kugler Publications, The Hague, The Netherlands, 2000, pp 67-74. Lasak JM, Sataloff RT, Hawkshaw MJ, Carey TE, Lyons KM, Spiegel JR. Autoimmune Inner Ear Disease: Steriod and Cytotoxic Medical Therapy. Accepted, Ear, Nose and Throat, 2001. IP: Logged |
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JulieNab unregistered |
Hi. I just discovered this forum and it makes me feel better knowing that there are others in the same boat. I am 42 years old and suddenly lost all the hearing in my left ear 20 years ago. It has never come back. For the last 10 years, I have also needed a hearing aid for my right ear as my hearing in that ear has progressively gotten worse. I have recently found out that I have a hole in my eardrum and a tumor in my right ear. My ENT says that he doesn't want to operate on my right ear until he absolutely has to (in otherwords until the tumor gets big enough to cause destruction) because they don't like to operate on people with only "one good ear." I am scared to death to have the operation at all because I am afraid I will lose the hearing in that ear also. Julie IP: Logged |
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Mike Member |
Well...It has been almost 6 months since I started this topic and had my surgery to repair the Fistula that caused my hearing loss. (Fistula was the result of commercial airplane flight from Las Vegas to San Diego!) I have not gained any hearing back and still suffer from severe Tinnitus. I hope everyone else is having better success than I am. QUESTION? Does anyone know anything about the chances of losing the hearing in my good ear. I have read on other sites that when one suffers from SSHL, especially when Tinnitus is involved, that the brain finally figures out that no sound is entering and shuts down the nerve. Unfortunately it also tends to shut down the nerve of the good ear as well. Has anyone here had this occur or have information regardinf this occurance? IP: Logged |
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ROCCO unregistered |
Mike, I've been to several ENT's and ALL of them say they never had a patient lose their hearing in the "other" ear after suffering from SSHL. This was also a big concern for me, and I continue to ask this question. I look at it this way- Lightening doesn't strike twice !!! The Rock IP: Logged |
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JulieNab Member |
Mike...I only wish it were true, but I had a SSHL in my left ear 20 years ago that left me almost completely deaf in that ear. At that time the hearing in my right ear was fine. For about the last 10 years I have gradually started losing my hearing in my right ear. It is at about 50% right now. None of the doctors I have seen have been able to tell me why this is happening. It is very scary. Julie IP: Logged |
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Sheena Member |
Hi Everyone, I've been reading the postings and have a question for everyone. Do any of your families have a history of hearing loss and if so what type? Should a "natural" loss of hearing occur in both ears? Is unilateral hearing loss "unnatural" showing some sort of problem be it a viral infection, acoustic neuorma etc.or could it be hereditary? I'm am now going to see a third specialist in October. My hearing loss has been progressive over the last year and an acoustic neuroma still has not been ruled out. Julie how are you coping with your tumor? I'm assuming it's an acoustic neuorma. Do you have any idea of what caused your inital hearing loss 20 years ago? Thank you for relating your story. It means alot to me that I can ask these questions to people who are going through the same ordeal. Best wishes to all! IP: Logged |
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00Swede Member |
Hello everybody. I just read this column for the first time and I am happy to learn so much. I am 31 yrs. old and 2 years ago, I learned that I have about 60% (right ear)and 40% (left) hearing loss. Since then I have lost more and now hear 50/20. I wear hearing aids which enables me to hear okay. I have not been diagnosed with anything but "hereditary reason" and would like to get suggestions from all you knowledgeable people where to educate myself about hearing loss reasons. I am so uneducated, please help!!! Thank you and remember when people around you get frustrated because you can't hear them, remember that it is hard for them too. [This message has been edited by 00Swede (edited 09-12-2001).] IP: Logged |
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JulieNab Member |
Sheena, My tumor is called a "cholesteatoma" and no, I have no family history of hearing problems. I really don't understand why this is happening to me. It was bad enough to lose the hearing in my left ear, and now to have trouble with my "good" ear is frightening! The doctor said that after my surgery I should be able to hear better in my right ear. Right now, I wear hearing aids in both ears but I am still having a lot of trouble hearing people. It is really hard to explain to someone that can hear fine how frustrating it can be to constantly ask people to repeat themselves and still miss 50-75% of the conversation. IP: Logged |
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Kathy Member |
Hi everyone, I just caught up on what is going on with everyone. I am sorry to hear that you have not had any improvment. I had another hearing test in August. I have had significant improvment. Considering that I had 100% loss initially. At 2 weeks I had greater than a 90% loss. At 4 months I now have normal hearing a the lowest 2 frequency, 50% hearing in the middle frequencies, and less than 10% hearing in the upper 2 frequencies. I can now understand speech much better. Before, I had no speech recognition, now I have 80%. I am also able to tell from what direction a sound is coming from. Unfortunately as my hearing has improved the tinnitus has gotten worse. I am not using a hearing aid yet. My ENT wants me to wait until my hearing stablizes. I go back in February. My tinnitus seems to get worse after I have been in a loud environment. That makes me think that a hearing aid might also make it worse. Has anyone had that experience? I can usually ignor it when I am engaged in an activity. When I go to bed, I have choosen to deal with it, by treating it like it is a sound like that produced by a sound machine. I have a static with chirps. I actually find it relaxing now, like listening to rain. This was a conscious decision on my part from the beginning. If I focused on the sound, and the fact that I could not stop it, I became quite distressed. Fortunately this is working well for me. My initial treatment involved decongestent for a few days, then I saw my ENT who put me on a medrol dose pak, steriod, and Nician. I took the Nician for 2 weeks, until I started having a reaction to it. My ENT feels that my loss was caused by a blood clot in my middle ear, but he is just guessing. Good luck to everyone. IP: Logged |
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KathyRN unregistered |
I too am late deafened in my right ear. I woke up one morning when I was 33 (38 now) and was puking my guts out. It was days before I could get out of bed without falling over and/or throwing up. Nothing could be done about my loss (they said) and it's a pain in the rear to not hear from that ear but I have adjusted better than I thought I might. There are tricks but background noise remains a problem. I'm a RN. IP: Logged |
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Chuck D unregistered |
On September 4, 2001, while sitting in the living room watching TV, I lost the hearing in my right ear. At first I thought it was wax build up. I used ear wax remover and it seemed to help. Approximately 1 hour later, the hearing went again. My wife took me to the Clinic here in Palm Springs that same evening. There I was diagonosed with an inner ear infection and given a prescription for e-Mycian and Allegra. 4 days later I went to see my Doctor and he said that the infection was gone, but there was Fluid behind my ear drum. He sent me to an ENT to have the ear drained. The ENT sent me for a hearing test and diagonosed me with "Sudden Sensorineural hearing loss". The ENT put me on 50 mg of Predisone a day. I'm coming up on 4 weeks of this living hell and am getting more and more disheartned. I'm starting to decrease the medication per the ENT and will be going back to Eisenhower Medical for an evaluation in 2 weeks. I too had never had any ear or hearing problems, but I must say that just prior to my hearing loss, I felt like I was coming down with a head cold or Flu like symptoms. I truly wish all of you out there the very best. I can relate and I know just how miserable you all feel. Thanks for listening, I do feel better since I now know that mine is not an isolated case. IP: Logged |
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