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Showing results for tags 'tinnitus'.
Found 3 results
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Hi I suffered a SAH 7 years ago and from the day I had the embolisation I have suffered dreadful migraines 2-3 days a week and constant tinnitus. . The neurologist has given me everything he can but nothing helps! Does anyone else still have long term headaches or migraines?
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Hi, I was wondering if anyone has started suffering from tinnitus since they've had SAH? I've never had this before but started to get it 6 months after my operation. I've seen an ENT specialist,my hearing test was fine and he said he was sure the tinnitus had been caused by the brain trauma. However, when I saw the neuro consultant a few days later he said no, the tinnitus wasn't caused by my op if it had been I would have had it since when the op was done. No one can tell me if it will be permanent. At neuro they checked all over my head and neck pressures,all ok. I see ENT again in sept.Gp has given me sleeping pills,but I know I can't stay on them for long.I don't sleep too great even with the meds. The tinnitus drives me insane, to cope with that on top of everything else at times brings me to my knees in tears. Wondered if anyone else suffers with this too since SAH?? SarahLou Xx
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My husband had a PMSAH at the end of December 2016. Three weeks after the event, he developed tinnitus that has become completely debilitating. What have others with tinnitus found to be effective in reducing (or, ideally) eliminating the tinnitus? My husband has tried acupuncture, chiropractor, diet changes, and hearing aids. The hearing aids made it worse, has anyone else experienced that? He's only had them for two weeks but wants to stop wearing them because they only seem to make everything worse. Thanks in advance for any help you can provide. Amy
