Curious to know if anyone else has noticed this.....if you put a finger in your affected ear and move it around quickly to change the pressure, do you experience nausea and dizziness? I do everytime, and it stops the second I stop moving my finger. It does not happen in my other ear.
That's actually the home test for PLF. Go get an official test and don't do it again as you can expand the fistula.
I have been able to do this for a few years, I assume it is part of the mm. I looked at perilymph fistula but do not have any other symptoms.
This happens to me. I'm bilateral. I've had a VNS in one ear and have had steroid injections in the other ear. The hole from the injections, after several years, never did heal. I can produce dizziness and nausea in the ear with the hole. I've been checked for a PLF. I've always thought it has something to do with the hole in my eardrum.
I have a similar issue. Almost threw up on the guy who was trying to fit me for a hearing aid because of that. I also have issues flying because of it. I brought it up the doctor and he blamed it on ETD (Eustachian tube Dysfunction). Could also be why I get the popping sound in my ear. Much worse in my MM ear...go figure. I had bad sinuses and allergies for years so I am sure it did a number. I had the doctor put a tube in my ear and it has helped with the pressure. I also looked int he ETD balloon surgery which is fairly new in the US. I believe Dr. Poe in Boston was the Pioneer. I dont really feel like a another surgery just yet. Hope this helps.
Dizziness Tinnitus Hearing loss pressure sensitivity sound sensitivity You don't have have these? How are you diagnosed with MM?
Yes, I do have those symptoms, but not unsteadiness which increases with activity and which is relieved by rest, and symptoms get worse with coughing, sneezing, or blowing their noses, as well as with exertion and activity.
Yes. I have to go easy with the cotton swabs also or I can get a little wave of nausea. I always assumed this was because of the increased pressure in the affected ear. A side note, my dad who has had MM for 20 years always talks about popping his ears (like when yawning or chewing gum) to relive pressure in his bad ear. Doing this has never helped me, assuming since popping your ear occurs in the middle ear and doesn't affect the inner ear workings. Thoughts?
I would agree it is he air pressure changing that creates the symptoms. It do find it odd I can only do it one ear.
I can't pop my ear. Ever. It was maddening at first but I have learned to live with it.... along with the constant ringing it's a ton of fun. One of the indicators that I am going to have an imminent attack is the ringing grows louder and the pressure increases.
I tried this and there was no response. I’m pretty sure my inner ear is damaged from all the 12 hour vertigo attacks. It can’t even work up a vertigo attack anymore so that may be why I felt nothing.
I'm very sensitive to changes in pressure--get the whole slew of symptoms: dizziness, nausea, stuffed ear, tinnitus. I don't fly anymore, and wear pressure-change-slowing ear plugs (https://www.alpinehearingprotection.com/earplugs/flyfit/) when I drive to high elevations--like over 500 ft. Once in the audiologist's office I was getting a tympanogram (I think that's the term--they blow air in your ear to test the ear drum), and I had a brief but dramatic wave of vertigo like the whole room rocked. My oto believes those things are from Migraine Associated Vertigo. Just based on the kind of nausea I get, that seems true to me.