posted
Used to be maybe twice a year. Now it's been twice in a week and a half. I'm focusing on mold now and am on a binder, working up.
My ent has always said it's my allergies and eustacian tube dysfunction. My ears have always felt a bit clogged, and I have tinnitus. Other than my short tinnitus spells, my hearing is excellent. I also have on off slight ear pains Some years ago, I had stabbing ear pain. That was terrifying
I knkw I have Lyme and Mycoplasma. I'm thought to have babesia and bart.
Is there anything I can do, evdn for just symptoms? I'm on levocitirizine, and both fluticasine and azalastine nasal sprays, all for allergies. This is scaring me. Posts: 603 | From sw suburbs of chicago, Illinois | Registered: Mar 2016
| IP: Logged |
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177
posted
6Hypnone
Here we go again with no one to defiantly tell us why this keeps happening. I have the same Infections as you, plus high EBV and low brucellosis. And it's my dreaded month, September. Aghhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh
I'm on the same nasal sprays and no progress so I feel your frustration. I also did low dose antigen therapy last year with my LLMD and no improvements. I take 2 oral anti-fungals without any benefit either.
But I do notice that when I take a Epsom salt bath (1/2 hour, 2 lbs Epsom), my sinus release a huge glob and I feel better. Don't know why but it's a temporary relief of the tinnitits and vertigo.
That disulfiram is looking better and better everyday. 💚
Posts: 2907 | From Florida | Registered: Nov 2016
| IP: Logged |
posted
You could try putting your finger in front of each ear and at the same time opening your mouth and quickly closing it. (sort of like clenching your teeth)
Do it 5-6 times.
My doctor taught me this when I had severe ear pains. It was like nerve pain.
Now if the pain hits, I do the open and close while putting pressure on my ears.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96173 | From Texas | Registered: Feb 2001
| IP: Logged |
posted
I am and have been for 3.5 years, but doesn't seem to make a diff. But that's pretty cool that's all it took!
Posts: 603 | From sw suburbs of chicago, Illinois | Registered: Mar 2016
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/