2007 - 2008
From Good To Bad
Seventeen years have now passed with no
problems and then seemingly out of nowhere, a few episodes of tinnitus, ear
pressure, vertigo and nausea return.
They end, again, after I vomit; they
subside on their own. My only remedy to thwart
an attack was to take a strong antihistamine
(first level) like Benadryl, which did the job but made me very tired. For awhile, I had no difficulties between
episodes. Then things changed. I
officially began menopause, I had just ended 3 very stressful years caring for
my mother and I was burned out after 38 years of working. My symptoms returned. I resumed my food elimination and rotation
diet but that did not help as it did before.
A new level of this problem showed its evil head. And it was bad.
2008 - 2012 The More Severe Stages of
Vertigo Appear - Becomes Central
and Peripheral
"And
she was blinded by the light. Cut loose
like a deuce, blinded by the light...but she'll make it alright" Bruce Springstein
On July 18, 2008 I awoke because I was
already slightly dizzy; the room was spinning. (The night before this episode I
had been to a wine and cheese tasting, had skipped dinner and was very tired
from the long day and hour long drive in each direction after work. I was dehydrated. This will be more meaningful later.) My
husband had already left for work so I was home alone. When I walked around, the vertigo seemed to
improve a little. I drank coffee and
water and had a light breakfast. Then
the nightmare began. The room was
spinning, I became quite nauseated and I had a severe, burning hot flash that left
me sweating. Then I began to vomit. And shiver.
I dragged myself to the bathroom because, I am sorry and of course embarrassed to tell you, I had
diarrhea. I got myself back to the den
floor and continued throwing up for over an hour. I could not get up. I did
not know how to stop the
vertigo. If I could just get to the
phone I would call 911. But the doors
were locked and 911 would surely use an
ax to enter. I dragged myself over to
the table and pulled the phone down to the floor and called my husband. It was barely audible but I managed to whisper,
"come home".
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As
soon as he arrived, he unlocked the doors and made the call. The paramedics immediately hooked me up and discovered
I had Atrial Fibrillation (A-Fib). I also had a high WBC (white blood cell
count). I had never had any heart condition or any
health issues. At the hospital I was put
on Valium and then everything was fine and I was sent home. They recommended follow-up with my ENT and a cardiologist. The only residual effect was fullness in my
right ear.
The Cardiologist gave me a good report and
stated my stress test did not reveal any issues. My cardiac and EKG tests were normal. The A-Fib was transient and non-recurring.
My ENT found my left ear
functioning within normal limits but a mild loss at 250Hz and 6000Hz in the
right ear. The other frequencies were
within normal limits. Also, I now
regularly had fullness in that ear.
Speech Discrimination was not affected as I had a 100% correct score in
both ears. She suggested I might have
Meniere's Syndrome and did not pursue another RAST test as she felt they were
no longer as sensitive a measure as in 1990.
I
remained well for one year, following my rotation diet, watching my salt and
taking antihistamines as needed (often).
My Primary doctor did not want me on diuretics because I have lower
blood pressure and they would make it drop even lower, which also can cause
dizziness.
In July and August of 2009 (one year
later) my hot flashes returned; the weather was quite warm and my vertigo
resumed. What is it about the hot summer
months? Do I get dehydrated? The episodes minimized when the cooler night
temperatures returned in September. Again, I relied on antihistamines. I was popping those pills regularly.
February 2010: I felt
I needed to see a specialist to try and solve this ongoing problem so I made an
appointment at the world renown House Clinic in Los Angeles. I drove myself there and then became very
dizzy sitting in the waiting room, under the lights. The
doctor gave me a pamphlet to read,
suggested a diuretic and said I had Meniere's Syndrome. He suggested I always
wear sensible shoes. (Thanks !) I relayed my issues
with low blood pressure and he said I only had one alternative: A shunt procedure - "A mastoid operation
is performed and a tube is inserted into the endolymphatic sac of the inner ear
to control abnormal fluid pressure", as is stated in their pamphlet.
( They drill into the inner ear through the mastoid bone and insert a shunt to
drain fluid.) After some questioning, I
found out that It has about a 60% success rate and may need to be done every
1.5 years. I declined. My audiogram now revealed a moderate loss in
the right ear for frequencies 250-1500Hz.
From February 2010 until June 2011 I lived on a lower salt diet and took Meclizine
every 12 hours to control the vertigo.
It made me very tired but I had no other choices, I was told, except the
shunt surgery. Then in June 2011
I had a new, more severe attack
that seemed to involve both my ear and more central areas in my head. Any prolonged eye movement like reading, any
quick head movements and exercise would set off similar attacks and Meclizine
had no effect. I felt pressure and
vibration behind my nose and eyes. My
eyes hurt. Sometimes I felt tingling in
my lips. The new level of attack was intolerable and sent me to the emergency
room where I was put on Valium for
several days (yes, I did feel withdrawal symptoms when I stopped them). Those pills gave me time to follow-up with an
ENT recommended by the hospital. He said
he could not and would not monitor me on Valium so they were discontinued. He
yelled at me about the Valium but he had no other solutions except to try a diuretic
(which I could not do) and he sent me back to my primary care doctor. He did not notice my shoes.
During this same time period I began more research on the internet. All information
about Meniere's Disease was the same from site to site and I still could not
take a diuretic. Since I was typing
"Vertigo" into the search box, I began reading about the connections
between migraine and vertigo, about Migraine Associated Vertigo (MAV) (even
though I had never had a migraine headache I did get occasional headaches, that
Advil could control) and about food and chemicals as triggers. I was seeing the words "silent migraine". The
symptoms in these scenarios were so similar and the treatment called for a
rotation and elimination diet. I still
was clinging to the fact that at one time, changing my diet did make a positive
difference, so this was appealing to me.
There seem to be another professional community - one that was linking migraines with Meniere's Syndrome and Benign Positional Vertigo and drippy noses and "sinus" headaches and even hearing loss. But none of my doctors were in the know. There were real discussions, backed by science, that I found at The Chicago Dizziness and Balance Clinic with Dr. T. C. Hain , The American Speech and Hearing Association (ASHA) Migraine and Vertigo/dizziness articles (ASHA.com), The Austin Migraine Support Group (excellent website at: fincher.org), The Vestibular Disorders Association (Vestibular Migraine or MAV) and several others around the country. *(Click Here)
There seem to be another professional community - one that was linking migraines with Meniere's Syndrome and Benign Positional Vertigo and drippy noses and "sinus" headaches and even hearing loss. But none of my doctors were in the know. There were real discussions, backed by science, that I found at The Chicago Dizziness and Balance Clinic with Dr. T. C. Hain , The American Speech and Hearing Association (ASHA) Migraine and Vertigo/dizziness articles (ASHA.com), The Austin Migraine Support Group (excellent website at: fincher.org), The Vestibular Disorders Association (Vestibular Migraine or MAV) and several others around the country. *(Click Here)
The university associated clinics and related
health organizations were making these connections, but not the community based
ENT physicians. These University clinics
all discussed "Vertigo", and that is certainly the most debilitating
part of my problems. Could it all be linked? I had many symptoms and some history related
to Migraine, but never had a migraine headache (except once a month, like
clockwork, three days before my period, for my whole life). I was getting dizzy
under fluorescent lights, from moving my eyes back and forth reading or at the
computer, and observing that abrupt up/down head movements would trigger attacks. These quick up/down movements could cause a
thud to the back of my head and a split second blindness - the lights went out
for just a second. By November, 2012, I had hit rock bottom. The medications (Meclizine and other
antihistamines) for vertigo were not working and I had no control over my
situation. I was taking them for 24
hours a day. I was having vertigo off and on, all the time. And nausea.
And worse. HELP. PLEASE. NOW. ( Click Here)
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