Friday, March 28, 2014

TRAUMATIC BRAIN INJURY STORIES

Migraines and dizziness after closed head injury

In 1997, I was in a car accident that left me with a severe closed head injury. I was in a rehabilitation program for about 6 months but was unable to return to work because of short term memory problems and assorted other problems associated with a head injury. I began to get migraines shortly after the accident, I was told this was associated with the head injury and was given...



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Glasses Made Me Feel Normal Again After A Traumatic Brain Injury

In July of 2006, I was hit above my left eye with a golf ball resulting in a TBI (traumatic brain injury). During my recovery, I was constantly nauseous and had the feeling of “sea-legs”. I also had headaches everyday and fatigue was a constant battle- in the first few weeks of the injury. I slept 18-20 hours a day. When I read, which wasn’t very often because of...

After over 8 years of seeing Dr Debby

First of all, I have been having problems for as long as I can remember. I had eye problems all of my life. Being dizzy with the headaches. The seizures. were just the start. When I was 22 years old I was hit in the head with a baseball bat. Closed head injury. I was in a coma for 3 months. It almost killed me. After that I just got worse. I was in and out of the hospital most of my life. I had all of the symptoms you could have with this disorder.
Around 8 years ago I went to an ear nose and throat specialest. And he recommended me to Dr. Debby. That would be the day my life would change. I made an apointment with her. And with in a month I had my new glasses. And just like that all of my symptoms went away. Dr Debby saved my life. I would recommend this group of Doctors to anyone. I am living proof.
- M.B., 49 y/o


11 years of misery ended with one visit

Nearly 12 years ago I was in a traffic accident, and several months later I was hit hard by a vicious dizzy spell. I had no idea what was happening to me. I was so nauseous I couldn’t eat, so dizzy I didn’t want to move. Prior to the attack I was healthy, fit, strong–a year later, I was obese from lack of activity (bad balance) and a bad diet (being constantly nauseous made me crave mostly sugar). My excellent attendance record at work was shot, and now I missed 3-5 weeks of work every year because of my inability to drive or even get out of bed. Even on my good days I had to fight nausea and to constantly be alert and grab things when I lost my balance.
I was sent first to University of Michigan’s Vestibular Testing Center, where I was told that “something” was wrong with my inner ears and “be grateful you don’t have cancer.” I was stunned by the lack of compassion or understanding of what I was enduring each day. Repeated visits brought no new treatments or relief, so I stopped going. Specialists were unable to help me. After receiving a formal reprimand for my poor attendance at work, I was desperate for a solution and got an appointment with a neurologist who was recommended to me because of his willingness to try new techniques. He suggested that the problem might be my eyes, not my ears, and referred me to Dr. Debby Feinberg.
I’m fortunate in that the clinic is only a 2 hour drive away. Within 15 minutes of putting on my first pair of glasses, the constant ache in my neck disappeared. The next day, for the first time in 11 years, I was able to stop taking my anti-nausea medication. I could walk in crowds again and not lurch around like a drunk. I could enter unfamiliar territory and not worry about where I was placing my feet. Family and friends had grown used to having to clutch my arm and guide me around like I was blind, and they still can’t believe the change. My mother is forever asking me, “You’re OK? You’re really OK in here, with all these people, looking around like this?” I used to keep my eyes fixed on the ground.
I’m still adjusting to my new glasses and my health insurance doesn’t cover the cost, but it’s well worth it to me to have my life back. I will be forever grateful to the doctors and staff here. I just hope the rest of the medical community will learn about vertical heterophoria and this treatment soon.


If you want more information on how you can be helped if you have this condition go to www.vsofm.com


Yolanda


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