Gail Devers
While training for the Olympic games, track star Gail Devers began to suffer from a number of mysterious symptoms: weight loss, dry skin and fatigue. She lived with them for years before being diagnosed with Graves' Disease. Her treatment was effective but led to another condition, hypothyroidism, and a different set of medications. Join Gail Devers as she shares the twists and turns of her story and her ultimate triumph.
[ANNOUNCER CALLING RACE; CROWD NOISE]
VOICEOVER: Before her Olympic Gold Medal performance
at the 1992 Olympic Games earned her the title "World's Fastest
Woman," sprinter Gail Devers had to jump hurdles far greater than those on
the track. In 1988 while training for the Olympic Games in
Seoul, she began to suffer from symptoms that resulted in deterioration of
both her body and her performance. GAIL
DEVERS: It took 2-1/2, almost 3 years for me to be diagnosed
with a thyroid condition. And the reason is because the symptoms
are so vague. In 1988 when I first started feeling that
something was wrong with me and didn't know what it was.
Didn't have an answer to it, but I was tired.
Couldn't make through my workout. Just
fatigued. My normal running weight was between 119 and 120 and I
had gone down -- at my worst under 85 pounds. I was going from
doctor to doctor and no one was giving me any answers. I mean
I've always had long fingernails and they got really brittle and
they'd break and wouldn't grow back. For me that
was the first sign that something's wrong. The exact symptoms
that I had would be dry hair, brittle nails, fatigue, insomnia.
I had menstrual problems where I was having three and four cycles a
month. As an athlete they say you're supposed to have
the opposite. Night sweats and I had problems with my
eyes. And those were probably the main symptoms I was
having. Psychologically and physically it was very
debilitating. I got to the point where I was pulling my
hamstring by jogging because you lose the extensor muscles. And
then psychologically like as an athlete, you know that you depend on your
body and now my body is letting me down. And there's no
answer for this. So it was very hard for me. Like the
word I use is "debilitating." You know people
thought I was crazy. Even I began to think that I'm
crazy. There is something wrong and can't somebody give
me an answer and there is no answer to be found. VOICEOVER:
After almost three years of searching for the cause of her ailing health,
Devers was diagnosed in 1991 with Graves disease, a form of
hyperthyroidism.
GAIL DEVERS: The hardest part about
having my Graves disease was not knowing. I mean I tell people
all the time. I mean it's unanswered question and
feeling of not knowing what you're going to do, what you can
do. In my heart, I had the desire to do everything that I had
written on paper for my goals and aspirations. But my body was
saying no. VOICEOVER: After undergoing radioactive iodine
therapy to disable her overactive thyroid, Devers was put on
levothyroxine, a thyroid replacement therapy, marketed under such brand
names a Synthroid, Unithroid and Levoxyl. GAIL
DEVERS: I have been on Synthroid since January of 1991, about
10-1/2 years. It's a very small pill. I take
it once a day every day for the rest of my life. I say it all
the time. It's a very small price to pay to have the
quality of life that I have.
VOICEOVER: Although oral
levothyroxine drug products have been used to effectively treat
hypothyroidism for decades, recent FDA regulatory issues surrounding
Synthroid, a popular form of levothyroxine, have created a controversy
that threatens to pull Synthroid off the market.