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    Doctors dismissed my health concerns and said I was training too hard. No one knew I was competing in the Olympics without being able to see the hurdles.

    By Kelly Burch,

    1 day ago
    https://img.particlenews.com/image.php?url=0It9c2_0ukBRatd00
    Gail Devers is a three-time Olympic gold medalist and struggled for years to get a proper diagnosis.
    • Gail Devers is a five-time Olympian and three-time gold medalist in track.
    • She dropped to 79 pounds due to Graves' disease between the 1988 and 1992 Olympics.
    • She won gold in '92 but was losing her eyesight because of a related condition.

    This as-told-to essay is based on a conversation with Gail Devers. It has been edited for length and clarity.

    I started running when I was 15. By the time I was in college, I was smashing records in the 100-meter hurdles and sprint, so no one was surprised when I made the 1988 Olympic team. I was 129 pounds of muscle and power, and I could dash through the hurdles in just 12.61 seconds, a time that would have been good enough to win a medal in the Games.

    But as the Olympics grew closer , I knew something wasn't right with my body. You don't need to be an athlete to have that power — you know your body better than any doctor you see once or twice a year.

    My hair was falling out , and I pulled a hamstring just from jogging. That should not have been happening. I started losing weight, and at the Olympics, I ran the slowest 100-meters I'd done in a competition. I wanted to succeed so badly, but my body just wasn't there.

    Doctors told me I was training too hard

    When I got home, I started seeing doctor after doctor. I would open the phone book and call a new doctor, hoping for an answer.

    All the while, people were talking about me. I had dropped to 79 pounds, and I looked incredibly sick. People asked me if I was anorexic or on drugs. Those comments hurt and left imprints that I carry with me to this day.

    Despite how obviously sick I was, doctors couldn't find an answer. Instead, they said it was my fault: I was training too hard , or I was stressed. But I knew that wasn't right, and I kept fighting to get an answer.

    I felt better, but my vision started to fail

    After two and a half years of arguing with doctors, I was diagnosed with Graves' disease , a condition that causes an overactive thyroid. I was so excited to have my life back on track — literally. I had qualified for two events in the 1992 Olympics.

    While I was feeling much better, I was living with a secret: my eyesight was terrible. It was like I was constantly looking through clouds. My eyes were always red, puffy, and bulging, so people asked if I had pink eye or allergies. I started wearing sunglasses everywhere. I always had a pair on my face and a spare pair on my head.

    https://img.particlenews.com/image.php?url=4F5N2I_0ukBRatd00
    Gail Devers competed in several Olympics before getting a diagnosis for her condition.

    Runners are taught to do the hurdles in rhythm: eight steps off the blocks, then jump; three strides between the hurdles; then five strides to the finish line. That became my mantra. I could run the hurdles faster than anyone else, even without seeing them clearly.

    It took decades to get a diagnosis

    At the 1992 games, I tripped on the final hurdle, a fall that became famous, but I took a gold medal in the 100-meter sprint. In the next Olympics, in 1996, I won gold again in the 100-meter sprint and a third gold medal in the 100-meter relay. I also competed in the 2000 and 2004 Olympics.

    I lived a charmed life and had an impressive career, but my eyesight was still failing me. I stopped driving at night. I remember once driving with my kids, being worried about their safety because my eyes were so bad that day. For a long time, I didn't even tell my husband how bad it was.

    No doctors could give me answers, so I assumed that my eye problems were related to my Graves' disease. Then, only two years ago, I was diagnosed with thyroid eye disease . Having a diagnosis meant I had answers and could get treatment that worked, in my case, from a neuro-ophthalmologist.

    I call my eye disease Ted, pronounced like the name. When you've been living with someone as long as I've been living with Ted, you have to give them a name. For a long time, I knew Ted was around, but I didn't know what to call him.

    I want others to know about thyroid eye disease. In my case, getting a diagnosis was a marathon when it should have been a sprint. Now, I'm running a relay, passing information that others can use to get their life back on track.

    Read the original article on Business Insider
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