“It’s an invisible disability,” Winter said. The hardest thing now is that people usually have no idea what her condition entails. Her hands and feet still tingle all the time, but it is much better than it was, she said. “I’m 20 years old and I can’t hold my bladder - it was embarrassing.”Īfter finally getting diagnosed, Winter was put on medication and started supplementing her diet with vitamins. “I thought I was going crazy,” said Winter. All the while, doctors had trouble figuring out what was wrong. She soon started having problems with sensation in her hands and legs, and finally had trouble controlling her bladder. Doctors diagnosed Winter with the illness in 2008, but she started feeling the symptoms two years before, when she suddenly lost vision in her left eye.
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