A Volleyball Friend Told Him He Has Rosacea
It wasn't unusual for Bob Vilsoet's face to get particularly red while he played volleyball. After all, the competition was usually fierce, and the game would get his blood flowing.
But when the facial redness persisted, and his face began to look red and "splotchy" all the time, he wondered what was up.
"I didn't know what was going on. The splotches resembled acne, but they just wouldn't go away," Vilsoet said. "It went on for about two years and I didn't do much about it." Then, as he prepared for a volleyball game one night, a friend approached him during a tournament. "Hey, I have what you have," his friend declared.
"I looked at him confused," Vilsoet said. "I didn't know what he was talking about." His friend went on to explain about rosacea. "His face had the same red spots that I had, and I knew I wanted to do something right away."
Vilsoet mentioned his plight to a nurse friend and she sent him copies of Rosacea Review. He then went to see a dermatologist who confirmed he had rosacea. He started using oral and topical antibiotics and learned that other factors that cause him to flush might aggravate his condition.
"The medication helped my face clear up considerably," Vilsoet said. In his particular case, Vilsoet finds his volleyball playing, although physically intense, doesn't pose much of a problem.
"Playing volleyball doesn't seem to bother me," he said. "In fact, if it wasn't for the game, and my volleyball friend, I wouldn't have my rosacea under control."
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The National Rosacea Society is interested in hearing personal success stories from readers who have been able to improve their lives through effective control of rosacea. In the coming issues of Rosacea Review, we'll feature some of these stories and personal tips. Please mail your success story to Rosacea Review, 800 South Northwest Highway, Suite 200, Barrington, Illinois 60010; e-mail to firstname.lastname@example.org, or FAX to: 847/382-5567.
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The National Rosacea Society is a 501(c)(3) nonprofit organization whose mission is to improve the lives of people with rosacea by raising awareness, providing public health information and supporting medical research on this widespread but little-known disorder. The information the Society provides should not be considered medical advice, nor is it intended to replace
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