“It was a disease I wasn’t familiar with," said Randy Tressler, physical plant manager, "so I needed to educate myself because I wanted to make sure just changing out lights, bulbs and fixtures would be enough or know if we needed to do other things,”
Through his research about the condition, Tressler learned that light-emitting diode (LED) lighting was safe for those suffering from the disorder. The campus had already started converting some of its older, fluorescent lighting to LED lights to meet sustainability and energy goals. A meeting was set up between Adams, his mother and members of the campus in the Arbuckle Technology building, an area already converted.
“He [Randy] did more research before we even met him than I think some doctors do before meeting Mackinly,” said Adams' mother, Kelly. “He realized, before I even told him, that LED lights were great.”
Following the meeting, Tressler and his department began working on a plan to help make Adams’ dream a reality. Over the summer, Tressler leveraged funding and donations from vendors so that multiple areas of campus could be converted to LED lighting sooner than originally planned. More than 700 bulbs and fixtures have been converted to date, with more planned in the future.
“I can remember how excited Kelly and Mack were that we already had a building that was LED,” said Adam Robinson, learning center coordinator. “That first meeting was an immediate motivator for me, and I think, for all of us.”
The journey to Penn State
Severe migraine headaches began to plague the Arnold youth almost daily when he was just seven years old. By lunchtime, he would have unexplainable reactions that caused him to be sent to the emergency room three to four times each month, and began failing in his schoolwork. He also suffered symptoms outside of school.
“We couldn’t figure out why, when he was little, we would get through the front doors of a store, and by the time we would get to the back of the store, he would be red and look like he spent eight hours at the beach without sunscreen,” Kelly Adams remembered. “It’s scary seeing your child like that and not know what’s going on and no doctor can tell you.”
Visits to more than 15 doctors in four states over a span of three years finally led Adams to the diagnosis of actinic prurigo with the help of a doctor in North Carolina who would reference a white board containing lists of the youth’s symptoms and test results. Many of those tests had to be run through the National Institute of Health’s Undiagnosed Diseases Program in Bethesda, Maryland.
Adams’ form of the condition is at the most severe end of the disease’s spectrum, and, to the family’s knowledge, less than 20 individuals in the world experience symptoms this acute.