Courtesy of The Eagle Press

“I asked to carry the American flag and lead the volunteer firefighters in last year’s Memorial Day parade,” recalls Travis Grogan. “It’s usually the rookie who gets to carry it, but I pulled rank.” Travis was an active member of the volunteer firefighters in Cambridge, NY, a town with a population of 3,500 people, until the symptoms of Wilson disease forced him to step away from the volunteer work that he loved.

Bewildering neurological changes

Three years earlier, Travis watched the parade from the sidelines sitting in a wheelchair. He couldn’t speak, feed or bathe himself, his vision deteriorated and his body twitched uncontrollably.

“We didn’t know what was wrong with him,” said James Grogan, Travis’s father. James had just retired and found himself providing continuous care for his son. As a single father, Travis could no longer care for his 6-year-old daughter so they both moved into his parents’ neighboring mobile home.

Travis worked as a cook after graduating from culinary school and followed in his father’s footsteps volunteering as a firefighter.

“Then his attitude changed and he kept getting pulled over by the police for erratic driving,” explained James. “He’d be driving all over the road and he could no longer do his job as a cook.”

Small town doctor searches for answers

James supports his son after WD symptoms develop

Travis was taken to the nearest emergency room in Vermont three times and prescribed treatment for a psychiatric disorder. However, the medications didn’t help. He lost the ability to control his movements and would scream and physically harm himself. It was in Vermont that a diligent doctor figured out what was causing Travis’s bizarre neuro-psych symptoms.

“The doctor didn’t know the cause, but he was determined to figure it out,” said James. “He was a bookworm and kept going to the medical library and he finally figured it out!”

Dr. William Tock thought he had the answer, and for confirmation, he referred Travis to an ophthalmologist. He did an eye exam and found Kayser-Fleisher rings, the tell-tale copper rings that are found in almost all people with neurological Wilson disease.

“We were overwhelmed by the Wilson disease diagnosis, but were glad to have one,” said James.

Wilson disease is a rare genetic liver disease that doesn’t allow the body to process dietary copper. Over time, the excess copper builds up in the liver, brain and other organs and can look like a liver disease, neurological disorder or psychiatric illness.

“I give all the credit to Dr. Tock,” said Travis. “this small town doctor figured it out, but he didn’t have experience treating it.”

The search to find the right treatment

Travis then traveled more than an hour to Albany, New York to be treated. He was prescribed the chelating drug penicillamine, which works by removing excess copper from the body. However, the dose was too high and he had troubling side effects.

“You know you have a rare disease when the doctors are searching on their phones for information,” said Travis. “Then one of them came across the Yale Wilson Disease Center of Excellence and called its director, Dr. Michael Schilsky. The first time I met him was over Zoom.”

He then traveled three hours to Yale and entered the Wilson Disease Patient Registry Study and was evaluated by hepatologist Dr. Uyen To.

“She took one look at him and said they needed to cut back his chelator dose,” recalls James. “She said the copper was coming out too fast, and she warned us that it would likely get worse before it got better.”

The Wilson disease symptoms did get worse, and he ended up needing a wheelchair. He was given hope that he would get better, but it would be a long process.

Fighting for his recovery one step at a time

Community support helped James fight for his recovery

Travis did get better and by the time the 2023 Memorial Day parade rolled around he was able to join it and ride in the cab of the fire truck. He had an even bigger goal for 2024:

“I wanted to lead the volunteer firefighters in the parade,” said Travis. “So, I started walking every day to build endurance and was walking up to three miles a day.”

How did it feel to accomplish his goal?

“It was emotional for all of us. I went from being in a wheelchair to the main guy leading,” said Travis. “My hand fell asleep carrying the flag about a quarter of the way in, and my glasses fell off at one point, but I didn’t want to give up.”

“People thought he wouldn’t make it,” said his father. But he did, though the family went through some very dark days. “I don’t know what we would have done without the support of our small town community, the church and firefighters who brought us food and helped us to cover expenses.”

Travis continues to work on his recovery from Wilson disease. He still experiences mood swings and he’s not back to work yet. He and his daughter have returned to their own mobile home and Travis is hopeful about his future.

“I’m so thankful there is medicine that works.”