Collaboration among a multidisciplinary care team at Mayo Clinic helped Julianne Vasichek successfully navigate not one, but two, rare liver diseases.
graduating from high school, Julianne Vasichek was eager to take her athletic talents
to the women’s hockey team at the University of Minnesota Duluth (UMD).
Julianne’s college career got off to a rocky start, however, due to a sudden
change in her health. “I was symptomatic my entire freshman year of
college while doctors tried to figure out what was going on,” she says. “But
I played through it.”
Diagnosed with ulcerative colitis, Julianne had a colonoscopy done a week before the Bulldogs’ 2001–02 NCAA Division 1 championship game. “That colonoscopy really helped spur me on during that game,” Julianne says. “We did win, but I was pretty worn down by the end of the year from playing through my symptoms.”
in Duluth, Minnesota, put Julianne on medication that kept her symptoms at bay
long enough for her to finish her playing career at UMD. That career included
another national title and tryouts for a spot on Team USA’s women’s ice hockey
team. “I tried out for the 2006 Olympic team but didn’t make the final
cut,” Julianne says.
that, Julianne moved east to take an assistant women’s hockey coaching job with Bowdoin College in
Maine. “I was thinking about still trying to play hockey
myself, but I started noticing throughout that year that I was just getting
more and more tired,” she says.
chalking it up to being “tired from life in general,” Julianne put
her increased fatigue out of her mind. “I just shrugged it off,” she
says. Then at the start of 2008, her skin began to feel itchy. “I was in
my early 20s and otherwise healthy, so again, I shrugged it off,” she
Julianne returned to Duluth a few weeks later to watch UMD host that year’s
national championship game, however, she couldn’t ignore her symptoms any
longer. “By that time, I was itching so badly I was cutting the skin around my ankles
she says. “It was at that point that I said, ‘Maybe I do need to get this
Facing a scary diagnosis
When Julianne got back to Maine, blood tests revealed a surprising cause for the itching. “I was diagnosed with primary sclerosing cholangitis,” she says. “It’s an inflammatory disease that causes scarring within my bile ducts that, in turn, makes the ducts hard and narrow. Over time, it causes serious liver damage.”
Julianne was told the damage eventually would require a liver transplant. “That was a scary thing to hear,” she says. “But my gastroenterology doctor in Maine said the disease usually progresses slowly, and that it could be several years before I’d need to start thinking about a transplant.”
“I knew people who had gone to Mayo Clinic, and I knew that’s where I wanted to go, too.”
At that point, Julianne decided she no longer could stay in Maine. “I didn’t feel like I knew where to go to get the care and treatment I’d ultimately need,” she says. “I knew people who had gone to Mayo Clinic, and I knew that’s where I wanted to go, too.”
put that plan into motion by calling her former coach at UMD. “I told her
about everything that was going on and that I’d like to come back and work for
UMD,” she says. “I thought that would be an ideal situation because
it would allow me to be closer to Mayo Clinic. Thankfully, it worked out.”
With her return to Minnesota set, Julianne’s next call was to Mayo Clinic to schedule an appointment. At Mayo Clinic’s Rochester campus, Julianne was placed in the care of John Poterucha, M.D., in the Department of Gastroenterology and Hepatology.
had some lab tests done before coming to Mayo. After looking at those, Dr.
Poterucha said things were looking good. He wanted me to come back in six
months for another checkup. But I asked if we could shorten that to three
months because I was still symptomatic and wanted to stay on top of things as
best I could, and he agreed.”
Getting to know her foe
meeting with Dr. Poterucha, Julianne returned to Duluth and immersed herself in
learning as much as she could about primary sclerosing cholangitis, or PSC. “I
also became active in trying to meet other PSC patients,” she says. “That
was huge for me because it helped me see I wasn’t the only one in the world
living with this disease.”
organized a benefit hockey game at UMD to create more awareness of primary
sclerosing cholangitis and raise funds for research. It was at this time,
however, that Julianne’s health really began to decline.
had some hospitalizations for infections between my initial consultation with
Dr. Poterucha and then,” Julianne says. “But we still weren’t talking
about a transplant because, even though the disease was progressing, the
therapies and treatments I was receiving were keeping things at bay.”
before the fundraiser, that changed. “I was sick that whole week,”
Julianne says. “But there was no way I was going to miss that game, so I
ended up making it through the weekend. But by Sunday night, I was feeling
pretty bad. “
went to the hospital. “They did scans, but they couldn’t find anything
abnormal,” Julianne says. “I had a lot of pain in my lower abdomen,
but they weren’t sure what was causing it.”
“In addition to everything else, I’d gained 30 pounds of fluid and had developed swelling around my brain. Everything was going south.”
and nausea medication helped her to feel a bit better, and then she was sent
home. Her care team at the hospital told Julianne to follow up with her
gastroenterologist as soon as possible. By the next morning, though, she was back
where she’d begun. “I was throwing up again, so I went right back to the
she was going through all of this, Julianne’s doctors in Duluth were keeping in
close contact with Dr. Poterucha and the rest of her care team at Mayo Clinic. That
contact intensified as Julianne’s health worsened.
had become apparent by Wednesday morning that I needed to be transferred to
Mayo,” Julianne says. “In addition to everything else, I’d gained 30
pounds of fluid and had developed swelling around my brain. Everything was going
was transported by air ambulance to Mayo Clinic. “I was assessed for
transplant immediately after we landed because, by that point, they knew my
liver was beyond repair,” she says.
Battling for hard-earned
Julianne and her care team were aware of the complications primary sclerosing
cholangitis were causing for her liver, an ultrasound revealed that another
problem was lurking in the background.
“A couple of my major veins were dark and not visible on the ultrasound, so my care team knew they were blocked,” Julianne says. “After more testing, they learned I’d also been living with a second rare liver disease called Budd-Chiari syndrome.”
and her team were stunned. “Having these two rare conditions together is
kind of ridiculous,” Julianne says. “The odds are more than 1 in a
million. Nevertheless, the disease had clotted several veins in my liver and
made my need for a transplant imminent, as my liver function was down to 20% by
for Julianne, her wait for a transplant would not be long. “All of this
happened on a Thursday, and the next day, my care team told me they’d found a
new liver for me,” Julianne says. “My transplant was then scheduled
for the next day, Saturday, Feb. 28, 2015, which happens to be Rare Disease Day
every year. I found that fitting.”
“After I woke up, Dr. Nyberg told me the new liver fit perfectly. I remember giving him and a whole room of other doctors high-fives after hearing that.”
in the course of the surgery, Julianne’s transplant surgeon, Scott
Nyberg, M.D., Ph.D., discovered another obstacle. “During
the transplant, Dr. Nyberg and the rest of the team saw that part of my colon
was dead, so they had to call in a colorectal surgeon to deal with that,”
W. Larson, M.D., had to remove 40% of Julianne’s colon
to allow Dr. Nyberg and his team to continue with the transplant. Fortunately,
the rest of the procedure went off without another hitch. “After I woke
up, Dr. Nyberg told me the new liver fit perfectly,” Julianne says. “I
remember giving him and a whole room of other doctors high-fives after hearing
With her new liver in place, Julianne and her care team spent the next few days waiting to see how her body would respond. “They were watching to see what the brain swelling was going to do,” Julianne says. “I’d also been on dialysis since arriving at Mayo, so we were all waiting for things to hopefully correct themselves with the new liver. It was, honestly, still pretty touch-and-go at that point. My care team still wasn’t sure if I was going to survive.”
thanks to the collaborative efforts of everyone involved in her care, Julianne
overarching team approach to patient care really shone through in everything surrounding
my care. I have no doubt that’s why I’m still alive today. That and, of course,
because of my donor,” Julianne says. “I’m just really thankful I live
close to Mayo Clinic now and have access to their care because it’s been lifesaving
more about Julianne’s liver transplant at Mayo Clinic in this video:
- Learn more about primary sclerosing cholangitis and liver transplants.
- Read about the Department of Gastroenterology and Hepatology.
- Check out the Mayo Clinic Transplant Center.
- Connect with others talking about transplants on Mayo Clinic Connect.
- Explore Mayo Clinic’s Rochester campus.
- Request an appointment.