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Nick Vojnovic was diagnosed with myelofibrosis (MF) in February 2016 and has been actively engaged with research about his condition since. He sought second opinions with multiple experts at several major medical centers around the country. While participating in a clinical trial, changes in his bloodwork were discovered, and he was recommended for stem cell transplant. Nick underwent a stem cell transplant in early 2017 and is doing well today.
Since his diagnosis, Nick has sought support through online communities to learn more about his condition and meet others in similar situations. He even began a support group of his own in central Florida for patients living with myeloproliferative neoplasms and finds connecting with others to be cathartic for all parties involved. Nick is a strong proponent of clinical trial participation and does his part to raise awareness about this rare condition through community efforts, local media and blogging.