It was not be coincidence that I sought out Board service with the CLF. For nearly two decades, I have been provided care to patients living with manifestations of Cutaneous T cell Lymphoma. It was in those very early day to day interactions with patients and their caregivers that I realized managing this disease called for "an expanded arm" to provide support/ education/ advocacy... and the CLF fit the bill !
I have witnessed tremendous foundational growth over the past several years. Educational platforms have been expanded, the website has been redesigned, and the research award program has taken flight.
Our (the CLF's) really ultimate goal for finding a cure and making life better for all affected with CTCL is rather ambitious.
But, why not dream big?
During the 20/20/20 campaign season, I am asking you to consider a donation of $20 to the CLF.
Take good care,