Whether you are newly-diagnosed or have been living with your diagnosis for a long time, our programs provide information that can help you improve and maintain your quality of life while living with cutaneous lymphoma.
Patient Educational Forums & Webcasts
The Cutaneous Lymphoma Foundation offers FREE Patient Educational Forums (PEF) to help patients, caregivers and others affected by cutaneous lymphoma receive accurate information about the disease. Forums are an opportunity to learn about current treatment options and research, connect with other people who share similar experiences, and obtain information about resources and support available. For those who can't attend in person, we provide a live webcast of the PEF with the opportunity to participate in event via the internet.
Denver, CO - Saturday, April, 2018
Details coming soon!
2-Day Patient Conference
The annual 2-Day Patient Conference is two days of learning, connecting and celebrating for patients, their family and/or friends. The 2-Day Conference offers clinical presentations, diagnosis-specific breakout groups, open Q&A discussions with clinicians as well as presentations related to daily-living topics. Unique to the 2-day is the time devoted to creating opportunities for attendees to connect with each other and build friendships with others also impacted by cutaneous lymphoma.
Bethesda, MD - Saturday - Sunday, June 23-24, 2018
Details coming soon!
Answers from the Experts...Live!
For many individuals it can be difficult to find answers to the questions they have about cutaneous lymphoma and its treatment. This FREE question and answer event with local expert clinicians provides patients, caregivers and others affected by the disease to ask their questions in a relaxed atmosphere. The events are held on a weeknight evening and are typically two hours in length with dinner included.
Upcoming events coming soon!
Patient Networking Groups Meetings
The Cutaneous Lymphoma Foundation created networking groups to provide patients and caregivers a place within their local community to meet, share and have opportunities to learn. The Foundation's networking groups are open exclusively to patients and their loved ones in order to provide privacy and encourage open communication.
CLF-DC Patient Networking Group
Fairfax, VA - Saturday, December 2, 2017
Annual Holiday Social
CLF-SLC Patient Networking Group
Salt Lake City, UT - Thursday, December 7, 2017
CLF-NYC Patient Networking Group
New York, NY - Tuesday, December 12, 2017
CLF-LV Patient Networking Group
Las Vegas, NV - Wednesday, December 13, 2017
CLF-OR Patient Networking Group
Portland, OR - Tuesday, January 9, 2018
Collaborative Partner Events
The Cutaneous Lymphoma Foundation provides a list of events held by our collaborative partners that may be of special interest to the cutaneous lymphoma community.
Lymphoma Research Foundation
Seattle, Washington, Saturday, November 11, 2017
Education Workshop: Mind Body Techniques to Cope with the Stresses of Cancer
November 15, 2017 - 1:30 - 2:30 pm (EST)
Available live over the phone or online as a webcast.