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.

Please Note: All event times are U.S. Eastern Time Zone (ET) unless otherwise noted.

Virtual Events

Come join us in a virtual setting as we share formal presentations from our medical professional community. Our webinars will most closely resemble our live programs as they will be clinically-based, educational information. Each webinar will include a formal presentation as well as an opportunity for the audience to ask questions following each topic. Events will require online registration. Spots are limited.

Research Roadmap
Wednesday, March 3, 2021

Research Update
Thursday, March 25, 2021

Treatment Options - Late Stage
Friday, April 16, 2021

Answers from the Experts: An Open Q&A
Wednesday, April 21, 2021

Biopsy Results
Thursday, May 13, 2021

For illustrative purposes only.
Panel Discussions

Join us in an informal virtual setting where we take a deeper, more exploratory look into a webinar topic. Our panels of experts will share their own perspectives on high level topics and engage our audience through question and answer opportunities. Events will require online registration; spots may be limited. 

Watch this space for upcoming panel discussions!

Facebook Live

Facebook Live events are live-streamed interviews hosted on the Cutaneous Lymphoma Foundation's Facebook page. Guest interviewees include cutaneous lymphoma clinicians and researchers, insurance experts, as well as patients and care partners -- and you'll have the opportunity to ask questions of our guests live!  We hope you will join us for these social media events. 

Facebook Live, TBA, 2021

Or join us on our YouTube channel: CutaneousLymphomaFndn

Networking Groups - Online Meetings

Meeting others who are affected by cutaneous lymphoma can be an important part of building a support network. The Online Networking Groups are be open to all patients, and family and friends of patients regardless of location. Registration is required and space is limited. 

Upcoming Meetings

  • February 2, 2021 - 7:00 - 9:00 pm ET
  • March 2, 2021 - 7:00 - 9:00 pm ET
  • April 6, 2021 - 7:00 - 9:00 pm ET
  • May 4, 2021 - 7:00 - 9:00 pm ET
  • June 1, 2021 - 7:00 - 9:00 pm ET

Please Note: All event times are U.S. Eastern Time Zone (ET) unless otherwise noted.

To register for an upcoming meeting: Register Online

Partner Events
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

Lymphoma Workshops are regional, one-day educational programs that provide information about lymphoma, diagnosis, current treatment options, and patient support issues.

Upcoming events coming soon

Triage Cancer 

Triage Cancer offers a series of FREE educational conferences for individuals diagnosed with cancer, caregivers, advocates, and oncology healthcare professionals. Learn valuable information about navigating practical cancer survivorship issues, from beyond diagnosis, into post-treatment survivorship.

Upcoming events coming soon

Patient Educational Forums

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 the event via the internet.

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. These FREE question and answer events with local expert clinicians provide patients, caregivers and others affected by the disease to ask their questions in a relaxed atmosphere. The events are generally held in the evening and are typically two hours in length with dinner included.

No new events at this time