Meeting others who are affected by cutaneous lymphoma in person can be an important part of building a support network. In 2013 the Cutaneous Lymphoma Foundation introduced patient networking groups to provide patients and caregivers a place within their local community to meet, share and have opportunities to learn. The groups are facilitated by a local volunteer leader. The Foundation's networking groups are open exclusively to patients and their loved ones in order to provide privacy and encourage open communication.
Patient Networking Groups are located in the following cities:
CLF-DC - Fairfax, Virginia (Washington, DC area)
CLF-LV - Las Vegas, Nevada
CLF-NYC - New York, New York
CLF-OR - Tualatin, Oregon (Portland area)
CLF-SLC - Salt Lake City, Utah
Visit the group's page for meeting location, dates and times.
If you are interested in forming a patient networking group in your community, please contact Tina Collins, Community Development Manager at 248.644.9014, ext. 5 or firstname.lastname@example.org.