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Cutaneous Lymphoma Foundation


The Cutaneous Lymphoma Foundation is an independent, non-profit patient advocacy organization dedicated to supporting every person with cutaneous lymphoma by promoting awareness and education, advancing patient care, and facilitating research. We exist to make sure that each person with cutaneous lymphoma gets the best care possible.

 

Patient Educational Forums

These live educational events held throughout the United States and Canada provide exceptional opportunities for people affected by cutaneous lymphoma to receive accurate information about the disease, learn about treatment options, clinical trials, have access to experts in the field and connect with others who are experiencing similar symptoms and quality of life issues. Learn more


2-Day Annual Patient Conference

The 2-Day conference is an expansion of our one-day patient educational events and provides a more in-depth program for patients, caregivers and medical professionals. The conference includes a full day of clinical presentations geared towards patients and caregivers, including updates on clinical trial opportunities and research in cutaneous lymphoma and a second day devoted to discussions of quality of life, including nutrition, exercise, living with the disease as a young adult or as a child, navigating insurance, as well as sessions of inspiration and hope for patients and their families.  The event also includes a Saturday evening networking reception and silent auction.  Learn more


Online Learning Center

The Cutaneous Lymphoma Foundation Online Learning Center provides patients, medical professionals and care givers with more targeted and personalized access to cutaneous lymphoma resources.  This new resource allows our constituents access to all of the Foundation resources, including videos presentations, from the comfort of their home or office.  Visit the Online Learning Center


Research Awards Program (RAP)

Young Investigators Award
Each year, the Cutaneous Lymphoma Foundation awards two travel grants under our Young Investigator Awards.  These awards are presented to new physicians and scientists in the field of cutaneous lymphoma research and assist them in attending either the American Society of Hematology Annual Meeting or the Society for Investigative Dermatology Annual Meeting, where they will present their cutaneous lymphoma specific research. Learn more

CLARIONS Research Award
The signature funding initiative of the RAP, is the CLARIONS Grant Program -  Curing Cutaneous Lymphoma by Advancing Research, Innovation and Offering New Solutions.  The CLARIONS Grant Program supports investigators interested in conducting innovative cutaneous lymphoma specific research.   Two grants are awarded annually to help uncover causes and improve the treatment and quality of life for patients. Discovering new avenues for better therapies and, one day, a cure for cutaneous lymphoma are key goals of CLARIONS program. Learn more


Newsletter Publications

The Cutaneous Lymphoma Foundation publishes a printed educational newsletter, the Forum, three times each year, as well as a monthly e-newsletter.  These publications provide relevant news, information and resources to patients, caregivers, physicians, researchers and the larger cutaneous lymphoma community.  Our publications are the only of their kind, dedicated to providing comprehensive news and information to people affected by cutaneous lymphoma.  Read the latest edition of the CLF newsletters

Brochures & Educational Materials

Each year the Foundation produces printed educational materials distributed to patients, caregivers, medical professionals and treatment centers. Thousands of pieces are distributed each year by mail and at all Foundation events, to provide our constituents with valuable information about specific diagnosis, treatment options, resources available by the Foundation and more.  Materials include the Patient’s Guide to Understanding Cutaneous Lymphoma, specific diagnosis Fast Facts and more.  Learn more
If you are interested in supporting the Cutaneous Lymphoma Foundation as a corporate partner, please contact Susan Thornton, CEO at Susan@clfoundation.org or 248.644.9014, ext. 3.
For general questions or more information about the Cutaneous Lymphoma Foundation, please feel free to contact us at:

Cutaneous Lymphoma Foundation
PO Box 374
Birmingham, MI  48012
(248) 644-9014
info@clfoundation.org
www.clfoundation.org

For questions specific to fundraising, please contact Susan Thornton, CEO at Susan@clfoundation.org or 248.644.9014, ext. 3.