CLL Society is an inclusive, patient-centric, physician-curated nonprofit organization that addresses the unmet needs of the chronic lymphocytic leukemia and small lymphocytic lymphoma (CLL/SLL) community through patient education, advocacy, support, and research. CLL Society is a leading authority for CLL/SLL cancer patients and care partners providing education and support services to help them navigate a CLL diagnosis. We provide essential education on treatment and care management options for CLL through monthly webinars and patient-friendly articles that cover the latest medical developments and other important topics in CLL. Our network of over 40 support groups across the US and Canada offers a safe space for patients and care partners to find emotional support and learn from others navigating the same experience. Additionally, our Expert Access^TM Program provides patients with the opportunity to get a free second opinion about their CLL from a world-renowned CLL expert. At CLL Society, we aim to ensure that no one has to go through a diagnosis of CLL/SLL alone. We believe SMART PATIENTS GET SMART CARE™.

Sign up for CLL Society’s This Week Email

CLL Society Support Groups for Patients and Care Partners

Expert Access™ Program

Test Before Treat Campaign

Peer Support Program

Emotional & Spiritual Advocate Program

COVID-19 Updates Specific to CLL/SLL Patients and Care Partners

CAR-T Therapy Brochure

CLL Society Webpage

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