CLL Society

Who has helped you the most? Is there a person on your CLL care team – a doctor, nurse, clergy or family member – who has made an invaluable contribution to your physical or mental health? This #NationalFamilyCaregiversMonth show your appreciation by honoring them with a donation in their name to CLL Society. Let them know what a difference they have made in your life, and at the same time, help us make a difference in the lives of all of us with CLL. https://bit.ly/4e7xvcV

Important changes are coming to Medicare Part D and Medicare Advantage plans in 2025. Learn about these updates so you can make the best choices for your healthcare needs. https://bit.ly/3YKhYtH

Fatigue is one of the most common symptoms of CLL. Understand what it could indicate about disease progression. https://bit.ly/48MlCrA

This #VeteransDay, we honor and thank all those who serve our country. Some U.S. military Veterans may have an increased risk of developing chronic lymphocytic #leukemia (#CLL). CLL Society has resources specific to supporting veterans with CLL, helping them navigate care within the VA system, and connecting them with fellow veterans. Learn more at: https://bit.ly/44Ygi12

For those living with chronic lymphocytic leukemia (CLL), seeing healthcare provider who specializes in treating CLL patients will improve their treatment outcomes. CLL Society's Expert Access program offers patients a free, second opinion, virtual consultation with a world-renowned CLL expert for a personalized care discussion. This free program is open to anyone with a CLL diagnosis. People who have participated before can re-apply for reasons such as new and worrying symptoms, new test results, or treatment decision discussions. Learn more at: https://bit.ly/3Lsj9qL

This study looked at the impact of vitamin D supplements for patients in the watch and wait period of CLL. https://bit.ly/3YT345z

CLL Society's Ask Me Anything Facebook Live is next Friday at 9am PT-12pm ET. Join us along with Dr. Alan Skarbnik and CLL patient advocate Michele Nadeem-Baker to get your CLL questions answered. This event is entirely dedicated to answering audience questions. Learn more and register at: https://bit.ly/3zWeU5y

This study aimed to understand which patients with chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) might be right for CAR-T therapy. https://bit.ly/4f1pR51

November is #NationalFamilyCaregiversMonth! This month, we honor care partners and the essential support they provide to those living with chronic lymphocytic #leukemia (#CLL) or small lymphocytic lymphoma (SLL). Whether it's offering emotional support, helping with household tasks, taking notes at doctor appointments, and so much more, their contributions make a significant difference. To all the care partners out there, THANK YOU for all you do. Tell us about an important #carepartner in you life in the comments below. CLL Society offers resources to support care partners: https://bit.ly/4fkT1Me #caregiving

During the European Research Initiative on CLL (ERIC) Annual Meeting, Brian Koffman presented on the needs of individuals with CLL. https://bit.ly/3Yv0WzC