CLL Society Inc.
@CllSocietyThe CLL Society is a 501(c)(3) formed to help meet the unmet needs of those living with #CLL and #SLL. https://t.co/PMtovq27vV
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Is there a person on your CLL care team – a doctor, nurse, or family member – who has made an invaluable contribution to your physical or mental health? This #NationalFamilyCaregiversMonth show your appreciation with a gift in their honor to CLL Society. 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. bit.ly/3YKhYtH
Fatigue is one of the most common symptoms of CLL. Understand what it could indicate about disease progression. bit.ly/48MlCrA
This #VeteransDay, we honor and thank all those who serve our country. 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: bit.ly/44Ygi12
We are proud to take a wholistic approach to supporting and caring for the well-being of those living with CLL/SLL! Thank you @clonoSEQ for featuring our resources for patients and care partners!
There’s more to a diagnosis than medical treatment. Thank you @CLLSociety for offering comprehensive support to those affected by CLL. Explore the "Living with CLL" hub for stories, advice & creative works from fellow CLL patients and caregivers: cllsociety.org/living-with-cl…
This study looked at the impact of vitamin D supplements for patients in the watch and wait period of CLL. bit.ly/3YT345z
CLL Society's Ask Me Anything Facebook Live is next Friday at 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: 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. bit.ly/4f1pR51
November is #NationalFamilyCaregiversMonth! This month, we honor all the essential support care partners provide to their loved ones with CLL/SLL. To all the care partners out there, THANK YOU for all you do. Explore our care partner resources: bit.ly/4fkT1Me #caregiving
During the European Research Initiative on CLL (ERIC) Annual Meeting, @briankoffman presented on the needs of individuals with CLL. bit.ly/3Yv0WzC
Happy Halloween! CLL Society wishes everyone a happy, fun and safe holiday celebration.
Learn about this combination therapy with the BCL-2 inhibitor sonrotoclax that is in development as a treatment option for CLL/SLL. bit.ly/3Ut3Rrv
Longtime friends and CLL patients Andrew Schorr and Dr. Brian Koffman reflect on their shared experiences navigating CLL and the importance of considering clinical trials. bit.ly/4hrb4lG
Learn about the bispecific antibody epcoritamab as a treatment option for patients with Richter’s transformation. bit.ly/3NIODL1
Why do treatments for chronic lymphocytic #leukemia (#CLL) sometimes stop working? Learn more about #BTK inhibitor resistance mutations in this activity with Dr. Jennifer Woyach. Test your knowledge to see what you learned & print an informational handout. bit.ly/3AhITF1
Are you aware of all CLL Society has to offer patients with #CLL? Watch our video, Your CLL Journey Starts Here, on YouTube to learn more about the wide range of programs and services we provide: youtu.be/mg_3gmwig_E
Come get your CLL questions answered at our "Ask Me Anything" Facebook live event on 11/15 at 12pm ET! CLL expert @ASkarbnik will join to answer questions along with CLL patient advocate @MicheleNadeemB Learn more: bit.ly/3zWeU5y
This retroactive study aimed to understand why survival rates differ between Black and White patients with CLL/SLL. bit.ly/3UjpREY
If you missed the recent webinar with Dr. Michael Choi and patient advocate Larry Marion about managing side effects from CLL treatment, you can catch the replay, presentation slides, and transcript here! bit.ly/3XPM12V
For those living with #CLL, considering health factors beyond their diagnosis is essential. One factor researchers are looking to understand better is the impact of CLL/SLL on bone health and the risk of fractures. bit.ly/4eLBsoP
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Who to follow
-
CLL Advocates Network
@CLLAdvocates -
Lymphoma Hub
@lymphomahub -
Matthew Davids, MD, MMSc
@DrMDavids -
CLLSA
@CLLSupport -
John P. Leonard, MD
@JohnPLeonardMD -
Toby Eyre
@tobyeyre82 -
Nitin Jain
@NitinJainMD -
Chaitra Ujjani, MD
@UjjaniC -
UK Chronic Lymphocytic Leukaemia (CLL) Forum
@UkCll -
CLL CANADA
@CLL_CANADA -
Jonathan Friedberg
@DrJFriedberg -
Joanna M. Rhodes, MD, MSCE
@drjoannarhodes1 -
Women In Lymphoma - [email protected]
@WomenInLymphoma -
Jeff Sharman
@jeff_sharman -
Kate Cwynarski
@CwynKate
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