Wow! more than 300 Cllers, a record, have signed up to watch the Patient Power/MD Anderson/CLL Global Foundation Town Meeting on Sunday 10/25. I am the in-person host and my care partner, Esther, is the online host. Hope you can join us, if you haven't signed up already. We'll have world famous experts to answer your questions and a crowd to help you know you are not alone. See you there in Houston or online! patientpower.info/event/cll...
Record Registration for CLL Online Eve... - CLL America Support
Record Registration for CLL Online Event from Houston
Written by
andrewschorr
To view profiles and participate in discussions please or .
Not what you're looking for?
You may also like...
Treatmant for cll
Hello!My name is Lidia.My husband has cll from 2012 and now his wbc is 140000 and the platelets are...
CLL diagnosis and diet
was Diagnosed with CLL a day after my 60th birthday party. I hadn't been feeling well for months. I...
Choice of doctors
Ok so I've got a real dilemma. I'm on W&W. I have two top CLL specialists in two sister hospitals....
I’m unclear what to think of my diagnosis
I’m new here and not clear about the diagnosis given on my Flow Cytometry, which classified me with...
I'm new to the site
I am 50, mother of 2 sons. Diagnosed CLL almost 3 years ago. I'm in the watch and wait category,...
Encouraging Tests on Green Tea Extract
Hubby about to begin Obinutuzumab infusions....feeling anxious
New here. After 10 years of CLL, Ibrutinib treatment needed for decreasing hemoglobin and platelets. 
Good News from the Doctor Venetoclax is working!
My Cll progression
