CLL Forum

Site participants, as you know, we have launched this new site due to the closure of the hosting platform of the current CLL Forum site. We have incurred some costs, and want to open up the opportunity for new site participants to donate money to the upkeep of the new site. Here are the costs that we have incurred to date, so that we can provide transparency:

Hosting at new site (for three years): $271 - this is at an introductory rate, and is expected to more than double after the first three years.
PayPal Transaction fees: Varies

If you would like to donate, please use the PayPal Donate button at the bottom of this page. If you would prefer to mail in a check, please send a private message to either drmoss_ca or JCreager.

Thanks
Jennifer and Chris

Did it Jen. Hope others join in too. Thank you to you and Chris for all this work!

Happy New Year!

Thanks so much!

Done! One problem, I think, is that the Donate icon is a bit hard to find.

Thank you! And thanks for the feedback, I'll play with the HTML a little more.

Well this explains why I had so much trouble finding site and logging in. I registered with new username and email and will definitely donate.

I was part of the BR treatment group back in 2015-2016. After 7 years without treatment, it is time for treatment. Looking at Acalabrutinib, Venetoclax and Obinituzimab, and a clinical trial.

Hi Ken, BR buddy! Welcome to the new forum! Good news is that there are lots of great treatments available, I should know, as I have had them all Good luck and definitely message me with any questions you might have.

Just donated as well. I'm thrilled to see this site up and running and, browsing through those registered, so happy to see old CLL friends. Many thanks to Chris and Jenn for all their work setting this up. Me ke aloha Lynn Samuels

Thank you, Lynn!

C.