← Return to Anyone else have Clonal Cytopenia of Undetermined Significance (CCUS)?

Discussion
Comment receiving replies
@j68eis

I have a diagnosis of CCUS as well. I chose to let my Doctors do the worrying for me. why worry about something we have no control over. I just had my 4th Bone marrow biopsy.
Like you my counts have been up and down for 30 years. Sounds crazy , I know. Sure I find it inconvenient to wear masks in many crowded places but it is what it is. I sometimes take my mask off just to feel comfortable. My advice, would be to hang in there and know you are not alone.

Jump to this post


Replies to "I have a diagnosis of CCUS as well. I chose to let my Doctors do the..."

Thank you for your reply and inspiration. I'm sorry you've been dealing with this for so long but glad to hear you've done so well. You do have a great outlook. I am in the medical field and easily find myself going down the rabbit hole of reading too much. Do you mind sharing your mutations and VAF?