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The trial I was in 8 yrs ago required frequent CT scans to

monitor the effectiveness of the drug on the size of my

internal nodes. Altogether, in the last 13 yrs I've had more

than 20 CTs; that also includes two cardiac ones with much

higher radiation levels. According to prevailing reliable

research, my chances of developing lung cancer are now 1 in

400. They're not great odds, but still greatly in my favor.

Meanwhile I've had 8 yrs of remission during which I've

hardly had to think of the word leukemia. No previous tx had

come close. Not to veer from our factual format, but that's

over 400 sunsets I've seen, countless wonderful moments with

family and friends and at least 3 life-changing adventures.

No treatment for CLL I know of comes without scary-sounding

risks but most of us don't go into trials unless we're

pretty sick and our alternatives are limited. I think you

should ask your doctor all the pro & con questions you need

to -- the " what would happen if... " ones and do some

research on your own re CT scans. It's important ask if the

trial actually requires them or is it the doctor's

preference? Can he reduce the number of them or use an

alternative means of imaging and still have the trial stats

be valid?

Once you have enough information, your husband should be

able to figure out what risks he can live. I don't regret

my decision but knowing what I know now about the cumulative

aspect of CT scans, I might not have been able to overcome

my fears. But with the knowledge that's out there now

doctors should be, and I mean damn well should be, much more

flexible about requiring CTs.

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