Hi Sue,

So sorry you had to "join" us! But glad that you found us; there is a
wealth of information that comes from the collaboration of many.

There are also Facebook groups that you may be interested in, also.

I have had CML for 3 years 9 months and what I can tell you is that it does
get easier with time, and that it also can be a roller coaster!

I have chronicled my journey in a blog. This is a post of questions that
you may wish to ask your oncologist.

Hope this helps!
Important Questions for the Newly Diagnosed
<http://www.leukemiasurvivor.co/2011/08/important-questions-for-newly-diagnosed.html>

Best wishes,
Michele

On Wed, Nov 12, 2014 at 8:23 AM, smgedit <[email protected]> wrote:

> I was diagnosed with CML a little over a month ago and had a bone marrow
> biopsy and started taking Gleevec last week.  I'm trying to learn as much
> as I can about CML and my oncologist is great about giving detailed
> explanations and answering questions. But I was wondering if anyone else
> ever got what I consider a strange reaction from others about my news. In
> the past week, I've had people say the following things to me which upset
> me a lot.
>
> "So what's the big deal? So you have to take a pill...I have to take this
> antibiotic for my tooth infection this week too."
>
> "There is so a cure for leukemia. Plenty of people are cancer free. You
> don't know what you are talking about."
> (This after explaining about the drugs and "response," vs. "remission."
> etc.)
>
> "Well I hope you have a speedy recovery. Good luck."
>
> I know I can't put my energy into dealing with this right now but it is
> weighing on my mind anyway. It made me happy to find this group online
> where I know people can at least "get" it and where some of you have been
> living with CML for quite a while.
>
> Anyway, that's my first post. Nice to meet you.
>
> Sue
>
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