newly diagnosed

[Guest guest]

I just found out I have CML with 138,000 white blood cells, haven't

seen an oncologist yet.

I'm wondering what's the most effective treatment? Can it be passed on

to my children/grandchildren? How does your life change with

treatment?

The only symptoms I had was vision programs and fatigue. I also seem

to have a lot of foam-like mucus in my nose and throat every morning.

Anyone else with this?

Thanks for responding. I'm still in the dark, trying to learn from the

web but need more information from other CML folks.

Thanks much,

Margaret