> Anyway, What can I expect taking Gleevec? Can I do normal 
activities? Yes, I have asked the doctor, But he's never had CML . 
Yes, He's a professional, but I think you know what I'm saying . Any 
advice would be appreciated....
>  
> Blessings !
>  
> Kelly Ann in Tennessee ...


Kelly Ann,

Your story touched my heart and I wanted to welcome you to the club 
that nobody wants to join! First of all, know that your feelings are 
completely normal. Secondly I would like to tell you about a website 
where you can learn a lot of good information about CML and gleevec. 
It is run by another CML patient named Jennifer that is also a 
member of this group. The address is www.cmlsupport.com 
It is a great site for new and old patients alike. 

As far as your insurance goes, they should have an appeals process 
that you can use to get them to pay more of the cost. Gleevec is now 
the standard front-line therapy to treat CML and is covered by most 
insurances. I pay a $75 a month copay and I know a lot of others pay 
a lot less depending on their insurance. 

Where are you being treated? Are you being seen by a CML expert? CML 
is a pretty specialized field and a lot of the regular hemo-oncs 
dont know much about treating it. I travel from Kansas to Houston 
twice a year to see a specialist at MD Anderson. And I know of a lot 
of others who travel to various centers around the country also. If 
you are not being seen by a specialist, that might be something that 
you should consider if you can afford it and if your insurance would 
cover it. 

Just remember, that your life is NOT over and that this disease is 
very treatable. Just think of this as starting a whole new chapter 
of your life that will include a lot more ups and downs than you are 
used to, but one that you can get through with the help of your 
family, friends, and this group!

Ask any questions that you can think of. Knowledge is power!!

Take care,

Trisha--age41
Parsons, KS
dx 9/99







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