Kelly - Have you ever looked into NeedyMeds.com? http://www.needymeds.org/
It's a nonprofit started by a doctor and they have aggregated information on
patient assistance programs that help with drug costs. Might be able to help
you with some of your costs related to the PAH. You could also contact the
Patient Advocate Foundation http://www.patientadvocate.org/ and The National
CML Society also assists CML patients with medical cost issues
http://www.nationalcmlsociety.org/contact-us
Sorry you are dealing with all this, hope you find some solutions, and soon!
Pat 

-----Original Message-----
From: [email protected] [mailto:[email protected]] On Behalf
Of kellyelise
Sent: Tuesday, April 10, 2012 10:05 AM
To: CMLHope
Subject: [CMLHope] Re: Tasigna Users

Thank you for your response, Susan. Quite frankly, it feels as though these
drugs are sucking the life right out of me. I hate them with a passion. Good
for you for managing so long without them. I am sorry you suffered such
awful side effects to the Gleevec. The insurance issue is a huge problem for
me, too. My PAH supplies are well over
$7,000 per month. My co-pay is $1,500 per month - which I don't have.
I suspect it will only be a matter of time before they cut me off. My co-pay
for the Tasigna is $3.30 per month - go figure. I have odd dreams where I go
off and live somewhere else with my closest friends and
children....paradise? lol

Marty - you are so funny!  Sometimes I think stepping in front of a speeding
bus would be a viable option...and then reality sets in and I know it is
not. Thanks for making me laugh!

18s,
Kelly

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