Guest guest Posted September 30, 2010 Report Share Posted September 30, 2010 Good Point because I knew my insurance company would not pay for clinical trials, therefore, even though it was being done through a hospital I never went to the hospital for treatments. I was seeing the doctor who was in charge at his office. My doctors office was put through as a consultation and then my blood work and BMB which was all done in the doctors office was submitted to the insurance company. The only thing was that the doctor was not allowed to give me my STI-571, and I had to go over to the hospital after my visits to pick up my months supply of my drug. This went on for 6 months, until STI-571 was approved by the FDA. Then I went back to my regular Oncologist and went from there. I am going back to 2000. I have no idea how these things work now. From: Lottie Duthu <lotajam@...> Subject: [ ] How do they know? " CML " < > Date: Wednesday, September 29, 2010, 2:54 PM  I am replying to Theresa Migut's question about insurance not paying for trial. I would like to know how an insurance knows when you are in a trial. I was already on Medicare when I was diagnosed 15 years ago, but no one has ever asked if I was in a trial or refused to treat me because I was in one. What they don't know won't hurt them. Bobby Doyle and I are running neck and neck on the number of trials we are and have been in. She is already in Phase 1 of the Ariad trial and I am waiting to get in Phase II and we talked about never being compensated for offering up our bodies to science in the hopes that drug will be an alternative to the other ones that didn't work for us, but we are fully covered by insurance. I have a co-pay at the beginning of the year for Medicare, but other than that, it doesn't cost me out of pocket. I am out a small fortune for traveling to MDACC for all these visits and I am almost afraid to figure out how much. I am out of pocket for all the insurance I pay, however. Maybe you should contact the Insurance Commissioner of your state and get his opinion. I remember when I read in the paper that my secondary carrier would no longer write policies in LA, I sent an email about midnight to the Commissioner's office. At 7:00 a.m. the next day he was calling me to tell me not to worry, they could not refuse to insure me, so I was covered. That was a relief to hear, so call someone, call anybody and you may get the information you are looking for. I'm the lady who always says " Don't give up " and I'm saying it one more time. Have you contacted the LLS or American Cancer Society. ACS has given me more information and assitance than LLS, believe it or not. Your senator or congressman? Keep us informed. Carpe Diem, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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