Guest guest Posted February 10, 2003 Report Share Posted February 10, 2003 It was recently diagnosed that my PA flare was not just seasonal but a progression of the disease. My RD said he would like me on Enbrel but first I had to fail on two other drugs for insurance to pay for Enbrel. He put me back on Mobic and started Azulfidine and said it would be atleast 2 mo for the Azulfidine to work. Then if that failed he would try MTX. So I am looking at several months of pain and also hoping these drugs fail so I can take Enbrel. It's crazy! The insurance company is determining my treatment, not my doctor. My RD " should " be able to prescribe a treatment for his 5 year patient. I trust my doctor and have always received great care and attention from him. However, some computer, fed my numbers will decide on my treatment program. I know there's little I can do but ride out the next couple of months. I just wanted to explain my frustration about paying such high premiums and having such little control over my treatment. Thanks for letting me vent. Savannah Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2003 Report Share Posted February 11, 2003 Hi, I fought that war this summer and won. My rheumy sent a letter to the insurance company and I hand delivered a copy of it to the HR Rep. at work along with harassing him everyday until I got what I needed. They had changes in the policy stating they would not cover any injectables not even insulin. Myself and one other employee of this large company are taking Enbrel and were on it when they made the changes. This stopped our Enbrel temporarily. Rheumy wrote in my letter that I had tried and failed all the drugs (naming every drug on their approved formulary list -- even ones I had not ever tried) and that Enbrel had been sucessful for me. I took the letter along with an article about Enbrel being the first and only drug approved by the FDA for PA to them and copies were sent to everyone concerned. I also wrote a letter stating how Enbrel had helped me and that without it I would end up crippled by this disease, that it was slowing the progression when all else had failed. I have Enbrel again since they changed the policy again because of this. That war began August 1st. I have just last week received the insurance booklet telling us what that new plan will cover. I was told we would get new books soon in about 3 weeks--it took 6 months. In the new book it states they will cover injectables but NOT BIOLOGICALS. I'm probably going to have to fight the war again this summer at the end of their fiscal year, as I was approved for a year. You can go to the Enbrel site for a copy of the article I gave them. It was very helpful in getting the help I needed. Also, an Enbrel rep will talk with your insurance company to help you get and or keep the drug. Cassie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2003 Report Share Posted February 11, 2003 Dear Savannah - I too had to go through the rigamarole of 3 NSAIDS failing to get Celebrex and then Enbrel was given to me with no trouble at all. The Dr actually had to change his diagnosis to osteo before the insurance would give it to me. So it sounds like many of the insurance companies insist on trying the less expensive drugs first. J [ ] Drug progression It was recently diagnosed that my PA flare was not just seasonal but a progression of the disease. My RD said he would like me on Enbrel but first I had to fail on two other drugs for insurance to pay for Enbrel. He put me back on Mobic and started Azulfidine and said it would be atleast 2 mo for the Azulfidine to work. Then if that failed he would try MTX. So I am looking at several months of pain and also hoping these drugs fail so I can take Enbrel. It's crazy! The insurance company is determining my treatment, not my doctor. My RD " should " be able to prescribe a treatment for his 5 year patient. I trust my doctor and have always received great care and attention from him. However, some computer, fed my numbers will decide on my treatment program. I know there's little I can do but ride out the next couple of months. I just wanted to explain my frustration about paying such high premiums and having such little control over my treatment. Thanks for letting me vent. Savannah Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.