Crossroads in brisirtivikishn insurance ...
After pumping two five years ago as part of phase III clinical trial in lupus, Lupus in continuing my remission. Instead of having to pump more every four to six months as expected, the first pair of enough to last for years. Improve my and my forgiveness was exceeded in clinical trials. Now my Lupus act again, we need to find new funding source ritoxan.
The first leg? Insurance companies. Pulmonary approval followed my insurance company ritoxan pump of my lupus, without success. For several weeks, health insurance companies will issue of inform my lung "was" only written rejection message.
Then, after many phone calls and conversations with the Director of medical insurance company, the company finally sent a message saying "no", but denied that the message is either a formal refusal nor approval. After further consideration of additional based on medical necessity, the insurance company "deny" message again this week.
My insurance company stated strongly that they do not cover payments ritoxan lupus, because they are considered experimental or survey of lupus, and that sufficient evidence to substantiate these criteria:
Show how scientific ritoxan ritoxan lobosbrovi ritoxan lobosbrovi effects to improve public health over standard Lupus midikationsobort ritoxan effectiveness outside survey settings
Furthermore, my insurance company to cover drug policy, based on the survey "medical coverage guidelines" for the company.
Here's bondogli catches and bureaucracy. Says the insurer does not appeal to the initial payments unless I get. Then after we submit a claim, they will reject the formally coverage. After they deny coverage, you can then appeal to their decision, but not to pronounce a message was rejected. Refusal to issue a denial of procedural block pre-treatment claim on our ability to appeal.
"Human beings are not ultimately responsible."
And frustrated by bureaucratic barriers, we continue to pray for approving medications that will get my Lupus under control. Blakinil webrdnizolon no longer dominates the seriousness of my lupus, it continues to escalate. We hesitate to return to transplant and cancer therapies, having begun my Lupus attack the central nervous system and liver.
We are still believes that an appropriate treatment will be available, even if that means going down a path differently from ritoxan. Perhaps that appeal ultimately taking longer than FDA approval pending from binlista. This new biological drugs are about to FDA approval of lupus, possibly as soon as possible in March 2011. Binlista may be available to help me and other Lupus patients who have exhausted most of those other therapeutic options soon.
Somehow, the words Lupus foremost experts seem appropriate for my situation:
"Remember that human beings are not ultimately in charge. As we have to fight with our daily lives, always ask the Supreme authority for help, too. Medicine won't do everything. But one day there will be a cure for lupus. "
Centre for Michelle Petri, Ph.d., M.P.H., Johns Hopkins arthritis. See, http://www.hopkins-arthritis.org/arthritis-info/lupus/#treatment.
Tags: biological, clinical trials, faith, illuminated, pump, lupus, medicine, prayer, pulmonary symptoms, steroid, ritoxan,
This entry was published on Monday 21 February 2011 at 8: 00 am and is filed under health, opportunities, and research. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your site.
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