**UPDATE!** Although I don't have a solution to my problem of my insurance company not wanting to pay for the replacement of my malfunctioning Vagus Nerve Stimulator yet, I do have some progress. My p-doc is currently compiling a letter to include with my own to my elected officials and to the Insurance Commissioner which includes a timeline of the clinical trials, FDA approval and other vital data about the VNS, along with the facts surrounding the entire situation. There's no guarantee of success, but this is progress.
If anyone has input or advice as to what my letter should (or should not!) say, by all means, PLEASE drop me a line! I'm open to all suggestions, thoughts, and comments. And if you're an elected official yourself, I'd like to hear from you as well. Wish me luck!
Tags: Vagus Nerve Stimulator VNS Insurance TRD Treatment Resistant Denial Remissi