I thought I would share something interesting that happened today.
I had LLMD appt. yesterday. I was put back on Zithromax and Flagyl. Zithro was increased to 500 mg.
When I first did this combo my insurance only agreed to pay for 20 tablets a month. LLMD office really had to push for that and it went to the review board with insurance.
I went to pick up new script at pharmacy yesterday and was told insurance would only pay for 4 pills a month.
I called LLMD office this morning and told them they needed to call my ins. and it would have to go under review again. Pharmacy called me this evening to tell me it was all approved.
I called LLMD office back and this is what they told me they did to get approval.
Instead of giving the insurance co. a diagnosis for lyme and co-infections they took every one of my 30 symptoms and matched it up with a code. The receptionist told me the insurance company quickly agreed to approve a 30 day prescription that is good for the next year.
Can you imagine the look on the review boards faces when they are presented with 30 diagnosis codes?????
I am really proud of my LLMDs office for doing this for me. I know it must have taken them awhile to pull all that together.
Just thought I would share something good for a change. It might be an idea for others to use in the future.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/