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I ask my insurance company if a provider is in-network. They are the ultimate source of correct information. And I sometimes call twice to be sure.
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Will be Pleased
I am sure you will be pleased with Mayo in Jacksonville. We have been there a number of times and currently my wife is in their
study to follow a certain medical problem in which they established a 10 program to follow that particular medical concern. Once you have become one of their patients you will be able to tap into their "Patient Data Base". This data base will provide you with the results of your last tests on almost a real time basis. It will also provide you with your schedules, etc. It is a great tool for the patient. All in all it is worth the two and half to three hour drive from the Villages. In addition to the Mayo In which use to be a "Residents Inn by Marriott" to stay at there is a "Courtyard Hotel" which is quite comfortable and is on the Mayo property and very available. We usually stay there as it is in good condition, has a small dining facility, etc. Hope all goes well.:wave: |
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Unique Was
Mayo has a sort of unique way of handling billing. No we do not have to pay up front. We also have BC/BS. Mayo will send the
billing to your insurance company and have the check sent to you and then Mayo will bill you what the insurance company paid you and you put the check in the bank and send amount to Mayo. Strange but it works fine.:wave: |
I had a similar surgery performed at the UPMC facility in Pittsburgh prior to moving here. My neurosurgeon recommended an annual follow up down here. Can I ask the name of the surgeon or head of neurosurgery that your husband used at Mayo. I know there is no one locally that can review my case. I had complications as a result of the surgery and am currently having Physical Therapy done to try and reverse a paralasys issue.
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The doctor here, who discovered my problem, called a specialist at the Mayo Clinic (while I was actually in his office), spoke with him and explained my situation and then told me I would get a call from Mayo. They called me the very next day, explained their billing etc., asked me some questions and then said I would be receiving a package in the mail. It was a three page itinerary of medical appointments over a two day period. My initial consultation was with the primary consultant, from there I went through an extensive physical, and from the results of that I had appointments with various specialists. I did not meet the actual person who did the surgery until the day before surgery, he just had all my information from the team of consultants I had seen. I got the distinct impression they work as a team, not a single doctor. So I rather think the best thing to do is to have your local doctor contact Mayo to get you in quickly, or to find a Neurosurgeon from their list of doctors on their website and go from there. By the way, if I remember correctly, at my initial visit I had an appointment with one of their financial people who explained their way of doing business. |
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post may be too late but here goes anyway....just got back yesterday from Mayo-Jax after seeing pain management for severe back pain that is inoperable until I get a lung transplant. I met with a neurosurgeon, Ronald Reimer, MD. He has performed back surgeries on transplant patients and, God willing I am fortunate to get a transplant, I will definitely be his patient for back surgery. He is direct and to the point during his visits and there is no "grey" areas when you leave his office.
Regarding accommodations, the Inn at Mayo, is overpriced for the convenience in my opinion. Several hotels in the area give a Mayo discount, just ask! Hope this helps! |
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I had back surgery at Greater Orlando Neurosurgery & Spine. Dr. Max Medary is the BEST. He accepts medicare and your supplement. I wouldn't go anywhere else for back surgery. He operates out of Dr. Phillips Hospital.
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I went through all of the interviews with the Mayo and gave them my medical records. They called yesterday and said I am not a candidate for surgery. This is because of scar tissue. They said that by going in and doing surgery they would risk making my pain worse than it already is. I am very disappointed to say the least since I have been pursuing this for almost a year with 4 different neurosurgeons and numerous tests. Finally someone explained to me the reasons behind their decision instead of just walking in the room saying no and walking right out the door. Still thinking about the neurostimulator but just haven't heard enough good feedback on it to make a decision. The good has to outweigh the bad.
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