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#1 | ||
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Senior Member
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Hi, wow sorry you had a bad time but if you check they give all imformation
on all of the Mayo Clinics,on the page on the Mayo hospitals. It did say something about,the insurance,and just curious why you didn't realize that there is a big differences in those hospitals,and that Dr. could of been fired. I was at the one in MN. and there's a big difference I'm sure,but I still check on the insurance before I make a appointment. I checked everything at the Cancer Hospital Barnes Jewish and the Drs. I would be seeing..If you don't have the time a family member could e-mail or call. I'm sorry you had such a bad time. Sue |
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#2 | ||
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Junior Member
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Hi,
I knew the Mayo in Scottsdale did not take Blue Cross of Arizona when the appointment was made. The trouble with out of network is as follows. If a bill is 5000, the carrier will only pay 60% or so of what they consider the usual charge of what the service should cost. So if their vision is 3000, they will pay 1800 of the bill. The poor patient needs to pay 5000-1800 for the balance of the bill. The doc told me that the Mayo in MN and Fla do take Blue Cross. I am sure that anyone could get a bad meal at a five star restaurant. I am sure most would have a good experience at the Mayo. My experience left me disappointed. Glenn |
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#3 | |||
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In Memorium
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Appreciate feedback on Mayo in AZ - my docs have told me to go to Mayo - but my only option because of costs, travel, etc - would be AZ - (I'm in Calif)... and they arent contracted with Medicare either (I'm on SSDI) - and they told me they would bill them but they may or may not pay the charge and I'd be completely responsible.... I have heard many good things about their amyloid program (my docs have gone back and forth on this with me - had a positive biopsy in the past they couldnt repeat so was considering it)... but never heard about their neuro department....
Also, if you received such poor care as a physician - and dont you think physicians tend to sometimes have more respect for each other when treating - that a "civilian" may even have worse luck????? Just curious, 'cause my docs are still talking about me going and I'd hate to get out there and have a similar experience???? ![]() |
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#4 | ||
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Junior Member
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Have you checked out UCLA? They are listed as one of the top ten neuro centers by US News and World Report. UCLA would likely have a contract with medicare.
I have seen four neurologists over the years. Half were quite strange. I have had good luck with the Barrow Neurological Institute in Phoenix AZ. Good luck, Glenn |
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#5 | ||
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Junior Member
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I tried scheduling an apt at Scottsdale Mayo in July and they finally called me in February to see a neuro there. I had become so tired of waiting that I began with another Scottsdale neurologist and have decided to give her a fair try before I go to Mayo, so I cancelled and postponed until summer. Their insurance is really bizarre as I'm on medicare with AARP supplement and still may have to pay some overages on allotted charges. Tom
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#6 | ||
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Senior Member
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Glenn ,
Do you have PN,and yes most neuro's are a bit odd,we have all mentioned that in one way or other. You live in a great area,have a friend who was a GP there. If you liked Barrow why didn't you stay there? I just wish you could tell us a little more about your problems and some of test you given..I'm glad you brought this up.Being a Physician doesn't always mean you will get better care.After being a nurse for 25 years,I've seen it go both ways. I not sure but didn't you have more of a pain problem in you spine? Nobody here would want to see anybody in pain. I wish you luck. Sue |
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#7 | ||
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Junior Member
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Sue,
I have had symptoms for over 20 years. They have been mostly mutifocal burning dysesthesias with some paresthesias and other neuropathic goodies thrown in. My neuro exams have been normal. I think the stress of having two foot operations in one month(10/07) really flared things up again, in terms of bad burning pains. The symptoms have waxed and waned. My Barrow doc feels it is a variant of small fiber neuropathy.....though I do not have any deficits. As many in the groups with this know the skin biopsy is a new quick diagnostic tool for this. There are also the expensive autonomic and sensory tests. Currently the Barrow does not offer these. In terms of the skin test my neurologist feels it has to be done by a good lab. He recommends only the labs at Mayo and Barnes in St Louis......thus the Mayo appt for another opinion. Unfortunately Mayo in Scottsdale does not offer the skin biopsy...only the other expensive tests. I have had the million dollar blood workup in terms of all the diseases with small involvement such as diabetes. I feel better now and did not want the out of pocket costs with the Mayo tests. They would probably tell me... idiopathic small fiber disease.....no cure anyway. Barrow has a new peripheral nerve attending who trained at Mayo Mn. Maybe he we set up the biopsy and other tests. Sorry for the long post. Glenn |
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#8 | |||
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In Memorium
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Glenn, I actually started my neuro experiences with them when I first got sick - they did great NCS/EMG's they even repeated the test twice in the same day on different machines cause they were doubting the results) and my sural nerve was sent to them for biopsy from another center and it was very thorough too, but often an appt would streach out for 6 hours waiting for resident to consult with attending - then they would eventually come back... their conclusion at the time (now they are quite a trek from me to get down there) - was "we've never seen someone's sensory nerves completely die in six months - and we will consult with other centers, etc... and get back to you"... never heard another word... if you have a name of someone that maybe I could get a private appt with that would be wonderful though - I know they have a PN support group that meets down there so they definately have an interest in it! (they definately do have contract with Medicare - Mayo was one of the few that didnt!
(in regards to UCLA I should add - I have gotten excellent cardiac care there, in addition to excellent MOHS surgery, and they have some of the best natured nurses and assistants I've ever come across) (I was hoping first Mayo cause then they could look at all at once - gatroparesis - cardiac - back pain - abd stuff, etc. instead of constant trips to different docs etc... I wish they would just toss me in the hospital even here and do all the tests at once - dont know why they just cant do that for people who have multiple issues and cant get around easily, etc... but I have a feeling has to do with insurance also!) Thanks Quote:
Last edited by BEGLET; 04-12-2008 at 04:34 PM. |
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