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#1 | ||
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Magnate
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I would call and ask why you at least deserve a reason. The PA I have dealt with seemed clueless. I am not saying this is all of them. I just feel many of us are too complex and we need someone who had more experience and higher degree.
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#2 | |||
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Member
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Update: it's not quite as bad as it seemed at first, but still not great. The neuro called me later and explained that he's just never prescribed the lidocaine for PN before (the PA said "he just doesn't", which sounded to me like "because I said so") and wasn't sure what was the correct dosage. He told me he would consult with other neuros in the practice to see what they say (he's very young BTW) but also said that I might want to ask the Dr. who originally prescribed the patches for more.
Then we had some other frustrating go arounds including his multiple deflections of my point that most people with PN have more than one medication because they are more effective that way. He didn't disagree, but he didn't suggest a second med, either. Arggggh! He wore me down for now. |
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#3 | |||
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Member
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Oh, two other things:
I'm not in an HMO. And what about the claim that a neuro-muscular specialist is the same as a PN specialist--that's bull isn't it? |
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#4 | |||
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Wisest Elder Ever
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There is a form of motor neuropathy... and I would think a neuro-muscular specialist would be good for that type.
But for plain old sensory? A regular neuro. You know we had a neurologist visit here at Forum Feedback and ask for ideas about patient help at his new neuro website etc. He listed all the topics and PN was not on that list. Considering how common this is, I was totally miffed: http://neurotalk.psychcentral.com/thread97228.html I think this sort of reflects how neuros feel about PN patients in general.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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#5 | ||
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Magnate
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Can you see someone else for at least another opinion and approach? It concerns me that for something so simple he needs to ask a co worker. With my neuro and nerve meds he started me with one at a time. Then I went to a pain doc/anestesolgist and he was more knowledgable with treatment in terms of meds etc. Have you thought of seeing one?
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#6 | |||
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Senior Member
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The pain clinic at Hopkins is in the dept of anesthesiology and the docs staffed there are anesthesiologists. I always felt that was kinda odd, but it seems to be a general consensus at many places. Maybe having to do with the vast knowledge of meds and their effects & s/e that the anesthetists need to know. Also, specifically in the area of blocking pain for surgery too.
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Bob B |
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#7 | |||
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Member
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Quote:
I have been treated in the Neurology Clinic at at one of the major medical universities since 2005. Last year they stopped treating PN in the Neurology Clinic and formed the Neuromuscular Clinic for treatment of neuropathy. The Neuromuscular Clinic has just been named as a Center of Excellence, by one of the leading neuropathy associations. I have tried to avoid reference to any names, so hope the above all makes sense. But, to sum up - Yes, you want to be treated by a neuromuscular specialist. |
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#8 | |||
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Member
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Thanks all for your ideas and info. I do still have that appointment with the neuro-muscular specialist, plgerrard, and now that you've filled me in, I will give him a try. I just have such a hard time knowing what to believe and what not to because I've been told so many different (and often opposite)things by different doctors and other professionals. But in particular, I'm concerned about this very young PN whom I've taken to calling Doogie. He's told me things that I know for a fact are not true.
Bob and daniella, what you both are saying seems to make sense too. I could easily see how those specialties could address PN as well. So the neuro called me back again and said that he found a 3% OTC cream that he had my local pharmacy order for me. I'll definitely try it. In the meantime, I got the doc who originally prescribed the lido patches, so in the end, I've gotten what I wanted. It seemed like a ridiculous way to do it, though. |
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#9 | |||
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Member
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Here's what I don't understand: as long as I've been reading here, I've been seeing people say that what you want is a neurologist who specializes in PN. I'm confused as to why I want a neuromuscular specialist then. Are they the same thing? Is there such a thing as a PN specialist?
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#10 | |||
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Member
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I think the Neurologists who specialize in neuromuscular disorders are the new PN specialists. I've been going to the Neurology clinic at Vanderbilt since 2004, but the beginning of 2009, they switched me to the Neuromuscular Clinic. Cleveland Clinic once had an actual Neuropathy Clinic. It is gone now, replaced by their Neuromuscular Center. I think their description of the Neuromuscular Center is better than Vandy's, so am quoting here:
Neuromuscular CenterI think the key point is they join forces. It is a good scenario for patients, because there is more exchange of ideas and knowledge than in the typical Neurology practice. |
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