I disagree with all of you who are saying that you have either stopped going to a neurologist or see one very infrequently. I saw Dr Kerr at John Hopkins for the first 10 years after coming down with TM. I go to my neurologist at least once per year to insure that my meds are the best they can be. New Medications and procedures happen all of the time....by seeing a neuro I assure myself that I am getting the best treatment possible. Just last week I changed to a new neurologist, Douglas Holland in West Long Branch NJ. Not only did he prescribe medical marijuana for me he also set up a test to inject baclofin directly into my spine and see over a period of 4 hours if it makes a noticeable improvement. If it does we may consider the baclofin pump....if it does not we will explore other options to help me better cope with my pain and discomfort.
    I head up the New Jersey TM support group. The main benefit of a support group is comparing doctors and medicines that others are seeing or taking and perhaps get some new ideas regarding treatment. At our last 2 meetings we had as a guest speaker the head of physical therapy who gave us many ideas of simple things we could do in our own homes to exercise as well as hospital treatments that could prove beneficial.
    I have had TM for over 15 years....and I have fought this condition every single day. I cannot walk very well....but I have learned that I can swim pretty good. I now swim one mile a day......and even if this is doing nothing for my TM it is at least giving me a great cardio workout. Finally I purchased a Golden Retriever......this 60lb dog forces me to walk at lease 1 hour every day.
    Start living or start dying!

All the best!
Rob in NJ



-----Original Message-----
From: rn11974 <[email protected]>
To: Tracey L. Black <[email protected]>
Cc: tmic <[email protected]>
Sent: Thu, Jan 17, 2013 10:55 am
Subject: Re: [TMIC] neurologist

My neurologist saw me less than 24 hrs after my tm attack; he quickly diagnosed me, gave me IV steroids for 7 days, saw me every day in rehab. I saw him every 3 months for over a year. Then I spoke with PCP about baclofen, and never went back.
He was charging $300 per office visit to my insurance, plus my $15 co-pay.



From: Tracey L. Black <[email protected]>
To: "[email protected]" <[email protected]>; tmic <[email protected]>
Sent: Thursday, January 17, 2013 10:20 AM
Subject: RE: [TMIC] neurologist

I agree Cheryl. My daughter, Ashlee, hasn’t been to a neuro since she was at KKI in Baltimore in 2006 and even then, they didn’t do any testing or anything on her. He never really even checked in on her while she was there for the 8 week program. Her PCP orders her Oxybutnin and if she gets a sinus infection or something along those lines, she goes to the PCP or Ready Care.
 
 
Tracey L. Black
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Hockley & O'Donnell Insurance Agency
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From: [email protected] [mailto:[email protected]]
Sent: Thursday, January 17, 2013 10:07 AM
To: tmic
Subject: [TMIC] neurologist
 
I haven't seen a neurologist in over 15 years. What's the point? My PCP orders my baclofen.
  Cheryl


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