I have not been to my neuro in at least 4 years.    My family doctor and Pain 
Management doctors take care of me far better than my neuro.    Once I was out 
of the hospital for a year or
two we quit going to him because he just did not do anything except ask how I 
was doing and then that was it.     Pain Management doc’s do sooooo much more!
Janice


From: [email protected] 
Sent: Thursday, January 17, 2013 5:38 PM
To: [email protected] 
Cc: [email protected] 
Subject: Re: [TMIC] neurologist

Rick,

Sorry, I thought that message was from Rob.  I am going to try the trial before 
the permanent pump.  Living with a broken leg is what is causing the pain.  I 
asked the Dr. about electrical stimulation etc. and she said to tackle one 
thing first.  I'm supposed to give them a week to call and set up the trial and 
if I don't hear from them in a week, I'm supposed to call the Dr. back.  I 
think it's kinda' lame, but that's the way it's supposed to work.

I'm updating my address book on AOL and wonder if I can have your full name, 
address and phone number.  You never know, I might want to send you a card or 
call you some time.

I love you too,
Jude in Michigan

In a message dated 1/17/2013 4:36:25 P.M. Eastern Standard Time, [email protected] 
writes:



  Jude, I allowing with you despite many trials of  pain meds have realized 
that I'm not satisifed  with them, I personally suggest that you try the trial 
pump before you undergo the actualy procedure. I  wish that we had neuros down 
here willing to do trials. , Only you know how bad it hurts, you need  help so 
I would atleast give ot a try. I care for you and I hate to know how bad you 
feel. Please help yourself no matter what it takes. I  love you and I really  
care. Rick

    
  From: "[email protected]" <[email protected]>
  To: [email protected] 
  Cc: [email protected] 
  Sent: Thursday, January 17, 2013 11:49 AM
  Subject: Re: [TMIC] neurologist


  Hi Rob,

  I am waiting for a phone call from my neurologist, who is setting up a trial 
for the pain pump, but he didn't mention anything about doing a trial with a 
hypodermic.  Do you think that I ought to call him?

  Judy in Michigan

  In a message dated 1/17/2013 11:21:50 A.M. Eastern Standard Time, 
[email protected] writes:


    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
    Certified Insurance Service Representative
    Hockley & O'Donnell Insurance Agency
    PO Box 3039, 132 Buford Avenue
    Gettysburg, PA 17325
    Phone:     717-334-6741, x 29
    Fax:       717-334-3414
    Office hours:   8:00 a.m. - 5:00 p.m. 
    My hours:       9:00 a.m. - 5:00 p.m.
        
    P Please consider the environment before printing

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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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