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]_ 
(mailto:[email protected]) >
To: "[email protected]_ (mailto:[email protected]) " <[email protected]_ 
(mailto:[email protected]) >; tmic <[email protected]_ 
(mailto:[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.
     (http://on.fb.me/hnofb) 
P Please consider the environment before  printing
 
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From: [email protected]_ (mailto:[email protected])  
[_mailto:[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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