I was lucky. The neuro on call in my HMO that Sunday had seen tm before,and I 
was diagnosed under 24 hrs from onset of symptoms. Started on 1 week of high 
dose IV steroids immediately. I believe that's why I can walk today.
     Cheryl in Easthampton,MA.

--- On Wed, 5/19/10, Patricia Cooley <[email protected]> wrote:


From: Patricia Cooley <[email protected]>
Subject: RE: [TMIC] RE: tmic-digest Digest V2010 #197
To: "'Janice Nichols'" <[email protected]>, "'Gerry Surette'" 
<[email protected]>, [email protected]
Date: Wednesday, May 19, 2010, 12:47 PM








I agree Gerry.  When I was in the E.R., the first doctor had no clue, but when 
the other one came on duty he ordered an MRI and knew immediately and I was put 
on steroids right away.  I am very thankful for the second doctor.
 
Patti - Wisconsin
 


From: Janice Nichols [mailto:[email protected]] 
Sent: Wednesday, May 19, 2010 11:03 AM
To: Gerry Surette; [email protected]
Subject: Re: [TMIC] RE: tmic-digest Digest V2010 #197
 

I don't understand how a doc can fool around for a year and not have a 
diagnosis.    All my docs had to do was delete by testing what I did not have, 
and do a spinal

tap and MRI to find what I did have.       How totally unfair to you.

Janice

 


 


From: Gerry Surette 

Sent: Wednesday, May 19, 2010 7:07 AM

To: [email protected] 

Subject: [TMIC] RE: tmic-digest Digest V2010 #197

 
hi Janet i know how you feel it took the dr.s close to a year to diagnoise tm 
I had to wait unti li was paralized to get any help
 

 



Date: Wed, 19 May 2010 04:47:54 -0700
From: [email protected]
Subject: tmic-digest Digest V2010 #197
To: [email protected]



--Forwarded Message Attachment--tmic-digest Digest                            
Volume 2010 : Issue 197

 

Today's Topics:

  Re: [TMIC] Neurontin                  [ "Janice Nichols" <jan...@centurytel ]


--Forwarded Message Attachment--
Date: Tue, 18 May 2010 22:36:24 -0500
From: [email protected]
To: [email protected]; [email protected]; [email protected]; 
[email protected]
Subject: Re: [TMIC] Neurontin

Janet,

I hope you get more help from the docs for your son and that he does get off 
the percocet easily.    Please keep us posted on both of you.

Janice

 

 


 


From: Janet Dunn 

Sent: Tuesday, May 18, 2010 1:00 PM

To: 'Pieter and Heather' ; 'Robert Pall' ; [email protected] 

Subject: RE: [TMIC] Neurontin

 

Hi Heather
 
Thanks for asking.  I just don’t know what to think.  After raising the TM 
alarm bells (significantly), the neurologist sent a letter to the family 
doctor, stating that the “problem” is organic in nature.  That the pain is 
coming from the brain itself, and not from the spinal cord lesion.  That he 
does have reduced feeling and strength.  That he does have decreased sensation. 
That it is not TM and not MS, but he does not know what it is.
 
Geesh, thanks for scaring the crap out of us.  He does have a lesion at T2.  He 
does have significant pain and weakness.  
 
They have put him on Baclofen 10 mg 2 times a day, and Carbamazepine CR 200mg 
twice daily.  The goal being to manage the pain and to get him off of the 
percocet.   The neurologist is hoping that he will heal, as he has youth on his 
side.  
 
Am I angry?  Yes.  Am I frustrated?  Yes.  This young man has been dealing with 
this for over a year now, and it has not gotten any better, and fortunately not 
much worse, other than the pain.  The prognosis is just what I said: hopefully 
he will heal. 
 
You would think, that in this day and age, when we can do so much, that somehow 
they could figure out what is wrong with him.
 
So, a big thank you to all of my TM family.  While this is not TM (sorry for 
passing that on, but that was the info that I had) this is a Spinal Cord 
Injury.  It does not change the tears that I have shed, and will shed.  I am at 
a loss as to what to say, do or think.
 
Janet
 


From: Pieter and Heather [mailto:[email protected]] 
Sent: May 18, 2010 10:09 AM
To: Janet Dunn; 'Robert Pall'; [email protected]
Subject: Re: [TMIC] Neurontin
 

Janet,

 

How did your son make out at the doctors?  Are they going to be putting him on 
some meds to help with his pain?  This has to be just so hard for him.

 

Heather in Calgary 


----- Original Message ----- 

From: Janet Dunn 

To: 'Robert Pall' ; [email protected] 

Sent: Monday, May 17, 2010 10:45 AM

Subject: RE: [TMIC] Neurontin

 
Hi Rob.
 
I couldn’t take neurontin.  I am on Lyrica, have been for four years now.  75 
mg a.m. and 150 mg p.m.  It has virtually stopped the banding, and the burning 
in the feet.  I am actually going to lower the dosage to 75 twice a day.  
However, that has been delayed because of my “inability to pace myself”  so I 
have paid for it  with high pain levels in my legs – but not nerve pain.  I am 
also taking effexor, welbutrin, and long acting oxycodone.  I supplement that, 
as needed, with regular oxy during the day – so if the pain is high – then oxy 
during the day, or baclofen, - it is a tricky road so I monitor my symptoms 
constantly.  
 
I am seeing a pain specialist in Vancouver BC  three times a year – he just 
writes a script for many months, and I fill as I see fit.  That is how it works 
here in Fort St John.  
 
Now, with my son exhibiting what the neurologist is labeling TM, I have no idea 
what the doctor is going to do here in town.  We will find out today – right 
now he is not managing his pain – he is simply coping with it – “ I am tough, I 
can take it” (he is 15).  He takes 2 percocet in the evening so he can walk the 
dog – he uses a cane.  
 
Good luck with the neurontin – my money is on the lyrica and the effexor – in 
combination they work wonderful.  I do not know what is in Cymbalta, and 
honestly – I will google it asap. 
 
Janet


      

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