That's what my neuro said. I was diagnosed with TM until I had a leasion
in my optic nerve (causing double vision) in 2007 then the diagnosis
became MS

 

BERNARD BUTCHER

Honeywell Engineering

516-577-5868

________________________________

From: Janice Nichols [mailto:jan...@centurytel.net] 
Sent: Thursday, June 10, 2010 11:46 PM
To: Dalton Garis; Laura Beaudin; tmic-l...@eskimo.net
Subject: Re: [TMIC]

 

Is it possible that with both brain and spine lesions that you have MS
rather than TM?                Janice

 

 

From: Dalton Garis <mailto:malugss...@gmail.com>  

Sent: Thursday, June 10, 2010 10:34 PM

To: Janice Nichols <mailto:jan...@centurytel.net>  ; Laura Beaudin
<mailto:laura.beau...@gmail.com>  ; tmic-l...@eskimo.net 

Subject: Re: [TMIC]

 

Janice;

I can function normally for spurts of time, but no stamina in the
muscles at all.  My lower legs and lower arms are hit with constant
aching and feel as if they were filled with hot lead.

My spine is very sore now with many different pains.  My diaphragm and
upper stomach area is burning and squeezing all the time.  I cant get
comfortable anymore, no matter how I sit, recline or lie down.

The biggest problem is with the attacks of spasticity.  They are overall
convulsions affecting all my muscles and causing me to arch my back and
legs backwards, then forwards, pinning my head aagainst my chest and
leaving me with no control over arms, legs and speech.

They ate almost epileptic fits, and likely caused by brain and spine
lesions.  I take Epanutin for this, which is an anti-convulsive
medication given to epileptics.  It works a little but the spastic
qattacks can come at any time.  I will feel it in my voice as I try to
talk and become halting in speech.  Then the back arches and the arms go
flying upwarrds.  This can last for 20 minutes or 6 hours, one
convulsion after another.  When it is finished with me all my muscles
and backbones ache and giv e me a lot of pain.

But I manage somehow and I am happy.  Life is all about solving
complications and problems, so, we get good at it.

I must stop now, as both my eye focusing and my fingers are quitting on
me.

Kind regards,

Dalton Garis
Abu Dhabi/New York


On 11/6/10 2:22 AM, "Janice Nichols" <jan...@centurytel.net> wrote:

Do you mind my asking what are you able to do?     Were your arms
affected and how did it leave you with walking/not walking?
Janice

From: Laura Beaudin <mailto:laura.beau...@gmail.com>  
Sent: Thursday, June 10, 2010 11:43 AM
To: Janice Nichols <mailto:jan...@centurytel.net>  ;
tmic-l...@eskimo.net 
Subject: Re: [TMIC]

All my docs and therapists are on the Spinal Cord Injury Unit of our
rehab hospital...definitely qualified. It sucks, but sometimes the best
efforts don't work. I was on this unit as an inpatient for 6 weeks last
summer, they were not able to get much back so the time ended up being
spent on how to adjust to changes and become independent in spite of it.


Transverse Myelitis IS a Spinal Cord Injury...just not a traumatic one
(ie, not caused by an accident). 

Laura

http://practical-homeschooling.org
www.laurascoolstuff.com <http://www.laurascoolstuff.com> 



On Thu, Jun 10, 2010 at 10:34 AM, Janice Nichols <jan...@centurytel.net>
wrote:


 
I am getting definite improvement with  PT.     My pain management doc
recommended a PT guy that  specializes with damaged spines (like us).
He  knows

what he is doing.    We are taking it  very slow because of the severe
back arthritis I have and the  myelitis.      I also do my exercises at
home in  between sessions.

Can you get a PT especially recommended by your doc  because of our
special  problem?          The hamstring  problem is definitely from
myelitis.

Janice

 
 
From: Laura Beaudin <mailto:laura.beau...@gmail.com>  
 
Sent: Thursday, June 10, 2010 11:14 AM
 
To: Janice Nichols <mailto:jan...@centurytel.net>  
 
Subject: Re: [TMIC]
 
 
 
 

Ditto...more bruising would be normal (and often is) if you  have
decreased sensation. As for hamstrings, mine are shortening and despite
PT, I can't get them flexible again. 
Laura

http://practical-homeschooling.org
www.laurascoolstuff.com <http://www.laurascoolstuff.com> 



 
On Thu, Jun 10, 2010 at 9:04 AM, Janice Nichols <jan...@centurytel.net>
wrote:
 


 
Also the  baclofen!             Good luck and keep in touch in New York.
Are  you going to live there now?

Janice

 

 
 
From: Dalton Garis <mailto:malugss...@gmail.com>  
 
Sent: Wednesday, June 09, 2010 11:44 PM
 
To: Janice Nichols <mailto:jan...@centurytel.net>  ;
tmic-list@eskimo.com ;  Leslie Garis <mailto:lga...@mindspring.com>  ;
Garis, Brooks (Darien,  CT) <mailto:brooks_ga...@ml.com>  
 
Subject: Re: [TMIC] 
 

I haven't;

But I was in very heavy labor  employment before returning to get a PhD
at aged 35, with lots of broken  bones, back fusions, hardware, the
works.  So, I wouldn't notice  anyway.

As to the hamstring, also, no.  For me the spasticity  and convulsive
attacks when I try to speak during stressful situations is  absolutely
the biggest problem.  And no one's heard of that.  But  I read about
this being a well documented effect of TM, that is, spasticity  in some
form, on the Johns Hopkins website.  I also have uncooperative  legs and
hands a lot of the time.

But I can't keep my left foot up  while walking now, so I wear western
boots with big heels.  They allow  me to walk without the need for a
foot brace.

Here's hoping I don't  get spastic in the airport or on the plane so it
doesn't get me grounded or  thrown off the plane today on my flight back
to NYC!!!  Hey, just  increase the Lyrica, right?

Dalton
Abu Dhabi/New York  



On 10/6/10 8:23 AM, "Janice Nichols" <jan...@centurytel.net
<http://jan...@centurytel.net> >  wrote:

 


Got a couple of  questions:

1.    Have you  noticed more bruising on affected areas of TM than you
had before  TM?

 
2.     Have any of you had problems with your hamstring since  TM?

Janice

 

 

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