Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 09-16-2009, 08:42 PM #16
GalenaFaolan's Avatar
GalenaFaolan GalenaFaolan is offline
Member
 
Join Date: Dec 2006
Location: Florida
Posts: 445
15 yr Member
GalenaFaolan GalenaFaolan is offline
Member
GalenaFaolan's Avatar
 
Join Date: Dec 2006
Location: Florida
Posts: 445
15 yr Member
Default

When a doctor states, "I can't find any organic cause for the symptoms." He/she means they can find no physical cause to explain the symptoms. Organic = physical in the medical world. Just another bit of medical terminology trivia, idiopathic = they don't know what caused it. Example, Idiopathic Pulmonary Fibrosis. No family history or other factors as to why someone has the disease. :-)

Quote:
Originally Posted by SandyRI View Post
Dear Dennis,

I can SO relate to your frustration and anger.

Perhaps he trained with the neurologist I saw a few months ago in RI at my GP's insistance because I was suffering with such severe head pain he wasn't quite sure what to do with me? That neurologist charged me a $25 co-pay to hear basically the same thing - in his report he stated "I do not have an organic alternative diagnosis to explain her pain, and wonder how much of this is caused by depression." This is because at the time I saw him he didn't observe any autonomic changes that he expected to see with, as he puts it, "chronic RSD, such as sweating, hair loss, changes in skin turgor, temperature and color, osteopenia or edema."

BTW - what does "organic" mean?

I recall him being upset with me because I did not want to add Tegretol to my list of meds. I had tried Lyrica and Neurontin and hated them both. I already take Topamax for head pain. And furthermore, one of my brothers suffered from a seizure disorder when he was younger and was on Tegretol for a while - it made him lethargic and caused him to gain weight. No thank you.

I only saw this dr. because my GP wanted me to - he prescibes my opiods and I've needed them increased over the summer because my pain has been severe on a number of occasions. Before I agreed to the appt with the neurologist, I think I SHOULD have asked whether the doc had any experience with RSD, how many RSD patients he sees a year, etc. There are several other neurologists in his office -perhaps one of them would have been better qualified to treat me. Live and learn.

My GP has asked me AGAIN to try to find a neurologist because he needed to increase my meds 2 weeks ago. A RI FB page had a suggestion for a RI neurologist, so I called his office. I asked the receptionist if the doc had experience with RSD and how many patients he took care of, etc. I also asked my GP if he had heard anything negative, and he hadn't. That's a lot more due diligence than I perfomed the first time around.

Not all doctors are alike. My GP wants me to see neurologists, that's the only reason I'm persisting. But the bulk of my care has been provided by a PM doc in Boston at ST. Eliz that I really like a lot (7 SGB, 1 LB, 2 lidocain infusions). He's board certified in both pain management and anesthiology, and is a Doctor of Osteopathy.

I think you may find that many people on this board use PM docs for their care.

Good luck, and never, never give up. Sorry you had such a *edit* day.

Sandy
__________________
Laugh until you cry, don't cry until you laugh.

Living, loving and laughing with RSD for 14 years and counting.
GalenaFaolan is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
AintSoBad (09-18-2009), Dew58 (09-17-2009), Hockey (09-17-2009), SandyRI (09-17-2009)
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Neurologist! jaynurse05 Myasthenia Gravis 1 03-10-2009 12:05 PM
Do you like your neurologist? DaleD Parkinson's Disease 24 07-22-2008 03:28 PM
Went to a different neurologist paula_w Parkinson's Disease 18 07-19-2008 08:55 PM
WC Neurologist????? inpain24/7 Layoffs, Unemployment and Worker's Compensation 1 05-07-2008 04:57 PM
Another Neurologist? Doodle bug7 Trigeminal Neuralgia 6 03-09-2008 05:30 PM


All times are GMT -5. The time now is 10:03 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.