advertisement
Reply
 
Thread Tools Display Modes
Old 12-22-2013, 07:04 PM #1
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Default Path of progression?

I have been diagnosed with poly neuropathy several months ago,I have no pain with it and after searching I finally found a neurologist who will see me.My question is this what is the normal progression of the disease...so far my left foot(where it started) left leg left hip and now my left shoulder is affected nothing at all on my right side and still absolutely no pain associated with PN
Does this indicate a certain type of PN or perhaps a pinched nerve or stenosis? I am hoping of all the experience contained on this board someone will be able to better educate me...
Thank you
Steph70 is offline   Reply With QuoteReply With Quote

advertisement
Old 12-22-2013, 07:52 PM #2
ElaineD's Avatar
ElaineD ElaineD is offline
Member
 
Join Date: Nov 2013
Location: North Carolina
Posts: 293
10 yr Member
ElaineD ElaineD is offline
Member
ElaineD's Avatar
 
Join Date: Nov 2013
Location: North Carolina
Posts: 293
10 yr Member
Default

Steph70,

I'm not an expert, and I'm sure that many people here will be able to tell you more than I can.

But I don't think there is a 'normal progression' of polyneuropathy. It isn't even possible to know what 'might happen' until you know what is causing it.

Poly neuropathy means that several kind of nerves are affected (as opposed to mono neuropathy) which is one kind of nerve damaged.

Most neuropathies are related to an underlying cause (damage, disease or genetic defect).

However, in a fairly high percentage of cases the cause of the neuropathy is unknown. Then it is called idiopathic, which means of unknown cause.

I have idiopathic poly neuropathy, which seems to be limited to my feet and legs.

But since I don't know what caused it, and it was profound when it was diagnosed, I don't know if it will stay where it is, or spread.

However, in the 4 years since it was first diagnosed, it hasn't affected other parts of my body.

I don't know for sure, but for most of us, we learn to live with a fairly high degree of uncertainty about progression, and often even about cause.

The fact that your polyneuropathy is asymmetric seems unusual to me. I look forward to others posting.

Hugs, Elaine
ElaineD is offline   Reply With QuoteReply With Quote
Old 12-23-2013, 07:50 AM #3
glenntaj glenntaj is offline
Magnate
 
Join Date: Aug 2006
Location: Queens, NY
Posts: 2,857
15 yr Member
glenntaj glenntaj is offline
Magnate
 
Join Date: Aug 2006
Location: Queens, NY
Posts: 2,857
15 yr Member
Default Polyneuropathy--

--just means that many nerve are affected.

This may mean one type of nerve in many areas of the body, which is typical of many metabolic and autoimmune neuropathies, or it could mean many types of nerves (sensory and motor, myelinated and unmyelinated) are affected (more typical of toxic neuropathies).

The location can sometimes provide a clue as to cause; as Elaine mentions, asymmetric neuropathies much more prominent on one side of the body than the other imply a less systemic cause and can point to compression or mechanical injury, particularly of the spinal nerve roots. All people with neurological symptoms should probably get spinal MRI's to see if this is where the symptoms stem from, as symptoms from spinal problems can absolutely mimic those of more systemic conditions.
glenntaj is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ElaineD (12-23-2013)
Old 12-23-2013, 09:42 PM #4
hopeful hopeful is offline
Member
 
Join Date: Aug 2009
Posts: 914
10 yr Member
hopeful hopeful is offline
Member
 
Join Date: Aug 2009
Posts: 914
10 yr Member
Default

Quote:
Originally Posted by Steph70 View Post
I have been diagnosed with poly neuropathy several months ago,I have no pain with it and after searching I finally found a neurologist who will see me.My question is this what is the normal progression of the disease...so far my left foot(where it started) left leg left hip and now my left shoulder is affected nothing at all on my right side and still absolutely no pain associated with PN
Does this indicate a certain type of PN or perhaps a pinched nerve or stenosis? I am hoping of all the experience contained on this board someone will be able to better educate me...
Thank you
Hi Steph70,
What is normal progression? That's the million dollar question. If only there was an answer. I have asked every doctor I've seen what the future may look like with my neuropathy and all have said they couldn't say with certainty. My neurologist said I can just tell you that you won't end up in a wheelchair. I'm still trying to figure out how he knows that. He didn't say.

I'm glad to hear that you are not in pain with it.
hopeful is offline   Reply With QuoteReply With Quote
Old 12-26-2013, 11:41 PM #5
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Default Progression

I was just wondering if there is a certain way this attacks you.Never having it till back surgery and having it roar up my left leg,my left hip and now left shoulder in 6 months after surgery seems to me to be a sign that something on my left side is screwy.Now considering my surgery was on the left side of L3.L4 and L5...I am just poking and hoping I can learn more about my problem beffore I see my first neurologist next month.I am learning a lot here about what my prep should be before I see him and I will be ready
Thanks for your answer
Steph70 is offline   Reply With QuoteReply With Quote
Old 12-28-2013, 08:25 AM #6
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb

Does cold treatment make your pain worse?

If if does you may have a type of neuropathy called RSD. (CRPS)

This is our RSD forum where you can ask the posters there about progression of pain, which sometimes happens with RSD.

In general PNers like cold treatments which will numb pain signals.
But if the nerves are reacting differently, as in RSD, they prefer, heat treatments. So this can be a diagnostic sign.

This is the link to our forum here:
http://neurotalk.psychcentral.com/forum21.html
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are 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.
mrsD is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
hopeful (12-30-2013)
Old 12-29-2013, 11:12 PM #7
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Default Progression

I have absolutely no pain in areas affected,warm feels good sometimes ice feels good,but neither of them causes me pain..I just have more and more of the left side of my body going numb.I have been using an interferential unit to run some low voltage through my leg--seems to be giving me tingles in areas that were completely numb..going to keep it up..will see a neurologist on the 9th,anxious to hear his assessment thank you
Steph70 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
hopeful (12-30-2013), mrsD (12-30-2013)
Old 01-09-2014, 09:30 PM #8
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Steph70 Steph70 is offline
Junior Member
 
Join Date: Nov 2013
Posts: 13
10 yr Member
Default Possible answer

Saw a neurologist today..he seems to think my neuropathy is not systemic but is coming from a slopped up surgery. He looked at my MRI after surgery and pointed out that I still had a badly bulging disc. He set me up for a bunch of blood work and will schedule more extensive EMG tests soon..The fact that all my symptoms were asymetric points him to a pinched nerve from a disc...It is amazing just how right the members of this group are
Quote:
Originally Posted by ElaineD View Post
Steph70,

I'm not an expert, and I'm sure that many people here will be able to tell you more than I can.

But I don't think there is a 'normal progression' of polyneuropathy. It isn't even possible to know what 'might happen' until you know what is causing it.

Poly neuropathy means that several kind of nerves are affected (as opposed to mono neuropathy) which is one kind of nerve damaged.

Most neuropathies are related to an underlying cause (damage, disease or genetic defect).

However, in a fairly high percentage of cases the cause of the neuropathy is unknown. Then it is called idiopathic, which means of unknown cause.

I have idiopathic poly neuropathy, which seems to be limited to my feet and legs.

But since I don't know what caused it, and it was profound when it was diagnosed, I don't know if it will stay where it is, or spread.

However, in the 4 years since it was first diagnosed, it hasn't affected other parts of my body.

I don't know for sure, but for most of us, we learn to live with a fairly high degree of uncertainty about progression, and often even about cause.

The fact that your polyneuropathy is asymmetric seems unusual to me. I look forward to others posting.

Hugs, Elaine
Steph70 is offline   Reply With QuoteReply With Quote
Old 01-09-2014, 09:56 PM #9
ElaineD's Avatar
ElaineD ElaineD is offline
Member
 
Join Date: Nov 2013
Location: North Carolina
Posts: 293
10 yr Member
ElaineD ElaineD is offline
Member
ElaineD's Avatar
 
Join Date: Nov 2013
Location: North Carolina
Posts: 293
10 yr Member
Default

Steph, amazing to be on the path for finding the cause!

The sooner you know what is wrong, the sooner you can perhaps address it and stop and even reverse the damage.

It is SO KEY to find the right doctors. And so very very hard to find BOTH the right kind of doctor and a very GOOD one of the right kind.

PLEASE keep us posted on what develops.

Hugs, Elaine
ElaineD is offline   Reply With QuoteReply With Quote
Reply


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
Am I on the right path? AddyNat Myasthenia Gravis 8 11-13-2013 11:24 PM
For Everyone in Irene's Path BlueCarGal Sanctuary for Spiritual Support 1 08-26-2011 10:47 PM
Hurricane IKE- all in the path Corkybird Sanctuary for Spiritual Support 17 09-16-2008 08:54 AM
Life's Path..... isobelle Creative Corner 1 12-07-2007 05:52 AM
Off the Beaten Path buckwheat Reflex Sympathetic Dystrophy (RSD and CRPS) 6 09-17-2007 06:06 AM


All times are GMT -5. The time now is 11:18 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.