advertisement
Reply
 
Thread Tools Display Modes
Old 09-25-2011, 11:41 AM #31
malawigirl08's Avatar
malawigirl08 malawigirl08 is offline
Member
 
Join Date: Mar 2010
Location: Scotland
Posts: 315
10 yr Member
malawigirl08 malawigirl08 is offline
Member
malawigirl08's Avatar
 
Join Date: Mar 2010
Location: Scotland
Posts: 315
10 yr Member
Default

Quote:
Originally Posted by Buttercup40 View Post
Hi Mrs D, he has the pn pain, burning, over sensitivity etc, also these electrical type pains. The pains in his shoulder, ankle and knee have only started this week.
The pain he is getting in these area's is different to the other pains. The only pain he can liken it to is, if you put your hand in snow or ice but more intense and painful?
Even though the Dr is concerned there is little more he can do if the neurologist will not see Mark sooner.
I feel the only other alternative will be to get him into hospital, which Mark is reluctant to do in case they transfer him to the neurology hospital which is about 45 miles away from our home.
Thanks Mrs D
Regards
Buttercup x
Hi Buttercup
I am also in the UK and it has taken me three years since diagnosis to feel as though I am actually getting someone listening to me - I hope your experience is better but my experience is that as long as referrals meet the 12week target of being seen you then are left to get on with it. I would recommend you try your best to get Mark admitted to hospital, even if it is 45miles away.Good luck.
malawigirl08 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Buttercup40 (09-26-2011)

advertisement
Old 09-25-2011, 11:51 AM #32
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

You know, it is a terrible thought, but severe PN in a person like this progressing rapidly, could be paraneoplastic.

Certain cancers cause PN like this.

Has he had a chest Xray?

http://www.uptodate.com/contents/par...rve-and-muscle
__________________
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
Old 09-25-2011, 07:03 PM #33
malawigirl08's Avatar
malawigirl08 malawigirl08 is offline
Member
 
Join Date: Mar 2010
Location: Scotland
Posts: 315
10 yr Member
malawigirl08 malawigirl08 is offline
Member
malawigirl08's Avatar
 
Join Date: Mar 2010
Location: Scotland
Posts: 315
10 yr Member
Default

Quote:
Originally Posted by malawigirl08 View Post
Hi Buttercup
I am also in the UK and it has taken me three years since diagnosis to feel as though I am actually getting someone listening to me - I hope your experience is better but my experience is that as long as referrals meet the 12week target of being seen you then are left to get on with it. I would recommend you try your best to get Mark admitted to hospital, even if it is 45miles away.Good luck.
I also meant to add the best thing my GP done for me was to refer me to the Chronic Pain Clinic, they took the time to look at my history and treat me, it has been very successful - you may find they will be able to do more for your husband than the neurologist - just because they give a diagnosis doesnt mean they will be able to provide a treatment but the Pain service treats the pain
malawigirl08 is offline   Reply With QuoteReply With Quote
Old 09-26-2011, 04:08 AM #34
Buttercup40's Avatar
Buttercup40 Buttercup40 is offline
Junior Member
 
Join Date: Jul 2011
Location: North Wales UK
Posts: 23
10 yr Member
Buttercup40 Buttercup40 is offline
Junior Member
Buttercup40's Avatar
 
Join Date: Jul 2011
Location: North Wales UK
Posts: 23
10 yr Member
Default

Quote:
Originally Posted by mrsD View Post
You know, it is a terrible thought, but severe PN in a person like this progressing rapidly, could be paraneoplastic.

Certain cancers cause PN like this.

Has he had a chest Xray?

http://www.uptodate.com/contents/par...rve-and-muscle
Thank you for this info Mrs D. I have checked out the information on paraneoplastic and thankfully I don't think Mark fits this? The Dr did ask Mark if he had visual disturbance or headaches etc.

He did have a chest X-ray about 3 mths ago, as the Dr suspected he had COPD. There was signs of COPD, but he had the blow tests done and the results were mild COPD.
I'm not going to let this lay, I will be back on to the Dr's if things don't start to settle down.
If anything else comes to mind, please let me know.
Hope your feeling better
Buttercup x
__________________
"During your times of trial and suffering, when you see only one set of footprints, it was then that I carried you" Anon
Buttercup40 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
mrsD (09-26-2011)
Old 09-26-2011, 04:18 AM #35
Buttercup40's Avatar
Buttercup40 Buttercup40 is offline
Junior Member
 
Join Date: Jul 2011
Location: North Wales UK
Posts: 23
10 yr Member
Buttercup40 Buttercup40 is offline
Junior Member
Buttercup40's Avatar
 
Join Date: Jul 2011
Location: North Wales UK
Posts: 23
10 yr Member
Default

Quote:
Originally Posted by malawigirl08 View Post
Hi Buttercup
I am also in the UK and it has taken me three years since diagnosis to feel as though I am actually getting someone listening to me - I hope your experience is better but my experience is that as long as referrals meet the 12week target of being seen you then are left to get on with it. I would recommend you try your best to get Mark admitted to hospital, even if it is 45miles away.Good luck.
Hi Malawigirl, It's over 12 wks since Mark was referred to the neurologist. I did speak to their department which is in Liverpool to ask how long he would have to wait for an appointment and the girl the other end shouted "how long is the waiting time in Wales!" She told me 3 mths, but when his letter first came they wanted him to wait until the end of Nov', I told them he couldn't wait this long and we would travel to Liverpool for an earlier appointment. They then found an appointment in our local hospital for 30th Sept', which has now been changed to 14th Oct'. Poor Mark almost cried when he read the letter!
I could see on Thursday that our Dr was not happy with the way Mark is suffering, but other than him faxing off a letter to the neurologist there is little more he can do.
I can't understand why they have not referred him to the pain clinic? The would seem a normal process to me!
Thanks for the input
Buttercup x
__________________
"During your times of trial and suffering, when you see only one set of footprints, it was then that I carried you" Anon
Buttercup40 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
malawigirl08 (09-28-2011)
Old 09-28-2011, 10:30 PM #36
Liftyourhands7 Liftyourhands7 is offline
Member
 
Join Date: Sep 2011
Posts: 180
10 yr Member
Liftyourhands7 Liftyourhands7 is offline
Member
 
Join Date: Sep 2011
Posts: 180
10 yr Member
Default I'm so sorry

I am so sorry to hear about your husband, Is there any way to get him to a Emergency room, that's what I did last week and they put me in the hospital immediately, I was able to get help very quickly, they did so many tests, sometimes it pays to go through the ER. I hope he feels better soon. Blessings, Jan
Liftyourhands7 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
atypical T.N. and typical T.N. Doodle bug7 Trigeminal Neuralgia 10 12-18-2015 01:35 PM
Cat drinking from faucet...not typical! mrsD Pets & Wildlife 3 09-28-2009 02:49 PM
It is not your typical boxing class Stitcher Parkinson's Disease 0 01-06-2009 09:00 AM
A Typical Oct Morn -- Not! SallyC Multiple Sclerosis 12 10-11-2007 08:07 AM
Typical Friday... colombiangirl1 Creative Corner 0 03-09-2007 05:30 PM


All times are GMT -5. The time now is 06:24 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.