Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 10-22-2013, 05:41 AM #15
kazzar1958 kazzar1958 is offline
Junior Member
 
Join Date: Sep 2013
Location: London, England
Posts: 48
10 yr Member
kazzar1958 kazzar1958 is offline
Junior Member
 
Join Date: Sep 2013
Location: London, England
Posts: 48
10 yr Member
Default

I was on it for five years from 2005 to 2010 and I know only too well how hard it is to come off. The withdrawal regimen my doctor suggested was way too fast and I had all the nasty side effects. I had to taper off using the liquid form for months which was hard to get hold of in Britain. At the time there was a lot of denial in the medical profession about how insidious the drug is.
I've had reasonable success with it. I'm still depressed but my extreme highs and lows have been removed. I feel very flat and lethargic but I've never had to deal with the prospect of a life changing illness and be stuck in a limbo of not knowing at the behest of the British healthcare system before. I can't afford to go private and I don't agree in principle. A free, on demand healthcare system available to all, paid for by everyone's taxes, is one of this country's most enlightened institutions. (I don't want to stir up a hornet's nest about Obamacare!)

The reason I'm taking it again is because my doctor thinks my body already knows it and it would therefore kick in quicker. At the time I was in favour of duloxitine bacause I had already read about it's pain relieving use in diabetic neuropathy. I thought I woud kill two birds with one stone so to speak, the pain and depression. I was a bit concerned about the dose of 60mg though as I thought it was a bit high (I'm on 20mg Paxil). I've since found out that dosages of different SSRI's are not necessarily comparable.

Anyway, on a different point, another problem I have at the moment is my voice. For the last month or so, I have struggled to talk in my usual low register, my voice keeps breaking. It's worse in the morning and on days when I hardly talk (easily done living on my own and being off work at the moment).
I mentioned it to my choir leader last week and she gave me some vocal exercises to do and said she thought it was nothing to be concerned about. I have also mentioned it to my therapist. She thinks it's stress related.
Predictably I've looked it up and started panicking when I saw nerve related conditions. I don't have a sore throat, I have no problems swallowing and I mentioned it to my doctor a couple of weeks ago. He looked at it and seemed perplexed by the symptoms but offered no diagnosis. I'll go again this week I think.

Karen
kazzar1958 is offline   Reply With QuoteReply With Quote
 


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
Scs permanent 7/10 tkayewade SCS & Pain Pumps 9 07-08-2012 12:45 AM
When do you know that your symptoms are permanent? SpaceCadet Traumatic Brain Injury and Post Concussion Syndrome 10 01-09-2012 02:04 AM
What are the chances of PCS being permanent? Cat&TheHat Traumatic Brain Injury and Post Concussion Syndrome 5 01-03-2012 03:02 AM
Is it permanent billy027 Thoracic Outlet Syndrome 5 10-25-2007 09:41 PM


All times are GMT -5. The time now is 02:37 PM.


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.