Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 10-30-2014, 09:46 PM #4
Jon_sparky Jon_sparky is offline
Member
 
Join Date: Jul 2013
Posts: 145
10 yr Member
Jon_sparky Jon_sparky is offline
Member
 
Join Date: Jul 2013
Posts: 145
10 yr Member
Default

Quote:
Originally Posted by en bloc View Post
Plaquenil may help with the fatigue and sometimes joint pain related to autoimmune disease, but not nerve pain. There is some research that indicates it can slow progression of some autoimmune processes, but it's hard to prove or track this when so little is known about the progression of AI diseases to begin with. Keep in mind that it take a good 6 months or so to start working. Make sure to get a base line ophthalmologist evaluation before starting the Plaquenil and then EVERY 6-12 months after that.

I'm glad you are getting some relief with the Cymbalta.

The skin biopsy can be repeated down the road if your continue to get worse...and maybe the borderline level will have changed...allowing you to qualify for IVIG or another treatment.
I went for my eye test yesterday, the Optimologist told me that the side effect of retina detachment takes 5 years to manifest, that it is accumlative. She called the 3 month test a benchmark, she has been in the field for probably close to 40 years. She said that the Rheumy's are over reacting, but a lot want a 6 month exam, to cover themselves. Anyway, passed the eye test, but still have to do the Field eye test in December, to complete it. She told me that my blurred vision was not coming from Planquil, or from any problem with my eyes, so maybe a manifestation of SLE also... I always thought the blurred vision was related to low blood sugar, but I have tested my glucose during the episode and it is normal. I also get blurred vision when I am have a allergic reaction to the new carpet in my office...
Jon_sparky 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
Punch biopsy tomorrow morning... Jon_sparky Peripheral Neuropathy 4 10-01-2014 05:08 PM
Accuracy of punch skin biopsy for nervedensity Synnove Peripheral Neuropathy 5 04-24-2014 10:29 AM
Has anyone had a skin punch biopsy for SFN? SuzieCue Peripheral Neuropathy 12 09-08-2013 01:22 PM
Saliva gland biopsy to diagnose PD--did anyone check for intestinal biopsy results? olsen Parkinson's Disease 0 01-11-2013 12:17 PM
Biopsy results EE03 Peripheral Neuropathy 13 11-06-2010 06:26 AM


All times are GMT -5. The time now is 04:59 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.