Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS.

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 02-05-2015, 06:14 PM #3
ArtandIron ArtandIron is offline
Junior Member
 
Join Date: Jan 2015
Posts: 22
10 yr Member
ArtandIron ArtandIron is offline
Junior Member
 
Join Date: Jan 2015
Posts: 22
10 yr Member
Default

Annie-- I have a question related to your cellcept comment. Would any anti-inflammatory alter the test results or just the strong ones like Cellcept? I've been on Mobic for years to help control the low grade fevers and joint pain to which I'm prone. Is there any chance that would have affected my results?

mrzt-- don't give up. The doctor at the ER told me there was nothing wrong with me. I felt a little vindicated when I got my PFT results. Was this doctor a neuro? Can you see your original doctor or ask for a referral to a different neuro?
ArtandIron 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



All times are GMT -5. The time now is 03:24 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.