Home Menu

Site Navigation



NeuroTalk Support Groups > > >

ME/CFS/CFIDS and Mycoplasma!

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 12-30-2007, 12:48 AM #10
shiney sue shiney sue is offline
Senior Member
  
Join Date: Mar 2007
Posts: 1,812
15 yr Member
shiney sue shiney sue is offline
Senior Member
 
Join Date: Mar 2007
Posts: 1,812
15 yr Member
Default
I seen it happen many times as a nurse,and i've seen Drs. who had
Drug problems. Thanks again C. you came through.and yes nurses have
been know to tell on Drs. Sue
shiney sue is offline   Reply With QuoteReply With Quote
 

« Previous Thread | Next Thread »
Thread Tools
Display Modes
Threaded Mode Threaded Mode

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
I got a question for all you cfids-ers... Idealist Fibromyalgia and Chronic Fatigue 6 01-19-2007 03:51 PM
Mrs D -- L-Lysine & CFIDS: can you help me? OneMoreTime Vitamins, Nutrients, Herbs and Supplements 5 12-05-2006 09:36 AM
Persistant Brain Dysfunction from CFIDS Brain Damage OneMoreTime Fibromyalgia and Chronic Fatigue 1 10-29-2006 01:12 AM
Hello CFIDS forum ! Wittesea Fibromyalgia and Chronic Fatigue 0 10-11-2006 10:44 AM


All times are GMT -5. The time now is 03:00 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.

 

All posts copyright their original authors.

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.

Home