Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 08-12-2009, 11:16 AM #25
notasperfectasyou's Avatar
notasperfectasyou notasperfectasyou is offline
Member
 
Join Date: Jul 2009
Posts: 104
15 yr Member
notasperfectasyou notasperfectasyou is offline
Member
notasperfectasyou's Avatar
 
Join Date: Jul 2009
Posts: 104
15 yr Member
Default

Quote:
Originally Posted by poetic license View Post
Thanks for this statement. I wish more people had the courage and control to take control of their own bodies. My doctor does not own my body, when my first neuro made it clear that he would not accept me to do something he did not approve, I switched to a neuro who is still mainstream but who says "it's your choice". Would love to hear more about your journey.
I don't quite know where to start. I have a ton of info I can post, but I also know that I'm new here.

I guess where I'm at is a place of uncertainty because I'm a long time poster at another board and I know when someone new shows up and has something completely new and different to say, it goes largely ignored. I can't blame folks for that, I'm guilty of it myself.

I don't want to come across like the sham-wow guy.

I also know that most all of us are "raised" on autoimmune therory. I've been there and done that. I know about, have posted about and read endlessly about cytokines, TH1, TH2, Macrophages, NK cells, etc. It wasn't until I got fed up with the neuro offering the same thing over and over again that I decided that there had to be others who wanted to find a path beyond what the neuro tells you. Funny thing is, there is.... and while many are up in arms over the heathcare debate, I feel that I've been trying to expose healthcare for a quite a while now.

I'm rambling. In a nutshell, my perspective on MS is so different, I know it is and I know it's hard to interest others when it all sounds like snake oil. But, it's not unique to me and there are published articles in real medical journals that support this approach. Ken
notasperfectasyou 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
Link between Alzheimer's Disease & Chlamydia Pneumoniae? Mark Hall Alzheimer's Disease 2 03-31-2008 05:40 AM
Link between CFS, FM & Chlamydia Pneumoniae? Mark Hall Fibromyalgia and Chronic Fatigue 0 03-23-2008 07:35 AM
Mycoplasma pneumoniae Infection and OCD: A Case Report Lara Anxiety and OCD 1 01-12-2008 03:53 PM


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