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


advertisement
Reply
 
Thread Tools Display Modes
Old 04-20-2010, 02:25 PM #1
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb

Quote:
Originally Posted by Kathie Glenn View Post
I have one question - why don't doctors tell you all of these when you are diagnosed? It seems like less time and money would be spent by doctors, patients and insurance companies if there was a comprehensive medical consult where the patient would go from doctor to consults - to talk about meds, nutrition and exercise. Wouldn't we all be better off and the doctors would see and hear less from us. Guess I am a little grumpy today.

Kathie Glenn
Basically it is because they are not trained in this aspect of life.
Dr. Weil who graduated from Harvard himself, is a vocal advocate on training doctors in nutrition. Some places are making an effort. Tufts university is one. Another is U.C. San Diego (where Vit D research is being made public) and U.C San Francisco where the Dept of Endocrinology is researching obesity and nutrition.
This video comes from U.C. SF and is a lecture being given to medical people there:
http://www.youtube.com/watch?v=dBnniua6-oM

I myself discovered many nutritional things myself, when we started with our first computer over a decade ago. I search and learn every day. Most doctors will not take that time, and also have internal prejudice about the internet. Many specialists do not like having their patients search the net for answers. Some very special ones like you see on Mystery Diagnosis on Discovery Health TV, are the exceptions. That program illustrates very painfully how long some patients go before being diagnosed correctly. There is one segment of a woman who went 10 yrs and saw many doctors and not one diagnosed her low B12. That is a sorry example of the quality of medical care in this country.

You have every right to be grumpy and angry! I get that way too!
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are 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.
mrsD is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
DesertFlower (04-20-2010)
Reply


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
raw food amit Peripheral Neuropathy 3 02-21-2010 03:14 PM
trying new food razzle51 Gluten Sensitivity / Celiac Disease 1 08-10-2009 07:37 PM
Favorite food and food you won't eat Earl Social Chat 46 04-28-2008 11:21 AM
The Future of Food BobbyB ALS 0 01-15-2007 02:32 PM


All times are GMT -5. The time now is 07:20 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.