advertisement
Reply
 
Thread Tools Display Modes
Old 02-23-2012, 08:45 AM #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 New genetic information on Vit D and MS:

This was posted today, on the PD forum.

Olsen always posts interesting things IMO.

http://neurotalk.psychcentral.com/thread165433.html

How this will translate to patients at the doctors clinically
is not yet explained.

But for MSers with MS in the family, it is interesting.
Active Vit D is available in a capsule, RX Rocaltrol.
__________________
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:
ANNagain (02-23-2012), Dejibo (02-23-2012), Jappy (02-24-2012), Natalie8 (02-26-2012), SallyC (02-23-2012)

advertisement
Old 02-26-2012, 01:54 AM #2
Natalie8's Avatar
Natalie8 Natalie8 is offline
Member
 
Join Date: Apr 2008
Posts: 900
15 yr Member
Natalie8 Natalie8 is offline
Member
Natalie8's Avatar
 
Join Date: Apr 2008
Posts: 900
15 yr Member
Default

Thanks for sharing this! I have MS and my mother has MS. I have been trying to get my sister to take Vitamin D (and get her level tested). But I think she is too afraid. Anyhow, I'll pass this along.
__________________
On Tysabri and love it.
.
Natalie8 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SallyC (02-26-2012)
Old 02-26-2012, 12:42 PM #3
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

I'm taking my D3 5000 daily and hope it's helping?????????
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Natalie8 (02-26-2012)
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
B 12 information skyspirit Multiple Sclerosis 8 04-30-2014 05:54 PM
does anyone have information about RSD maryam71 General Health Conditions & Rare Disorders 1 07-31-2009 11:28 PM
23 and me genetic analysis information paula_w Parkinson's Disease 28 04-15-2009 01:00 AM
Insurance Companies Should Have Access To Genetic Information Stitcher Parkinson's Disease 1 06-10-2007 06:12 AM


All times are GMT -5. The time now is 01:48 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.