Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 05-22-2010, 02:18 PM #1
girija girija is offline
Member
 
Join Date: Nov 2006
Location: southern tip of west coast
Posts: 582
15 yr Member
girija girija is offline
Member
 
Join Date: Nov 2006
Location: southern tip of west coast
Posts: 582
15 yr Member
Default vit D

hi All,
After reading about Vit D and PD posted here, I had blood Vit D test done along with others tests. My blood Vit D is very low and it is considered a Vit D deficiency state. My neurologist agrees that could explain some of the problems I had in the last year. Unfortunately I dont have prior vit D values. I am on extra, mega doses of Vit D now and I am monitoring my symptoms.

I dont remember who posted about Vit D......whoever you are THANK YOU
Anyone else with a similar story?
Girija
girija is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
imark3000 (05-22-2010), Shake 'Em Up (05-24-2010)

advertisement
Old 05-22-2010, 03:14 PM #2
paula_w paula_w is offline
In Remembrance
 
Join Date: Aug 2006
Location: Florida
Posts: 3,904
15 yr Member
paula_w paula_w is offline
In Remembrance
 
Join Date: Aug 2006
Location: Florida
Posts: 3,904
15 yr Member
Default yes - identical

hi girija,

i just went thru exactly the same thing. Tested very low and taking 2000mg a day now. And you are in San Diego and I'm in Florida, both sunny places!

I went after reading about it so much here too.

paula
__________________
paula

"Time is not neutral for those who have pd or for those who will get it."
paula_w is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
girija (05-27-2010), imark3000 (05-22-2010), Shake 'Em Up (05-24-2010)
Old 05-26-2010, 09:07 AM #3
Jaye Jaye is offline
Member
 
Join Date: Aug 2006
Location: The Left Coast
Posts: 620
15 yr Member
Jaye Jaye is offline
Member
 
Join Date: Aug 2006
Location: The Left Coast
Posts: 620
15 yr Member
Default Sunshine used to be my nickname in high school!

I posted about vitamin D a couple of times in the last few months, but I was by no means the first to do so. A researcher of my acquaintance mentioned having my D level checked, and I had seen a scientific paper on it, too. i found several references to it in forum archives, too.

Sometimes it seems like we're all so intent on finding The Cure, or at least the Answer That Explains Everything, that we forget what we CAN do for ourselves NOW.

Vitamin D3 is the appropriate form of D to take, I was told, and it makes me feel noticeably better. My internist put me on 50,000 IU per week for six or eight weeks (I forget which), and then 1000 IU per day indefinitely.

If anyone reading is thinking of taking vitamin D, do please have it checked first, as too much is as harmful as too little.

Jaye
Jaye is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
girija (05-27-2010), violet green (05-28-2010)
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



All times are GMT -5. The time now is 02:03 PM.

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.