Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 07-07-2009, 03:29 PM #21
Conductor71's Avatar
Conductor71 Conductor71 is offline
Senior Member
 
Join Date: Jul 2009
Location: Michigan
Posts: 1,474
10 yr Member
Conductor71 Conductor71 is offline
Senior Member
Conductor71's Avatar
 
Join Date: Jul 2009
Location: Michigan
Posts: 1,474
10 yr Member
Default

Quote:
Originally Posted by Damsee View Post
...

One thing I posted recently and that disappeared strangely enough is the need to have some global web place for personal effect/counter-effects of all experiments we make on ourselves.
i'm thinking about a web site that would collect all the stats/records of each one's experiments with plants/vitamins/medicines/molecules and allow us to better decide based on other's experiences and global stats.
What would you thing about that?

I'll keep you posted
Cheers

Damsee
Yes, I'm reviving an old post, but has anyone followed up this idea? I think it's a great suggestion. Not only would it help PWP but who knows how this data might be mined to aid research in the future?

- Laura
Conductor71 is offline   Reply With QuoteReply With Quote

advertisement
Old 07-07-2009, 05:13 PM #22
reverett123's Avatar
reverett123 reverett123 is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default

Quote:
Originally Posted by Conductor71 View Post
Yes, I'm reviving an old post, but has anyone followed up this idea? I think it's a great suggestion. Not only would it help PWP but who knows how this data might be mined to aid research in the future?

- Laura
This is one that I have intentions to follow up on eventually. The problem is how to get some standardization of data. I have my own website where I may host it, but it might fit in here as well. PLM lists what members claim to be taking but it is almost useless. I'll call it The White Rat Project.
__________________
Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
reverett123 is offline   Reply With QuoteReply With Quote
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
Mucuna warning! rosebud Parkinson's Disease 76 12-25-2010 10:41 AM
Mucuna and dyskinesia Tom5C Parkinson's Disease 18 09-05-2008 03:26 AM
mucuna clue? reverett123 Parkinson's Disease 1 08-01-2008 10:41 PM
Mucuna info Ibken Parkinson's Disease 1 05-23-2008 01:57 PM
Zandopa, Mucuna? sunflower4u Parkinson's Disease 0 12-12-2006 12:04 PM


All times are GMT -5. The time now is 06:21 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.