Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 09-07-2012, 08:30 AM #1
Jim091866 Jim091866 is offline
Member
 
Join Date: Oct 2006
Location: Central Florida
Posts: 520
15 yr Member
Jim091866 Jim091866 is offline
Member
 
Join Date: Oct 2006
Location: Central Florida
Posts: 520
15 yr Member
Default Do you ever stop responding to levodopa?

I wonder if the body ever stops responding to levodopa. I have seemed to find a somewhat consistent timing and dosage of my levodopa (generic by Teva) that I can be relatively stable at w/o dyskinesia or a great amount of off time. Believe it or not if I do feel off or a little bit stiff I have confidence that it is just a while and my body will respond. In thinking of the long term does the body ever stop responding to levodopa. My reasoning is surely I will have to increase the dose as time goes on but does the body ever NOT respond to the med? I guess that you could probably reach a point where the slightest bit of overmedication would cause dyskinesia but that is a response-No? So do you ever develop non responsive Parkinson's where you are just off? Wouldn't want to find out.
For those that are wondering I take 1 1/2 25/100 when I get up then 1 tab every hour. It's a little bit at a time and I stay loose and dont get dyskinetic. My thinking is the medication stays in my body for about an hour. So in the morning I "prime" my body with an hour and half's medication. Then I maintain that level throughout the day. I use the alarm on my phone. I don't have the ups and downs of a roller coaster as if I were trying to spread out the doseage.
Jim091866 is offline   Reply With QuoteReply With Quote

advertisement
Old 09-07-2012, 08:42 AM #2
Jim091866 Jim091866 is offline
Member
 
Join Date: Oct 2006
Location: Central Florida
Posts: 520
15 yr Member
Jim091866 Jim091866 is offline
Member
 
Join Date: Oct 2006
Location: Central Florida
Posts: 520
15 yr Member
Smile I wanted to add...

This only seems to make sense. A little bit at a consistent level. Duh? I have even gone out on short errands and forgot my walker at home. It is a little bit harder to keep up with the pills and alarms but I got used to it. When the alarm goes off I take a pill and erase that alarm. If I am wondering
"did I take that pill or not", which seems to be the biggest problem, I look to see if the alarm has been erased. I also have a daily diary icon on my phone where I log in 0930 and put xxx's for the 930 medication. Hey, it works for me. Another benefit I have found is that I pretty much don't have to worry about what I eat, the next dose is only at most an hour away.
Jim091866 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
Drug interactions of Coumadin, Comtan, Carbidopa And Levodopa, Carbidopa And Levodopa lou_lou Parkinson's Disease 0 06-23-2011 11:50 PM
Not responding to simulus! Numbnow Traumatic Brain Injury and Post Concussion Syndrome 2 12-22-2008 08:41 PM
Partner not responding to Stimulus Numbnow New Member Introductions 4 12-22-2008 10:47 AM
responding to a neurotalk forward email DiMarie Community & Forum Feedback 6 03-21-2007 12:54 PM


All times are GMT -5. The time now is 02:51 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.