Parkinson's Disease Tulip


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 05-17-2015, 06:59 PM #1
leonore leonore is offline
Junior Member
 
Join Date: Apr 2008
Location: Brooklyn, NY
Posts: 57
15 yr Member
leonore leonore is offline
Junior Member
 
Join Date: Apr 2008
Location: Brooklyn, NY
Posts: 57
15 yr Member
Tongue Rytary: Success? If so, how? I'm stumped

I'm having a tough time making Rytary work for me, but so want it to! With 16 years of PD under my belt, and Stalevo 75 or 50 (plus Azilect and Tasmar) every two hours, I was hoping Rytary would give me longer On's and gradually replace Stalevo. Well, not so fast!
I was doing pretty well without Rytary until late afternoon, with pretty good on's, assisted by 3 miles daily on exercise bike, plus high-intensity bursts making my On's even better. But.... my unpredictable, fluctuating Offs were bad in the evenings, even after a nap, (which help sometimes.)
So I decided to try the highly touted Rytary,under my neuro's supervision, beginning with a week of replacing 2 pm Stalevo with Rytary, next week replacing a 4 pm Stalevo with Rytary, etc.
Well, the first week, and still now by the fourth week, Rytary takes a good 4 hours to kick in, and thus I get a terrible Off until my next planned dose of Stalevo 2 hours later. Adding a second dose at 4 pm meant I was Off for 2 doses, so I went back to one per day, and played with the timing, switching my dose to 6 pm or 8 pm. It does seem to last about 3 & 1/2 hours when it finally works, and I think that the next day, my On's are better.
But I can't bear the 2 Off hours until it kicks in, and then I get bad dyskinesias when it does. I tried taking it at 4 am, but ended up with awful dyskinesias which kept me awake, and dyskinetic throughout the next day.
Anyone???
__________________
“WHEN I DARE TO BE POWERFUL, TO USE MY STRENGTH IN THE SERVICE OF MY VISION, THEN IT BECOMES LESS AND LESS IMPORTANT WHETHER OR NOT I AM AFRAID.”
Audre Lorde: (1934-1992) African American, lesbian-writer/poet/warrior, who gave us the gift of her courage, before cancer stole her away
leonore is offline   Reply With QuoteReply With Quote
 


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
Stalevo - Stumped rd42 Parkinson's Disease 30 08-28-2009 08:20 AM
Stumped and Looking for Answers rossy Epilepsy 1 08-02-2009 11:31 AM
Still stumped dmplaura Multiple Sclerosis 9 08-27-2008 08:28 AM
Stumped watsonsh Computers and Technology 4 07-11-2007 11:55 PM
Stumped again jamietwo Gluten Sensitivity / Celiac Disease 5 11-18-2006 03:49 PM


All times are GMT -5. The time now is 01:35 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.