CARBIDOPA AND LEVODOPA vs ENTACAPONE

Hello! Been awhile since I posted, but this reddit has also one of the greatest interim helps compared to some of the doctors I've visited. I just want to thank the docs ahead of time <3 33 male, 6 foot, 230 pounds Over the past few months (since late Jan), I've been oversalivating, difficulty sw

Help! Progressive neurological syndrome in 69M — possible MSA. Hello, I’m seeking advice regarding my 69-year-old father with progressive neurological symptoms since 2018. Aftet extensive testing, a second neurologist said it's almost certain it's MSA. **Patient:** * Male, 69 y/o * Onset: Feb 2018 *

I apologize if this is long. I truly do not know where else to go. My mom is 68. She was diagnosed with Parkinson’s in 2016 but may have had it a couple years before then. They do believe she has Parkinson’s dementia. She is on carbidopa and just started entacapone as the wearing off was very bad.

He’s just been prescribed this and am slowly phasing it in so he’ll be on 3 tablets a day on top of current meds. Not sure if they are helping much so far and also whether he’s just having a bad week, or the side effects are showing their lovely selves. I was told they could make him more confused a

Edit: Posted this in the wrong subreddit, mods took it down and made me post it over here. Made this post last night. Here is my life story and background into my experience with being a Parkinson’s caregiver. And I have about had it. Basically asking for any pointers/tips/help at this point. I (F23

I was diagnosed 2 years ago. Stuffness in my right extremities. Have been taking Rytary with entacapone and sometimes I feel like the meds do nothing. I haven't really progressed according to my neurologist. I exercise every day. 4 days a week of running and 3 of weight lifting. Anyone had a simila

At this week's checkup the MDS asked if I wanted to try entacapone for extending 'on' time. We already do a mix of regular and ER C/L. Her only concern was that it might worsen issues with excessive daytime sleepiness. If you've tried it, or if you provide care to someone who has, what was the exper

Hi everyone – hoping to get some perspective from others who’ve been through similar medication changes with Parkinson’s. My dad was diagnosed with Parkinson’s about 2 years ago. His pattern has mostly been motor-predominant PD with freezing of gait (FOG) as his main issue – especially when starting

I have been on this new ‘journey’ for months now. I am 6 months postpartum with my third child and about 3 months ago I developed rashes around my eyes and all over my arms and hands. I had sudden weight gain/inflammation. Went to check basic labs and of course everything was ‘normal’. Went back 2 w