Rytary - update : Hi all! I hope everyone... - Cure Parkinson's

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Rytary - update

MissRita profile image
11 Replies

Hi all! I hope everyone is well!

? On Rytary - anyone have the following: constipation, gut distress/distention, massive insomnia, and heart racing?

I’m finding that I have to take 2, plus 1 capsule of Mucuna.

Interestingly enough and something that none of my doctors see as common is anal/rectal and gastric neuropathy. Any information is helpful!

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MissRita profile image
MissRita
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11 Replies
Tmarsella profile image
Tmarsella

What strength is your RYTARY? I start with MUCUNA at 3:am ish. And 195 RYTARY around 6-7am. Then RYTARY 145 3-4 hrs later, Then MUCUNA when needed before 3rd 145 around 2- 3pm then again around 6ish. Also B-1 thiamin , D-3, Mg, ALC, NAC, OM-3 with LND and 10 mg of Meltonin and ASPIRIN 81. L-serine and MANNITOL in am. No constipation. Dx 4 yrs, age 80

MissRita profile image
MissRita in reply to Tmarsella

Rytary 23.75-95 MG, i’m supposed to take up to six a day and I can barely take 4 because if I took any more I would never sleep. The insomnia and constipation are just brutal.. it’s bad enough that it makes my blood sugar dip and my blood pressure rise.

After some more research I did find out that levodopa carbidopa has a mild stimulant to it and there in lies the reason why any LC always makes my body tremor worse. .LC and Mucuna both make my heart race and give me a boost but quite frankly it’s like taking ADHD medication.

Hikoi profile image
Hikoi

What is gastric neuropathy?

MissRita profile image
MissRita in reply to Hikoi

Well think about neuropathy in your feet and your hands and now transfer that to the gastric portion of your body including the anal rectal area. It’s not fun.

Hikoi profile image
Hikoi in reply to MissRita

I think you are talking about what is common in PD - and I know as gastroparesis. It may be knon by both names or it may be different. I have trouble with the muscles not working in my gut but havent neuropathy type symptoms which I describe as tingling and numbness in my feet.and hands.

MissRita profile image
MissRita in reply to Hikoi

I do not have gastroparesis and I’ve been tested for it. I thought that was the case originally many months ago but after being tested for it and looked at for it they said I do not have it.

Hikoi profile image
Hikoi in reply to MissRita

Interesting! I have self diagnosed so how do they test.?

park_bear profile image
park_bear

High-dose thiamine restored my normal gut peristalsis. I discuss that and other things to remedy constipation here: healthunlocked.com/cure-par...

Also some useful comments.

MissRita profile image
MissRita in reply to park_bear

Thx!!

661marina profile image
661marina

About your gut distress: Have you been on any acid reducer prescriptions recently? I have those symptoms after being on Prilosec for about 6 months. It ended up being SIBO. If you don't get enough acid to digest your food, the food will ferment and rot in your small intestine. It causes horrible issues.

MissRita profile image
MissRita in reply to 661marina

Omg maybe!!! I’ve been taking papranizole which is the generic version of Prilosec. I’m going to try and see what happens. I wondered about that! Thank you so much for suggesting it.

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