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Real members of MyParkinsonsTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
September 6, 2025
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A MyParkinsonsTeam Member

Have you talked to your doctor about Duopa, it's Carbo/Levodopa in a suspension form that comes in cartridges and they are then hooked to a pump, which feeds you medicine throughout the day. It does require having a jpeg tube placed in your abdomen but that is a small price to pay if it works for you like it has for me. ABBVIE has a website on it called DUOPA.COM
Check it out. If you think it might be right for you, contact me on here and I will share my experience with Duopa. I've had it since October 2022. I don't know what your symptoms are, but I was on 24 pills a day and was only getting 10 "on time" from each dose. My off periods were alot more prevaalent than my "on period". It has made life so much better. I pray this helps you. They also have mentors that you can call and talk to, that should be able to answer you questions. But, again, I am happy to share my story with you. Just contact me🙏💕

September 6, 2025
A MyParkinsonsTeam Member

Thank you Anita. It's my husband, Ed who has PD. I’m his wife and caregiver.

September 7, 2025 (edited)
A MyParkinsonsTeam Member

CherylJollie I am sorry that you are having a hard time. You will be in my prayers. Hugs and I pray they find something that works for you.🙏🫂🙏

September 7, 2025
A MyParkinsonsTeam Member

Thank you. Yes, have been on Duopa for 18 months. Duopa was not working as well as it did initially, so tried the Vyalev. Vyalev didn’t work, so back on Duopa. Problem is, many days dyskinesia starts up early in the day, so have to stop the Duopa, then off time sets in. Can usually restart the Duopa and extend day a little longer. Have tried reducing continuous rate to prevent too much build up, sometimes this works and sometimes it doesn’t. Every day is it’s on day and not one day is the same. I’m living a life of predictable unpredictability. There is Apokyn, Doctor recommend, although many side effects associated with the medication. One day at a time is what’s left. Hoping for a miracle and cure for this dreadful disease.

September 7, 2025
MyParkinsonsTeam

When Parkinson's medications aren't providing adequate symptom control, there are several potential options to discuss with your neurologist:

Here are some medication adjustment strategies
• Modifying [[treatment:levodopa/carbidopa:55d534f51fcaa397470006dd]] timing or dosage to reduce "wearing-off" periods
• Adding Show Full Answer

When Parkinson's medications aren't providing adequate symptom control, there are several potential options to discuss with your neurologist:

Here are some medication adjustment strategies:
• Modifying [[treatment:levodopa/carbidopa:55d534f51fcaa397470006dd]] timing or dosage to reduce "wearing-off" periods
• Adding medications like rasagiline or entacapone to extend dopamine activity
• Trying amantadine to help control involuntary movements
• Considering clozapine for hallucinations management
• Exploring sleep medications like clonazepam or melatonin if needed For those with advanced Parkinson's, device-assisted therapies may be worth exploring:
• Continuous [[treatment:levodopa/carbidopa:55d534f51fcaa397470006dd]] infusion pump delivery to the small intestine
• Apomorphine infusion or injection for "off" periods

Remember to always discuss any treatment changes with your healthcare provider to determine the best path forward based on your specific symptoms and needs.

September 6, 2025

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