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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.

Does Anyone Take Rytary For Their Parkinsons

Does Anyone Take Rytary For Their Parkinsons

posted 17 days ago
A MyParkinsonsTeam Member said:

If you are interested in what I have please message me. Last I checked without ins. It was @1200.00 per month with my insurance I think it was @4or5 hundred a month.

posted 16 days ago
A MyParkinsonsTeam Member said:

Didn’t work for my husband.

posted 9 days ago
A MyParkinsonsTeam Member said:

never heard of it

posted 16 days ago
A MyParkinsonsTeam Member said:

Hi Carolyn... I'm new here so don't know the ropes yet. Sorry to hear about your husband. I have helped two of my friends who lost their husbands. A grief support group is very helpful. My prayers are with you.. . My husband Bill is on Rytary 48.75, three times/day, along with C/L The doctor gave him samples. She said it is very expensive. I called my insurance, but they said it is not in their formulary. The doctor has to send in the script and then they will review it and let me know how much it will cost. The doctor also said I can apply to the drug company to see if they will be able to help. ♥️

posted 16 days ago
A MyParkinsonsTeam Member said:

The reason I ask is , my husband took it before he passed away last week. I have several bottles totally unopened and wanted to see if anyone could use it. If I send them back they will just throw them away.

posted 17 days ago
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