← Return to Is anyone using Rytary?

Discussion

Is anyone using Rytary?

Parkinson's Disease | Last Active: Oct 15, 2023 | Replies (82)

Comment receiving replies
@dianalee

Yes, I am a Caregiver Partner for someone with PD...And with the financial assistance of the PAN Foundation I was able to get Rytary for him with no out of pocket $$$...He has gone from a frequency of Sinemet and Comtan every 2+ hrs, to Rytary every 4-5 hrs...for us, it has been a "win win."

Jump to this post


Replies to "Yes, I am a Caregiver Partner for someone with PD...And with the financial assistance of the..."

Hello @dianalee

I see this is your first post. Welcome to Mayo Connect!
Thank you for sharing about Rytary. Thanks also for sharing information about financial assistance through the PAN Foundation. Good information for us all. I would also encourage to join Connect's Caregivers discussion group.

Who or where does one call or email for the connection with the PAN Foundation to get Rytary with no out of pocket $$$? It is very expensive; just paid $367. for 30 days for a regimen of 4 MG95 capsules (I'm in the doughnut hole right now, and will be paying $1,100. per 90-day period. Right now my neurologist is touting its benefits, buy so far (after 8 weeks, or so, on the drug) I am feeling so-so,only.