My dad [M69] had been taking ReQuip since his diagnosis over 7 years ago and has had a good quality of life at a 12mg dose (4mg x 3 times a day) in addition to his usual Madopar dose. Since May 2024 he was tapered down to a single 4mg dose in the morning to combat his dyskenisia but now experiences debilitating freezing and fatigue. I have reached out to his specialists but some 2 have retired and the PD nurse was the one who recommended the change of dose and will follow-up with him by telephone in 1 year.

Does anyone else think this is a mistake or had a similar experience with ReQuip?

I understand ReQuip is immediate release so not having a consistent dose throuought the day seems unorthodox and he is displaying symptoms of withdrawal (DAWS). I'd like to get my dad back to a manageable state as his quality of life has dropped significantly since the change.

He has tried a slow release option (Ipinia) but it had adverse side effects. I am pressing for more attention from the professionals but would love to hear from this great community. Thank you and blessings xo