I'm starting to think something isn't working as it should- should I ask to have meds changed as I'm not able to increase Requip (almost at max dose)
Honestly @A MyParkinsonsTeam Member, there is so much going on in the body that affects how we respond to the meds. We should be keeping a detailed log of what we eat, when we take our meds, when we drink coffee, (alcohol), exercise, go to sleep, etc. A friend finds that taking protein with her tablets has a negative impact.
I am one who as changed meds, the process was interesting as I was weaned off the one drug (Ropinirole) and slowly introduced to the new drug (Pramipexole). I felt pretty good on the lower doses.
wishing you well on your journey!
I've been to see the Neuro and he's put me in Entacapone to "boost" my Levodopa (Madopar) I assume I'll stop Madopar and start on Stalevo but who knows?
Thanks Keith, I've got Neurologu this Friday and Parkinson's Nurse the week after - was just wondering if anyone has been / or still is in the same position
Hi @A MyParkinsonsTeam Member, best to speak to your Parkinson's Nurse or neurologist.