If you look at someone’s profile there’s a part that says what meds they’ve been on and the side effects

@A MyParkinsonsTeam Member, I have been diagnosed 19 years and presently take carbidopa/levodopa plus Ropinirole & Amantadine. If you read side effects of practically any medicine, not just Parkinson's, you will never take any medicine. It's like GinnyJ said you have to get a doctor you trust. I was tried on Rasagline, but had side effects and had to stop taking it, but side effects went away. Every medicine has "potential" side effects. With this disease we are all going through trial and error one day at a time. Depend on the doctor to prescribe and find what works for you, but, ultimately put your faith and trust in the Lord!!!

Love & prayers in Christ, .Robert

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A MyParki...

@A MyParkinsonsTeam Member ... HELLO my Friend, l'm sorry not to have responded sooner, but alot has been going on, And to be honest, I've just felt like, giving up..? At times..? My Laptop, Crashed on me.? Then my phone got wet, and l had to get a new one, 3-Days after that, l knocked the new one off in a bucket of liquid, l had by the side of my bed...? Luckily by the Grace of God, l had a screen protector and case for it, and grabbed it and took it apart really quick and it was alil wet inside, but it still works, but bot that good ? Anyway you asked who was on sinimet ? I take it, alot, that's All I take for the PARKINSON'S DISEASE , l take 25/100 every 2-Hours, and One 50/200 CR, AT BEDTIME.
I ALSO HAVE A DEEP BRAIN STIMULATOR, ON Both sides of my brain. I used to take several different types of med medications, but I didn't like the side effects, SO l hyst slowly cut them out and I found l didn't really need them, and actually I have been able to fun better, with out all the 3ztra, garbage they had me on.

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A MyParki...

I take carbodah 1and1half tablets 4 x a d really helps.

There’s also a spot on the site for drs that people have had