Has anyone with PFS been diagnosed with Parkinson's disease?

My biggest scare is Propecia has given me Parkinson’s disease. I have NOT been diagnosed but do plan on seeing a neurologist. I quit 8 months ago. The twitching in my hands and forearms was really bad and yes was worse as I slept. The type of twitching I had was my hands would suddenly shake for a moment as I slept and my shoulder, lower back, or leg would jolt. Those decreased a lot over time and the shaking hands during sleep is totally gone. Now I am suddenly getting muscle twitches all over my body day and night, and once in a while I get that “pill rolling twitch” that is known as an early sign of Parkinson’s disease and it really scares me. It’s not constant and only happens for a min or two every couple of weeks. My hands and feet hurt like they have arthritis. My forehead gets greasy from time to time as well. I am terrified. My forearms, wrists, and hands always feel weak. So weak that one time my right hand started shaking just holding a beer. Another time my right hand started shaking while I had it leaning against a laptop, below the keyboard.

Other than that I can deal with the rest, my penis functions just fine. In the beginning I had reduced semen but that appears to be better now, even though my wife has had 2 miscarriages since I quit. I did get eye floaters, that really sucks but I can deal with it. Sometimes my eyes get stabbing pains.

The list of things that has happened to me over the last 8 months seems endless. In the beginning I had a very scary situation with my throat. It would start involuntarily swallowing in my sleep. In addition I would start taking a sudden involuntary deep breath during sleep. The swallowing thing went away and the sudden breaths got much less frequent and sever however once in a while as I sleep the involuntary breath will still happen on a lesser scale. At one point when I dried my left ankle after a shower the towel felt like it was ripping off my skin. At one point I had moments of sudden tingling running through my head, down my spine through my feet, itchy skin, I would get hot flashes down my right leg. Those all got better though. In the last 2 months I developed tinnitus (constant ringing in my left ear) but that now is starting to get less, it comes and goes. In the beginning I could not sleep, I would dream non stop and hear song lyrics playing over and over in my head. One time I woke up from a dream where my head felt like it was exploding. I would have light flashes in my closed eyes as I slept. Those have passed as well. However I still dream all night but I sleep well. I feel like it is much easier these days for my arms to “fall asleep” when I sleep. I’ll wake up and my hand will have partial pins and needles that go away if I reposition of shake it off. I can cause my biceps to twitch if I flex them really hard. After I flex, they will twitch for a couple of min. Another thing that comes and goes is I’ll feel like more should be coming out when I take a crap. I don’t feel constipated, but just feels like there should be more. I have high blood pressure and have gained 30-40 pounds cause I am too depressed to work out anymore. I try very hard to remain positive and every time I get a new side I stay positive that it will pass like most all of them have. I tell myself this is just another thing from PFS and I don’t have a deadly disease. Ultimately I am just terrified that I have early onset of Parkinson’s and that’s what terrifies the most. I keep telling myself in 5 years this will all be in the past.

Any response would be greatly appreciated, thank you so much.

Robin Williams was on Finasteride and also diagnosed with Parkinson’s disease. Im worried about this as well because ive noticed my hand shaking on a few different occasions.

Is there proof he was on Fin?

Yes it was listed on his tox report. They of course didn’t think it had anything to do with his death.