u/fireworks1985

That's it, in the title: What's the difference between a $5k Theracycle and a 200$ recumbent bike from amazon? TIA

That's it, in the title: What's the difference between a $5k Theracycle and a 200$ recumbent bike from amazon? What does "forced" mean? TIA!!

i know that when you're medicated with levodopa, (i'm taking the "regular" rx, not extended release) your symptoms are meant to be suppressed, ideally. then when the meds wear off, the symptoms may reappear. but when i forget to take my meds, i don't feel ANY different than when i take them every 4 or 5 hrs...?? i am 59 y/o F, diagnosed less than a year ago & medicated for about half a year. i'm just wondering why i don't see any return of symptoms even if i only take the levodopa twice (instead of thrice) daily. [symptoms prior to medication=slightly altered gait (can't be any more clear than that, it just felt "weird" when i walked); slowness of movement (i ate REALLY slowly); stiffness (like when moving out of a corner i took many small steps instead of just walking out like a normal person); lack of arm swing when walking; & it was hard to brush my teeth] but when i miss a dose, i still can brush my teeth fine & don't notice any change in gait, my arms swing fine. husband said, Maybe the effects of the meds are cumulative? but i told him NO that's not what i keep reading. am i mistaken? i almost want to stop the meds to see what i notice but i think my neuro wouldn't like that! any insight is welcome! TIA

diagnosed in august of last year, 58 y/o then, now 59. cried at diagnostic appointment, got 2nd opinion (& confirmed with dat scan) & after a while thought i was getting close to accepting my "new reality." but i'm still having problems believing that this is my future. i'm grieving the loss of the future i was looking forward to, retiring as a somewhat fit & healthy "older" lady. now i'll be a less fit...shaky? stiff? falling? older lady. neurologist called my case "mild" now, & said it WILL get worse but there's no way to predict how fast nor how bad symptoms will progress. i keep reminding myself that i was gonna get less mobile & old lady-ish anyways (due to just plain age/gravity/decrepitness) AND that i shouldn't assume the worst AND that i should enjoy the fact that right now i'm not shaking, i'm not stiff (after starting levodopa), no one could guess i've got this. but in the dark moments it's very hard not to worry. i'm prone to pre-worrying anyways, so here we are. and yes, i know that there's no value in assuming the worst, & i know i have to exercise, & i know stress makes things worse. what's my point here? there is no point! (see the orange bar above, it says rant!) i'm just putting this here coz i don't know anyone with PD & i can't keep complaining to my husband, i feel bad enough for him. to be clear: i'm only seeking commiseration, as misery loves company. thanks for listening! sorry for rambling...

In the new episodes, the first responding uniform keeps telling the detectives that MLI found blah blah. Who is MLI?

Past experience tells me I should lead with this: I'm not seeking advice (thus, not flaired with "Questions/Advice") just asking if this is typical. I know, I know, everyone is different. Having said that: About 4 or 5 pm of a work day I feel like I could fall asleep in my Archie Bunker chair. I probably shouldn't sit in a recliner then, but...I think I could go to bed w/o dinner & just fall asleep if I let myself. Now, at my age 58F, I play that fun game of: Is this PD? Or menopause? Or just old age? (Or am I sick!?) Doesn't help that aforementioned work day is teaching 2nd grade. Isn't fatigue a symptom of PD? I read that your body gets tired due to all the movements, but I have very minimal physical symptoms--no tremors, just slow moving w/o meds & occasional (usual night time) mild spasms so...? Anyone with me? Just asking coz you're the only people with PD that I know!! (Have not "come out" yet IRL) THANKS!

The ONE common thread when researching PD is that patients MUST exercise if you have any hope of coping with symptoms. So, after the initial shock of the diagnosis, I started doing so full speed ahead. But two things are bugging the heck out of me: 1) I'm 99 percent sure I'm NOT exercising (I run/walk/run & elliptical) at the recommended 80-85% heart rate AND 2) When I don't exercise at all some days due to fatigue and/or apathy I feel VERY guilty, like I'm not fulfilling my required treatment. Not looking for advice, as I know the solution is: JUST DO IT, I guess I'm looking for commiseration ,,, does anyone else feel like this sometimes? TIA!