I’m not on the meds and have no tremors. This Doctor probably speaks for the Pharmaceutical companies

I think this bull crap because… 1. 99.99% of doctors and researchers say PD can’t be cured (dead brain cells are permanently dead) 2. How do you know your Parkinson’s is “completely reversed”? I dare you to answer this.

What’s the name of the medicine for your dad Parkinson’s

Click and search #DrMadida for medicine.

What is the medicine name? dophamine?

Immensely!! My husband exercises 45 minutes to an hour a day and he's doing pretty well, along with vitamin supplementation.

Which medicine u got

Please tell me I wanna see if my dad would be a good candidate, I’m suffering watching my biggest hero suffer 😢

It's not fair that you build hope and leave everyone hanging. Please disclose the treatment/medicine that you got. It will definitely help someone. Thanks 🙏

I think these comments are some sort of spam, guys. I see them on a lot of Parkinsons video commentary and they never elaborate. No idea why they even post them 🤷

@@KN-bx9nt you are unwise and know nothing. Why won’t I voluntarily tell people about what can help them. I know how terrible this disease are and how my Dad suffered with it before he got cured. You are just a hater and devil incarnate.

Hi can u tell me the medication please it will be very helpful for my father also

What did you do to get rid of the symptoms. I'd love to help my brother

Click and search #DrMadida for medicine...

Ive seen same comment on other threads. Might be selling a miracle

Can you pl advise the treatment you have to your father and he became alright.. Jaiswal

Funny you should bring this up at this time. My long-time partner, Theresa, who is 85 was diagnosed with Parkinsons about a year ago. She was "freezing" up when going from one room to another quite often. They started her on Sinemet. One tablet 3 times a day. It stopped the freezing symptom within 3 weeks and she continues with no "freezing" of gait. Never had any tremors to speak of. They wanted her to increase the dose to 1.5 tablets, 3 times a day for several weeks, and then 2 tablets 3 times a day. We declined,, as the "freezing gait" did not return on the 1 tablet, 3 times a day. However, late this fall (October of 2023) she had several episodes of thinking our cat who died 2 years ago was in the house. Also, one day she opened up the back door and called for him. She also thought two of her grown children were in the next room on several occasions. I then made an appointment with the physician's assistant and told her about these hallucinations. She said the Sinement could be the cause of it. even at this low dose. She said to cut back the third dose of the day to a 1/2 tablet for several weeks. If the hallucinations do not return, eliminate the third daily dose completely. If the gait freezing comes back resume the third daily dose, from none to 1/2 tablet, and report back. Everyone with this disease is different I guess.

A tip: Be more active, do more fast walking and avoid slips. Just never get bedridden or wheelchair bound

At long last someone I can relate to. My sentiments exactly. I was told take this but didn’t forget your anti nausea tablets first. I have Diazepam 10 mg as a muscle relaxant, Pregabalin 6 / 10 mg daily for nerve pain, Zopiclone 2/ 7.5 as a night time sedation 15 mg Methadone as pain relief and Mitazapine as an antidepressant. Of cause you cannot drive or operate machinery. These meds taken at a much lower dose would guarantee a great nights sleep minus the hallucinations. Stops all shakes , . I feel fine . My symptoms are minimal and under control. I have started watching everyone taking pd meds, I was shocked . I do know it’s a progressive disease but listening to a poorly man talk about loosing the muscle in his tongue and fearing he may choke to death doesn’t lift one’s spirits. I was diagnosed in Nov 2017 . I cannot understand why a cure hasn’t been found. My son thinks it’s because the disease is associated with elderly men with one foot in the Grave.

I think Theresa is a fortunate lady to be diagnosed at 85 . ❤

This is a superb comment. I take a similar approach for similar reasons. If you simply mask symptoms you can’t learn to manage those symptoms. Still, I’ve learned I can’t manage without medicine. A diabetic can’t substitute will-power for insulin. PD treatment isn’t a one-size-fits-all thing. Do what fits YOU!

How are u now??

@@kookpg7629 Im doing ok, Nerve conduction showed reduced signal going to my hands, but its due to the ulnar nerve. Still get numb in my hands but the shaking has reduced. The muscle spasms have reduced through out my body too. Regarding my back, turns out i have re activation of bone marrow in my back still unclear what that means seeing a specialists soon, as well as a couple of bulging discs.

So this doc is saying patients will freeze up and die. That hasn’t happened to my neighbour or to my aunt. The late stage of the disease would be different of course. Yes this doc would be a great undertaker.

It works for me. It might not work for you if you were misdiagnosed as having Parkinson's.

People in their 50s these days don't seem to realize that supporting two generations of people (grandparents and parents) is a lot of work. Especially when most of today's generation won't have kids to "pawn it off"

!

Get up very slow while holding on to something. If dizziness occurs, sir back down. I never get straight up from a lying position. Sit on the side of the bed for awhile to see if you're dizzy or light headed. Slow down and think how you are feeling before getting up. Good luck.

Hello Lindsay. I just read your comment. Am commenting from Nigeria. My dad is suffering from Parkinson's, Diabetes, prostate etc etc. Which has caused UTI. The frequent urination is a source of worry, as my mum is overly burden. Most nights, when I visit, I find myself having to stay awake all night because I have to take my dad to the bathroom to urinate. Pls from your experience, is there anything we can do to lessen the burden ?