"Those who fight Parkinson's with knowledge always find solutions" -Dr. Rana Dr. Rana is a world renowned Canadian Neurologist who is founder of the World Parkinson's Program (WPP). The World Parkinson's Program is a Canadian charitable organization which provides FREE medications, educational literature, and walking aids around the world to improve the lives of those affected with Parkinson's disease. Dr. Rana is the director of Parkinson's Clinic of Eastern Toronto, and is also the founder of Dr. Rana Parkinson's Foundation, which provides multilingual educational literature and lectures about Parkinson's disease. Dr. Rana strongly believes that educating Parkinson's patients about this condition helps them to improve their quality of lives.
NOTE: The information provided by us is ONLY for the educational purposes. You should follow the advice of your treating physician. We are not responsible for any consequences arising from use of any of the information.
‘‘I am not only happy am alive but also glad that "DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease(PD) with their herbal treatment. My smile is so bright because I am happy 😊..’’
I'm sorry my husband was diagnosed with Parkinson's disease almost 3 months ago and I totally disagree with you doctor. As a matter of fact a few of my husband's specialists have concurred to keep him off of meds for as long as possible. He exercises almost 45 mins a day and attends physical therapy. He's staying off of them hopefully for a long time
Sinemet made me sick so I stopped it. I take mega benfothiamine and magnesium theonate which help more than pharma drugs. You doctors should learn about more natural medicine.
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine🌿 🌿🌿from Dr Madida that truly works that helped treat, cure and reversed all his symptoms…My Dad is well again.
Great things Dr Madida on RU-vid has being doing for mankind, I undergo his Parkinson disease treatment plan for weeks and my Parkinson Disease was completely reversed...💫💫
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.
I can't exercise because of orthostatic hypotension. I am bedridden 90% of the time. I sleep from fatigue that is so bad I can't even stay awake most of the time. I haven't gotten a parkinsons diagnosis as of yet but I'm progressing quickly. I have a Dr apt soon and I will bring up parkinsons it runs in my family. As well as multiple sclerosis
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms•••My Dad is completely okay and healthy now..
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms••My Dad is completely okay and healthy now.
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.
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms•••My Dad is completely okay and healthy now.😊
I noticed Parkinson's symptoms about 10 years ago when my voice would "collapse" for no reason - and I was a public speaker! Now I have all the symptoms and refuse to take pharmas/meds when my doctor told me that one of the possible side effects of the pills he recommended I take was hallucinations. Oh, yeah. Sounds wonderful. I'm all about playing russian roulette with my consciousness.
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.
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 was diagnosed over four years ago and I am yet to take medication regularly. I will save it until I really need it and have developed other methods of managing my symptoms and slowing their progression. So far so good... I will not win this battle but I will fight it on *my* terms.
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!
The peptide treatment can induce alcohol reliance, this can lead to headaches in the morning, ( hangovers) …once you realize this, drinking water with the booze will lessen the hangover. Also restricted use of alcohol can reduce headaches. The nausea can be reduced by restricting use of peptides to a reasonable amount. Sleep 💤 is a symptom of the disease so try to start the day in 7am, and stay awake till noon.
Doing a nerve conduction soon, shaking fingers, i also said to the doctor that when im going to bed and lying on my back it feels like my body especially around my chest feels like its vibrating. My father had it, i guess i have to wait and see if its got me too
@@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.
Hey @denadavisteam4197 ... Ask your father's neurologist about the dosage of dopamine medication. Carbidopa/levodopa plays a role as it does tend to lower blood pressure, If reducing the dosage is possible, without negatively affecting the presence of PD symptoms, then a small reduction may help with your father's situation. Also, we with PD should be drinking at least six full 8 ounce glasses of water daily as this will tend to raise one's blood pressure throughout the day. This works for me.
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.
I have early Parkinson's at age 73, and have suffered with insomnia. I now use a grounding mat aka an "earthing mat" (amazon - earth and moon co. approx 60 dollars) to place my bare legs on for several hours while watching tv/reading before bed. It has helped me to get a good night's sleep of 7-8 hours for the past 2 weeks. Love it
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"
My dad has Parkinson’s, and he is constantly dizzy. The doctor seems to have no solution for it all though they have tried taking him off of blood pressure medicines. The problem he has is when he rises his blood pressure drops. Do you have any solutions for that . He fell and hit his head
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 ?
