What are the different stages of Parkinson's disease?
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- เผยแพร่เมื่อ 12 พ.ย. 2019
- For more information on this topic, visit the Parkinson's Foundation website: www.parkinson.org/Understandi...
Parkinson’s disease (PD) impacts people in different ways. Not everyone will experience all the symptoms of Parkinson’s, and if they do, they won’t necessarily experience them in quite the same order or at the same intensity. There are typical patterns of progression in Parkinson’s disease that are defined in stages. Joseph Jankovic, MD discusses those patterns in terms of the forms and stags of Parkinson's disease.
Helpful resources:
- Parkinson’s Foundation Helpline: 1-800-4PD-INFO (1-800-473-4636) | Helpline@Parkinson.org | www.parkinson.org/resources-s...
- Resources for those who are new to Parkinson’s disease: www.parkinson.org/living-with-parkinsons/new-to-parkinsons
- Aware in Care hospital safety kit: www.parkinson.org/resources-s...
- PD Health @ Home programs: www.parkinson.org/resources-s...
- Información en español: www.parkinson.org/espanol
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What is the Parkinson’s Foundation?
The Parkinson’s Foundation makes life better for people with Parkinson’s disease (PD) by improving care and advancing research toward a cure. In everything we do, we build on the energy, experience and passion of our global Parkinson’s community. Learn more on our website: www.parkinson.org/
Excellent video explaining the stages of Parkinson's
Me
Se puede escuchar en español
@@charleneanderson6137 😅
My husband who had been diagnosed with Parkinson’s disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from natural herbs centre . com after undergoing their Parkinson’s natural protocol. God Bless all Parkinson’s Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.
I would have helped to know this about 55 years ago when my father developed PD. Useful video.
It is total suffering from Stage 2 onwards. This might help. Take Vitamin B1 to tackle jerking body, quivering mouth and tightening of toe muscles.
For my case I usually take 2 tablets each time, once a week.
There are times, seldom, I take 2 tablets each time twice a week.
We are developing and researching the benefits of infrared laser therapy on the gut and back of neck - to assist with PD symptoms - stimulate the gut brain axis - and improve sleep, motor skills, mood, sense of smell and the very common gut issues associated with PD. The PDCare Laser is used 3 times a week for 20 minutes only - and is approved in Europe and Australia/NZ.
Excellent video, thank you.
Excellent! Terrifying, so appreciated!
Parkinson’s, in and of itself, is not fatal. 80% of PD patients develop dementia, and that IS fatal. Unfortunately, some PD medications can cause cognitive impairment.
I’m not a doctor, but I played one at home caring for my wife for over 17 years who had Parkinson’s, and later developed dementia.
I'm sorry to hear that about your wife. I was diagnosed fairly young (33) with severe obstructive sleep apnea. I'm not overweight and it does not run in my family, neither does PD. However, a year after my OBSA diagnosis, I've noticed internal tremors, trouble handwriting and foggy cognitive ability. Also, staring off into the distance, and not really wanting to socialize with anyone other than close friends(maybe because I'm just getting older) These things are what led me here, where I am trying to learn what early onset PD symptoms people have noticed. My great grandmother died at the age of 78 from dimentia. I'm trying to piece this all together. My diet isn't perfect but I would say it is good. I guess in the end it doesn't matter, there is no cure for PD and only treatment. So I guess just wait until things become bad, like loosing my balance often, or not being able to move very well, before going to see a doctor.
@@bobscott7253 What are the most dangerous foods to stay away from that makes PD worse? I hope they don't include my occasional pleasures (like oatmeal-raisin cookies and ice cream)
Appreciate your kindness.
@@htunlin2000 Thank you for your curiosity for inquiring that I may supply you with more information that could be beneficial. Here’s an “Actual Factual.” If you have Parkinson’s remember, you die WITH Parkinson’s, not FROM it. In very advanced cases, difficulty in swallowing can cause patients to aspirate food into the lungs thereby leading to pneumonia or other pulmonary conditions. Also, 80% of PD patients develop dementia, which is fatal.
As for your question regarding what foods you should eliminate in your diet, no artificial sweeteners. If you are a soda drinker, STOP IT! They are full of toxins, and one of the worst things you can put into your body, ESPECIALLY, if you have PD. Water is the best drink on the planet you can put in body. It hydrates every cell and lubricants the joints. If you are a smoker, QUIT! I don’t have to tell you cigarettes are toxic and full of carcinogens. Of course eating organic (which is expensive) is the best way to go. Eating foods that are rich in antioxidants are also very beneficial. Dark leafy veggies, fruits like blueberries and cranberries are especially good.
Grains, nuts, dark chocolate, and kidney beans are beneficial.
Consider your intake of Omega-3 fatty acids, and vitamin D, the “sunshine vitamin.” Consider supplementing with calcium to help maintain strong bones, to minimize breaks from falls, oh yes, falls are inevitable.
Here’s a tip that really helped my wife with her walking. Get a song in your mind and walking to the beat or rhythm will help your stride and gait. It helps with “freezing.”
Familiarize yourself with obstacles around the house, this will help you negotiate your movements.
Exercising is very important. I can’t stress that enough. The old saying, “use it or loose it,” should not be ignored. Any exercise is better than none in preventing joint stiffness. Just stretching can be beneficial.
If you play an instrument, that can be relaxing and relieves stress. ***Learn to laugh more, laughter is a natural antidepressant and stress reliever*** Doing crossword puzzles can force the brain to focus and improve memory.
Develop a routine, make it a habit….BE DILIGENT!
As I’ve said before, I’m not a doctor, but I played one at home, and my wife’s neurologist was very impressed from the knowledge I gained from extensive research. HOWEVER, consult your doctor before starting any of what I’ve suggested. But, I truly believe starting this kind of regiment may slow down the progression of PD going from one stage to the next.
I’m not going to sugar coat it, but my heart goes out to you for the many challenges and frustrations that lie ahead. Be prepared for mood swings, usually caused by some medications, but recognizing these aspects will allow you to better cope with your unfortunate disease. Lean on the LORD for strength and endurance, and He will get you through this. I hope I’ve given you a lot of food for thought, and yes, an occasional cookie or ice cream won’t hurt…..unless of course you’re also diabetic. If you’re not, you deserve to treat yourself.
God bless
@@bobscott7253 Thanks for the great advice from your personal experience. I'm going to print it and put it on the refrigerator door as a daily reminder.
What's the most scary is my throat gets lazy and sometimes I have to consciously remind myself to swallow or I start choking on my own saliva seeping into my windpipe, causing severe coughing.
I had to reduce any source of distractions when I am focusing on a task, or I worry I might have an accident. I have to be mindful and concentrate.
@@bobscott7253 aaa
I have a movement of my hands its little by happening evrytime .im 34 years now .is it Parkinson's disease
Thank you for teh video. It's easy to follow and understand.
Glad it was helpful, Vanessa!
Thank you so much for sharing this info.. When I was a kid around 7 year old I noticed that my right hand is shaking after I wrote maybe I got tired so I just let it go.. but what I worrying is now that I'm already 25 year old it is still shaking and both hands.😔 I wish it won't get worst..
I think it is anxiety or imsomnia
Essential tremor
Try propranolol
With stand your hope :)
~Please talk to your doctor~
I don't have parkinsons D, that I know of
I have chronic dysautonomia, autonomic nervousystem dysfunction. when I sit or stand fir more than five minutes, my blood pressure bottoms out. Many symptoms similar to parkinsons disease.
I've not had a lot of help despite seeing cardiologists=3.
None of which took my sitting standing blood pressure.
Eventually my condition was realised ( Diagnosed) by an Angel GP.
Even do, with all of the medications and life style modifications I'm still very sick daily.
My father also had these symptoms for his entire life. No diagnosis. Poor guy. 😢
My diagnosis took 30 years my daily issues prior to fludro cortisone were. Slow drop in bp ( 5 to 10 minutes latent)
40 points.
Visaul aura, misdiagnosed as Silent migraine or visaul + vestibular migraine. MAV
And possible epilepsy.
Due to the overriding symptom being semi loss of consciousness, who can only ramble like a drug affected drunk, gait and dizziness, walking and thinking with as much "brain ability" of a zombie. alziemers patient would be more apt. I also have muscle ticks and tremors
It's a nightmare fir the patient and family who has to rescue you when you've lost awareness of where you are, who you are, and you have no warning as the dynptoms creep up slowly.
Not all patients have slow progressing symptoms.
But thise who do can be in daily danger.
It horrible!!!.
I feel privileged that I live in a country that has free medicine and have a great medical system and support to help live life with a disability.
It's not a perfect system. If it was I'd have had a system where rare disease was easily recognised.
Long covid has sadly shone a light on my rare disease as long covid is often ( Dysautonomia)
Yes, yes it is
We In the dysautinomia community were upset to think hundreds of thousands of people will now suffer with dyautinomia and have Drs and specialists not know what it was.
Dysautonomia patients knew it!! We heard long covid stories snd knew emediately what it was.
So very sad. I pray others do not have to wait for treatment. That Drs and specialists now see the signs and listen to their patients.
Sending love to all who suffer daily chronic illness.
God help us all!! 😢.
Small tremors in hands ,arms like to go up for no reason that I know of ,or swings weird, left arm that is .Left hand is where it started ,a lot of muscle weakness ,hard to chew ,hands stop working ,Aphasia ,and my thoughts drop when I try to think to hard .Just started seeing neurologist ,did eeg ,all good I think .Still Un diagnosed .
My father is in bed for a month with the Parkinson and memory loss , also in brain MRI we got to know the disises about brain atrophy, is there any chance of recovery??
My father in law is in a care home with Kate stage Parkinson’s.
He can eat fine but shakes a lot and is having regular falls and cannot walk without a zimmerframe. Mentally is not well either and has frequent urine infections.
What is the life expectancy of someone at this stage?
there is a cure. Supplements can send Parkinson's into remission for good
I wish there was a cure for PD.
There is
@@aribabatony4035 and what is that cure? My mother is at Stage 5 with Parkinson’s Disease, and we were looking to see if she could be a candidate for DBS (deep brain stimulation) but at her current age of 82, she did not meet the criterion. It’s just a horrible disease that sucks almost the life out of you both mentally and physically. 😞
@@Saltynutz333not sure how I stumbled across this video but just wanna say I hope she’s doing alright, wish you the best
@@Saltynutz333 my mom is having this at 45 age. Just 45 😰
It a very beautiful thing to see myself healthy again after using remedy from Dr Ake on TH-cam, I finally got cured of my Parkinson's disease with his herbs med and I can tell how great my health has turned out so far.
Thank you 🙏 ❤️
Hello, what are the incidence and prevalence rates for PD in the US? Does it affect males more than females? Thanks
it does affect more males than females in the US.
Hi Domantas - Parkinson’s is diagnosed more commonly in men than in women.
I’m 22. Diagnosed with RSBD. Rare for my sex and age. I’m noticed all of these symptoms. Very early on-set. I will have to make a dr appt. however the nearest one is 2 hours away
2 hours is not bad distance, do your treatment but alas there is lock down.
How are you now?
I was not aware that my left hand was slightly tremouring, while at rest, until my family pointed it out, and stated I'd had it for at least ten years. Now I'm 81, and not aware of any worse tremour, My doctor sent me to a specialist, who said i showed symptons of Parkinsons, but not enough to affect my driving. Having prescribed a drug, that MIGHT affect my driving, I decided to not take the drug, ( this was 4 months ago ) and my slight tremour of the left hand is not noticeable. During this period, I DID have a spell of Inner ear inbalance, which is also a lot better. I think I'll tough it out.
what about medical Marjiana
there is a cure. Supplements can send Parkinson's into remission for good
I have a question I have seen a tv commercial that says you can see things that are not there with Parkinson's I am experiencing this a lot and am have trouble with my balance my nanna had Parkinson's should I worrie?
May I ask what do you see?
Normal things really like my wife or dog from my corners of my eyes don't know if I should worrie
@@julianmoody9768 I would suggest that you definitely let you Dr know what you are going through.
@@julianmoody9768there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
Is there a connection between Parkinson's and orthostatic hypertension? Its getting to the point where my dad can't even stand up to use the urinal without convulsing and passing out. I can always see it coming and I sit him down until it passes.
Hi there - Orthostatic hypotension is common in PD and affects 15 to 50% of patients. We have more information here: www.parkinson.org/blog/research/passing-out
Am Bismark Acheampong and lives at boston,Boston, have pD that I feel like dieing
I would like to know, is Hallucination a part of Parkinson?
Seeing stranger in home who are not really there. Seeing Dead persons who appear real. Being tortured by children sticking them with shall objects or constantly shouting cold water on them. Etc?
Hi Linda - Here's more information about hallucinations as part of Parkinson's disease on our website:
www.parkinson.org/Understanding-Parkinsons/Symptoms/Non-Movement-Symptoms/Hallucinations-Delusions
Thank you so much. I will definitely read this.
You should definitely talk to someone about that
@@earth_is_a_prison Thank You So much. Will do. 💕
@@sathmijayasinghe9424 same as my mother. People trying to kill her. Holding her hostage. My father passed in 1992 and she is seeing him with his new girlfriend and another child. Etc etc etc.
My siblings and I are trying to figure things out. We try to make sure someone is with her at all times. If you get any info you think will help please share. We need all the education we can get.
There is a vitamin by the name of "Melatonin". We give that to her at night. It is helping her to rest a little more once she gets to sleep. God be with and help you and your family with your Grandfather. 💕
There are many different symptoms related to Parkinsons. The non-motor symptoms of low mood, brain fog, poor sleep and therefore fatigue probably deserve more attention generally...
77 66 6yg
I think i have that😭
@@chanaiiH it's best to get properly assessed by a neurologist, and commence lifestyle interventions and natural treatment options as early as you can.
Was this an analogue recording?
Hi there - This voiceover is from Dr. Joseph Jankovic, MD.
Is involuntary closing of eye lids due to Parkinson’s?
Hi there - Some people with Parkinson's disease report trouble voluntarily opening the eyes, known as apraxia. We have more information on our website here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/vision
Besides taking Levodopa, there is not much can be done. Physical therapy has only limited effect, as patients tend to have little to no motivation.
Dignitas Switzerland will take Parkinson’s patients. I suspect I’m in the early stages of this disease or something similar. I can’t say I have a noticeable hand tremor though. I might someday, or perhaps slot into the PIGD subtype.
@@cam553 ml. Mlkplh8tit ui ITV out uh 7io. Nook vou by 99l
@@calvinmarr3379 ?
Have to agree with your comments. The biggest issue I see is keeping the patient optimistic and participating in helping themselves….. motivating him to do for himself in the absence of others pushing him to it…. Especially right now with lack of visits from friends (purely COVID driven) and no possibility in participating in their favourite activities…. In this case, riding his motorcycle and hunting, :(
there is a cure. Supplements can send Parkinson's into remission for good
4:03 late onset with gait and cognitive/dementia
My father in law is in a care home with Kate stage Parkinson’s.. he cannot walk without a zimmerframe and cannot get up without assistance. He is hallucinating and seems delusional at times. It’s a Brutal disease and I can’t help but wish it is over quickly. My fear is that he continues on for years like this. He’s having multiple falls. Can anyone provide some experience on life expectancy at this point?
Hi Billy - Parkinson’s disease impacts people in different ways. Not everyone will experience all the symptoms of PD; even if people do, they won’t necessarily experience the symptoms in quite the same order or at the same intensity. We encourage you to reach out to our Helpline to discuss further: 1-800-4PD-INFO (473-4636) | Helpline@Parkinson.org
Sounds just like my dad. I often wonder if his time is up. The less cruel thing would be for him to slip away peacefully.
I got parkinson now ill be 65 april.1 my syptons are getting harder to deal with quickly i have 3 children and devorced question what do you know about turning glieal cells of the brain into neurons human trials i was into cbs in my 4yr honorably dis charged duty at a young age 17 yrs
there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
My father 59, A PD patient had a fever last month and is unable to walk now..
Any suggestions?
Hi there - We encourage you to discuss this with your father's doctor. If you need assistance getting connected to care, we encourage you to email our Helpline: Helpline@Parkinson.org
Is peripheral neuropathy an early symptom of Parkinson's? Thanks.
Hi Charlie - Here are the 10 most common early symptoms of Parkinson's disease: www.parkinson.org/understanding-parkinsons/10-early-warning-signs
No. That’s associated with diabetes or chemotherapy mostly. MS maybe another possibility.
low B vitamins. especially B1 can cause Peripheral N.
I have PD since 2010 and my feet are killing me. They feel cold most of the time inside but not to the touch. Some days they're ok. Today is not one of them. What could be the cause?
@@invoxicatedthere is a cure. Supplements along with a good diet can send Parkinson's into remission for good
Plsss help my mother
We are here for you! Know that you can reach out to the Information Specialists staffing our Helpline by emailing Helpline@Parkinson.org. More information at www.Parkinson.org/Helpline
there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
I think I have early onset of Parkinson's. I'm in my mid 40s. I have slight hand tremors in both hands and chin tremors when I'm sleeping face down. Watching from London UK.
Hi - Here is a list of 10 signs that you might have the disease. No single one of these signs means that you should worry, but if you have more than one sign you should consider making an appointment to talk to your doctor: www.parkinson.org/understanding-parkinsons/10-early-warning-signs
there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
I have PD but don’t fit into either of these groups!
omfg don't scare me like that what symptoms do you have...?
Mostly stiffness and slow movements. Like I’m moving in water while up to my neck in it?
@@ohblimey21 oh, i'm sorry to hear that it's not fair that you have to go through that also I was being kinda rude i'm sorry.
@@ohblimey21 have you ever had concussion?
@@cam553 nope 👎
There is hope in the drugless treatment being tried in Ayurveda in Kerala State for complete cure
Great
I’m 25 and my hands get shaky and my legs sometimes especially when I intend to meet someone or talk to someone. It can get intense when I’m thinking about something and sometimes when I’m just not doing anything and I have focus on the part that shakes (ie hands and legs) it gets shaky . Is this a sign
Nah I think it’s just anxiety mate, it happens to everyone and focusing on something that you think is wrong with you will only make you think it’s worse, that’s what anxiety does to you but if you want to be sure you’re not getting PD go see a doctor or something but I’m sure you’re fine lol
@@comm04bangr98 I can’t move half of my face or at least smile correctly (not that I remember the last time I smiled in my entire life) since I was on a fight and someone broke my nose in middle school. I’m 28 to 29 now and I still can’t seem control half of my face. What should I do?
@@comm04bangr98 forgot to add that when I tried to move that side of the face or smile I get a immense pain in the jaw as if it will reach my brain and lock it. Is terrible
You have anxiety my friend
To much iced coffee.
I love my new INBRIJA inhaler. Anytime I feel an off period I just use my inhaler and I’m back on within minutes of using it.
Sir
I wissen there was a cure for RLS too.
Can alcoholism cause Parkinson’s ?
Hi Anita - Here is information on our website about our current understanding of the causes of PD: www.parkinson.org/understanding-parkinsons/causes
How long can you live with Parkinson's disease?
Parkinson’s, in and of itself is not fatal. Some people have been known to live 15-20 years with PD. However, 80% of patients develop dementia, and unfortunately, that is fatal.
It effects different people in different ways and times. Sad to say, but within time, dementia will take its toll.
My dad lived about 2 years after he had this disease
@@bobscott7253 Hi Bob, did your wife ever have really painful legs that also felt very heavy? I'm diagnosed with Parkinsonism last Sept
I've noticed a rapid progression of leg fatigue and everything I lift seems heavy. Does any of this sound familiar that your wife might have had?
@@toryberch My wife had Parkinson’s for 17 years. Oddly enough, at no time did she have the uncomfortable shakes that usually come with PD. There were times she would begin to shake, but when I called her on it, she would stop shaking. So, she did have control over it when she became aware. This would happen at bed time only from time to time.
There was a time her legs felt as you described. Her neurologist felt my wife may have had the beginnings of neuropathy, so she prescribe a medication for that. However, she was only on that medication for about 6 months, as she was doing therapy at the same time. I don’t remember the exact medication, but if you’re interested I can look back at her meds. Hope this helps.
@@bobscott7253 thanks Bob for answering so quickly
I have Gabapentin for my neuropathy symptoms.
I'm am sorry for your loss
You sound like you were a very caring caregiver.
Can I ask, how long did she live with her diagnosis until her death?
My brother is stage 5 and has started seeing demons coming out of his walls..and also children running in snd out of his carehome bedroom..hes scared and confused
Know that we're here for your brother and your family. 🩵 We have information on managing hallucinations in Parkinson's disease at www.parkinson.org/understanding-parkinsons/non-movement-symptoms/hallucinations-delusions.
Hi
Please help my mother too. Im from Philippines.thank you
Hi Shaika - Know that we are here for you & your family with educational resources & emotional support! You can reach out to our free Helplien by emailing helpline@parkinson.org with any PD questions or to talk to professionals who understand. parkinson.org/Living-with-Parkinsons/Resources-and-Support/Helpline
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@@ParkinsonDotOrg
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@@ParkinsonDotOrg .u
@@ParkinsonDotOrg thank u for this information. My father has been diagnosed with PD when he's 55 years old and now he's 68 and the illness get worsened. What medicine can control his tremor?
I be got Parkinson's disease and am 24 years old and I don't how I got it
Hi there - While much is still unknown about the causes of Parkinson's disease, scientists believe a combination of genetic and environmental factors are the cause of PD.
We have more information in this video that you may find helpful: th-cam.com/video/jxpMs-eBaBM/w-d-xo.html
You can also visit our website for more information on Young-Onset Parkinsons: www.parkinson.org/understanding-parkinsons/what-is-parkinsons/young-onset-parkinsons
there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
Well shit now i know i have the pigd form of parkinson's
Me too. This video is so pessimistic for us. At least I know now why the levadopa doesn't make me feel better, and often worse.
My mom is in 3rd stage what should we do?? Moms Age 45+ 😔😔😔
What symptoms she have
Do dbs surgery
there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
My hand’s shaking a bit is it normal or is it just because I a bit cold
Hi - Here are the 10 most common early symptoms of Parkinson's disease. No single one of these signs means that you should worry, but if you have more than one sign you should consider making an appointment to talk to your doctor: www.parkinson.org/understanding-parkinsons/10-early-warning-signs
How do people with this disease sleep at night with that constant moving around all the time. 😳
Hi Marcia - We have tips for better sleep with PD on our website: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/sleep-disorders
So in other words there is NO cure. 😢
No cure yet.
Although there is currently no cure, treatment options vary and include medications, lifestyle adjustments and surgery. More information about Parkinson's disease can be found on our website: www.parkinson.org/understanding-parkinsons/what-is-parkinsons
there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
@@vodatube2591there is a cure. Supplements along with a good diet can send Parkinson's into remission for good
Your memory starts to leave body and start to not see anything as real
Hi there - Know you can find information on cognitive changes that may accompany PD on our website here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/cognitive
My brother has Parkinson’s he’s only 53 it’s a bad disease
Know that we're here for your bother and your family if we can be of assistance 🩵 We have many free resources for those living with Parkinson's disease and the people who love them at www.parkinson.org/resources-support.
My Granny passed away becuz of Parkinson :(
We're sending our condolences to you and your family, Lia 💙
How long she had been having the disease... please.
Hi there - Parkinson’s disease impacts people in different ways. Not everyone will experience all the symptoms of PD; even if people do, they won’t necessarily experience the symptoms in quite the same order or at the same intensity.
For more information, please contact our free Helpline: 1-800-4PD-INFO (473-4636) | Helpline@Parkinson.org
Im 17 but i fell like i had slight shaking
Probably just your diet. Low blood sugar or iron perhaps.
Same for me I thought it was about low blood sugar but it isn't cz it's here everyday it doesn't leave
No cure
Va drs have no idea as to treatment. Never know about new medicines just keep prescribing the same meds. Try to tell them about all of boyfriends symptoms. Deaf ears.
He can sleep 15 hrs each day, no energy just eats sleeps and si t s infront of tv. Tell the drs and no advice. Va needs help with their medical staff.
Hi Linda - Please reach out to our Information Specialists if we can be of assistance with referrals to healthcare professionals and local resources near you: 1-800-4PD-INFO (473-4636) | Helpline@Parkinson.org
If you even think you have one see a doctor
Yeah, one stage is called Joe Biden!
😂
Lol good one
My husband diagnosed of dementia... Then Dr's prescribed him of 3 medications...i was suspecting that it's the side effect of the medicines but seems it's PD... pls help😭😭everytime I look at him shaking makes me cry
@@noyb7051 thanks very much
@@mariusbadenhorst4147there is a cure. Supplements along with a good diet can send Parkinson's into remission for good