Are there different types of Parkinson's?
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- เผยแพร่เมื่อ 29 มิ.ย. 2024
- Dr Michelle Hu from University of Oxford discusses identifying different 'types' of Parkinson's, which may respond very differently to the new treatments that are currently being developed.
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I read recently of a group of Doctors examining the blood taken from dozens of Parkinson patients...tests revealed all had little or no Vit. B in their
Systems. I never could take the B's either and have Parkinson's now at 88 yes. Taking loads of brewers nnuitritional yeast flakes everyday and believe this
Has definitely slowed things down. Hope this is a help for you all.
Interesting discussion.
Just Thank You, GREAT INFORMATION AND VIDEO. I have Parkinson's finding information is hard. Your doing a Great Job on this, I'm 62 fighting it. Walking and working is helping.. Happy Easter.
THANK YOU and thank you this is GREAT INFORMATION. Thank You.
I like hearing of natural bins and helps
من أفضل الفيديوهات عن مرض باركنسون. لقد تكلمت عن تفاصيل دقيقة منذ بداية المرض وحتى مراحله المتقدمة. جميع ماذكرت من تفاصيل وقعت لوالدي رحمه الله.
I know somebody who is clinically diagnosed with Parkinson's in 2022. He is 80 years old. He can hardly walk. His disease progressed until he was bedridden for more than six months. Now he can get up from his bed stand up and walk very slowly towards (somebody of course is assisting him holding his arms) the living room where he can sit on his rocking chair. I did some research and found out that no drug is available yet as of December 2022. How can this be possible? Only want to share my experience with this disease. Maybe this can help with your research.
Did you get any answer for your question? if so please share.
The illustration at 19:00 is illegible even when blown up to full screen on a nice, crisp 23" monitor. Too bad, eh? Anyone suggest where the same information can be found?
Yes!
Before diagnosed Parkinson first symptoms: extreme premature ejaculation and 2008 diagnosed overactive thyroid ( Graves' disease ) I believe must be connection with thyroid and Parkinson disease ! Low dopamine : premature ejaculation
My thyroid level was high when I got Parkinson disease I had mini stroke it took 2 minutes ruined my life stupid thyroid specialist said coincidence but I don't believe him
2008 diagnosed overactive thyroid and 8 years didn't do any treatment rai or operation 2016 February I had mini stroke and boom Parkinson hit me I was shocked..
@@16borabora Oh wow! I never would have thought that thyroid would be linked to the production of dopamine.
I know, Parkinsons, is a progressive neurological condition, but not everyone does. So, explain to the viewer, What this is, And what it means> Not Just, Parkinsons. But dementia, Overall.
This is glorious, I've been looking for "can parkinsons be detected by a blood test?" for a while now, and I think this has helped. Have you heard people talk about - Piyaliyah Prominent Prepotence - (do a search on google ) ? It is an awesome one of a kind guide for discovering how to reverse Parkinsons disease minus the hard work. Ive heard some awesome things about it and my colleague got amazing success with it.
Can only access a clinic visit once or twice a year?? What does that say about the UKs socialized medicine? Glad I live in the USA!
we are ecstatic you live their too Thom....... clogging up their system
I have Parkinson disease, if I was to leave my body to the scientist, can they use a dead corps to do any types of research or experiments with it. I fell if they could use it to save a animal, it could be a wonderfull gift to the future , to know it helped others makes it a wonderfull thing to know i could help 1 more time.
Hi Ray, thanks for your comment. You can donate your brain... If you're based in the UK then we run a brain bank - there's more info here www.parkinsons.org.uk/research/parkinsons-uk-brain-bank If you're based in another part of the world then there may well be an equivalent research centre, so it's worth doing some research. Best wishes to you.
Is PSP A form of PD?
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I have a question for the speaker my parkinson is rigidity, I walk slowly, I have difficulty to march, dance, walk. in this moment ,I arrived to walk, but I'm very tired,, I am taking a pill and a half a day of carbidopa levodopa and a pill of mirapex 3mg treatment 3 years ago. I am 57 years old. I began 7 years a go. I am from colombia, please, tell me What kind of parkinson do I have? thanks for your answear.
Helmer Moran im o
parkinsons
Helmer Moran of
You ask this question after watching a video that supposedly describes just that. Well, like you I couldn’t tell which was which either. This women may be tops in her field but getting the right info across seems to elude her
Start eating liver every day and see what happens. Any liver will do.
the persistent coughing is annoying--- good presentation
Any thoughts on ambroxl😊
My knowledge of Parkinson's is pretty shaky.
It
Find this very interesting, i was diagnosed in 2016, but last year was told i havent got parkinsons, i had a dat scan and it came back ok, yet i have all the symptoms of Parkinson’s, its become very frustrating and very difficult for me as iv no support or help now , im getting worse ,
Hi Susan, sorry to hear you're struggling. You may find calling our helpline useful on 0808 800 0303
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My mom had all of a sudden extreme physical deterioration and my mom had CT scans and was told that they didn't see any deterioration. I think unfortunately she was not being tested for Parkinson until recently and being it progressed so quickly. I wish we caught it early enough to help slow down the progression of symptoms
@@parkinsonsuk thank you , its been awhile and since they have changed there mines, its been four years since i was first diagnosed
I had a Dat Scan a week ago and can't get the doctor call me to explain
Taking warm milk with Turmeric powder with a pich of black pepper helps me to feel body relaxed. Is it wise to continue?
Multiple system atrophy
Parkinson’s is in my family my father had it without dementor, his younger brother had the condition but with dementor. I seem to have inherited Parkinson’s . I am reluctant to get diagnosed because i don’t want to start medication for the condition.
Hi Jeanette, we're really sorry to hear that you've had to go through so much with your father and brother and also now dealing with a potential diagnosis. Remember that our helpline is available for anyone affected by Parkinson's on 0808 800 0303. That might be a good place to start for any advice about your situation. Wishing you all the best
Help me Parkinson's
Help me Parkinson's disease sir
I was diagnose for parrkinsonism after a stroke until now i hope i will be healed with your informaton god bless i ama filipina senior. Citizen
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Lots of speil and not enough substance to her talk. 6:21
I got tremors, Parkinson & Alzheimer's runs in my family, I hate both, I have the tremors,,,,,
The new versvvÿion c
I thought ‘ maybe this will tell me something new. Well,was I wrong . Just the same old story. Tell us there are all these new techniques out there . But never what they are! Yes there’s new tests and what do they do? TELL ME SOMETHING THAT IS USEFUL TO ME THE REASON YOU ARE MAKING THS VIDEO! I’m missing this important point. What the f is it! This 3 minute test sounds good. What’s it called and where do I get it? The people you are talking to I hope were Parkinson’s illiterate. They would have learned something. I however , a person with Parkinson’s , learned nothing useful. Thanks
My mother has Parkinsons. She has undergone 7 YEARS of altering this medication and that medication and changing dosage from 50mg twice a day, to 100mg once a day, to 25mg 4 times a day, to xyz xyz times a day. Like popping smarties. The doctors always give this bullshit excuse that "everyone is different so it'll take time to work things out". Bullshit man. You've spent years studying your field, and you're telling me that my mother is the only one still struggling like she is? Bullshit man. I've seen the doctors other patients with Parkinsons, and they are right as rain essentially from the get go, yet, you can't figure out how to help my mother? Is she really such an outlier? It is so very clear that these doctors don't know a damn thing about what is going on, yet they still try and treat her like a kid playing around with a little puppet. Hell, I wouldn't have spend years studying to prescribe 50mg twice a day... Oops, no OK, let's change that to 25mg 4 times a day, because you get it, if we divide 100mg per day into 4, you get 25! Magic! It's like these effing doctors are praised for doing the absolute least amount of work, because "everyone is different". It's so tiring man. My mother has recently undergone a deep brain stimulation procedure to try and help with the Parkinsons (again, all the other patients that her doctor has had has been right as rain a couple days after), yet my mother was bedridden for 2 weeks, with extreme dyskinesia, and she was in an extremely delusional state for 1 whole week. She was neglected and is now doing even worse before her supposed miracle dbs procedure. Let alone probably the millions that has been spent on trying to manage this godforsaken condition. I've only seen my mother get worse and worse at each point of intervention and it is breaking down my soul. I want to fucking die every day, but what's even the point of that? This women in the video spews the exact same rubbish that thousands of other doctors spew, "we're doing this trial to try this and that, and we've got these people, with different types of Parkinsons (of which you clicked to watch, yet fuck you, I won't tell you what they actually are), but here are these technologies that we say will make you better, but really we just want all of your money. We don't actually care about you nor your mother and how you end up, we would just very much like your money to support this research so that we can go and bauble on for another 2 or 3 decades with absolutely nothing to show for it, but hey! Everyone is different right? Yes! We spent millions making everyone around us all the worse off for the sake of our research and our tummies, and our conclusion is that everyone is different! It's not like little Suzie would tell you any different, even though she is only 5 years old, but atleast we stole millions off of you! Thanks for that! Now we're stealing your mental resources to try and find out about the different types of Parkinsons, but again yeah, we aren't going to tell you that of course."
Absolutely disgusting how doctors and medical professionals nowadays make so much money for absolutely fuck all. My mother is suffering and will continue to suffer in the absolute slowest pace possible. It is just so inhumane. 20 minute appointment once or twice a year of you're lucky. Bugger off mate. Just bring the coffin so I can lay in it already. I HATE doctors with all of my heart. I hate the medical profession.
@@mikeandre7364Mike, hope you have solved this, but you are correct. And its lousy how they go about things modern times seem worse. Everyone i knew that had this suffered terribly.
No one has the secret if they did, it would shut down research car facilities loss to medicine field.
If u had to, look at cultures that are healthy and dont have this and mimick that plus any restoritive type things to improve nerv function
Michael Wallace seems to be a very unhappy camper. Michael leave your negative attitude at home don't put it into the public square, mate you need to put a sock in it.
Is light headness, a common symptom of Parkinsons?
This is where I fell we need to clone animals for research reasons. Cloneing is more like a created creature created for a reason. Cloned creatures were not created under love. Love is the most powerfull sense we have.
Cognitive brain damage from Parkinism