The International Parkinson and Movement Disorder Society (MDS) is a professional society of clinicians, scientists, and other healthcare professionals who are interested in Parkinson's disease, related neurodegenerative and neurodevelopmental disorders, hyperkinetic movement disorders, and abnormalities in muscle tone and motor control.
Hey there.I remember Doctor Jonathan Carr from way back at Groote Schuur hospital days when we were much younger I worked as a hospital porter that time and I had seen him as a medical student this shortish guy with his short than usual white doctors type coat and this very neat short haircut he looked real British type looking.This was in the 80s
I am on Ingrezza which reduced some of my symptoms but I continued to have mouth movement looking like I was chewing gum. My doctor told me that gingko biloba had a few promising studies. I am now taking this supplement with continuous success in eliminating my tardive mouth movements.
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 a gain..”
My nephew who has Autism has been prescribed antipsychotics for the majority of his life, movement disorders created by these poisons have made his life a living hell, trying to get a psychiatrist to wean him off these poisons is difficult even his latest quack just isn't listening to our concerns and I'm definitely not going to ever put any other poison in to his body to try and correct his issues, big pharma creates a problem and then sell other poison to resolve a problem they created, great business ploy to create another market, it's all pseudoscience, if only a psychiatrist had never seen him life would have been better for him.
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 was not diagnosed with Parkinson’s in 2017 but lately my eye movement is never been good but now I have to move my head rather than my eyes whether it looks like inside it up or down reading is very difficult driving I moved my head. I can’t move my eyes so whenever I move my check, my rearview mirror is so I’d be mirrors. I must move my head. Also I have tremors but not so bad but lately I find myself rocking back-and-forth when standing still, also I have a tendency to fall backwards. I was wondering if it is thought I have been diagnosed. I recently seen a nuclear ophthalmologist so I’m hoping to get some answers on my eye movement. If there’s any help you can give me it would be greatly appreciated. Thank you for your video. It’s been very helpful. My stuttering is hard so it’s hard to get this message out. Thanks again for all you do.
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
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.
Sir. Maddam. I would like speak about. The care the learn the about. The. Comes. In zig zag walk and. Colour yellow. Zig zag line. Walk. Balancing manner. Thanks. Medico
I would not forget about a good naturopath who has experience in the link between tics and diet/environment. In my experience pediatricians and neurologists were not that helpful as the only suggestions they had were either medication or CBIT, neither of which actually help the underlying problem.
Hello, Dr. Fung. I was diagnosed with DRD. I would love some resources to help me as I deal with this diagnosis as my symptoms seem to be worsening. Thank you.
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 got TD 4 years ago from anti nausea Reglan, metoclopramide aka maxalon.. You are the 1st person to understand it can happen from antimetics. Most people deny it and give to pregnant women.. my youngest two children have Tourette's Tourette's. Please continue to help us.. I couldn't begin to imagine if somebody was in mental health, then medications doing this to them. Feels so cruel
I have bipolar depression, anxiety, ocd. I was born with tourette's syndrome too. After being on Depakote for a couple years, my tics progressively got way worse!!! It was finally pinpointed that I have TD. It has made my life miserable. I do not wish this on anyone. I would go back to my normal tics any day. Has your TD been managed, or do you find it difficult? I am still looking for a positive way to manage both bipolar disorder and my TD.
@@stephensullivanii1295 thank you so much for commenting. I've just been to the neurologist and have TD with the Twist of dystonia.. originally when this first happened it was getting me down and the GP wanted to put me on antidepressants. I refused to go on them because I read PubMed information and it was not good news. I think Professionals are true idiots and uneducated when it comes to giving us drugs that make our condition worse. It should be criminal. I wouldn't wish it on anybody either. Within professional ignorance, it is wished upon us with more drugs that give us enhanced movement disorder. One of the cruelest things is that they don't listen.. I feel so grateful to have a new neurologist, who is taking every complaint seriously. He is sending me for a nerve conductor test first week of December. This will also check for spasms as well as nerve signals. I'm not really sure how it works. Gosh hanging there mate because I know how terrible it can be mentally. I speak to a psychologist once a month and it helps keep me stable and accept what's going on. I refuse to take any drugs that make me worse.. In your case that might be difficult due to the bipolar. My sister has been diagnosed with (cycloclimia?) bipolar.. she has OCD and a few other things happening but not sure she was at the diagnosed properly
Brilliant audio with a Nigerian-born neurology giant and erudite professor of Neurology of the University of Lagos. A very experienced and great mentor in the field of Movement disorders.
