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Hi Michael, on March 5, 2024 my husband was diagnosed with Parkinson's disease by a neurologist. That particular neurologist did a DaT scan per my request and an MRI. DaTscan showed decreased dopamine but the MRI showed normal age related changes. Moving on to a movement disorder specialist ( 2nd visit) it is definitely now believed do to my husband's severe autonomic involvement and quick deterioration, it most likely is MSA,. I've been beyond devastated over this. Many hopes and dreams have been vanquished in our early retirement years. Thank you for all of your educational material friend.🙏

My husband is being worked up for lewy body dementia vs Parkinson's disease. Along with his many other symptoms, he has recently started having a runny nose and sneezing, sneezing, sneezing. Poor man. He doesn't deserve this.

Thank you so much for the valuable information. Just wondering how much Vitamin B1 is needed in the treatment.

My B6 levels are about 90 ng/ml. I don’t take any supplements and it’s almost 6x the upper limit of normal. Is this level considered toxic? I have neuropathy in one side of my upper extremity but I have had several injuries. I thought I was just damaged from having 4 surgeries on one side.

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Very interesting

I’m 49.5 and have been going through the rapids of clinical testing lately. My question to you is why wouldn’t Cannabis therapy be considered as a means to put off Levodopa treatment as long as possible? I mean actual Cannabis that’s clean, tested and are the proper ‘terpenes’ to treat the disease accordingly. When I hear you explain why dyskinesia happens, I also wonder why I’ve never seen my Father with it who got diagnosed in 1997’. I believe he did or still takes Amantadine but I’ve never witnessed him have any movements like that and he’s 87 now. I’ve told my Movement Disorder Specialist at Stanford that I use Cannabis for my tremors and to sleep, etcetera and she kinda said ok but I could tell American Medicine isn’t ready to leap forward by any means, even with the MJF foundation in which I just started the PPMI study. That study which is put together by 2 Doctors themselves, goes above and beyond and very paralleled to my own research in the last 30 years since I was diagnosed with “Chronic Fatigue” by the same neurologist that diagnosed my Father with Parkinson’s 2 years later. We will soon find out if it’s a “coincidence” or not but what I’m pretty tired of hearing for the last 30 years is “Your too young to have problems”. Or someone telling me the small percentage of chances both my Father and myself have it. Cardiologist, Neurologist, and even some General Practitioners will comment like that.. You have to ask yourself if they are just trained to stay blind and silent? Generation X is dying faster than the Boomers, Alcohol and Heart related issues may be at the top. This all while being Gaslit by Baby Boomer Doctors, However I think we found where the actual problem lays and with enough UA-cam videos we can show other perspective patients what their real options are whether others agree or not. 🙏🏼

Any recommendation for medicine/supplement to speed up the nerve healing process ? I've seen people talk about hydration, exercise for recovery but no one has suggeted any medicine that could help speed up the nerve healing.

My husband has Parkinson’s, and we acquired a very nice unit from InLight therapy. They have a channel ( InLight, PJ Cardona)you can watch, and have introductory videos live every couple months where they give discounts and sometimes offer sone giveaways. In my work in dentistry, photobiomodulation is a growing support system across the board, and I did a lot of research. This company is FDA registered and has been in business 40 years. The units are well made, we’ve had ours for close to 2 years and no wear or issues. It has a warranty of two years, I believe, but they will do repairs for a flat fee. We have a unit that has red, blue, and near infrared. We were able to purchase a unit that can run 6 active pads at a time, so are able to both use it simultaneously. Very well made, I use it for pain(hip, arm, neck, muscle strain) and he wears the helmet and uses other pads on back, abdomen, neck. My results are impressive for relief, but my needs are not complex like Parkinson’s. I feel it is helping him, and am grateful to be able to take advantage of the opportunity. They have an array of choices, and we’ve been happy with the support they offer. Good luck and good health to every one of you.

What could cause Dyskinesia other than medication side effects? I'm currently waiting for an appointment with a movement disorder specialist. I have symptoms of Parkinson's but also have Dyskinesia sometimes.

Thanks!

Great info. Thank you

I have a red light hat been using it for3 months How would I know if it's helping Who knows But hey why not use it It can't do any harm 😊

You rock! You’re so very helpful and all. We appreciate you. <3 <3

The problem is in the duodenum and liver, which are not working properly to be absorbed into the blood. If the person has intestinal dysbiosis, H pylori, high ferritin, vitamin B complex deficiency, such as B2, B3, B5, B6, B7, B9, B12, minerals, zinc, copper, magnesium, selenium, VANADIUM, chromium, molybdenum, nothing will help. Only vitamin B1, Thiamine, I also recommend using a probiotic from the brand Vivomixx, 450 billion. I recommend using a biofilm disruptor and Bio-MAMPS together with Biointestil, Eurekol, and Corebiome!!! If the person has high ferritin, do a 400 ml or 500 ml bloodletting.

How about Stem cell therapy?

Thank you for learning the lecture. I did have fun

My father was diagnosed with Parkinson disease at 70 years old. He always had a shake in his hands and runny nose and sneezing all my life growing up . He never left the house without his big hankershift. He lived till he was 91 and always runny nose and that big handkerchief in his pocket till the day he died. He had seven kids and not one has Parkinson diagnosis or any of the symptoms he had all my memory of him.

michael j fox was on the good wife and gave several examples of unmedicated episodes. and we all love michael j fox, and his endurance,

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I tried everything under the sun for my Parkinson's and focused ultrasound surgery fixed me in the time it takes for a long lunch. It's been 3 years without tremors. See my film Tremor Documentary 2022 . It will blow you away. Promise. This doctor is the best!

I was first diagnosed with Parkinsons and then later NP hydrocephalus. After shunt surgery I no longer take or need CL. Understand as many 20% of Parkinson diagnosis or actually NPH.

NO CURE. Just talk

Talk forever. The reality NO CURE.

you are dufus you have no idea about B6

will it help with MSA - Multiple system atrophy?

Having observed him for a number of years I believe John Pepper did not have Parkinsons. He had essential tremor; he did not have a resting tremor but an action tremor. He became so convinced of his own story that he did two world tours telling people that drugs are not necessary, fast walking is the answer. He has never been able to produce the study he quotes. I don't think he has seen a paper on it; he attended a presentation at the first Parkinson's congress and the review of that presentation is what he quotes as evidence. His story has changed and evolved over the years. What is true is that he was removed from his position as chair of Parkinsons South Africa because the neurologists did not believe him, instead thought he was using his position to promote his book. He did not take levadopa for any length of time because it did not help. The drug he took the longest was selegiline which I think for him worked as an anti-depression med more than a PD med. He had been going to the gym for an hour a day for many years and increased it to 90 mins a day but stopped because he was not getting any better. On the insistence of his wife he joined her weight loss, walking group. At the time this all happened he was depressed. His business was not doing well. He resigned. With the absence of stress and the addition of an anti depressant and regular exercise (walking) he got better. When he asked the last neurologist he saw whether he had PD the specialist said you don't have idiopathic Parkinsons. John decided he had another type of Parkinsons though he didn't know what it was. He was so invested in his story that he made it real for himself and his many followers. You did well to be wary.

Perhaps vit b 1 and l glutamine also magnesium glycinate helps for restless legs all muscle needs that are robbed by this disease 😊

I did not respond to levidopa so I doubt I have PD. But what difference does it make what the disease is or is not, if there is no cure?

Thanks for this great video! A few months ago a neurologist diagnosed me with early onset dementia - I had just turned 55, but I've had some symptoms for awhile now, mostly what my husband has noticed. Recently the neurologist is talking about it possibly being LBD because other tests came back negative. Instead of visual hallucinations, I have olfactory hallucinations, which we told her in the beginning, but she's not discovering. Also I have Rem sleep disorder, but again, I've had that a couple of years. They've scheduled a neuropsych test for me in February. How does a neuropsych test diagnose LBD?

I have this condition, after about 2 years from diagnosis, especially when going outside in cold weather.

Is there anything you can do for burning mouth due to parkinson?

Which magnesium is best for PD tremors please?

I’d love to hear. NPH and Parkinsonism compared. Dignosed w NPH because of falls incontinence memory and gait. Then Dr told me to also check into PD My MDS said not Parkinson’s but need genetic test ! I first started falling backwards about 10 years ago damaged my spine hit my head. I’m sure… but still can’t get a definite answer. I did have the surgery for NPH, but I’m still having all the symptoms and even worse my short-term memory has completely gone! I’m 77 and hope to stay with my grandchildren a little longer.. but this is not a good way to live ,,: Always fatigued, no energy apathy depressed. have major depressive disorder. Just so ready to give up

Sir any treatment available Parkinson disease

Great topic as usual Dr. Hyland❤

Dr M i just wish der was a cure for PD😢 like yesterday already..iam very tired of being sick tired etc.

I meant United States I want to visit United States

hi brother i am so happy to watch your video thank you i really wanted to come and visit england

Thank you, Dr. Hyland. This is very beneficial information. I appreciate and thank you. I've shared it on my community page. I hope all are doing well. 🧡🦋✨