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Is it linked to Neuroleptic Malignant Syndrome ?As in genetically ?Do you know Dr ?I had NMS 2 X second time a TBI after a coma and all the stiffness ,dosorganisitaion mine I think my left I sure have weakness and stiffness /I am breaking bones here ?I had an MRI in This year and now changes that should not be there at my age I have to go back -For a blood test ,then another memory tests enough to make anyone cry ...I am falling over walking into walls -It's 💩..I just thought I would mention this is a horrible illness ..

Is this lady a doctor

How old can you be effected by this?

I recognize now that my brother in law had LBD. The progression and timeline lines up perfectly. Tnx.

Satan’s inspired label “dementia”into reality is @ a God level with Jesus in heart intuition. Not connected to soul, avoided heart honesty vulnerability, existed hiding in the mind over lifetime, avoided processing their trauma, detached from emotions, avoided dealing with truths, living lies, living in delusion, illusion & denial. That’s as a starting point. Of course if you don’t know what soul is & exposing it over your life, embracing your God given unique personality, then yes you are going to become a stuck in mind zombie not connected to soul. The reality is though, it was their karma for their life & they weren’t meant to get it in a lifetime yet. Not until you discover the connection with the real God human Jesus in heart intuition do you truly get the depths of soul & sovereignty with a saved soul & salvation from exposing your soul. Bible followers too, they become just as much zombies in mind if they don’t get soul also. It’s no joke soul is everything!

The suggestion about placing psychiatric meds on an "allergy" list is terrific. Thank you.

Incredible presentation 🙏🏼❤️ thank you so much!

This is the most informative video on LBD that I have seen. Be sure to save this one.

Marvelous presentation. I was diagnosed as having LBD about a year ago. - - Carrie P.

I have LBD, with a bit of Parkinson movement inclusion. Drs like YOU that try to PROMOTE THEIR OWN BELIEFS ABOUT LBD, should be called into question. It saddens me that you state LBD is a component of Lewy Body Dementia.... As I lose memories, valuable family memories, AND EVEN FORGET HOW TO TYPE (lack of key recollection), cooking ingredients, etc..... YOUR CASUAL ANALYSIS THAT IM DEALING WITH A COMPLICATION/SYMPTOM OF PARKINSONS DISEASE, IS LAUGHABLE!!!!!!

Can you do these if you already have an 11cm peritoneal hernia?

what about the mercury in the high fatty fish? And for leafy green veggies are microgreens included? thx

I am a PT student and I do appreciate this type of information, especially en this rare pathologies

This seems pretty obvious that Joe Biden is suffering from this

Dealing with family members currently with these symptoms. Especially the sudden change in behavior and facial expressions. Very good info here 👍

I can also read this from the computer

I heard that carnivore diet can treat dementia, what about this type of dementia?

I can’t figure out if you’re being tickled under the table.

This is still a lot of subjective clinical diagnosis. Some people with PD don't even have tremors or dementia. Basically you have two different doctors finding symptoms of the same disease effecting different parts of the body. This is similar to cancer. The diagnosis needs to simpler than this. This is why so many people are going years without help because doctors are not willing to commit to a diagnosis. The criteria for diagnosis is ridiculous.

Thank you, doctor.

I do love your explanation. I am in the process of going for a reassessment. They first diagnosed PD after Dat Scan. I also have loss of Swallowtail Sign on MRI. Didn’t respond much to Levodopa. Dx of MCI before PD. Main issues are attention memory and fatigue, tons of autonomic, I have fallen, etc. Question is, docs are deciding between MSA and LBD. Apparently MSA does present with MCI at the beginning in 47% of people. How do you determine if someone has MSA or LBD? What kind of tests should I expect? Thanks !❤

Would've been interesting and probably helpful but couldn't hear with volumr turned all the way up.

My father has recently been diagnosed with lewy body dementia about a month ago. His noticeable symptoms were like noticed by anyone in June or the end of may. He seemed to be fine and his normal self till one day he had passed out on his way to get the mail from the mail box and woke up in the yard (no one was with him at this time but he was fine and we got him checked for stroke signs and all that. From that day on he started to not act right. His memory is there but he's not fully there. He gets stuck in repeated cycles of the same thoughts over and over. He got to a point where he says he was seeing like shadows of people at night and during the day his property and house he said everything looked different and that there was like a glare type of thing or fog in the shy or something like that. All of this seemed to have come out of nowhere. We had to get him into a very nice nursing home that's close to the family because there's no way he can live by himself and I, nor anyone else, is able to live with him so it's just something we had to do. We go to see him everyday. He's absolutely not the same person. I hate it. He used to be just the nicest and most passive person who never really even raised his voice but now he is either non talkative and just out of it or sometimes he's just like aggressive, not like angry or violent but like abrasive like I guess rude for lack of a better word.

I got more information in this video than I did from all the medical staff at the VA. I wish I had found this video earlier. The most I got from the nurse practitioner at the VA clinic was: "You know you're going to die before your husband because of the stress of being a caregiver." She was even wrong on that front also, I'm still here and my husband passed in 2022. I never got a diagnosis from the VA, but all the information in this video points to LBD.

You were great! Thank you 🙏 One question I have though - you posed the question is it probable or possible DLB and then only went through the criteria for probable. What’s on the list for possible or what’s the difference? 🤔

Thank you!

You spoke to so much of my father. Thank you!

Possibly due to a metabolic issue, where the mitochondria becomes faulty and fails, creating no normal pathway for oxygen resulting in a secondary route that is less efficient, this causes macrophages to go out of action, cells multiply, Good diet including cruciferous veg can help and remove sugar that feeds the condition. Global study indicate a genetic link, and COBALT study looking at Memantine

Hi Hannah. Feel free to set up an exercise session on you tube,and then Ignore all the questions there after.

this is wonderful - - thank you!

How soon after stoma surgery can I start these exercises?

Excellent, thank you so much!!

The best vdo on dementia and thank u mam for such a detailed nd comprehensive vdo with simple language thanks again God bless u.

❤

This just happened to show up in my feed a year later....excellent job! My brother (we're 11 months apart). I don't get to see him much but this summer I noticed he had a tremor of his left hand. I mentioned my cat from years ago that only he knew. I was mentioning how she was feral and found me 3 days days after moving. He remembered I had her on a pink leash and took her everywhere. Nothing could be further from the truth. I'm still confounded and worried.

thanks you, great talk - these constant airplanes would make me mad 😠

How many reps if each exercise should be done and how frequently throughout the week? Thanks!

Thank you. That was a wonderful informative video! 👌👄👌

My dad was diagnosed with Alzheimers. Seemed to be more to it than that, but I'm not a doctor. It was the woman at the local health food store who first suggested Lewy Body after I listed off his symptoms. I started researching LBD and it seemed to be a better fit. Nobody would listen to me. Long story short, my dad and wife moved to another city. Dad very quickly took a turn for the worse and ended up in hospital. The first time a doctor walked into his room, without even examining him, the doctor said LBD. My Dad had a living will. It stated "do not feed me if I cannot feed myself" Very quickly my dad lost the ability to speak or use his hands. He starved to death. It was a terrible thing to bear witness to. I had to keep telling myself that it would be worse to watch a big, strong man turn into a vegetable. I read somewhere - I think it was Mayo or John Hopkins - that Alzheimers medications can kill LBD patients. This may also have contributed to my dad's rapid decline.

Please doctor We need treatment approch What is the best for pt with DLBD Is it rivastigmine or donepizel Or memantine ? Can be used together ? Or should be used alone? What about depression? What about psychosis? Please doctor

if have UTI, the frequent trips to the bathroom will be the exercise

I only wish I had had this information before my mother passed away from Lewy Body Dementia & Parkinson’s in July of 2014. Nobody knew or didn’t share helpful information so it goes without saying her life would have been much better if we had known more details about LBD & PD. Now at least I have this info in case it turns out that I have inherited the possibility of getting LBD/PD. Thank you very much for this video.

This looks interesting but for starters the sound is terrible. I have my volume turned all the way up and it's still really soft.

Responding to your call to action. At the time of my car accident, 38 years ago, my major work was senior social worker, but then now with Severe Traumatic Brain Injury. Depression, dementia etc are the next expected processes to possibly happen too my body now. Call to action can be in just that one area of your professional interest, or could be in any other area of social action. In the early years of my activism, 38 years ago, we created various brain injury organizations. Personally my interests moved to ethnic differences in life policies: expectations, individual or social involvements. Call to action can be as an individual person, quietly or obviously. My Hakka heritage (one of the Chinese ethnic groups) tends to be as a puppeteer, working on the superstructures, rather than being the obvious front person. Which ever method of call to action works, direct or indirect, both are needed.

I can’t help but keep noticing how beautiful you are. I’m listening to you to try and educate myself on what’s going on with my dad 🙁 but seeing you light up the room helps hear this sad information

Thank you for sharing. This is quite helpful in understanding our mom, who's been struggling with symptoms for years, but cannot get a diagnosis.

Thank you for being sweet while u r explaining this.

My Mom is having auditory hallucinations but not visual. She was diagnosed with Dementia.

Dr. Fleisher, Your video is fabulous and I found it extremely helpful in understanding some of the progression I was seeing in a loved ones condition. I would love if you could make another video that touches on some additional subjects such as whether you have seen another underlying health condition (i.e. cancer or its medications) lead to the "parkinsonism" symptoms that begin in the brain stem - or if the development of Lewy Bodies and proteins is not something triggered by anything else. Are there any hereditary trends in neurodegenerative diseases? I would also like to know what symptoms tend to present as the lewy bodies migrate from the brain stem to the rest of the brain, and is that painful for the patient (i.e. can they feel the lewy bodies spreading - akin to a bad headache etc.) I would also like more information of end of life quality of life and caregiver tips. Lastly, can you discuss more of the differences with Lewy Body dementia and vascular and frontal lobe dementia...

I wish every doctor could communicate and explain complicated things as well as you do. Thank you!!!!!