Neurodegenerative Disease Seminar
Neurodegenerative Disease Seminar
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Creutzfeldt-Jakob disease (CJD)
Creutzfeldt-Jakob disease (CJD)
Переглядів: 2 333

Відео

Amyotrophic lateral sclerosis (ALS)
Переглядів 446 місяців тому
Amyotrophic lateral sclerosis (ALS)
Spinocerebellar ataxia (SCA)
Переглядів 3096 місяців тому
Spinocerebellar ataxia (SCA)
Myasthenia Gravis
Переглядів 336 місяців тому
Myasthenia Gravis
Spinal Muscular Atrophy (SMA)
Переглядів 396 місяців тому
Spinal Muscular Atrophy (SMA)
Wernicke's Korsakoff Syndrome
Переглядів 1076 місяців тому
Wernicke's Korsakoff Syndrome
Chronic traumatic encephalopathy (CTE)
Переглядів 176 місяців тому
Chronic traumatic encephalopathy (CTE)
Infantile Neuroaxonal Dystrophy (INAD)
Переглядів 1146 місяців тому
Infantile Neuroaxonal Dystrophy (INAD)
RBD
Переглядів 96 місяців тому
REM Sleep Behaviour Disorder (RBD) is a disorder of dream enactment.
Alzheimer's Disease
Переглядів 56 місяців тому
Alzheimer's Disease
Friedreich's Ataxia
Переглядів 1616 місяців тому
Friedreich's Ataxia
Huntington's Disease
Переглядів 86 місяців тому
Huntington's Disease
Multiple Sclerosis
Переглядів 596 місяців тому
Multiple Sclerosis
PSP - Progressive Supranuclear Palsy
Переглядів 326 місяців тому
PSP - Progressive Supranuclear Palsy
bvFTD - Behavioral Variant Frontotemporal Dementia
Переглядів 2,5 тис.3 роки тому
bvFTD - Behavioral Variant Frontotemporal Dementia
MELAS - Mitochondrial Encephalopathy Lactic Acidosis & Stroke-like Episodes & Seizures
Переглядів 5 тис.3 роки тому
MELAS - Mitochondrial Encephalopathy Lactic Acidosis & Stroke-like Episodes & Seizures
Spinal Muscular Atrophy (SMA)
Переглядів 2673 роки тому
Spinal Muscular Atrophy (SMA)
Progressive Supranuclear Palsy (PSP)
Переглядів 1923 роки тому
Progressive Supranuclear Palsy (PSP)
REM Sleep Behaviour Disorder
Переглядів 1874 роки тому
REM Sleep Behaviour Disorder
Brown-Vialetto-Van-Laere Syndrome
Переглядів 1,4 тис.4 роки тому
Brown-Vialetto-Van-Laere Syndrome
Creuzfeld-Jacob's Disease
Переглядів 1634 роки тому
Creuzfeld-Jacob's Disease
Multiple Sclerosis (MS) Rap
Переглядів 4134 роки тому
Multiple Sclerosis (MS) Rap
Wernicke Korsakoff
Переглядів 4144 роки тому
Wernicke Korsakoff
Parkinson's Disease
Переглядів 224 роки тому
Parkinson's Disease
Lewy Body Dementia
Переглядів 534 роки тому
Lewy Body Dementia
Behaviour Variant Frontotemporal Dementia
Переглядів 6 тис.4 роки тому
Behaviour Variant Frontotemporal Dementia
ALS presentation video
Переглядів 2164 роки тому
ALS presentation video

КОМЕНТАРІ

  • @catbee1452
    @catbee1452 Місяць тому

    My husband is all this but he has severe short term memory loss. I've heard of people having more than one kind of dementia.

  • @HelenHarris-r7b
    @HelenHarris-r7b 2 місяці тому

    Jackson Brenda Garcia Daniel Wilson Scott

  • @AhmedIislamRevertMuslim
    @AhmedIislamRevertMuslim 4 місяці тому

    This disease is very painful, I saw it with my own eyes. My father had Frontotemporal dementia, (bvFTD) He passed away on 12 January 2024.😞 What Is Frontotemporal Dementia ?(bvFTD) Shrinkage of the front part of the brain is called frontotemporal dementia (bvFTD). Frontotemporal disorders (FTD), sometimes called frontotemporal dementia, are the result of damage to neurons in the frontal and temporal lobes of the brain. bvftd symptoms are personality changes, patient loses weight, has memory loss, cannot eat on his own, cannot wear clothes, cannot walk and has sleep problems In frontotemporal dementia, the patient also suffers from Apahsia Means loss of voice.he can't speak Science has just found out that there is no cure for this disease, why this disease occurs, science still does not know. Quran had told about dementia 1500 years ago. This is one of the signs of Allah Click This Link & see video-ua-cam.com/video/-MHRbIejyrA/v-deo.htmlsi=pumN2a_SpbS6f8nS

  • @fallmar05
    @fallmar05 5 місяців тому

    My sister just recently passed from this."Emotionally" devastating experience to go thru. Hope more people become aware of this disease. Knowledge is "progress" towards a treatment one day(god willing).

    • @shellbacksclub
      @shellbacksclub 2 місяці тому

      So sorry for ur loss. I just lost my uncle 6 months ago to CJD. It's unbelievable.

    • @fallmar05
      @fallmar05 2 місяці тому

      @@shellbacksclub Thank you for your condolences. It is consoling to know that there are others who truly understand this unique experience and that we share our grief in our great loss. May your loved uncle as well as my wonderful sister know a truly peaceful sleep now and wake to a glorious day. A healing thought.

    • @vtj2e
      @vtj2e Місяць тому

      Sorry for your loss. My mother is also diagnosed with cjd. Her memory is rapidly detoriating. How long is the life span of person having this disease

    • @fallmar05
      @fallmar05 Місяць тому

      @@vtj2e So sorry to hear about your mom having this unforgiving disease. You have my heart and that of others who have gone thru this experience with their loved ones. To answer your question the duration from showing symptoms of falling,memory loss and other to eventual passing is around 6 months often less. Diagnosis is often only confirmed well into this span. I hope you can give her every bit of love that you can during this time for the ordeal will be haunting and heartbreaking."Be strong" for her. I will pray for her and you. Take care.

  • @jeremiahbaker6396
    @jeremiahbaker6396 6 місяців тому

    Thank you

  • @markgentry6688
    @markgentry6688 8 місяців тому

    Thank you ❤

  • @SR-bw3sc
    @SR-bw3sc 11 місяців тому

    The music is a bit intense.

  • @Ilyxs
    @Ilyxs Рік тому

    I have MELAS myself and this is one of the best videos for people who want to learn something about MELAS

  • @lacypatterson5984
    @lacypatterson5984 2 роки тому

    The sad thing is when you are fighting for them Everyone else thinks you’re the problem OR isn’t ballsy enough to stand up

    • @catbee1452
      @catbee1452 Місяць тому

      No. Kidding. They don't believe things are as bad as you say they are. Total lack of support. Our daughters are afraid to talk about their dad's dementia, let alone offer me support.

  • @nonacee5065
    @nonacee5065 2 роки тому

    Very simplistic view of FTD.

  • @louisegalluzzo1749
    @louisegalluzzo1749 2 роки тому

    So it has been pointed out to me that you may not have intended to sound flippant by your usage of 'just neuron death', which I accept, but I would urge you to be more mindful in future as this is a devastating disease. That said, I do applaud you bringing it to the attention of people as no one seems to have even heard of it.

  • @nicksteini
    @nicksteini 2 роки тому

    Very informative, thanks

  • @andreagoodman5414
    @andreagoodman5414 2 роки тому

    This is my JAM

  • @eileenking9987
    @eileenking9987 3 роки тому

    Thank you for this information. It answers a lot for me .

  • @dilsalange
    @dilsalange 3 роки тому

    Me gustaria en espanol

  • @louisegalluzzo1749
    @louisegalluzzo1749 3 роки тому

    You pissed me off at the me off at the ’just neutron death’. You clearly have never had anyone closer to you with this.

    • @nicksteini
      @nicksteini 2 роки тому

      She didn‘t mean „just neuron death“ as disrespectful. It‘s simply the medical definition of atrophy :)

    • @louisegalluzzo1749
      @louisegalluzzo1749 2 роки тому

      @Kimmy Anfo yes, because I care what you think. You clearly don't get it, see Furtuna has made a polite response which made me realise the girl in the video is not intentionally being disrespectful. How exactly is staying my opinion rude? How is it irrational to be bothered by language which to me, an autistic person who takes things literally, trivialises a disease which my mother has and has had a devastating impact on our family?

  • @user-ii3vn8tn3q
    @user-ii3vn8tn3q 3 роки тому

    Couldnt it be that I just don’t like people?

  • @violet9853
    @violet9853 3 роки тому

    my relative turned into a horribly mean, spiteful and revenge minded psychopath, telling lies all the time, it was so hurtful and unjustified. 😥 oh and he would never go see a doctor... because he "knew" there was nothing wrong with him.

  • @touchofzen8428
    @touchofzen8428 3 роки тому

    There is some evidence, that you can revers TAU or other Proteins accumulating in your brain - 🧠 Dale Bredeson wrote a great book called "The End of Alzheimers" and it can give hope for people with other forms of dementia.

  • @paulflint6254
    @paulflint6254 3 роки тому

    I have a diagnosed mental illness but would like a brain scan to find out if it's something else. Would love to know how to go about doing this as my behaviour has really deteriorated recently and I'm losing control, thanks

    • @Orourke-r7v
      @Orourke-r7v 2 роки тому

      My loved one, who has FTD, saw a neurologist

    • @paulflint6254
      @paulflint6254 2 роки тому

      @@Orourke-r7v thanks , i think i was just mentally ill.

  • @LoriAnneHarris
    @LoriAnneHarris 3 роки тому

    you should have explained that is is usually a defect in the mitochondrial DNA and not the nuclear DNA double helix most people think about, (that you showed)

    • @deannafrankton9532
      @deannafrankton9532 3 роки тому

      To answer your question: it is due to copyright laws and availability of free and or paid images.

  • @LoriAnneHarris
    @LoriAnneHarris 3 роки тому

    why did you never show the mitochondrial DNA structure

    • @angelinarobert622
      @angelinarobert622 3 роки тому

      it's not double helix DNA. it's the wavy structure inside the Mitochondria. 🤔 why not show the mutation an A to G or Guanine molecule next to Adenine like wikipedia.org/DNA/ page does? Now that's chemistry. all we are is 100's of trillions of atoms. 🤔 you'll need a Quantum Computer to figure us out.

  • @dollytelgote2738
    @dollytelgote2738 3 роки тому

    I am from India,I got diaganosed with same 3 days ago..let me know if I can help

  • @agelinagozes6365
    @agelinagozes6365 3 роки тому

    HOW MY HUSBAND GOT CURED FROM Amyotrophic Lateral Sclerosis (ALS). I lost my Dad to ALS 5 years ago, he suffered from the dreaded disease for 6 years with his doctor telling us he can’t be cured and all the therapies and life support machines could not save him and 3 years later my husband was also diagnosed of the same disease and I was devastated he fainted when the doctor read the diagnosis because he knew how deadly the disease is. His condition worsened and he was unable to move and he was confined to the chair the direction the disease has taken with his body is the gradual deterioration of the “Bulgar muscle,” which controls breathing, swallowing, voice, and tongue movement. His neck muscles have weakened to the point that he can’t hold his head up and the left side of his body is weaker than the right , the doctors told me all his muscles were dead, he was able to eat via a machine because he could not swallow anything. I searched and tried different neurologists and different medicines none worked and I was so scared to lose my husband. While running up and down seeking a solution I met my friend from third grade and saw me all worked up, we got talking and in the process of discussion I told him all I am facing. He felt sad and told me about Dr. Sani who was able to cure his cousin. I was interested and he gave me his contact. I contacted him and he sent me his medicine and in a space of 4 weeks he was up on his feet again and in 6 week here covered fully. He can do normal things like walking, eating, without any assistance whatsoever. I am so amazed at the potency and effectiveness of his medicine. I decided to share my story for you not to lose hope or feel your world has ended. Simply contact him by Email: perfectherbalcure@gmail.com OR WhatsApp / call +2348118184266

  • @stefanlehmann7699
    @stefanlehmann7699 3 роки тому

    Honestly speaking the only research that the ’scientists’ will always do involves the increase of big pharma profits. They will never cure any disease permanently for them to make more money by keeping people reliant on drugs, and they will do everything possible to discourage others from trying other medications like herbal medicine but I thank God for my friend who directed me to Dr. Sani.I am happy to inform you all that I am finally free and completely cured of ALS (amyotrophic lateral sclerosis) after using Dr. Sani herbal mixture, the formula works like magic .Always learn to follow your heart, refuse to be discouraged because there is no problem without a solution . I am back on my feet even stronger than before thanks a lot to Dr. Sani. You can also contact Dr.Sani to eradicate diseases like diabetes, high blood pressure, stroke, infertility, tuberculosis, skin disease, hepatitis, fibroid etc.You can reach him through his WhatsApp number on: +2348118184266 or via Email: perfectherbalcure@gmail.com

  • @catherine7147
    @catherine7147 3 роки тому

    My husband passed away last November from some form of this disease. We never received a complete diagnosis and certainly never had any guidance. My husband started experiencing many of the characteristics mentioned in his early 50’s. Despite seeing 6 different neurologists and several neuro psychiatrists, He was told he had severe depression most often. He was given medications and some seemed to help with behavior issues. In July of 2020, a neurologist gave him a pamphlet and said he may have a type of FTD. He had accompanying gross and fine motor difficulty and experienced many falls and injuries. He was an environmental geologist and missed working. He died at age 66 at home with his dog at his side. This was a very good explanation but care in the real world is lacking.

    • @jenniferrobinson1792
      @jenniferrobinson1792 2 роки тому

      I am experiencing these symptoms. It’s difficult to get a diagnosis. It’s worse for my friends and colleagues than for me. I can’t imagine what you endured.

    • @catherine7147
      @catherine7147 2 роки тому

      @@jenniferrobinson1792 thank you and I hope you can find some help managing the symptoms.

    • @FresnoRays
      @FresnoRays 5 місяців тому

      I'm sorry if I sound insensitive, but what was it like living with him? At what phases of the disease was he unable to have full conversations anymore? At what phase was he unable to speak full sentences, and when did he get reduced to groans and moans when it came to speech? I'm doing a college project over the summer and I want to learn more about ataxia in bvFTD.

    • @catherine7147
      @catherine7147 5 місяців тому

      @@FresnoRays The disease developed slowly the first 5 years. He was still able to work however he was losing the ability to complete reports due to word finding difficulty. Over the next 4 years, he would answer slowly and had more significant word finding problems, This was frustrating to him and he would avoid conversations at times. Some days he was more verbal and some days unable to speak . He never fully lost speech until the last few weeks of his life. At that point, he was sleeping a lot. I hope this information is helpful to you.

    • @FresnoRays
      @FresnoRays 5 місяців тому

      @@catherine7147 How is the progression like? Is it exponential or is it a a gradual decline

  • @MrSmokeTheBongAlong
    @MrSmokeTheBongAlong 3 роки тому

    Actually like the lyrics. The voice not so much but yeah got the same shit.

  • @hussainalhumud
    @hussainalhumud 3 роки тому

    I'm from Saudi Arabia and I have a 14-month-old girl with the same syndrome I want to contact the child's family to benefit from their experiences.

  • @amandafurlong1079
    @amandafurlong1079 4 роки тому

    who's the creator

  • @amandafurlong1079
    @amandafurlong1079 4 роки тому

    this is AMAZING

  • @bobinab8925
    @bobinab8925 4 роки тому

    Thank you for posting this! There is not many recent videos on RBD. I’m 23 and have had this disorder since I was 12 years of age.