What are the symptoms

Does insulin resistance cause the gene mutations to occur or would a gene mutation cause insulin resistance?

If C9ORF72 Gene mutation (chromosome 9) causes FTD, would this change the outcome of child inheritance?

Brain 40% natural animal fat + more cholesterol required by the brain, what are we eating? high carbohydrates = SUGAR,,the killer of brains.......

Umm. It’s a good informative video. Umm

He youngest in history to get ftd under 18 forced under chemicals

Frontel cortex gone 16 Holes temporal lobe thinning coursump collisim butterfly pattern look like Demita to me

Sad

Is there no middle stage?

Amei esse médico... Falou tudo que eu precisava ouvir 👏👏👏👏👏

Great content. You should repackage it to a more attractive video presentation. I nearly passed over it simply because of the dull appearing powerpoint etc.

Thank you from the bottom of my heart. I needed to hear what you have said. I am working on feeling what I feel, not stuffing what I feel. You are a wonderful human being. Thank you for your compassion. ♥

We make good progress by using mykotherapy medicinal mushrooms (in Germany). They are working like "soothing" and as nerve stabilizers. Also detox and anti-inflammatory. VERY helpful! Plus: We pick them for free in our local forest. 👍👍

My mother is 89 and violent. She refuses water and food now. Really horrible things she says. She's been in mental ward for 6 weeks, no one will take her, she's actually frightening. She had mental illness before the dementia. We don't know where we go from here.

Brain toilet. Lack of CSF drainage.

Would blood clots in brain 26 years ago rear their head as FTD ?

My wife started mental change a couple of years ago of normal bi-polar towards child like with this absolute need to cut in font of me like a 3 year old needs to cut in front of daddy. Also not doing what I asked but progressed to, I asked her to look on her right but instead looked left. Now major problems finding the right words to incapable of knowing what I ask her to do. Five years ago I have gone from what the heck is she doing now to softly guiding her to where I want her. She is now 59 years old. 10 years ago or so she would combine words sorparate but ment sort and separate.

Amazing speech I was deeply moved thank you 😊

Great information...

Thank you for the information.

Will same symptoms exist for multiple neurofibromatosis type 1 along with tumours in the whole spinal tiny ones and extra large tumour in the dorsal region edema in the hippocampus region and thigh region. How to distinguish whether it is due compressing of the whole body due tumour damaged nerves viens tmcells muscle mass bone density or dementia or any health issues

Omg so u telling me tau is not causing FTD dementia and the doctors have no idea what causes FTD?

With Aphasia,my patient doesn’t answer any questions. Yes may mean no and no means yes. She tries to make sounds but 90% of sounds are unintelligible. Can’t tell if she is in pain. I want to help but don’t know what she is trying to tell me. Very good presentation

This guy has issues. Knocked the mic with his sleeve and didn't put it back in place.

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: [email protected] OR WhatsApp / call +2348118184266

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: [email protected] OR WhatsApp / call +2348118184266

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: [email protected] OR WhatsApp / call +2348118184266

3

Watching in 2020 learned a lot since this vid was made but dementia is still relentless.

What a beautiful soul 🙏🏻

g00d vid

Um um um uh da um da da. Speaker needs to learn how to speak properly and stop using those annoying fillers. He sounds uneducated

Q

A lot to think about. A lot of interesting points. Thank you

Picks which this is affects my family male line

Trump's word finding problem / FTD symptom: "I know words, I have the best words"

Does #Trump have this?

We tryed to help my..Dad he was caring for mother ...it killed him in the end ...my mom is in a carehome now at 90 she had pnewmonia ..got over it in last stage ....caregivers take care of you---- you could go first!!!

You are a wonderful speaker, you are an even more wonderful human. I love your heart and I'm so thankful you share it with the world. THANK YOU! ,

Yeah the panel or controller had to be replaced. Support call required unfortunately.

My laptop screen is having the same problem. Did you find the solution? Please tell me.

I am not going to watch anymore on the Shrinkage of both frontal regions of brain. Why, when a Dr. diagnosis me. I will live as I am. To much for me is to much! Everything about me can all be healed back to the original coding if I could just get there... Meaning the trueness of me. It was my Birth Right. I have just lost it. Due to all the Karmic debt I had to carry from this and pass life. But, it can back to the original format.

www.dementiatookmymom.com

The most beautiful and touching speech, thank you so much, I am the care giver for my husband with FTD and I love what you said

Thank you.

kzbin.info/www/bejne/jpTRnaiCoMlsaa8

Why try to prevent infections and pneumonia when the patient is at end stage dementia? Isn't it better to allow these things to happen and shorten the suffering? Surely they have no quality of life.

Excellent talk, thank you.

Super helpful and humane. For those of us dealing with caregiving for a loved one with FTD. Thank you Dan :)

*Thank you for uploading this!*