This disease took everything from me... My best friend and cousin. Was fine one day and woke up and snapped then passed away within 3 weeks. Extremely cruel disease.
It is extremely rare, affects 2 in a million people a year. My lovely mum passed away from it 4 years ago, she was only 56. I'm just glad it is rare as it's horrible.
@@dxublexxsplicitxxsplicit4943 nah, nothing wrong with his English, must be you, bro. I don’t see why you’re making this point, he said his beloved mum passed away and that he is glad that it is a rare disease since it is horrific.
My Grandma passed away from this. It was terrible and happened so fast. When her first symptoms started we all thought it was just from a concussion from falling in the snow but it quickly grew worse and worse :(
@@SotonbrainhubUk1 Atypical L-BSE and H-BSE cause SCJD. C-BSE can propagate either SCJD or NVCJD subtypes. My dad died from exposure to Atypical L-BSE after being a butcher for 47 years. It caused SCJDMM1-2. From diagnosis to death was 29 days.
Plz I want to ask a question ❓ one of my family members had CJD disease...just One month she enters to Coma ? My question is is it the final stage of this disease or is it normal because as I know the ❤ year with this disease (now she has 3 months with it ) ?
My mom has CJD… she’s 47, we thought she was just overwhelmed by work and needed rest… after 3 months, we ran some tests and it turns out she has 30 months to live, max… This disease is atrocious…
I don't know exactly when my sister got CJD but she has been in a coma now for about 4 weeks; feeding tube was removed about 9 days ago; she is in hospice now at a facility in Michigan. An autopsy is going to take place. She is 60 years young.
@@kayleighgriva4817 5 months later now, she can barely walk. She’s mentally completely disabled, but still smiling and laughing when she’s not having paranoia. I hope your nan still has a smile on her face. Sending you love too!
My uncle just passed away from this earlier this morning 11/6/22. He was diagnosed in September they thought he had a stroke and he went downhill fast. I really hope that a treatment is able to be developed.
Oh, man. I am so sorry! I know how you are feeling, a bit. My mother died January 3rd, 2021 from Dementia and something I don't want to state yet until is official. It was made worse and very quickly so, by COVID-19 and the quarantine. I can only imagine the hell you went though and I hope your mother did not suffer for a long time. My thoughts are with you. I hope you have the chance to grieve properly in all this COVID-19 mess. If you ever need to talk, DM me. Peace!
I dont know why youtube only recommended this video to me now, but I'm sure glad they did cuz this is amazing. clear and informative without any fluff. this is what im looking for on this site. Edit: the self promotion is a bit much and breaks up the video a bit too much imo
CJD runs in my family. I just found out today.. Ive already lost my aunty from CJD, now my grandfather is dying from it, and im currently chronically ill and I have to get a test to see if I have CJD.
@@cofiking23 I don't know. I got referred to a geneticist for the test, but I have to wait a little while longer to go get the test. Apparently it's a blood test, and if there's a possibility of you having CJD, they then take some fluid from your spine and test that.
@@ahsenaftab6220 well I'm no longer having an existential crisis over it. I have a genetics appointment in September to see if I have it laying dormant. My grandpa has passed, he was in hospital for CJD and then he got covid at the same time. Which is pretty unlucky. But things aren't too bad. He lived a long life and as morbid as it sounds I'm glad he passed quick. He was gone within a month. Seeing what my aunty went through living with CJD for a whole year and a half is living hell. CJD isn't really something you want to live with. So in a way I'm glad he went quickly. But thank you man, I'm just lucky to live in an era with modern day medicine.
My mother has dizziness last December but now she's catatonic admitted in the hospital and rapid body deterioritation we don't know yet the definite finding since all her lab tests are negative , waiting for the results of her Anti-NMDA receptor and protein 14-3-3 😔 it's so hard not knowing what treatment plan/protocol she'll undergo yet..
@@bayle3942 I wouldn’t say it’s not curable. Well perhaps in our lifetime it is but as technology becomes more advanced we might be able to find a cure for it in the future.
Yes. Something that can recognize im gon a say probably programmble particles. Or tiny bots that can search and destroy. We are bit closer but still need time
@@cryonic8215 prions are hard to destroy most drugs won’t work it doesn’t destroy them but the only way prions can be destroyed are by heating them up to 900 degrees Fahrenheit or bleach
I’m 95% certain I’ve got variant cjd, I’ve had these symptoms that are identical to it since September 2020, symptoms are muscle twitches sleep disturbances visual disturbances with a blind patch now occurring in my left eye, and some weakness in my right leg.
I've also been deathly afraid too of this disease, i may not quite know much as i am not a medic or qualified expert but sometimes the weakness around the leg may or may not be a sign of another neurological sickness such as a brain tumor, sometimes the cases of this disease tend to be much more quick (a couple of months to enter an advanced stage of this disease from most cases) and fortunately if the news of a brain tumor are presented then maybe, just maybe, You Will survive and overcome the sickness rather than perish to this fatal yet unique disease. I hope that You are fine for the next few months and perhaps You should go ahead and check for the spinal fluid test or a brain scan as perhaps You could have a chance to keep going with us.
I had a brain scan last may and it was all clear, you see with this blindness setting in it can only be vcjd, but thanks for wishing me the best you’ve been a breath of fresh air with your words👍✌️🙏👌
Let's say that i have been way too paranoid of it since a thing that happened on September, where i felt confused and from then and now there hasn't been any form of evaluation other than psychological and blood tests (it's important to say that i'm a young person who tends to be paranoid) but despite how soon it may be, that has been a thing that traps my mind into a cycle of paranoia and anxiety about it, despite having almost no symptoms (sometimes small balance problems and forgetting things where soon after i can remember them) i pretty much want to be safe for i haven't enjoyed my life enough and have yet a lot to lose...
My hypothesis: excess iron (hence old people) likes to bind to protein, resulting in misfolding of the prion protein. As this goes on, the prions tie up heat shock proteins in the brain which are supposed to deal with misfolded proteins. So this reinforces accumulation of prions. This explains why it is 'transmissible' by injecting prions: the prions also tie up the heat shock proteins. But if they continued the experiments, they would probably see that these cases tend to resolve because no inherent misfolding problem. Solution: iron chelation. The 1993 Bueler paper showing that knockout mice are immune to inoculation with prions actually supports my idea, because they also found that heterozygous knockouts were also resistant. Which makes no sense unless you assume it's a quantitative phenomenon. Clearly, half as many prion proteins would still be infected. Instead, what is probably happening is prions do not propagate misfolding. Instead, prions naturally misfold. And disease is only an outcome of an imbalance of heat shock folding proteins to misfolded prions. In the experiment, the injected prions plus natural misfolding overwhelmed the heat shock proteins, leading to accumulation. But in the heterozygous case, the injected prions and naturally misfolded prions were not enough.
Nice video, but I think you might, next time, want to be a tad more clear on the "mad cow disease" issue. Human beings can NOT get Mad Cow Disease or BSE. I know you didn't say that, but 2 people I was watching with inferred (whether or not you implied it) that you could get Mad Cow Disease from cows. (but still learned a lot watching this video!) A human being can NOT get vCJD from eating the muscle meat, which is ground beef, steaks, roast... or milk products. They must eat NERVE TISSUE from the cattle, like spinal cord or brain. Yuck! I'm not sure if you've heard of the Fore people of Papua New Guinea, but they have a funerary rite in which they perform endocannibalism on certain members of the dead. Relatives would bury the family member and days later exhume the body to eat it, with the warrior men eating the "choice pieces of meat" like the arms, legs, and muscle parts of the body and the women and children eating the brain and other areas. The whole body was consumed, maggots and all. They wanted to return the life force of the relative to the tribe and family. This act caused a sickness called transmissible spongiform encephalopathy (TSE), or prion diseases, of which CJD is the most frequent. They call the sickness from this Kuru, meaning "to shake or tremble." or negi-nagi, which means silly or foolish person. The disease makes people laugh at weird intervals and is also called the "laughing sickness." This tribe stopped the funerary rite in the 1960s and recently, the last victim of this disease was thought to have died. What is amazing is that the Fore people developed a "naturally occurring prion protein" that confers somewhat of a resistance to TSE, and they only found this in the area and in people where Kuru was epidemic. This is a genetic evolution that scientist believed only just happened and over about 10 generations! That is damn amazing. Many tribes practiced some form of anthropophagy , or cannibalism, in history. I'm sure there is much more to this that I'm unaware of, but it is a fascinating research!
@@scienceium5233 Yes,you are correct. That is a good point to make, but in the US and other "developed countries" it is extremely rare. The risk is so low, that statically, it is about nothing! If people are still freaked out about the possibilities, they should get only "muscle" meat. I believe it is under 200 people worldwide that have developed BSE. That is damn low per the amount consumed, but it is still a good point that it does exist so playing it careful, if you're worried, is a good idea! The rendering machine (I think they're called that) that strip the meat off the bone are designed to strip as much as they can down to the bone, so chops, roast, and steaks are the safest, T-bone steaks are the ones in that category you might want to use a little caution with. The "T" in T-bone meat comes from the area where the vertebrae in the backbone meet the rib, and that "meeting point" can contain small pieces of spinal cord. Can you think of anything I missed? That was a good point. Thanks for correcting me!
@@scienceium5233 Well, on the animal population, at least. Creutzfeldt- Jacob Disease is not transmissible from human to human, thank goodness! BSE (Mad Cow Disease) is also not transferable from human to human, other than through cannibalism or infected tissue. But yes, it would be devastating to farmers and parts of the economy.
My close aunt sadly passed away from CJD. It was shocking to see how quickly it progressed and how quickly it debilitated her. After her passing, we got a call from the Ministry of Health stating that we had absolutely no choice but to cremate her, which neither we nor most importantly my late aunt wanted. After a lot of begging, they finally gave us the option to bury her as long as she was bolted into a certain metal box that they were going to bring and place her in following the funeral that was instructed to be completed the very next day. It was extremely difficult to plan and negotiate all this in literally an hour of her passing. She's definitely missed 😢
He was a notary, he could remember articles of law, recite different mortage particularities but could not compose a phone number or write a letter. There was electrical storms in his brain. His face made stange twitches. He could not process the steps to go to the bathroom, he had small moments of clarity, the last time he looked at us and said: kaput! He tried to say something but nothing came out. Then he could not swallow, then he was given what they call "comfort care".
My mother passed away from CJD, which is a human form of mad cow disease and there is no cure. It is a 1/1 million likelihood of contracting this. It was originally diagnosed as Alzheimer's but it came on so aggressively within four months she was gone. We needed answers, so we had an autopsy done on her cerebrospinal fluid which confirmed the presence of cjd prions. At that time, 14 years ago, we were told the only way to contract this disease was through a blood transfusion but the medical community has found a variant form of cjd that can People can get from eating tainted beef (BSE). I have another theory that she may have gotten this disease from taking a supplement containing bovine testes extract. I guess we'll never know but I have a feeling we're going to see an increase in this awful disease in the near future
It was more rare in that prior to ‘pandemic’, it was 1 in a million but when my sister died, it was stated 3 in a million but the number just continued to get greater and greater.
People with experience of it are more likely to look it up. 1 to 2 in every million in uk get it. 131 deaths in 2020, if I’m remembering that right. It’s not that many. 57 million is the population. 131 out of 57 million. 26,000 from flu with pneumonia died in 2019 in England and Wales. We tend not to panic about that one. I don’t know where you are but stats will be around the same. Less even maybe if out of uk as we had the whole vcjd shenanigan.
Plz I want to ask a question ❓ one of my family members had CJD disease...just One month she enters to Coma ? My question is is it the final stage of this disease or is it normal because as I know the ❤ year with this disease (now she has 3 months with it ) ?
In theory yeah, (although you would be dreadfully unlucky to get both). Rabies is a virus, it will travel retrogradely along motor neurones to the brain. Not sure it would worsen cjd symptoms, but that might be the least of your worries!
Im sure that you would die a lot faster with having both as your brain gets turned into mush. Both prions and viruses wreaking havoc to your brain cells. Those both have got to be the two worst diseases you can have. Rabies is worse because you have merely weeks, with CJD at least you can still potentially live up to a year and have time to complete your bucket list before you go
Hello ! I will be 17 on June 13 , I got a brain mri in 2023 March it came clean doctors said it may be anxiety but the symptoms have got worse slowly slowly, I have muscle weakness and little muscle loss , myopia in right eye , little stammering and hearing problems and short term memory loss tooo I don't know what it is
Do u have sleep disoder or emotional disorder too ? I have sleep disoder, some kind of memory loss and emotional disoder too Idk what kind of shit im having too XD also im not depressed at all Its just i cant feel much thing and dont have any negative thought in my head
Is this contagious? My mum died 10 years ago of this. As we did not lnow we never protected oueselves with gloves when chnginh disper, I slept with her. My aunt died this week of this. I am si scared
@@MindStrider34 my aunt yes!!!!!!!! She had Pfizer . My mother did not. She died 10 years ago 2010 after a trip to Uk in 2008. 1 year after strated w symptoms.
@@ingridjocelynab1 I'm sorry for your loss. There is proof the symptoms of mad cow disease is almost exactly the same with the vaccine. I don't think nothing will happen to you unless you take the shot.
i knew a woman who died from this a couple years ago. the comments saying they know someone who died from it all seemed to have died within the last few years. i’m wondering how this is happening so many years after chernobyl
I love to see medical dramas shows and web series and I want to become a doctor in future I listen this disease name in k drama emergency couple so I excited to know about disease
@@XenoZeduX yeah , unfortunately prions are hard to destroy , but thanks to natural weathering and decay degrades prions over time rendering them less infectious ,containing the spread is hard but not impossible ,but what we really needs is a cure to all variants of prion disease, i hope scientists can make that happen
specific prnp mutations (gene which encodes prp protein) can cause prp made to have chemical imperfections which lead to instability and therefore a heightened chance of misfolding into infectious prions@@Pazuzu82
This disease took everything from me... My best friend and cousin. Was fine one day and woke up and snapped then passed away within 3 weeks. Extremely cruel disease.
Very sad 😞
I am sorry for your loss.
Hello, I'm from Russia, can you please tell me your friend got sick for only 3 weeks? And how old was your friend?
read a book called virus mania 2021
download it for free from Z library
Im sorry for your loss, was this back in the 80/90s Europe?
The fact that from googling this, most cases are caused by “no apparent reason” is terrifying.
It is extremely rare, affects 2 in a million people a year. My lovely mum passed away from it 4 years ago, she was only 56. I'm just glad it is rare as it's horrible.
@@fayeb6593the way you worded that makes it seem like you wanted her to suffer. I know that's not the case but your English is a little off
@@dxublexxsplicitxxsplicit4943?????????????? ur tripping lol
@@dxublexxsplicitxxsplicit4943 nah, nothing wrong with his English, must be you, bro. I don’t see why you’re making this point, he said his beloved mum passed away and that he is glad that it is a rare disease since it is horrific.
@@dxublexxsplicitxxsplicit4943Not so. You’re just inconceivably stupid.
My Grandma passed away from this. It was terrible and happened so fast. When her first symptoms started we all thought it was just from a concussion from falling in the snow but it quickly grew worse and worse :(
Very sorry to hear that, you are right - it is a cruel disease.
@@SotonbrainhubUk1 Atypical L-BSE and H-BSE cause SCJD. C-BSE can propagate either SCJD or NVCJD subtypes. My dad died from exposure to Atypical L-BSE after being a butcher for 47 years. It caused SCJDMM1-2. From diagnosis to death was 29 days.
Plz I want to ask a question ❓ one of my family members had CJD disease...just One month she enters to Coma ? My question is is it the final stage of this disease or is it normal because as I know the ❤ year with this disease (now she has 3 months with it ) ?
My mom has CJD… she’s 47, we thought she was just overwhelmed by work and needed rest… after 3 months, we ran some tests and it turns out she has 30 months to live, max…
This disease is atrocious…
Devastating news, I'm sorry that is happening and I don't even know you.
I don't know exactly when my sister got CJD but she has been in a coma now for about 4 weeks; feeding tube was removed about 9 days ago; she is in hospice now at a facility in Michigan. An autopsy is going to take place. She is 60 years young.
@@karenjohnson4805 I’m so sorry for your sister… I hope you are surrounded by family during these challenging moments…
We thought my nan was having a mental breakdown. She's now unable to walk. Whether your Mother is alive or not still, sending you love and healing
@@kayleighgriva4817 5 months later now, she can barely walk. She’s mentally completely disabled, but still smiling and laughing when she’s not having paranoia. I hope your nan still has a smile on her face. Sending you love too!
My uncle just passed away from this earlier this morning 11/6/22. He was diagnosed in September they thought he had a stroke and he went downhill fast. I really hope that a treatment is able to be developed.
My grandpa passed away due to this disease a few years back. I wish I could have gotten closer to him. :(
I can recommend a powerful man who can help you with herbs and healing spell like he also help me
I'm sorry for your loss
The other comment is from a bot I think
@@israelakisin5201 Wtf is that going to do?
@@israelakisin5201 herbs can stop prions, yeah no. Your stupid, get off this website, step away from the computer, and go to college.
My mom died from this disease a year ago. Extremely cruel disease
Oh, man. I am so sorry! I know how you are feeling, a bit. My mother died January 3rd, 2021 from Dementia and something I don't want to state yet until is official. It was made worse and very quickly so, by COVID-19 and the quarantine. I can only imagine the hell you went though and I hope your mother did not suffer for a long time. My thoughts are with you. I hope you have the chance to grieve properly in all this COVID-19 mess. If you ever need to talk, DM me. Peace!
I dont know why youtube only recommended this video to me now, but I'm sure glad they did cuz this is amazing. clear and informative without any fluff. this is what im looking for on this site.
Edit: the self promotion is a bit much and breaks up the video a bit too much imo
Thanks for the kind words and the constructive feedback…Noted!
CJD runs in my family. I just found out today..
Ive already lost my aunty from CJD, now my grandfather is dying from it, and im currently chronically ill and I have to get a test to see if I have CJD.
but what is the test for it?
@@cofiking23 I don't know. I got referred to a geneticist for the test, but I have to wait a little while longer to go get the test. Apparently it's a blood test, and if there's a possibility of you having CJD, they then take some fluid from your spine and test that.
@@bingbong7241 how you doing now man?
@@ahsenaftab6220 well I'm no longer having an existential crisis over it. I have a genetics appointment in September to see if I have it laying dormant. My grandpa has passed, he was in hospital for CJD and then he got covid at the same time. Which is pretty unlucky.
But things aren't too bad. He lived a long life and as morbid as it sounds I'm glad he passed quick. He was gone within a month. Seeing what my aunty went through living with CJD for a whole year and a half is living hell. CJD isn't really something you want to live with. So in a way I'm glad he went quickly.
But thank you man, I'm just lucky to live in an era with modern day medicine.
My nan has it and we are wondering if its familial. Good luck to you. If we both end up with it I wish us speedy deaths!
My mother has dizziness last December but now she's catatonic admitted in the hospital and rapid body deterioritation we don't know yet the definite finding since all her lab tests are negative , waiting for the results of her Anti-NMDA receptor and protein 14-3-3 😔 it's so hard not knowing what treatment plan/protocol she'll undergo yet..
How has it gone?
My Dad too, he is suffering in hospital without any physical response. There is nothing to do except waiting for him to fly to the heaven.
This is really scary I hope there's a cure for this in the future
I believe I read something where due to it being in the brain, it can only be slowed down.
@@bayle3942 oh so it's impossible to make a cure?
@@UglyPotato34 I believe so unfortunately
@@bayle3942 damn that sucks
@@bayle3942 I wouldn’t say it’s not curable. Well perhaps in our lifetime it is but as technology becomes more advanced we might be able to find a cure for it in the future.
Do you think it will ever be possible to create a drug that attacks this specific protein and not good proteins?
Yes. Something that can recognize im gon a say probably programmble particles. Or tiny bots that can search and destroy. We are bit closer but still need time
@@da-yp1wu like monoclonal antibodies?
Nothing's impossible.. Just have to change the way we see things😅
Лечить бкя не смогут не когда, бкя это смерть
@@cryonic8215 prions are hard to destroy most drugs won’t work it doesn’t destroy them but the only way prions can be destroyed are by heating them up to 900 degrees Fahrenheit or bleach
Thank you Kent as expected ..well done
I’m 95% certain I’ve got variant cjd, I’ve had these symptoms that are identical to it since September 2020, symptoms are muscle twitches sleep disturbances visual disturbances with a blind patch now occurring in my left eye, and some weakness in my right leg.
i really hope that you are fine because this disease is horryfing
The truth is I kind of am fine, I can swallow I can walk talk, I just need the doctors to take me more seriously, and I appreciate your concern.
I've also been deathly afraid too of this disease, i may not quite know much as i am not a medic or qualified expert but sometimes the weakness around the leg may or may not be a sign of another neurological sickness such as a brain tumor, sometimes the cases of this disease tend to be much more quick (a couple of months to enter an advanced stage of this disease from most cases) and fortunately if the news of a brain tumor are presented then maybe, just maybe, You Will survive and overcome the sickness rather than perish to this fatal yet unique disease.
I hope that You are fine for the next few months and perhaps You should go ahead and check for the spinal fluid test or a brain scan as perhaps You could have a chance to keep going with us.
I had a brain scan last may and it was all clear, you see with this blindness setting in it can only be vcjd, but thanks for wishing me the best you’ve been a breath of fresh air with your words👍✌️🙏👌
Let's say that i have been way too paranoid of it since a thing that happened on September, where i felt confused and from then and now there hasn't been any form of evaluation other than psychological and blood tests (it's important to say that i'm a young person who tends to be paranoid) but despite how soon it may be, that has been a thing that traps my mind into a cycle of paranoia and anxiety about it, despite having almost no symptoms (sometimes small balance problems and forgetting things where soon after i can remember them) i pretty much want to be safe for i haven't enjoyed my life enough and have yet a lot to lose...
My hypothesis: excess iron (hence old people) likes to bind to protein, resulting in misfolding of the prion protein. As this goes on, the prions tie up heat shock proteins in the brain which are supposed to deal with misfolded proteins. So this reinforces accumulation of prions. This explains why it is 'transmissible' by injecting prions: the prions also tie up the heat shock proteins. But if they continued the experiments, they would probably see that these cases tend to resolve because no inherent misfolding problem.
Solution: iron chelation.
The 1993 Bueler paper showing that knockout mice are immune to inoculation with prions actually supports my idea, because they also found that heterozygous knockouts were also resistant. Which makes no sense unless you assume it's a quantitative phenomenon. Clearly, half as many prion proteins would still be infected. Instead, what is probably happening is prions do not propagate misfolding. Instead, prions naturally misfold. And disease is only an outcome of an imbalance of heat shock folding proteins to misfolded prions. In the experiment, the injected prions plus natural misfolding overwhelmed the heat shock proteins, leading to accumulation. But in the heterozygous case, the injected prions and naturally misfolded prions were not enough.
Nice video, but I think you might, next time, want to be a tad more clear on the "mad cow disease" issue. Human beings can NOT get Mad Cow Disease or BSE. I know you didn't say that, but 2 people I was watching with inferred (whether or not you implied it) that you could get Mad Cow Disease from cows. (but still learned a lot watching this video!) A human being can NOT get vCJD from eating the muscle meat, which is ground beef, steaks, roast... or milk products. They must eat NERVE TISSUE from the cattle, like spinal cord or brain. Yuck!
I'm not sure if you've heard of the Fore people of Papua New Guinea, but they have a funerary rite in which they perform endocannibalism on certain members of the dead. Relatives would bury the family member and days later exhume the body to eat it, with the warrior men eating the "choice pieces of meat" like the arms, legs, and muscle parts of the body and the women and children eating the brain and other areas. The whole body was consumed, maggots and all. They wanted to return the life force of the relative to the tribe and family.
This act caused a sickness called transmissible spongiform encephalopathy (TSE), or prion diseases, of which CJD is the most frequent. They call the sickness from this Kuru, meaning "to shake or tremble." or negi-nagi, which means silly or foolish person. The disease makes people laugh at weird intervals and is also called the "laughing sickness."
This tribe stopped the funerary rite in the 1960s and recently, the last victim of this disease was thought to have died. What is amazing is that the Fore people developed a "naturally occurring prion protein" that confers somewhat of a resistance to TSE, and they only found this in the area and in people where Kuru was epidemic. This is a genetic evolution that scientist believed only just happened and over about 10 generations! That is damn amazing. Many tribes practiced some form of anthropophagy , or cannibalism, in history. I'm sure there is much more to this that I'm unaware of, but it is a fascinating research!
sometimes meat containes nervous tissue in small amounts
@@scienceium5233 Yes,you are correct. That is a good point to make, but in the US and other "developed countries" it is extremely rare. The risk is so low, that statically, it is about nothing! If people are still freaked out about the possibilities, they should get only "muscle" meat.
I believe it is under 200 people worldwide that have developed BSE. That is damn low per the amount consumed, but it is still a good point that it does exist so playing it careful, if you're worried, is a good idea!
The rendering machine (I think they're called that) that strip the meat off the bone are designed to strip as much as they can down to the bone, so chops, roast, and steaks are the safest, T-bone steaks are the ones in that category you might want to use a little caution with. The "T" in T-bone meat comes from the area where the vertebrae in the backbone meet the rib, and that "meeting point" can contain small pieces of spinal cord.
Can you think of anything I missed? That was a good point. Thanks for correcting me!
@@kiastar67 yeah agreed
@@kiastar67 the thing is that if an outbreak were to start it would be devastating
@@scienceium5233 Well, on the animal population, at least. Creutzfeldt- Jacob Disease is not transmissible from human to human, thank goodness! BSE (Mad Cow Disease) is also not transferable from human to human, other than through cannibalism or infected tissue. But yes, it would be devastating to farmers and parts of the economy.
The PM and the rest of us thank you
Pipe line LNG needs checking .and as well as twitter feed
My close aunt sadly passed away from CJD. It was shocking to see how quickly it progressed and how quickly it debilitated her. After her passing, we got a call from the Ministry of Health stating that we had absolutely no choice but to cremate her, which neither we nor most importantly my late aunt wanted. After a lot of begging, they finally gave us the option to bury her as long as she was bolted into a certain metal box that they were going to bring and place her in following the funeral that was instructed to be completed the very next day. It was extremely difficult to plan and negotiate all this in literally an hour of her passing. She's definitely missed 😢
He was a notary, he could remember articles of law, recite different mortage particularities but could not compose a phone number or write a letter. There was electrical storms in his brain. His face made stange twitches. He could not process the steps to go to the bathroom, he had small moments of clarity, the last time he looked at us and said: kaput! He tried to say something but nothing came out. Then he could not swallow, then he was given what they call "comfort care".
My mother passed away from CJD, which is a human form of mad cow disease and there is no cure. It is a 1/1 million likelihood of contracting this. It was originally diagnosed as Alzheimer's but it came on so aggressively within four months she was gone. We needed answers, so we had an autopsy done on her cerebrospinal fluid which confirmed the presence of cjd prions. At that time, 14 years ago, we were told the only way to contract this disease was through a blood transfusion but the medical community has found a variant form of cjd that can People can get from eating tainted beef (BSE). I have another theory that she may have gotten this disease from taking a supplement containing bovine testes extract. I guess we'll never know but I have a feeling we're going to see an increase in this awful disease in the near future
Everyone saying it’s rare but all the comments on many videos say their family member had died from it. Not so rare
It’s about 1 in 750k I think
much more often, 4-5 per million
Still rlly rare
It was more rare in that prior to ‘pandemic’, it was 1 in a million but when my sister died, it was stated 3 in a million but the number just continued to get greater and greater.
People with experience of it are more likely to look it up. 1 to 2 in every million in uk get it. 131 deaths in 2020, if I’m remembering that right. It’s not that many. 57 million is the population. 131 out of 57 million. 26,000 from flu with pneumonia died in 2019 in England and Wales. We tend not to panic about that one. I don’t know where you are but stats will be around the same. Less even maybe if out of uk as we had the whole vcjd shenanigan.
Plz I want to ask a question ❓ one of my family members had CJD disease...just One month she enters to Coma ? My question is is it the final stage of this disease or is it normal because as I know the ❤ year with this disease (now she has 3 months with it ) ?
my father in law suffard from this disease now and admite in aiims in india ....suggest me where is the treatment possible
I remember hearing about this back in October 2018
I can recommend a powerful man who can help you with herbs and healing spell like he also help me
Is this other comment from a spam bot?
Short and precise 👍
Thank you for the info
If someone has this can they get rabies? Will it make their brain swell still? Would it worsen or hasten the effects of cjd?
In theory yeah, (although you would be dreadfully unlucky to get both). Rabies is a virus, it will travel retrogradely along motor neurones to the brain. Not sure it would worsen cjd symptoms, but that might be the least of your worries!
Im sure that you would die a lot faster with having both as your brain gets turned into mush. Both prions and viruses wreaking havoc to your brain cells. Those both have got to be the two worst diseases you can have. Rabies is worse because you have merely weeks, with CJD at least you can still potentially live up to a year and have time to complete your bucket list before you go
Hello ! I will be 17 on June 13 , I got a brain mri in 2023 March it came clean doctors said it may be anxiety but the symptoms have got worse slowly slowly, I have muscle weakness and little muscle loss , myopia in right eye , little stammering and hearing problems and short term memory loss tooo
I don't know what it is
Get it checked again
Do u have sleep disoder or emotional disorder too ?
I have sleep disoder, some kind of memory loss and emotional disoder too
Idk what kind of shit im having too XD also im not depressed at all
Its just i cant feel much thing and dont have any negative thought in my head
@@accnew8649 kind of May be I don't know , do you have foamy urine or other kidney issues
Is this contagious? My mum died 10 years ago of this. As we did not lnow we never protected oueselves with gloves when chnginh disper, I slept with her. My aunt died this week of this. I am si scared
Did she take the covid vaccine?
@@MindStrider34 my aunt yes!!!!!!!! She had Pfizer . My mother did not. She died 10 years ago 2010 after a trip to Uk in 2008. 1 year after strated w symptoms.
@@ingridjocelynab1 I'm sorry for your loss. There is proof the symptoms of mad cow disease is almost exactly the same with the vaccine. I don't think nothing will happen to you unless you take the shot.
@@MindStrider34 so interesting. My aunt starting to get sick a week after the shot. She lost memory 1.5 months later. And died 14th of June
Hello, maybe you have a hereditary mutation? And how much was your aunt sick, and how old was she and your mother when they died? Thanks in advance
Terrifying..
Many have these symptoms after having the Covid vaccine. Several scientist suspect the vaccines are causing prion disease for some people.
This is one of those times where I’m glad I was born in 2001 post cattle regulations.
My father passed away due to this bloody cjd 😔
Hi, I'm from Russia, how much was your father sick, and how old was he?
I came here after watching batman Arkham knight
Me too
i knew a woman who died from this a couple years ago. the comments saying they know someone who died from it all seemed to have died within the last few years. i’m wondering how this is happening so many years after chernobyl
What’s this got to do with Chernobyl?
This isn't about chernobyl
@@monetum1392 all goes back to descent of european cows during chernobyl
@@thedoc6413 ^
Has nothing to do with radiation but a disease in animals. It's biological not radiation damage.
Consuming contaminated meat bocomes primary cause for CJD now a days.
I love to see medical dramas shows and web series and I want to become a doctor in future I listen this disease name in k drama emergency couple so I excited to know about disease
Nice, I have 10 years of Holby City on VHS, will definitely hold its value I reckon.
Genetic is beautiful play..game on
Anyone here still eats beef after knowing cjd ?
No, but we shouldn't forget about other animals; it is spreading to a lot of other herd animals
@@XenoZeduX yeah , unfortunately prions are hard to destroy , but thanks to natural weathering and decay degrades prions over time rendering them less infectious ,containing the spread is hard but not impossible ,but what we really needs is a cure to all variants of prion disease, i hope scientists can make that happen
You're gonna get it from eating brains of other animals, not tainted meat.
I can recommend a powerful man who can help you with herbs and healing spell like he also help me
I'm vegetarian
why am i attracted to this disease???
You're being warned in your spirit. I think there may be a crossover of covid and CWD, or something similar.
U wot m8
Same for me, i mean, its just interesting for me, and i research it much, but def not attracted😂
@@choccybirb 🎯🎯🎯😳
bro what. i dont think thats how it works@@choccybirb
I did not understand why he suddenly could not do something as simple as composing a phone number!!! He did not either.
Plague Inc. players when Prion Mega-Brutal😳😳😳‼️‼️‼️🐄🐄
according to my DNA i have a heightened risk of getting CJD lmao
That's scary
How can they know that just by finding out your DNA is?
specific prnp mutations (gene which encodes prp protein) can cause prp made to have chemical imperfections which lead to instability and therefore a heightened chance of misfolding into infectious prions@@Pazuzu82
If your family had it
Danielle Plains
King Estates
Stracke Crossing
Miller Jessica Lewis Angela Garcia Brenda
Beier Meadows
100% deathrate
scary ffi is more scary
r/interestingashell
for more info pls contact chris pomfrett ( ex. umist) or myself............good video btw..........
How