My father who is currently 89 years old was diagnosed with multiple sclerosis when he was 68, ever since he has although been living a peaceful life and it hasn't really impacted him, although he has eye vision loss and has hurt himself a couple of times due to his lack of vision, i took him to his local doctor and the doctor said he was going to be fully blind by the time he turned 70, but I'm glad he could still see after all these years, he does wear glasses though.
I'm not a medical student but I have MS your video just explained the parts I understood so much that even going to MS events never did about why some of the newer DMT's target things like B & T cells. Great video ,
man I've had MS since I was 17 (I'm 32 now) and your video taught me more than most of the informative stuff I was given when I was diagnosed. you're doing amazing things, dude. keep on being amazing!
@Penny migraines can really mess with you, but I don't think any of those are really symptoms aside from the numbness - which wouldn't ever really go away.
I'm doing my MSc Clinical Neuroscience in the UK and your videos are extremely helpful and supportive. I just want to thank you a lot! Please continue the fantastic work to do
I’m in the hospital and just diagnosed with MS. She was such a fun and thoroughly informative explanation. It answered all my questions so far and was so easy to follow. Thanks so much!
Cure yourself with the paternal pheromone (source from any man's face). Just be sure to handle it with care, plenty of ventilation and wear a respirator collecting the pheromone (tare, rub his face with chewing gum, weigh, record about 10mg/dose and as tolerated.)
hello sir. My name is axel, 24 years old from Algeria. im 2018 i went to dentist to fix my teeth then went home after probably a week i started feeling numbness in my hand, troubles speaking, and diplopia. the the symptomes relieved without any meds, after almost 8 months i started having symptoms like lost in balance, troubles speaking clearly, diplopia again, and lost in taste and smell. i went to many doctors and they requested an MRI on my brain and spinal chord. the MRIs showed that i have demyelinating lesions on both spinal chord and CNS, been through a spinal tab and the IGg index was positive awell, and in the serology test i ve found that i have been infected of with HBV and the viral load was extremely high 9.42 log. i started taking the antivirals, and continued my diagnosis for the brain infection, been through a second spinal tab for HBV serology of Celebro spinal fluid and the results were positive after a year if research i have been diagnosed with MS and stared taking interferons which i couldnt handle. stopped it under doc's supervision and now am back on it since theres no alternative and no much meds here in Algeria now i have two questions if u may - can the hbv cross the bbb ? - did the hbv trigger my brain dymelination? i ve been searching lately and i found this article about ADEM, and started wondering whether i might mistakenly diagnosed. i would really pleased if answer, am so lost and cant find answers to my case. thank you so much.
I am trying to get my BSN and I am thrilled that I found your channel! Your teaching method is great for me because you have a way of simplifying the science and pathophysiology behind the disease. You are a true lifesaver! Thank you!
Thank you so so much. I had my first MS relapse 12 years ago, but thanks to you, I know more about my condition than I ever did before in one single beautiful video.
Brilliant presentation. I ended up on this site because the 34 yo son of a good friend of mine has recently been diagnosed with MS. This has been very informative, thank you.
i actually don't know how I would pass my physio master without you! It baffles me how amazing your brain is; how on earth do you remember so much detail about so much stuff!
Thank you sooooo much for your invaluable RUclips’s! I was diagnosed w/ MS 2/2021 at age 63. Doctors suspect I’ve had MS since at least 1987 … when I was diagnosed UCLA Jules Stein w/ pars planitis. I consulted 3 neurologists + numerous specialists (Mayo AZ, Cedars, USC + UCLA) over 3 1/2 years before diagnosis. Initial symptoms that came + went over time: bi lateral leg weakness, toe tingling that moved up the legs to waist, calf spasticity, fatigue, hand + foot tremors, difficulty speaking + eventually on hot day (88°) significant difficulty moving legs. My age + bilateral symptoms are both less common, causing delay in diagnosis. So grateful to you for helping educate about MS. If I can ever support your efforts, please know it will be my pleasure + I welcome contact.
Right On! Amazing Prof Zach... I am also impressed with his knowledge and verbal ability to simplify complicated things. Did he just eat the textbook or what? :)
Thank you so much for this detailed video. I’m a patient with a “mystery disease” with specialists that all want to pass the buck and none of them are coordinating so I’m binging youtube videos hoping for an aha moment. I’m already diagnosed with several things, but none of them fully explain my debilitating symptoms. I was an OR nurse working in Robotics and Informatics and having the time of my life. At 32 I got a virus and all hell broke loose. I’ve been looking for answers for 6 years and haven’t been able to work. I would have diagnosed myself by now, but it’s affecting my memory and executive functioning so I can’t keep it together long enough to see it clearly. My husband has since left me and I’m waiting on disability, but I should have been diagnosed and on proper treatment years ago. I’m appalled by the state of our the medical system. I appreciate doctors like you that care so much and take the time to explain in detail because that’s what helps make a diagnosis for patients with complicated profiles. I wish to God I could find doctors that dont just run a CBC and say you’re normal because the labs say so and if you ask for more they say it’s all anxiety. 🙄 I got lucky with one great cardiologist that they nicknamed “the brain”….he’s very much like you. He discovered I had several conditions under the umbrella of Dysautanomia and sent me to a Dysautanomia clinic where I found another doctor who is loads more helpful than most, but has no time to explore additional diagnosis because there are so few Dysautanomia clinics and now they’re overloaded by covid longhaulers. Will you please please please add a video on Dysautanomia and coexisting conditions like EDS and mast cell disorders to your neuro playlist? It’s incredibly life altering as it is, and despite these not even being that rare, doctors are not recognizing them. Last time I checked, it takes an average of 7 years for diagnosis! There are so few Dysautanomia clinics that many of us have to cross several state borders to get help. I’m lucky to be in Washington where we have 2, but they’re so backed up that I can only get 2 appointments a year and med management is a nightmare. Despite my official diagnosis, most doctors look at me like I’m crazy when they see my symptoms list. Our patient support groups have thousands of posts from women being told they’re “just anxious” and need therapy and a life. Its so cruel. We need more awareness and I’m sure any of the organizations such as Dysautonomia International would pay you to do a video just for the awareness it would bring. One other video request I have is possibly something you don’t do on your channel, but the Autistic community desperately needs the attention of medical students and doctors. The mortality rate in this group is terrible. There are so many barriers for this group to even reach a physician, but even when they do, they struggle to communicate and are misunderstood. Many die very young and there is a very high suicide rate. Alexithymia (which is common even in the general population) makes it really difficult to feel, understand and explain what is happening in the body so a physician needs to assist these patients with extra questions and prompts. It’s important to raise awareness because health problems are rampant in the autistic community due to lifelong trauma and being prone to certain conditions. It would be wonderful if you could add a video about consults and how to treat certain patient populations. I’ve recently been diagnosed with Autism myself and realized that it has been a contributor to my delayed diagnosis. Hopefully you can help these two patient groups out 🙏🏻
I've been researching a lot about the immune system after finding myself quite interested with the Vaccine debate and understanding the underlying processes in our body. It is shocking how complex they are and how long it has taken to develop this level of understanding of all the cell types and interactions and its quite fascinating. My father has MS and is unfortunately in the severely disabled group with an EDSS Score ~9. I'm still in the first few minutes of this video but wanted to say I love that you are that kind of unassuming extremely intelligent person who is comfortable just being you. I also love your enthusiasm and way of presenting information! So cheers!!
When you mentioned that macrophages can reach neurons through the brain blood barrier at 11:48, that made me remember that sometimes spirochetes can invade and remain inside macrophages. Excellent lecture!
Ninja nerd, this has explained so much to me. Easier to follow than my lectures, as I'm more of a visual learner. I just may get to write something worth marking now. Thank you.
Hi, I was diagnosed with MS this August, at only 16 years. I've been trying so hard to find out more about what's happening inside my body, especially as I would like to pursue medicine. This video was absolutely INCREDIBLE - thank you so much for the detailed explanations!!
Hey, I hope you are doing fine. If you don't mind can i ask you what were your symptoms before diagnosis and what tests you went through to confirm that you have ms.
Not sure how I ended up here since I am neither a doctor nor I have MS (though I know a bit about it) but this was an absolutely fabulous video. Your students are blessed to have someone so gifted in clear explanation.
I'm going to make a statement : ) I think you should get a Nobel prize for your work! and I'm absolutely serious. The effect you have is tremendous - Currently almost 2 million people follow you. But more so, a lot of them are doctors, researches etc - and each of them effect hundreds/thousands of people lives. I know academies committees have an "old school" way of thinking and there isn't a category for what you do. But our world has changed so much and maybe there should be - and you Sir are effecting millions of live world wide!
Ninja Nerd, thank you for this video. I was diagnosed with highly-active disease (HAD) RRMS in Oct. of 2019 and this far and away the best video I have ever seen on MS. I do not have a medical background, but I have read extensively since my diagnosis. This is the most approachable video I have seen and I have already sent it to my MS specialist for her to share with her patients. From one nerd to another, if you haven’t heard/read about autologous hematopoietic stem cell transplantation (aHSCT) for MS, I encourage you to do so. It is fascinating and I believe this is the closest thing to a cure that we have. Thanks again for the video!
I was diagnosed with Lupus thirty years ago. Yet now I also have MS at 64. I have been diagnosed only recently, yet I had early symptoms in my forties. However I experienced terrible nerve pain in my left leg in January 1st this year and now three months later I have severe foot drop and spasticity.
Thank you for this video! I am not a medical student however just an RN and this video is outstanding. I am one year into my dx and you do a fantastic job on explaining the disease process.
I have a research paper that I am working on regarding this and I am so grateful for this video, not only did it save me some reading time but you made the process of understanding this disease very manageable and fun!!!
ive never seen ur channel before looking this up and finding this video but i gotta say this is one of the best videos in regards to medical science biology and chemistry that i have ever seen in my life and thats saying a lot because im an absolute nerd for understanding things on a nuanced level ur insane dude keep it up
I have come to the point where I like these videos before even watching, cause I do not ever want to risk forgetting to like the video after watching it.
I appreciate you Pr. ZACH MURPHY for every single one of your videos. Professor! Could you make a playlist all about Testosterone replacement therapy and explain what happens while being on/off TRT and all the benefits and dangers at cellular level to the body. And in fact how to best start a PCT after a certain time of Testosterone injection use.
Thank you so much for this video. I was recently diagnosed and didn’t understand a bit of it so it shows how talented and passionate you are to keep my attention! I just kept thinking of all the memes with the confused faces, that was me! All I heard was “a really crappy perfect storm in the body that makes no sense.”
Thank you! I have recently been diagnosed with MS and have been struggling with understanding my disease and why my body doesn’t work the same in more. I’m very fortunate that I have a mild case, listening to you answered many of the questions I kept asking myself. Thank you for helping me feel better about not understanding why things have changed for me.
Excellent, detailed, clear, and complete presentation that is understandable by a non-medical student, like myself. thanks! so much important detail above most sources people go to first, like wikipedia.
Okayyyy so i did commented few hours ago and had to come back to say this…so at 1st I started studying my professors slides and it was just confusing and I wasn’t understanding so I decided to watch a RUclips video 1st then go back to the lectures so i saw ur this video well i have heard alot about ur channel but i never watched a complete video just because i find it long and i feel I don’t have that much time well today I decided to watch and it was AMAZING! I understood to the point that it surprised me well why I’m back is because i went back to my professors slide and i was BLOWN-AWAY!!!! Like i was saying wat will be in the next slide because of how much i picked from this video…YOU ARE AMAZING and thank you soo much for helping alots of us….well now I’m rooted subscriber because this will always be my 1st stop before my professors THANK YOU AGAIN and i wish u and the entire team Goodluck☺️☺️❤️❤️❤️
That video was awesome and you are very talented at education. I am not native speaker of English but i really understood %95 of the stuff that explained. Really thank you for that service to present to us.
Fantastic, Diagnosed with Tumefactiv MS (RRMS) in Nov 2021. Lesions on Brain, Brain Stem and Spine. the Trifecta. Love learning about MS and digging deep. This is clear concise and hit so many points. Currently on Ocrevus or the Ocrelizumab. Knowledge is power and you sir are doing it! thank you so much.
Please look into Dr. Terry Wahls. Her book has helped me a whole lot. I don’t take any medicine for my MS. All it was doing is making me more Flaccid and Lethargic. Tons of side effect. I changed my food intake and a couple of supplements helped me (CoQ10, Acetyl-Carnitine, and Alpha Lipoec). I’ve had significant changes. I also included waves of antioxidants. Hope this helps
@@BlasianGoddessTM77 I have the Wahl's protocol and looked into MS Hope/ Matt Embry. I didn't do strict Wahl's but intend on taking DMT and eating right. Left hip isn't cooperating today
I take CoQ10 and acetyl Carnitine. And others too but the acetyl Carnitine helped my fatigue a ton!!! I am going to try alpha lipoec. I love learning from others thanks so much for your comments.
My niece has been suffering with MS for almost 20 yrs but I have seen her go from being able to walk to the loss of her left hand and leg and depends on her mum doing almost her personal needs. She has to have daily physiotherapy but sometimes it's a ginacial issue that can result in her kt getting her necessary physics. So your videos are interesting like her to make comm with you .
As a medical student recently diagnosed with MS, this is a double benefit for me!
Wishing u remission and strength doc
Thanks so much for watching. We wish you all the best ❤️
Get well soon dear 🙂
I am a medical student with MS too. I wish you all the best.
@@umerbinshabir9819 wishing the best for you, my dear!
You are passionate and ispiring. An entire generation of med students can't thank you enough.
As a medical student, i've never found any medical content better than yours, keep it up
Unbelievable how much effort, knowledge, love and passion you put into this video. You are inspiring. Thank you!
Medicine is so easy with ninja nerd lectures
My father who is currently 89 years old was diagnosed with multiple sclerosis when he was 68, ever since he has although been living a peaceful life and it hasn't really impacted him, although he has eye vision loss and has hurt himself a couple of times due to his lack of vision, i took him to his local doctor and the doctor said he was going to be fully blind by the time he turned 70, but I'm glad he could still see after all these years, he does wear glasses though.
I'm not a medical student but I have MS your video just explained the parts I understood so much that even going to MS events never did about why some of the newer DMT's target things like B & T cells. Great video ,
You have a gift of teaching. I am studying for my Certified NeuroScience exam and have been watching your videos...truly amazing!
i live with my grandmother and she has had ms for years. This has been really helpful understanding what she is going through. thank you
man I've had MS since I was 17 (I'm 32 now) and your video taught me more than most of the informative stuff I was given when I was diagnosed. you're doing amazing things, dude. keep on being amazing!
@Penny migraines can really mess with you, but I don't think any of those are really symptoms aside from the numbness - which wouldn't ever really go away.
How are you doing now?
I'm doing my MSc Clinical Neuroscience in the UK and your videos are extremely helpful and supportive. I just want to thank you a lot! Please continue the fantastic work to do
I’m in the hospital and just diagnosed with MS. She was such a fun and thoroughly informative explanation. It answered all my questions so far and was so easy to follow. Thanks so much!
Take all my med school tuition fee like you rightfully deserve. You make things make sense so well. Kudos to the whole team and God bless you all. ❤😊
I was diagnosed with MS one year ago. Cannot wait to watch.
Cure yourself with the paternal pheromone (source from any man's face). Just be sure to handle it with care, plenty of ventilation and wear a respirator collecting the pheromone (tare, rub his face with chewing gum, weigh, record about 10mg/dose and as tolerated.)
@@TogetherinParis bro?
As a neurologist, I love this discussion and his entire content. He kills it, better than I could do.
hello sir.
My name is axel, 24 years old from Algeria. im 2018 i went to dentist to fix my teeth then went home after probably a week i started feeling numbness in my hand, troubles speaking, and diplopia. the the symptomes relieved without any meds, after almost 8 months i started having symptoms like lost in balance, troubles speaking clearly, diplopia again, and lost in taste and smell. i went to many doctors and they requested an MRI on my brain and spinal chord. the MRIs showed that i have demyelinating lesions on both spinal chord and CNS, been through a spinal tab and the IGg index was positive awell, and in the serology test i ve found that i have been infected of with HBV and the viral load was extremely high 9.42 log. i started taking the antivirals, and continued my diagnosis for the brain infection, been through a second spinal tab for HBV serology of Celebro spinal fluid and the results were positive after a year if research i have been diagnosed with MS and stared taking interferons which i couldnt handle. stopped it under doc's supervision and now am back on it since theres no alternative and no much meds here in Algeria
now i have two questions if u may
- can the hbv cross the bbb ?
- did the hbv trigger my brain dymelination?
i ve been searching lately and i found this article about ADEM, and started wondering whether i might mistakenly diagnosed.
i would really pleased if answer, am so lost and cant find answers to my case.
thank you so much.
I am trying to get my BSN and I am thrilled that I found your channel! Your teaching method is great for me because you have a way of simplifying the science and pathophysiology behind the disease. You are a true lifesaver! Thank you!
SAME!
It always amazes me how I can learn more from you for free than I can in my doctorate. You are great! Thank you!
Thank you so so much. I had my first MS relapse 12 years ago, but thanks to you, I know more about my condition than I ever did before in one single beautiful video.
And did you experience any other relapse after that?
@@RahulRaj-up5ql no I haven't at all.
Unbelievable how much effort, knowledge, love and passion you put into this video.Thank you
You’re the GOAT of teaching of medicine and all other specialties. ❤
Awesome breakdown. As a 55 Y/O just diagnosed you really simplify enough even I get it. I thank you.
Brilliant presentation. I ended up on this site because the 34 yo son of a good friend of mine has recently been diagnosed with MS. This has been very informative, thank you.
i actually don't know how I would pass my physio master without you! It baffles me how amazing your brain is; how on earth do you remember so much detail about so much stuff!
Every time I watch a new video,I get fascinated by how genius your explanation is, thank you so much
This was life changing information. My sister was diagnosed with MS last week. Can’t wait to share when she is ready.
Thank you sooooo much for your invaluable RUclips’s! I was diagnosed w/ MS 2/2021 at age 63. Doctors suspect I’ve had MS since at least 1987 … when I was diagnosed UCLA Jules Stein w/ pars planitis. I consulted 3 neurologists + numerous specialists (Mayo AZ, Cedars, USC + UCLA) over 3 1/2 years before diagnosis. Initial symptoms that came + went over time: bi lateral leg weakness, toe tingling that moved up the legs to waist, calf spasticity, fatigue, hand + foot tremors, difficulty speaking + eventually on hot day (88°) significant difficulty moving legs. My age + bilateral symptoms are both less common, causing delay in diagnosis. So grateful to you for helping educate about MS. If I can ever support your efforts, please know it will be my pleasure + I welcome contact.
It's good that you have such a diagnosis at 33
22 pages in our textbook simplified in a 54 min lecture. Thank you so much, Zach and the whole Ninja Nerds Staff. 😊
Right On! Amazing Prof Zach... I am also impressed with his knowledge and verbal ability to simplify complicated things. Did he just eat the textbook or what? :)
Which textbook are u following?
22 pages woah 😨
at least you all have this chapter, in our curriculum we don't have this essential lesson, not even little mention of multiple sclerosis in any form.
Thank you so much for this detailed video. I’m a patient with a “mystery disease” with specialists that all want to pass the buck and none of them are coordinating so I’m binging youtube videos hoping for an aha moment. I’m already diagnosed with several things, but none of them fully explain my debilitating symptoms. I was an OR nurse working in Robotics and Informatics and having the time of my life. At 32 I got a virus and all hell broke loose. I’ve been looking for answers for 6 years and haven’t been able to work. I would have diagnosed myself by now, but it’s affecting my memory and executive functioning so I can’t keep it together long enough to see it clearly. My husband has since left me and I’m waiting on disability, but I should have been diagnosed and on proper treatment years ago. I’m appalled by the state of our the medical system. I appreciate doctors like you that care so much and take the time to explain in detail because that’s what helps make a diagnosis for patients with complicated profiles. I wish to God I could find doctors that dont just run a CBC and say you’re normal because the labs say so and if you ask for more they say it’s all anxiety. 🙄 I got lucky with one great cardiologist that they nicknamed “the brain”….he’s very much like you. He discovered I had several conditions under the umbrella of Dysautanomia and sent me to a Dysautanomia clinic where I found another doctor who is loads more helpful than most, but has no time to explore additional diagnosis because there are so few Dysautanomia clinics and now they’re overloaded by covid longhaulers. Will you please please please add a video on Dysautanomia and coexisting conditions like EDS and mast cell disorders to your neuro playlist? It’s incredibly life altering as it is, and despite these not even being that rare, doctors are not recognizing them. Last time I checked, it takes an average of 7 years for diagnosis! There are so few Dysautanomia clinics that many of us have to cross several state borders to get help. I’m lucky to be in Washington where we have 2, but they’re so backed up that I can only get 2 appointments a year and med management is a nightmare. Despite my official diagnosis, most doctors look at me like I’m crazy when they see my symptoms list. Our patient support groups have thousands of posts from women being told they’re “just anxious” and need therapy and a life. Its so cruel. We need more awareness and I’m sure any of the organizations such as Dysautonomia International would pay you to do a video just for the awareness it would bring. One other video request I have is possibly something you don’t do on your channel, but the Autistic community desperately needs the attention of medical students and doctors. The mortality rate in this group is terrible. There are so many barriers for this group to even reach a physician, but even when they do, they struggle to communicate and are misunderstood. Many die very young and there is a very high suicide rate. Alexithymia (which is common even in the general population) makes it really difficult to feel, understand and explain what is happening in the body so a physician needs to assist these patients with extra questions and prompts. It’s important to raise awareness because health problems are rampant in the autistic community due to lifelong trauma and being prone to certain conditions. It would be wonderful if you could add a video about consults and how to treat certain patient populations. I’ve recently been diagnosed with Autism myself and realized that it has been a contributor to my delayed diagnosis. Hopefully you can help these two patient groups out 🙏🏻
Every time I watch any new video of you, I get fascinated by how understandable your explanation is, Thank you so much
I've been researching a lot about the immune system after finding myself quite interested with the Vaccine debate and understanding the underlying processes in our body. It is shocking how complex they are and how long it has taken to develop this level of understanding of all the cell types and interactions and its quite fascinating.
My father has MS and is unfortunately in the severely disabled group with an EDSS Score ~9. I'm still in the first few minutes of this video but wanted to say I love that you are that kind of unassuming extremely intelligent person who is comfortable just being you. I also love your enthusiasm and way of presenting information! So cheers!!
When you mentioned that macrophages can reach neurons through the brain blood barrier at 11:48, that made me remember that sometimes spirochetes can invade and remain inside macrophages. Excellent lecture!
Ninja nerd, this has explained so much to me. Easier to follow than my lectures, as I'm more of a visual learner. I just may get to write something worth marking now. Thank you.
Hi, I was diagnosed with MS this August, at only 16 years. I've been trying so hard to find out more about what's happening inside my body, especially as I would like to pursue medicine. This video was absolutely INCREDIBLE - thank you so much for the detailed explanations!!
Hey, I hope you are doing fine. If you don't mind can i ask you what were your symptoms before diagnosis and what tests you went through to confirm that you have ms.
Not sure how I ended up here since I am neither a doctor nor I have MS (though I know a bit about it) but this was an absolutely fabulous video. Your students are blessed to have someone so gifted in clear explanation.
Zack, your are just perfect! The medical world is blessed.
I'm going to make a statement : )
I think you should get a Nobel prize for your work! and I'm absolutely serious.
The effect you have is tremendous - Currently almost 2 million people follow you.
But more so, a lot of them are doctors, researches etc - and each of them effect hundreds/thousands of people lives.
I know academies committees have an "old school" way of thinking and there isn't a category for what you do.
But our world has changed so much and maybe there should be - and you Sir are effecting millions of live world wide!
Ninja Nerd, thank you for this video. I was diagnosed with highly-active disease (HAD) RRMS in Oct. of 2019 and this far and away the best video I have ever seen on MS. I do not have a medical background, but I have read extensively since my diagnosis. This is the most approachable video I have seen and I have already sent it to my MS specialist for her to share with her patients.
From one nerd to another, if you haven’t heard/read about autologous hematopoietic stem cell transplantation (aHSCT) for MS, I encourage you to do so. It is fascinating and I believe this is the closest thing to a cure that we have. Thanks again for the video!
Thanks so much for the additional information for us to look into. We wish you the absolute best and have a great rest of your weekend!
Probably one of the most interesting ninja nerd videos I've seen so far, I understood everything once and from the start, thank you Zach💜💜
Best doctor ever. You're beyond my achievement. We need really MENINGITIS LECTURE
I just thanked god that you had covered this topic. As a final year med student, so much grateful. Thank you 😊
Very informative for a non-medical student and a 48yr old suffering from symptoms, somewhat unexplained. Thanks
wow. Simply WOW. Stunned and so grateful for you.
I could watch you all day
This Doctor is a genius. Thank you
I was diagnosed with Lupus thirty years ago. Yet now I also have MS at 64. I have been diagnosed only recently, yet I had early symptoms in my forties. However I experienced terrible nerve pain in my left leg in January 1st this year and now three months later I have severe foot drop and spasticity.
Thank you for this video! I am not a medical student however just an RN and this video is outstanding. I am one year into my dx and you do a fantastic job on explaining the disease process.
"Just" an RN? Don't undervalue yourself! - TG
You taught me alot about my disease 💯, ty ty. After cov it got worse, we are working on it. Drs are low, staff, prayers 🙏 to us all.
In nursing, but these "overkill" videos absolutely make me a better nurse. Side note: Wife has been a doctor for 17 years and loves these too
What a gift!! you are inspiringly educational, with gratitude!
I have a research paper that I am working on regarding this and I am so grateful for this video, not only did it save me some reading time but you made the process of understanding this disease very manageable and fun!!!
You are such a good teacher, i hope you teach somewhere, bc the way you explain things, the knowledge and the effort is amazing.
Please do a video on Lupus!!! If there is anything I can do on my end to make this happen let me know!
Wow. Amazing how much this guy knows. I have secondary progressive. My poor sister had remit/remis and just died of complications. ..
Our condolences for you and your families loss - TG
your teachings are so passionate, I love your classes, Thank You.
Excellently explained in simplified manner even pharmacist get benefited with your illustrations
I’ve been following u from Tunisia (a small country in Africa) and I think u are AWESOME !! ❤️❤️❤️
ive never seen ur channel before looking this up and finding this video but i gotta say this is one of the best videos in regards to medical science biology and chemistry that i have ever seen in my life and thats saying a lot because im an absolute nerd for understanding things on a nuanced level
ur insane dude keep it up
Awesome lectures and great professor , I love the way you teach. I even introduced ninja nerd to my patients 🥰🥰🥰
I have come to the point where I like these videos before even watching, cause I do not ever want to risk forgetting to like the video after watching it.
try watching this video at x2 speed with a hiphop drumbeats (80bpm) on the background. Has a different ring to it..and amazing enough, he's on beat!
The best teacher, the best video, the learning revolution!
I appreciate you Pr. ZACH MURPHY for every single one of your videos. Professor! Could you make a playlist all about Testosterone replacement therapy and explain what happens while being on/off TRT and all the benefits and dangers at cellular level to the body. And in fact how to best start a PCT after a certain time of Testosterone injection use.
Best teacher ever
As physician I'd have like to have ela teacher like you. For real!
First video I've ever seen from you and I am just blown away so clear and concise thank you this is amazing
I was waiting for this..thank you so much ninja nerd💜
You are an amazing teacher. Thank you so much Ninja Nerd. Love and much respect!
thank you for making stuff much easier to understand:)
You have a great way of teaching .. better than a lot of college professors 👏🏽👏🏽👏🏽👏🏽 keep up the good work 🤍🤍🤍🤍🤍
wow very clear explanation! I'm still in HS but this vid makes medical school level stuff understandable to me
Your love for medicine is shown in your lectures Ninja nerds are the best👏🏻👏🏻👏🏻
I liked it, you explained everything about multiple sclerosis in an understandable way, I think
You are amazing! I never studied medicine but find it fascinating and i can understand everything you show :) your passion is evident ❤
Thank you so much for this video. I was recently diagnosed and didn’t understand a bit of it so it shows how talented and passionate you are to keep my attention! I just kept thinking of all the memes with the confused faces, that was me! All I heard was “a really crappy perfect storm in the body that makes no sense.”
Thank you! I have recently been diagnosed with MS and have been struggling with understanding my disease and why my body doesn’t work the same in more. I’m very fortunate that I have a mild case, listening to you answered many of the questions I kept asking myself. Thank you for helping me feel better about not understanding why things have changed for me.
Excellent, detailed, clear, and complete presentation that is understandable by a non-medical student, like myself. thanks! so much important detail above most sources people go to first, like wikipedia.
Ooooo mam great. I love explanatory power. Better than high rank university professors. Excellent excellent and excellent
I'm so great full for your mere existence, you have saved so many of my exams ❤️
Okayyyy so i did commented few hours ago and had to come back to say this…so at 1st I started studying my professors slides and it was just confusing and I wasn’t understanding so I decided to watch a RUclips video 1st then go back to the lectures so i saw ur this video well i have heard alot about ur channel but i never watched a complete video just because i find it long and i feel I don’t have that much time well today I decided to watch and it was AMAZING! I understood to the point that it surprised me well why I’m back is because i went back to my professors slide and i was BLOWN-AWAY!!!! Like i was saying wat will be in the next slide because of how much i picked from this video…YOU ARE AMAZING and thank you soo much for helping alots of us….well now I’m rooted subscriber because this will always be my 1st stop before my professors THANK YOU AGAIN and i wish u and the entire team Goodluck☺️☺️❤️❤️❤️
Can't imagine studying medicine without your videos ")❤
Como estudiante de MD solo puedo decir GRACIAS POR EXISTIR!
That video was awesome and you are very talented at education. I am not native speaker of English but i really understood %95 of the stuff that explained. Really thank you for that service to present to us.
Thank you so much for explaining this to me. It is making it easier for me to understand why I am the way I am
GOOD JOB IT TOOK ME 60 MINS TO UNDER SANDER IT WILL HELP ME WITH MY SOUTS SIA :)
Had to pause the video real quick for an obligatory “I love you”
Carry on
absolute and only love for this channel
Got the golden play button congrats 💪
even before actual starting of video i hit like button ' cause i know definately m gonna like the lec
the best tutorial ever
Thank you from Libya ❤❤🇱🇾🇱🇾🇱🇾
Yeeeesssss - I love y'all and I had scoured your channel for this topic in the past. I'm so excited it's up now!
You guys are absolute legends! Thank you!!
ur teaching style is so cool .......
Fantastic, Diagnosed with Tumefactiv MS (RRMS) in Nov 2021. Lesions on Brain, Brain Stem and Spine. the Trifecta. Love learning about MS and digging deep. This is clear concise and hit so many points. Currently on Ocrevus or the Ocrelizumab. Knowledge is power and you sir are doing it! thank you so much.
Please look into Dr. Terry Wahls. Her book has helped me a whole lot. I don’t take any medicine for my MS. All it was doing is making me more Flaccid and Lethargic. Tons of side effect. I changed my food intake and a couple of supplements helped me (CoQ10, Acetyl-Carnitine, and Alpha Lipoec). I’ve had significant changes. I also included waves of antioxidants. Hope this helps
@@BlasianGoddessTM77 I have the Wahl's protocol and looked into MS Hope/ Matt Embry. I didn't do strict Wahl's but intend on taking DMT and eating right. Left hip isn't cooperating today
I take CoQ10 and acetyl Carnitine. And others too but the acetyl Carnitine helped my fatigue a ton!!! I am going to try alpha lipoec. I love learning from others thanks so much for your comments.
All Your videos are top-notch. Could you make a video on Amyotrophic lateral sclerosis?
One of the best ways of studying! Greetings from Buenos Aires University, Argentina :)
Thanks for everything
My niece has been suffering with MS for almost 20 yrs but I have seen her go from being able to walk to the loss of her left hand and leg and depends on her mum doing almost her personal needs.
She has to have daily physiotherapy but sometimes it's a ginacial issue that can result in her kt getting her necessary physics.
So your videos are interesting like her to make comm with you .
thank you ninja professor zach
AMAZING!!!!!!!!! Thank you so much. Greetings from Poland