I lost my older brother due to MG this year.. he was only 27yrs old he was diagnosed at 21 .. This is a very heartbreaking disease I watched my brother loose his life slowly for 6yrs .. I'm not even ready to talk about it but not for one day was he sad he lived every one of those days to the fullest hheyi i thought i should let everyone who has this to get up and beat the odds against you
So, so sorry. My mother has this - she went for taking no medication to being in an ICU for six weeks on a vent! They wanted my sister & I to pull the plug but we refused. She recovered & is doing well considering everything. She can’t do much without shortness of breath - but refuses to stop, just takes little breaks. I am proud of her.✌🏽😎🌄
@@jabedbbsnot really in sever cases it weakness all skeletal muscles of the body including the diaphragm which is necessary muscle for your respiratory system so MG (Myasthenia gravis) can cause Respiratory failure and death Also sometimes people who has thymoma ( cancer of the thymus gland ) or other disease cause Myasthenia gravis and people might die by the other disease or the by the MG
I have been diagnosed in 2020 and also had thymoma which is the tumor of thymus gland and was removed I only spend 25 days in hospital and was recovered in one year, but was only taking 2mg of prednisone and 250mg of Mycophenolate mofetil for 2 years, and again in March 2023 my symptoms got worsened and doctors thought my meds needs to increased then after 2 months resting at home one day I had a fall due to going up the stairs then in hospital and scans done to see if any broken bone due to the fall then found out thymoma has grown back which is called (drop metastasis ) and this time was in diaphragm so it’s removed again but this time the symptoms was very bad I have been in ICU for 8 days and had respiratory failure and all together 10 weeks in hospital and still recovering at home and reducing prednisone and recovery this time was very challenging and taking longer than the initial diagnosis 🥹😌
Awesome video.. im now a 51 y/o male .i was diagnosed with MG when i was just 25. Took a ton of tests to figure out why i was having so much weakness. It was horrible. Eventually had a thymectomy at 27 .after a few months had very little weakness. Now some slight weakness if i push it. But certainly liveable. So greatful.
How was it diagnosed and what kind of symptoms? Is this like tight muscle feeling or eye strain fatigue (but for me one eye) it feels my eyebrow but mainly near temple on one side is tight and heavier. Im in vision therapy also for binocular vision issues. Im not sure if this or just weak eye and tight face muscles from eye and tmj.
@@user-zk8ck3my3l started with drooopy facial muscles. I always looked angry. Or frownng but wasnt. most of the time anyway. 😆 then it moved to my arms and legs. I couldnt walk very well well. very weak...sorry about the delayed response I just saw ur comment..im 54 now. still feeling fine. hope u r too!
Prayers to you I was diagnosed January 3 of this year 4 days before my 39th birthday just took sick suddenly had the surgery on January 15 an 2 IV IGs Plasmapheresis I spent almost 4 months in the hospital an now I will be goin to New Orleans to start a form of chemo treatment 🤷🏽♀️
@@rakeishaanderson-rhok how was it diagnosed and what symptoms? My one eye strains and fatigues. My eyebrow and temple feel tight and heavy and eye is tad lower but i can lift my eyebrow. Sound similar or no?
My father in law was diagnosed with this yesterday, he is 67 with no other health issues. We thought he was having a stroke. Symptoms were double vision for a couple of days the slurring speech and difficulty swallowing. He is hospital and has a feeding tube. Treatment has been started and has done well over night. So happy it has been recognised so quickly with treatment started
Thank you so much for providing this information is very helpful I am Amaya stenia gravis patients and all the information I can retrieve is so very appreciated
Thank you for sharing the information about a disease that is not well known. I was diagnosed with MG when I was 16 (currently 19) and I'm glad that I'm able to live without any serious problems after my thymectomy (beside muscle weakness). Thank you!
Hello, I am Manum Imran i am working on a documentary on Myasthenia Gravis. My mother was diagnosed with this disease 5 and 1/2 years back and i lost her on 30th June 2019. If any of your family member or relative has this disease currently or previously can you please help me out in research work?
So informative. I was diagnosed in 2008. Now I am 71 years old and feeling the essence of this disease on my body. I so appreciate this now. I have information now.
Let me also say that I was misdiagnosed by a Neurologist and my PCP immediately sent me to the Mayo Clinic and I got the diagnosis on my third day after testing and treatment started immediately. Please ask questions, referrals. I was there until 2015. What an awesome medical facility with caring and Great Doctors.
Hello sir, my mom also have this, firstly she was miss diagnosed as Motor Neuron Disease. But now they confirmed that it's MG. So can you please tell me, what type of treatment you are taking.
Thank you for a well-structured and amazing video. I not only have a clearer understanding about the disease- myasthenia gravis, but also unsmderstand the our purpose in treating these patients
Very helpful video and I loved the visuals , I have a quiz today on MG, GBS, Post op atelectasis and TBI. I feel more confident for the quiz after reviewing your video so thank you 😊
Hello, I am Manum Imran i am working on a documentary on Myasthenia Gravis. My mother was diagnosed with this disease 5 and 1/2 years back and i lost her on 30th June 2019. If any of your family member or relative has this disease currently or previously can you please help me out in research work?
I have was diagnosed January 3 an I have been through the IV IG 2 times an Plasmapheresis had the thymus gland removed an in now in myasthenia crisis they’re planning to do a form of chemo in a couple of weeks! This is something hard to live wit goin from never having health problems now can’t do for myself at times!
@@hechmihamza9080 for ne the hardest part is even after 5 years i'm still trying to love the person i am now. Ppl often ask me why so serious "how comes u dnt smile in pix" not knowing i can't physically smile no more. MG took one thing i was known for, my smile. Been hard to accept that this is me now but i am still learning
@@keavingray8334 yeah we have much in common bro imagine havin' it since ur birthday nothing is normal in ur life neither childhood nor adulthood but it got worse the last 4 years it's like im completely diffrent person always feelin' weak been in the house for long long time can't remember the last time i sat with my neighborhood homies doing our stuff im lucky i have one true freind always pays me a visit at house and i always ask him about how the outsideworld change during the recent years im a muslim so icant even pray properly whenever i wake up i dont have much power to even wash my face every single morning i have to take my medicine wait for like 30 to 40 min for my body to regain some strenght and that's how life's going thank god anyways 😊
@@hechmihamza9080 this is one of those morning that i woke tired, feeling like i just want to lay here all day but i been laying for too long so i fight my way out of bed. We have life and we just gotta fight. I've educated so many ppl about MG, so many ppl are not aware of what it is. But i'll keep u in my prayers bro
This is very interesting. I recently read a study in which children developed AChR-Ab (acetylcholine receptor antibodies) after being vaccinated with the live-attenuated Japanese encephalitis vaccine (LA-JEV) under China's childhood immunization schedule which led to them developing MG (myasthenia gravis). This suggests that AChR-Ab develops after exposure to viruses such as encephalitis. Now I have also read that nicotinic acid deficiency causes cases of acute encephalopathy so I would be curious if administration of oral or intravenous nicotinic acid would have a therapeutic effect on MG caused by AChR-Ab? Nicotinic acetylcholine receptors, or nAChRs, are receptor polypeptides that respond to the neurotransmitter acetylcholine and at the neuromuscular junction they are the primary receptor in muscle for motor nerve-muscle communication that controls muscle contraction... So wouldn't the administration of nicotinic acid possibly be a treatment for MG caused by AChR-Ab since nicotinic acid would block the antibodies?
Great video, you should include that there are sero-negative Myasthenia Gravis patients as well as they just found that the Angrin antibody is associated.
Thank you for this wonderful video. When seeing a patient with myaesthenia, the differential has to include Lambert-Eaten syndrome, motor neurone disease, botulism, myotonic dystrophy and thyroid ophthalmoplegia.
Very great and impressive video! can u cleary state the indication for thymemoctomy and difference between cholinergic crisis and myasthenic crisis .Thanks
Thank you for this detailed video about MG. The major question that I did not find an answer is: What is triggering the body to produce antibody for it self ?.
Thank you for this explanation with images. It would also be good to talk about the effect of high dose of Vitamin D3 in treatment of MG and other autoimmune disorders.
Just as an update - I read that edrophonium tests are no longer routinely performed due to the likelihood of developing bradycardia. I think serum acetylcholine receptor antibody analysis is the standard now - am I correct in thinking this?
You can use neostmine .5mg added with glycopyrolate .2mg as IM route for clinical diagnosis. More accurate if added antibody positivity(always need not be positive). There can negative anti Ach Antibody test with Positive Anti Musk Antibody.( testing is costly)Even there are cases both negative
@@juliadanielle6882 thanks for asking no not cured as a matter of fact ive been diagnosed with a second nuerological disorder called nuerofibromotasis and so God can keep me on my toes ive got a spot on my brain which has been declared not cancerous and a spot on my right lower lung, but havent been tested on that yet. So lol yeah I'm quite busy
@@user-zk8ck3my3l eye doctor then confirmed by a neurologist just had my worst day to date every muscle in my body was twitching feel like ive had a extensive workout. Totally worn out now
@@jerryjustice8026 im in vision therapy and the dr didnt mention it, ill ask but i guess he would know? I know my eye is a bit weaker and i have binocular issues due to misalignment then saw this and wondered but maybe not the cause. Will see, thanks! Do they just look at you or do testing?
Was diagnosed in 2001 ,but I'll since 1985 ,my weakness came upon me ,couldn't lift anything so weak ,my neck I had to use a towel for support, that why they thought I had lupus ,flushing in face ,I had urticaria, edema, all going on at the same time ,doctors didn't know what was happening to me, not until 1991 ,I had so much chemical in me ,not until 2001 when lost my voice, did they know it was MG. Thank God I have meds for it ,this is a brief story about how many things can cause MG,.
I suffer from the disease, I can't get up myself or raise my hand. I was in good health and move, but I was falling a lot and when I sat in a wheelchair, my situation deteriorated.2013😢
Thanks for the info. I suffered from ocular Myasthenia recently. I felt so depressed. I had droppy left eyelids. Does a occcuplastic surgeon can fix my droopy eyelids?
Iam a M.G.Patient since 20 Months.I have taken 40 injections of IVIG when I gone under M.G.CRISIS. and now some how alright. At present I am on medication of 1. Gravitor 60 tabs 1. 1. 1 Halfen hour before meals. 2. M.M.F. 750 mg 1. O. 1.
@@lasyasrinidhikavuri8340is this non curable 😢. And also tell me how are you managing this MG & can medications help control sever symptoms. Please reply me
@@ZeroToFinals your videos are better than osmosis contentwise. They missed many important points that you didnt. This channel can do much better with bit more aesthetic and better presentation. Thx too
thanks a lot. I got for myself info about Low density lipoprotein receptor related protein. probably that is why anticholesterolemic medications damages muscles.
This is because of the antibodies production in the thymus gland...called T cell... It tends to attack the acetylcholine...Thus it is the autoimmune disorder
Is have ocular myastenia and after changing to a whole food plant based diet I had 90% remission of symptoms. I have not had any new symptoms after 10 years on my diet.
This was good, but "Presentation" section only addressed symptoms above the neck. For generalized MG (which many cases develop into), or the 10% of people who present primarily with diaphragm weakness, it's not a good description, nor one that would help first responders or an emergency department to suspect and diagnose these MG patients. They would have missed my family member's MG. Thankfully, 2 out of the 3 neurologists he's dealt with were very aware of this, and are treating it correctly.
Man, I feel sorry for people who have this disease-NO FUN! I'd personally be making fun of myself when my symptoms got bad. Then again I probably couldn't laugh while in respiratory failure 😂 Still would have to find ways of lightening up 😆 Great description video. Thank you.
I lost my older brother due to MG this year.. he was only 27yrs old he was diagnosed at 21 .. This is a very heartbreaking disease I watched my brother loose his life slowly for 6yrs .. I'm not even ready to talk about it but not for one day was he sad he lived every one of those days to the fullest hheyi i thought i should let everyone who has this to get up and beat the odds against you
So, so sorry. My mother has this - she went for taking no medication to being in an ICU for six weeks on a vent! They wanted my sister & I to pull the plug but we refused. She recovered & is doing well considering everything. She can’t do much without shortness of breath - but refuses to stop, just takes little breaks. I am proud of her.✌🏽😎🌄
brother this disease makes u weak, but its treatable , why he die for this disease
May his soul rest in peace man
@@jabedbbsnot really in sever cases it weakness all skeletal muscles of the body including the diaphragm which is necessary muscle for your respiratory system so MG (Myasthenia gravis) can cause Respiratory failure and death
Also sometimes people who has thymoma ( cancer of the thymus gland ) or other disease cause Myasthenia gravis and people might die by the other disease or the by the MG
I have been diagnosed in 2020 and also had thymoma which is the tumor of thymus gland and was removed I only spend 25 days in hospital and was recovered in one year, but was only taking 2mg of prednisone and 250mg of Mycophenolate mofetil for 2 years, and again in March 2023 my symptoms got worsened and doctors thought my meds needs to increased then after 2 months resting at home one day I had a fall due to going up the stairs then in hospital and scans done to see if any broken bone due to the fall then found out thymoma has grown back which is called
(drop metastasis ) and this time was in diaphragm so it’s removed again but this time the symptoms was very bad I have been in ICU for 8 days and had respiratory failure and all together 10 weeks in hospital and still recovering at home and reducing prednisone and recovery this time was very challenging and taking longer than the initial diagnosis 🥹😌
Awesome video.. im now a 51 y/o male .i was diagnosed with MG when i was just 25. Took a ton of tests to figure out why i was having so much weakness. It was horrible. Eventually had a thymectomy at 27 .after a few months had very little weakness. Now some slight weakness if i push it. But certainly liveable. So greatful.
watch this : ruclips.net/video/cKueSxaamQo/видео.html
How was it diagnosed and what kind of symptoms? Is this like tight muscle feeling or eye strain fatigue (but for me one eye) it feels my eyebrow but mainly near temple on one side is tight and heavier. Im in vision therapy also for binocular vision issues. Im not sure if this or just weak eye and tight face muscles from eye and tmj.
Very informative. Thx
@@user-zk8ck3my3l started with drooopy facial muscles. I always looked angry. Or frownng but wasnt. most of the time anyway. 😆 then it moved to my arms and legs. I couldnt walk very well well. very weak...sorry about the delayed response I just saw ur comment..im 54 now. still feeling fine. hope u r too!
Your date n time of birth?
I live with myasthenia gravis for almost 13 years, this video was really helpful for more info. Thanks a lot!
Prayers to you I was diagnosed January 3 of this year 4 days before my 39th birthday just took sick suddenly had the surgery on January 15 an 2 IV IGs Plasmapheresis I spent almost 4 months in the hospital an now I will be goin to New Orleans to start a form of chemo treatment 🤷🏽♀️
@@rakeishaanderson-rhok Prayers to you too! Hope everything will go right for you :)
@@rakeishaanderson-rhok how was it diagnosed and what symptoms? My one eye strains and fatigues. My eyebrow and temple feel tight and heavy and eye is tad lower but i can lift my eyebrow. Sound similar or no?
@@user-zk8ck3my3lhow are you today?
My father in law was diagnosed with this yesterday, he is 67 with no other health issues. We thought he was having a stroke. Symptoms were double vision for a couple of days the slurring speech and difficulty swallowing. He is hospital and has a feeding tube. Treatment has been started and has done well over night. So happy it has been recognised so quickly with treatment started
Howw
Thanks for making this. You just made it all crystal clear for us, And honestly i don't feel that anybody could have delivered it better.
Thanks!
I just found out about a relative's musk MG diagnosis. This was a such a detailed video for being under 11 minutes. Thank you!
Who are these people who dislike such videos 🙄.. this was pretty helpful for quick revision!!
theyre a bunch of haters lol
I m mg pataint and I need some help if u r a doctor plz help me
@@CHANDANKUMAR-bu7cu where do you reside?
@@CHANDANKUMAR-bu7cu hi, how are you feeling now? Have you been able to get cured? there's a doctor who can help you dr isibor on youtube!!!
The ones who disliked are the professors who failed to deliver such presentation lol
Thank you so much for providing this information is very helpful I am Amaya stenia gravis patients and all the information I can retrieve is so very appreciated
Sir, you are one of the best med. student life saver
Thank you for sharing the information about a disease that is not well known. I was diagnosed with MG when I was 16 (currently 19) and I'm glad that I'm able to live without any serious problems after my thymectomy (beside muscle weakness). Thank you!
Hello my sister just had her surgery today...how do you feel after the thymus gland removal?...are you better now??
Hello, I am Manum Imran i am working on a documentary on Myasthenia Gravis. My mother was diagnosed with this disease 5 and 1/2 years back and i lost her on 30th June 2019. If any of your family member or relative has this disease currently or previously can you please help me out in research work?
So informative. I was diagnosed in 2008. Now I am 71 years old and feeling the essence of this disease on my body. I so appreciate this now.
I have information now.
Let me also say that I was misdiagnosed by a Neurologist and my PCP immediately sent me to the Mayo Clinic and I got the diagnosis on my third day after testing and treatment started immediately. Please ask questions, referrals. I was there until 2015. What an awesome medical facility with caring and Great Doctors.
Hello sir, my mom also have this, firstly she was miss diagnosed as Motor Neuron Disease. But now they confirmed that it's MG. So can you please tell me, what type of treatment you are taking.
Thank you for a well-structured and amazing video. I not only have a clearer understanding about the disease- myasthenia gravis, but also unsmderstand the our purpose in treating these patients
thats great to hear. thanks
Amazing video. Explained A to Z in a simple manner. Thank you dear.
Very helpful video and I loved the visuals , I have a quiz today on MG, GBS, Post op atelectasis and TBI. I feel more confident for the quiz after reviewing your video so thank you 😊
Hello, I am Manum Imran i am working on a documentary on Myasthenia Gravis. My mother was diagnosed with this disease 5 and 1/2 years back and i lost her on 30th June 2019. If any of your family member or relative has this disease currently or previously can you please help me out in research work?
I have was diagnosed January 3 an I have been through the IV IG 2 times an Plasmapheresis had the thymus gland removed an in now in myasthenia crisis they’re planning to do a form of chemo in a couple of weeks! This is something hard to live wit goin from never having health problems now can’t do for myself at times!
Been living with MG for 5 years now and trust it hasn't been easy
i got it since birth 22 years now
@@hechmihamza9080 for ne the hardest part is even after 5 years i'm still trying to love the person i am now. Ppl often ask me why so serious "how comes u dnt smile in pix" not knowing i can't physically smile no more. MG took one thing i was known for, my smile. Been hard to accept that this is me now but i am still learning
@@keavingray8334 yeah we have much in common bro imagine havin' it since ur birthday nothing is normal in ur life neither childhood nor adulthood but it got worse the last 4 years it's like im completely diffrent person always feelin' weak been in the house for long long time can't remember the last time i sat with my neighborhood homies doing our stuff im lucky i have one true freind always pays me a visit at house and i always ask him about how the outsideworld change during the recent years im a muslim so icant even pray properly whenever i wake up i dont have much power to even wash my face every single morning i have to take my medicine wait for like 30 to 40 min for my body to regain some strenght and that's how life's going thank god anyways 😊
@@hechmihamza9080 this is one of those morning that i woke tired, feeling like i just want to lay here all day but i been laying for too long so i fight my way out of bed. We have life and we just gotta fight. I've educated so many ppl about MG, so many ppl are not aware of what it is. But i'll keep u in my prayers bro
hi, how are you feeling now? Have you been able to get cured? there's a doctor who can help you dr isibor on youtube!!!
Thank you for the informative video. I am a nursing tutor and the video was very much helpful.
Yeah, my favorite youtuber posts again! You have made my weekend! Thanks!
Awesome! Thanks! Keep up the great work on your channel as well
Awesome! Thanks! Keep up the great work on your channel as well
@@ZeroToFinals thank you! I am slowly improving 😅👍
thank you so much. You explained it more clearly than anything else I've found.
Excellent information.. a true help here in the RUclips and greatly reliable.. thumbs up bro👍
Thanks Edwin
Really really helpful and beautifully explained.... Thankx for such lectures..... I'm thankful...Keep it up👍
Wow, very clear and straight to points!. Thanks😊
Thank you for this video, knowing someone with this it puts it in a way I understand.
This is a remarkable excellent explanation of a serious disease......so easy to follow and well illustrated.
This is very interesting. I recently read a study in which children developed AChR-Ab (acetylcholine receptor antibodies) after being vaccinated with the live-attenuated Japanese encephalitis vaccine (LA-JEV) under China's childhood immunization schedule which led to them developing MG (myasthenia gravis).
This suggests that AChR-Ab develops after exposure to viruses such as encephalitis. Now I have also read that nicotinic acid deficiency causes cases of acute encephalopathy so I would be curious if administration of oral or intravenous nicotinic acid would have a therapeutic effect on MG caused by AChR-Ab?
Nicotinic acetylcholine receptors, or nAChRs, are receptor polypeptides that respond to the neurotransmitter acetylcholine and at the neuromuscular junction they are the primary receptor in muscle for motor nerve-muscle communication that controls muscle contraction...
So wouldn't the administration of nicotinic acid possibly be a treatment for MG caused by AChR-Ab since nicotinic acid would block the antibodies?
interesting idea, definitely worth researching
Makes sense, we grow our own tobacco for nicotine, for friends and family, if they get sick with Viruses or side effects from jab.
@@amlebr80 Nicotinic acid is just another name for niacin vitamin B3.
Great video, you should include that there are sero-negative Myasthenia Gravis patients as well as they just found that the Angrin antibody is associated.
This video helped me a lot. thank you very much!
Thank you for this wonderful video. When seeing a patient with myaesthenia, the differential has to include Lambert-Eaten syndrome, motor neurone disease, botulism, myotonic dystrophy and thyroid ophthalmoplegia.
Very great and impressive video! can u cleary state the indication for thymemoctomy and difference between cholinergic crisis and myasthenic crisis .Thanks
Thanks for your videos! they are really great for revision!
Very good explanation easy to understand.. very nice
Thanks so much! This is a big help for my MSGD today :)
Thank you for the great video, as always!
Loved the way it is explained.💯🌻
thanks!! i could practise my english and vocabulary medicinal with your videos.
I'm having pyridostigmine for past 2 months and still no improvement in symptoms.
Thank you for this. It has certainly broadened my understanding of the topic.
awesome video! gives better understanding for what i have learned in class
Wonderful explanation! Thank you so much!
Thank you so much. It helped my SGD.
Thank you for this detailed video about MG.
The major question that I did not find an answer is:
What is triggering the body to produce antibody for it self ?.
Good question but we have no answer 😑
Some says, it could be caused from an infection. But nobody knows really why
I believe mine was triggered by Covid.
Thankyou sir for u r clear explanation 👌I loved somuch, thanks a lot ❤
really glad you liked it!
It was a good video, it would be great if you could cover seronegative myasthenia gravis. Thank you
that very very amazing -- that subject so hard and you explain so clear and easy
thanx
First lecture attended at your channel... It's great ☺️👍 keep it up.
Amazing video really helped me, thanks!
Thank you for this explanation with images. It would also be good to talk about the effect of high dose of Vitamin D3 in treatment of MG and other autoimmune disorders.
Oh could you please explain me what happens? Thank you a lots ☺️
Wow!! I loved so much!! Thanks a lot. It's very interesting.
Very nice presentation sir ❤
Just as an update - I read that edrophonium tests are no longer routinely performed due to the likelihood of developing bradycardia. I think serum acetylcholine receptor antibody analysis is the standard now - am I correct in thinking this?
I suspect you are right, but I haven't looked into it in detail
yes you are correct they are using prostigmin instead of edrophonium as far as ı konw.
You can use neostmine .5mg added with glycopyrolate .2mg as IM route for clinical diagnosis.
More accurate if added antibody positivity(always need not be positive). There can negative anti Ach Antibody test with Positive Anti Musk Antibody.( testing is costly)Even there are cases both negative
@@amv29 Thanks for the information!
Fantastic video Really helpful
U will be the future millioner I promise..
Is there any link to statins?
I had memory loss after taking statin medication. Then developed Myasthinia gravis.
I just got diagnosed today interesting and helpful information
hi, how are you feeling now? Have you been able to get cured? there's a doctor who can help you dr isibor on youtube!!!
@@juliadanielle6882 thanks for asking no not cured as a matter of fact ive been diagnosed with a second nuerological disorder called nuerofibromotasis and so God can keep me on my toes ive got a spot on my brain which has been declared not cancerous and a spot on my right lower lung, but havent been tested on that yet. So lol yeah I'm quite busy
How were you diagnosed?
@@user-zk8ck3my3l eye doctor then confirmed by a neurologist just had my worst day to date every muscle in my body was twitching feel like ive had a extensive workout. Totally worn out now
@@jerryjustice8026 im in vision therapy and the dr didnt mention it, ill ask but i guess he would know? I know my eye is a bit weaker and i have binocular issues due to misalignment then saw this and wondered but maybe not the cause. Will see, thanks! Do they just look at you or do testing?
Great video ! Reaaly helpfull! If you can make one about lateral sclerosis amyotrophic, it would also be really helpfull :)
I'll add it to my list. Glad you liked it
Watch all Videos from RobertRowenMD...a real eye opener!!! here is just one of them : ruclips.net/video/cKueSxaamQo/видео.html
Was diagnosed in 2001 ,but I'll since 1985 ,my weakness came upon me ,couldn't lift anything so weak ,my neck I had to use a towel for support, that why they thought I had lupus ,flushing in face ,I had urticaria, edema, all going on at the same time ,doctors didn't know what was happening to me, not until 1991 ,I had so much chemical in me ,not until 2001 when lost my voice, did they know it was MG. Thank God I have meds for it ,this is a brief story about how many things can cause MG,.
Sorry you have to go through all that! How are you today?
@lisa4471 not good I have a carcinod, which affects everything, I'm still fighting on all fronts of my illnesses
Thank you. Very clear and informative 🎉
Keep going, that's really great !
brilliant video ... thanks for clarification
Thank you so much, this is most helpful
Thank You! I live in a small city, and I don't think the Neurologists stay up to date on this, so I have become my own researcher lol
Very usefull..thank you so much👍👍..whould like to have similar videos on vitamin deficency
10 mins are more important than 3 hours at school.
Thanks for this helpful video!
I suffer from the disease, I can't get up myself or raise my hand. I was in good health and move, but I was falling a lot and when I sat in a wheelchair, my situation deteriorated.2013😢
Thank you for the information. Really helps
Thank you ❤️❤️ it was a good Video
Many thanks from Egypt ♥️♥️♥️♥️♥️😀
Thanks!
watch this too : ruclips.net/video/cKueSxaamQo/видео.html
Thank you very much doc 🤍🤍🤍🤍
Thank you so much 👍👍👍 that's just a great pleasure to watch your cool videos ❤️
Thanks!
I have myasthenia gravis do you
Best illustration sir
Autoimmune conditions are absolutely terrible!! 😔 😢 I hope someday hopefully soon can ve found the cause and jow to stop autoimmune conditions. 🙏🏽🕯️
you are absolutely fantastic THANK YOU
Thanks for the info. I suffered from ocular Myasthenia recently. I felt so depressed. I had droppy left eyelids. Does a occcuplastic surgeon can fix my droopy eyelids?
How was it diagnosed?
This video has been very helpful
Iam a M.G.Patient since 20 Months.I have taken 40 injections of IVIG when I gone under M.G.CRISIS. and now some how alright.
At present I am on medication of
1. Gravitor 60 tabs
1. 1. 1
Halfen hour before meals.
2. M.M.F. 750 mg
1. O. 1.
@@lasyasrinidhikavuri8340is this non curable 😢. And also tell me how are you managing this MG & can medications help control sever symptoms. Please reply me
Someone told me I might have MG because one eye sags and my lip is crooked. I’ve never noticed it before but now I see it in pics. 😔
Make an appointment with neurologist and have them do the blood work required to diagnose. Also check if you have a thymoma.
U r just amazing
Well done👍💯👏
Um ur new subscriber also liked ur lecture 🤞
Thank you, this was very helpful
this can behelpfull too : ruclips.net/video/cKueSxaamQo/видео.html
You can put this under neurology list too.
Thats true. Thanks!
@@ZeroToFinals your videos are better than osmosis contentwise. They missed many important points that you didnt. This channel can do much better with bit more aesthetic and better presentation.
Thx too
@@eget4144 Thanks! Super busy working on books at the moment, but once I get back to RUclips I hope to go all in with the production
It was very very useful and beneficial... thanks 🔥
thanks a lot. I got for myself info about Low density lipoprotein receptor related protein. probably that is why anticholesterolemic medications damages muscles.
May i know why thymoma is linked to MG? Or how does it cause MG to occur in thymoma patients?
This is because of the antibodies production in the thymus gland...called T cell...
It tends to attack the acetylcholine...Thus it is the autoimmune disorder
Is have ocular myastenia and after changing to a whole food plant based diet I had 90% remission of symptoms. I have not had any new symptoms after 10 years on my diet.
Very helpful for my refreshing!
This was good, but "Presentation" section only addressed symptoms above the neck. For generalized MG (which many cases develop into), or the 10% of people who present primarily with diaphragm weakness, it's not a good description, nor one that would help first responders or an emergency department to suspect and diagnose these MG patients. They would have missed my family member's MG. Thankfully, 2 out of the 3 neurologists he's dealt with were very aware of this, and are treating it correctly.
Thanks for this concise video
So beautiful and soothing voice 😋🤩👏
Thank you!
perfect explanation, thank you
Video is really helpful 👍
Liked it, thanks you are talented
Very helpful video sir.
Very good explanation
Thank you so much , that was very helpful
In 70 yr old, with mild symptoms like fatigue of masticating muscles and mild ptosis, what ll be the prognosis?
Do you have a video of amyotrophic lateral sclerosis?
Having symptoms. Had polio and was in iron lung when younger. Would this contribute to the disease?
No mention of the congenital form 😢
Man, I feel sorry for people who have this disease-NO FUN! I'd personally be making fun of myself when my symptoms got bad. Then again I probably couldn't laugh while in respiratory failure 😂 Still would have to find ways of lightening up 😆
Great description video. Thank you.
What is happening to you now hope ur fine
Great Job! Thank u! Keep on! Maybe some physiology lectures that is more common in usmle examens?
Thanks Miri. I plan on trying to cover everything in time, although it will be a massive amount of work!
I have myasthenia 4 -5 years I had seziers for 22 years haven't had any in 2 years