Dr. Tubridy thank you for your *amazing* neurology history and examination videos -- I am an M3 in the United States and your lectures are nothing but strings of pearls. Thank you UCD for putting these lectures online and to all the patients in your clinics who made these videos possible. Thank you again Dr. Tubridy
From a doctor, what a brilliant series. Thank you to the patient and Dr for this video. I still come back to this from time to time to brush up on my knowledge!
much appreciated, a very eye opening video presention toward learning MG. Patient was great as well giving clear history and was following instruction with ease. Very glad tat Dr Tubridy gave clues on how assess for differential diagnosis as well thanks a lot for sharing.
Excellent PACES teaching, many many thanks. For those extra points in the viva part, remember that IVIg is pretty much as effective as plasma exchange in this condition.
Antibody more commonly seen in focal myasthenia gravis is against muscle specific receptor tyrosine kinase and in generalised more common in against acetylcholine receptor . Excellent teaching doc 🙏🙏
In September 7 2020,my father was diagnosed with MG and the doctor immediately on the next day Started the treatment of plasmapheresis (series of 5 plasma infusion every alternate day) but before the 5th infusion my father passed away.he had fatty liver but he had taken good care of diet & exercise. I just want to know,Dr, what the treatment he gave is correct?? When he knew my father had fatty liver and heavy dosage of medicine can give him side effects.... infact he didn't even give us the guidance nor the chance to understand the severity of disease which we had never heard off. I feel really guilty till to this day that we should not have taken him to that doctor....
So it may be a case of Occular myesthenia...Should not we exclude other dd like Occular myopathy or occulopharyngeal myopathy or GBS ( Miller Fischer syndrome)??
@@kaynatkhan7560 pyridostigmen is anti cholen estrase long duration ,but I think patient take atropine before it to block muscurane resceptors (sorry for Bad English )
Can't express how thankful I'm for this very informtive videos . Thank so much for every one helped make these vids and specially thanks to dr tubridy .
To the uploader, please help me. Do you know how to find Dr. Niall tubridy? I badly need his help. I am from Philippines and my doctors find it hard to distinguish what disease I have. They keep giving me test and yet no answetd were found. They suspect it as myasthenia gravis. Please help me
Very good explanation sir .Is there any possibility to cure this my brother is having this disease and his age is 23 now....is it possible to cure this permanently..
Hi, I was diagnosed with MG in January 2012. Shortly after the diagnosis I switched to a vegan diet after reading about auto immune disorders in the book The China Study, by T. Coin Campbell. My symptoms slowly mitigated over a four month period. I now have slight throat and facial muscle impairment but the drooping eyelids and double vision are gone. Eliminating animal protein and excess fat from my diet made all the difference in my recovery.
Well Dr. I don't sell or promote books. However after 4 months on a whole food plant based diet 95% of my symptoms have gone away. My only object is to inform people that this diet may work for them and there are no bad side effects. So maybe you should check it out and possible help people get well.
Dr. Drake Ramoray With all the "cures" out there (baking soda, coconut water, coconut oil, spirulina, juicing, vegan diets, vegetarian diets, raw diets, no sugar diets) why is anyone sick at all if it's that easy? These diseases are as old as the hills and will most likely plague the human race till the end of time.
John Kammer Sorry for your diagnosis. I work in a six-Doctor neurology office and see patients every day battling an array of neurological issues. There is no harm in changing ones diet but patients need to be aware the of all the 'quack' stuff on the Internet (especially any supplements being touted as having supposedly been kept 'secret' by the medical community). Before doing anything drastic always discuss it with your doctor first.
Hi Tracey, Sorry to hear about your condition. I am so surprised that you are vegan and acquired an auto-immune disorder. From all I have read over the last four years, it seems you need a leaky gut and some type of partially digested animal protein to get MG. When I got MG I was taking a lot of ibuprofen and having protein smoothies with dairy milk and whey protein. As a vegan do you consume any processed foods? Processors sometimes have whey or other dairy protein way down on the ingredient list. Good luck with your tests, stay vegan, and your symptoms may get better.
I'm 25, and I may be diagnosed with MG.. I have the same issue, my eyelid droops in evening or when I'm stressed & my doctor told me it's very rare in this age.. I'm preparing myself for EMG tests.
Dr. Tubridy thank you for your *amazing* neurology history and examination videos -- I am an M3 in the United States and your lectures are nothing but strings of pearls. Thank you UCD for putting these lectures online and to all the patients in your clinics who made these videos possible. Thank you again Dr. Tubridy
What are you doing now? I mean what residency are you in?
That smile of a patient despite suffering, is a win for a doctor...you are a rockstar doctor 🤘🤘
From a doctor, what a brilliant series. Thank you to the patient and Dr for this video. I still come back to this from time to time to brush up on my knowledge!
much appreciated, a very eye opening video presention toward learning MG. Patient was great as well giving clear history and was following instruction with ease. Very glad tat Dr Tubridy gave clues on how assess for differential diagnosis as well thanks a lot for sharing.
This neurology teaching cannot be any better. Thank you.
Great demonstrative videos with a level of insightful knowledge that you always had in the art of teaching medicine
Excellent PACES teaching, many many thanks. For those extra points in the viva part, remember that IVIg is pretty much as effective as plasma exchange in this condition.
This is incredibly useful as part of preparation for the MRCP PACES. Thank you
Good thing there are still some doctors who are inquisitive about what their patients report. I don't see that very often.
I wish this Dr lived in Missouri.. He knows his stuff!
No kidding!!!
Very informative and great approach to the unilateral ptosis . Thank u sir
Amazing teaching. Thanks for sharing.
Antibody more commonly seen in focal myasthenia gravis is against muscle specific receptor tyrosine kinase and in generalised more common in against acetylcholine receptor . Excellent teaching doc 🙏🙏
Thanks, Doctor Tubridy! Brilliant demonstration as always.
If the blood tests were negative would you still do the other tests?
Amazing video
That video has helped me. Thank you
Can a muscel biopsy tell if you have MG
Amazing teaching
Excellent demonstration.
I’m impressed by both of you. Great work on this video doc. :)
Really useful video-thanks.
In September 7 2020,my father was diagnosed with MG and the doctor immediately on the next day Started the treatment of plasmapheresis (series of 5 plasma infusion every alternate day) but before the 5th infusion my father passed away.he had fatty liver but he had taken good care of diet & exercise. I just want to know,Dr, what the treatment he gave is correct?? When he knew my father had fatty liver and heavy dosage of medicine can give him side effects.... infact he didn't even give us the guidance nor the chance to understand the severity of disease which we had never heard off. I feel really guilty till to this day that we should not have taken him to that doctor....
So it may be a case of Occular myesthenia...Should not we exclude other dd like Occular myopathy or occulopharyngeal myopathy or
GBS ( Miller Fischer syndrome)??
Great differentials for ptosis. Extremely helpful. Thank you.
Olá, Qual foi o diagnóstico desse senhor ??
Here in 2024 thank you for an amazing resource - lots of love post IMT from London
Is there any treatment for dropping of eye lid or any medicine. I have done all the test and MRI. So please give me any advice for this treatment
Pyridostigmine is very effective if poor response go for steroids and if diabetic or immunocompromised mycophenolate mofetil can be given
@@kaynatkhan7560 pyridostigmen is anti cholen estrase long duration ,but I think patient take atropine before it to block muscurane resceptors (sorry for Bad English )
Great video!
Thanks to the patient
We are so grateful to our patients who make themselves and their conditions available to help train the next generation of doctors.
Amazing !❤
Excellent video for med student.. thanks professor
Excellent video. Thank you very much
that was a very informative video!
can this channel arrange similar videos for conditions related to other organ systems?
Thank you Dr Tubridy!
Wow 😮 great xplanation thank you
Can't express how thankful I'm for this very informtive videos . Thank so much for every one helped make these vids and specially thanks to dr tubridy .
Thank you Professor also the patient.
Very good 😌
Thank you very much for this! Your neurology teaching helped a lot in my preparation for paces!
From 5:50 - Thats your PACES discussion!
Very very useful ! Few words, but very precise
Thank you so much I learned alottt from your videos 😇I haven’t learned that much ever from my class😅
very helpful and informative sir !!!!! thanks for providing us the practical knowledge
Why is it unilateral
Hello Dr I have MG disease and I really need a help how can I reach you am from Kenya
We regret that we are not able to conduct online consultations or offer medical advice. Please see your own physician.
really good
To the uploader, please help me. Do you know how to find Dr. Niall tubridy? I badly need his help. I am from Philippines and my doctors find it hard to distinguish what disease I have. They keep giving me test and yet no answetd were found. They suspect it as myasthenia gravis. Please help me
Robbie Thomas thanks for the information
I watch your videos before reading topics in neurology :)
thanks to the patient!
To the doctor
Very impressive, thanks.
woww! that was great professor, i hope you keep doing this kind of videos. thank you very much!
Very helpful. Thank you!
Very informative
Thank you so much.. informative
Very good explanation sir .Is there any possibility to cure this my brother is having this disease and his age is 23 now....is it possible to cure this permanently..
@Pablo Dc can you share the details ....and you got cured permanently from mysthenia gravis? How long you got suffered?
@@saravananms1883it is cure mythenia gravis .my sis hd this disease plz share information
Very very useful
this was amazing thank you!
Queria tanto a tradução
tem a legenda em ingles, você pode pegar cada frase e ir traduzindo no google tradutor...
Your neurological physical exam videos are really excellent. Thank you.
sir I am Myeas thenia grevis petition sir please suggest me some tips please
TKS very practical!!!
great. thank you
thank you a lot
I don't even want to be a doctor, and I was impressed with the doctors range of words.
Great teaching session. Very clearly explained. Would love more of these for other conditions as well. Thank you :)
Exactly what I have. I am so sorry sir that you suffer from OMG as well.
Hi,
I was diagnosed with MG in January 2012. Shortly after the diagnosis I switched to a vegan diet after reading about auto immune disorders in the book The China Study, by T. Coin Campbell. My symptoms slowly mitigated over a four month period. I now have slight throat and facial muscle impairment but the drooping eyelids and double vision are gone.
Eliminating animal protein and excess fat from my diet made all the difference in my recovery.
Another Vegan with their own agenda promoting more books. Niggapleazz.
Well Dr. I don't sell or promote books. However after 4 months on a whole food plant based diet 95% of my symptoms have gone away. My only object is to inform people that this diet may work for them and there are no bad side effects. So maybe you should check it out and possible help people get well.
Dr. Drake Ramoray With all the "cures" out there (baking soda, coconut water, coconut oil, spirulina, juicing, vegan diets, vegetarian diets, raw diets, no sugar diets) why is anyone sick at all if it's that easy? These diseases are as old as the hills and will most likely plague the human race till the end of time.
John Kammer Sorry for your diagnosis. I work in a six-Doctor neurology office and see patients every day battling an array of neurological issues. There is no harm in changing ones diet but patients need to be aware the of all the 'quack' stuff on the Internet (especially any supplements being touted as having supposedly been kept 'secret' by the medical community). Before doing anything drastic always discuss it with your doctor first.
Hi Tracey,
Sorry to hear about your condition. I am so surprised that you are vegan and acquired an auto-immune disorder. From all I have read over the last four years, it seems you need a leaky gut and some type of partially digested animal protein to get MG. When I got MG I was taking a lot of ibuprofen and having protein smoothies with dairy milk and whey protein.
As a vegan do you consume any processed foods? Processors sometimes have whey or other dairy protein way down on the ingredient list.
Good luck with your tests, stay vegan, and your symptoms may get better.
I'm 25, and I may be diagnosed with MG..
I have the same issue, my eyelid droops in evening or when I'm stressed & my doctor told me it's very rare in this age.. I'm preparing myself for EMG tests.
are you ok? my eye lid started dropping and I'm scared what it could it be..
Do labs , often there are antibodies positive .
Is there any possibility to cure this disease permanently...
@@o1-preview I'm good.. my test was negative.. but still my left eyelid droops :(
How are you? Did you get your test done?
@@saravananms1883 I don't think so..
As per my research it can't be cured permanently
I say I say ashley
amiga cherished500 l