How are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation and Ayurvedic medicine
@@laxmangupta2268 how are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation
I wish they would really stop showing me ads to do with a therapist when it has nothing to do with my muscles and things like that knowing that i was diagnosed with that when I was born. I don't even want to have to discuss any of this for anyone to make out like I had to explain this and having to prove this to people has been going on a lot lately even before. I didn't know I had to keep specifying.
Also note that muscular dystrophy can also occur from a nonsense mutation. Which means that the mother does not have to be a carrier for her child to get muscular dystrophy. My brother has duchenne, and my mother was tested, and is not a carrier. To prove that point further, me, a female was also tested, and I am also not a carrier. Keep that in mind as well :) its also pronounced like (DO SHEN) :P
I recently got diagnosed with the same thing, no explanation... made a support group that will hopefully grow fast! Join us and share your story! m.facebook.com/myotoniasupport/
my father ,his brother ,sister and his dad all had and passed from mytonic dystrophy . such a bad life to live with It . I was adopted to stop the gene
My brother In this Muscle drophy at age of 40 years now. We all family is concerned about him. Such a silnice disease killing your muscle and Other health issue inside and outside. Please suggestion Dear
I couldn’t stay 2 months not able to perceive or taste anything and with ringing on my both ears. I quickly used a herbal supplements from Dr Madida and I got my lost sense of smell, loss of taste back and all the buzzing, disturbing sounds inside my ears all stopped.
DMD can take place in several different ways not just by a deletion. There can be a duplication as well causing the phenotype of DMD. You are not pronouncing it corectly. There is no "e" at the end. It is just Duchenne. A lot of your information is incorrect. I hope RN's are not using this for their understandings. I suggest you consult PPMD before making any more videos on MD disorders. Thank you for bringing about awareness of Duchenne.
I have been diagnosed with two types of MD...my son has many of the MD traits - can't run, trips, balance issues, weak core muscles, facial/drools...he was diagnosed with Fragile-X as well. My doctor says that there is a connection between the two: MD+ Fragile X. Have you heard of this? Thank you for your video. It was helpful to me.
Dude that was really well put together! I'm doing an assignment on Duchenne Muscular Dystrophy and your video helped me heaps, you explained it better than wikipedia! Thanks again!
Keypoints- Selfnote: Duchenne : symptomatic around age of 5. X linked recessive. Caused by producing rotten Dystropin which support the membrane. Then membrane damaged and Ca++ leakes inside which causes cell death , apoptosis then tissue necrosis. Patients have increased lordosis, weak abdominal and psoudohypertrophic calves. Walk abnormal and on fingertips. BEKERS MUSCULAR DYSTROPY is less severe form of DUCHENNE M.D. MYOTONIC MUSCULAR DYSTROPY is symptomatic in adults. it is coused by DMPK gene( type 1 CTGx3) and CNBM( Type 2 ) gene in chromosome 19. The problem is muscles cannot relax . These patients can also devolop cataract, Mental retardation and Heart problems. Has a typical face dismorphy( Tense cheeks, alopacia, and in chin)
I have muscular dystrophy. I can't go up the stairs, can't stand while sitting, can't run ,I live in Indonesia .Iam age 28 .please help I want to play like a normal person again.
So if we have girl embryo that is know as a carrier of DMD , could we return this embryo without the fear she will be developing same symptoms as a boy that sick with Duchenne?
I am a big fan of your videos... I am a little bit worried that some people will understand that at 3:21 the couple will always have this combination meanwhile it is a chance they'll have some of it or even a single one of it... Sometimes all offspring are diseased males or totally healthy ones and so on
Thank you, very informative in a short video, I like these kinds of videos. I was able to follow what you were saying, even without understanding it. If this makes sense? Which tells me that you’ve done a very good job.
My grandson Joshua has DMD, he is 18yrs old, and l'v read lots of information on the ill ness, but found your vidio to be more intresting and thanks cus I've understood more by watching it, well intresting and put together,
"Are you a med student"+"No, I'm studying medical science". This doesn't add up. 0o How can you be studying medicine, yet not be a medicine student? Hrmpfh, the pathological norms of language messing with us.
I study medical science too, its medicine without the patients and dead body parts. we study the science behind the medicine. its geared towards people who go into medical reasearch.
Thanks very nice Video! i have muscle dystrophy fascioscapulohumeral muscle - do you know anywere in world that i can get Tratment? that can make my muscle stronger?
I heard if you have a mutation in your gene due to certain exon, they can perform exon skipping treatment on you which can slow down muscle loss and also combined with drugs this treatment can cause increase in muscle growth. I hope you get some sort of treatment.
I m sorry but this video was terrible. The genetics were poorly explained and unnecessary. Also the "protruding stomach" isn't only because of weak trunk muscles, but in fact also functionally aids walking.
Wow, nice way of being a horrible person, GREAT JOB AT THIS!! You are like the only one who is dissing this video, also thank you for explaining one slight difference that is not necessary to know, that is not the content explanation necessary here, I would like to see you do something better, quit projecting your own insufficiencies onto a brilliant mind. Bravo. If you want to suggest ways to improve by all means, this is a NICE AND HELPFUL way to let someone know constructive criticism. But this? You sound like a spoiled rotten brat that does not believe in themselves. Which is a shame because you too have the ability to be brilliant. In other words, if you don’t have something nice to say, then don’t say anything at all. I hope you learn from this and grow instead of lashing out as a child. 🙏🏼💙✨
Hello, My son just turned 8 years old. He has a symptom of the Duchenne types. He is tiptoeing still. He falls very easily. Lately we noticed he is falling more often for no reason. His doctor referred him to Stanford and they're planning to do a DNA (gene) test. Please advise if there is anything else we should do. We are really confused.
Sir my diagnosis is going on still but according to my history doctors are saying about mitochondrial myopathy because some of symptoms of this disease is showing in my body. My treatment is going on from AIIMS New Delhi India.
I will never forget the day I came across dr igho channel on RUclips , I will always keep it memorable, thank you doctor for helping me cure my muscle dystrophy & pain completely , and putting a smile on my face , you made me feel more alive like never before , Thank you Dr igho
2020 trying to pass RN school, thank you Armando!!!
I have duchenne muscular dystrophy and I am 13 years old and I am still walking
I am of 18
I can walk but can't run
How are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation and Ayurvedic medicine
@@laxmangupta2268 how are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation
I wish they would really stop showing me ads to do with a therapist when it has nothing to do with my muscles and things like that knowing that i was diagnosed with that when I was born. I don't even want to have to discuss any of this for anyone to make out like I had to explain this and having to prove this to people
has been going on a lot lately even before. I didn't know I had to keep specifying.
Very nice.. thank u very much.
Really helpful! thanx!
Here is how to pronounce Duchenne, google, howjsay duchenne
No bro, just studying medical science:)
Dude you ROCK!!!!!
Nice presentation.
James
Also note that muscular dystrophy can also occur from a nonsense mutation. Which means that the mother does not have to be a carrier for her child to get muscular dystrophy. My brother has duchenne, and my mother was tested, and is not a carrier. To prove that point further, me, a female was also tested, and I am also not a carrier. Keep that in mind as well :) its also pronounced like (DO SHEN) :P
Duchenne
The only place in the world where they cure all incurable diseases.
ruclips.net/video/V5NHB7PSFxE/видео.html
Yogh se Arram mile sakte hai bas
Amazing, where were you when i started nursing school?! :D thank you!
Thanks this helped with my project a lot
Hello anyone watching this in 2020?
Thanks for your video
You are doing a good job
I Found out just 30 min ago I have MMD thank you this was more than the doctor told me
I recently got diagnosed with the same thing, no explanation... made a support group that will hopefully grow fast! Join us and share your story!
m.facebook.com/myotoniasupport/
Am humbled by the facility with which the DMD is explained in a comprehensive language and drawing.
Thank you.
omg thank u. Ive been on houndred different websites and no one was even close to explain what happnes in the cell but u safed my life! ty :)
Jazakallah khair May Allah bless u with the best for this🤲
my father ,his brother ,sister and his dad all had and passed from mytonic dystrophy . such a bad life to live with It . I was adopted to stop the gene
My brother In this Muscle drophy at age of 40 years now.
We all family is concerned about him.
Such a silnice disease killing your muscle and Other health issue inside and outside.
Please suggestion Dear
Sweety...Please watch Bruce Lipton....I know you mean well but, there are some things not right. LOVE you anyway
I couldn’t stay 2 months not able to perceive or taste anything and with ringing on my both ears. I quickly used a herbal supplements from Dr Madida and I got my lost sense of smell, loss of taste back and all the buzzing, disturbing sounds inside my ears all stopped.
DMD can take place in several different ways not just by a deletion.
There can be a duplication as well causing the phenotype of DMD.
You are not pronouncing it corectly. There is no "e" at the end. It is just Duchenne. A lot of your information is incorrect.
I hope RN's are not using this for their understandings.
I suggest you consult PPMD before making any more videos on MD disorders.
Thank you for bringing about awareness of Duchenne.
Hi. I am from nepal and I am suffering from Becker muscular distrophy.
Ajay Deula god bless you
It seems me too.. from India.
WE TREAT MD AYURVEDA TREATMENT AND WE WILL HELP IT OUT SEND DETAILS hispharma@gmail.com or call 9818903387
I have been diagnosed with two types of MD...my son has many of the MD traits - can't run, trips, balance issues, weak core muscles, facial/drools...he was diagnosed with Fragile-X as well. My doctor says that there is a connection between the two: MD+ Fragile X. Have you heard of this? Thank you for your video. It was helpful to me.
yes X chromosome is the real cause of MD.. what's your sons age now?
WE TREAT MD AYURVEDA TREATMENT AND WE WILL HELP IT OUT SEND DETAILS hispharma@gmail.com or call 9818903387
Thank you for sharing this informative research in such a well laid out style of teaching
Question, can a patient have becker muscular dystrophy and Atherosclerosis? If so what is the chance of living a long life?
But with adequate care many men with Duchenne can reach 40i or even more.
Contact doctor Akhigbe for your cure with his herbal medicine
Email him now
Please update any cure of this disease if any in previous couple of years...
I have Duchenne Muscular Dystrophy is there any treatment I want help please
myotonic dystrophy is the same as STEINERT disease ??
thanks for uploading, you're a great teacher!
Dude that was really well put together! I'm doing an assignment on Duchenne Muscular Dystrophy and your video helped me heaps, you explained it better than wikipedia!
Thanks again!
Based on your info on this will a alkaline diet reserve this?
Please tell me about your research assignment.
Thank you! Great explanation and illustrations.
2012trying 2 pass the primary exam of anesthesia big like 👍
Anyone is watching this video for bio project?
Keypoints- Selfnote:
Duchenne : symptomatic around age of 5. X linked recessive. Caused by producing rotten Dystropin which support the membrane. Then membrane damaged and Ca++ leakes inside which causes cell death , apoptosis then tissue necrosis. Patients have increased lordosis, weak abdominal and psoudohypertrophic calves. Walk abnormal and on fingertips. BEKERS MUSCULAR DYSTROPY is less severe form of DUCHENNE M.D. MYOTONIC MUSCULAR DYSTROPY is symptomatic in adults. it is coused by DMPK gene( type 1 CTGx3) and CNBM( Type 2 ) gene in chromosome 19. The problem is muscles cannot relax . These patients can also devolop cataract, Mental retardation and Heart problems. Has a typical face dismorphy( Tense cheeks, alopacia, and in chin)
My son has muscle dystrophy plz help my son 🙏🙏🙏🙏
Can you please do a session on transverse myelitis and multiple sclerosis ? Thank you
Can this not happen to female children???
Can you make a video explaining ullrich and bethlem congenital muscular dystrophy?
I have muscular dystrophy. I can't go up the stairs, can't stand while sitting, can't run ,I live in Indonesia .Iam age 28 .please help I want to play like a normal person again.
So if we have girl embryo that is know as a carrier of DMD , could we return this embryo without the fear she will be developing same symptoms as a boy that sick with Duchenne?
2021 prepping for my exams (in the next 10 days)And I will win
Thanks Armando ❤️
I am a big fan of your videos... I am a little bit worried that some people will understand that at 3:21 the couple will always have this combination meanwhile it is a chance they'll have some of it or even a single one of it... Sometimes all offspring are diseased males or totally healthy ones and so on
There aren't just 3 types of muscular dystrophy, there's a plenty of them. Also consider variables that can make much more of them......
im doing a research paper on muscular dystrophy, would you be able to link to me some sites that you used to get this information?
Thank you, very informative in a short video, I like these kinds of videos. I was able to follow what you were saying, even without understanding it. If this makes sense? Which tells me that you’ve done a very good job.
Thank you so much for this wonderful video! Really gave me a clear understanding >_
how to differentiate muscular dystrophy and muscular atrophy?
Why didn’t you go into detail about BMD? I think that information would have been very helpful instead of generalizing it
very well structured! well done
"psuedo-hypotrophied, i think thats a word" that totally made me laugh
Pseudohypertrophied. Correction
sir please give me some treatment for this
Hey Armundo, where can you get the image for this video? It'd really help me with med school to get it and put it up!!!!!!!!!!
My grandson Joshua has DMD, he is 18yrs old, and l'v read lots of information on the ill ness, but found your vidio to be more intresting and thanks cus I've understood more by watching it, well intresting and put together,
"Are you a med student"+"No, I'm studying medical science".
This doesn't add up. 0o How can you be studying medicine, yet not be a medicine student? Hrmpfh, the pathological norms of language messing with us.
Please update your older videos
if people are interested, there are also several forms of dystrophy that arise via problems with protein glycosylation and trafficking
one of the best myology vids out here thanks!
#DRIYAREMOSES HERBAL HEALING
I study medical science too, its medicine without the patients and dead body parts. we study the science behind the medicine. its geared towards people who go into medical reasearch.
But you didn't even really cover Myotonic Dystrophy!
actually, there is no distrofin at all in muscle fibres in DMD, but i Beckers there is abnormal distrofin!
Thanks very nice Video!
i have muscle dystrophy fascioscapulohumeral muscle - do you know anywere in world that i can get Tratment? that can make my muscle stronger?
I heard if you have a mutation in your gene due to certain exon, they can perform exon skipping treatment on you which can slow down muscle loss and also combined with drugs this treatment can cause increase in muscle growth. I hope you get some sort of treatment.
I m sorry but this video was terrible. The genetics were poorly explained and unnecessary. Also the "protruding stomach" isn't only because of weak trunk muscles, but in fact also functionally aids walking.
Wow, nice way of being a horrible person, GREAT JOB AT THIS!! You are like the only one who is dissing this video, also thank you for explaining one slight difference that is not necessary to know, that is not the content explanation necessary here, I would like to see you do something better, quit projecting your own insufficiencies onto a brilliant mind. Bravo. If you want to suggest ways to improve by all means, this is a NICE AND HELPFUL way to let someone know constructive criticism. But this? You sound like a spoiled rotten brat that does not believe in themselves. Which is a shame because you too have the ability to be brilliant. In other words, if you don’t have something nice to say, then don’t say anything at all. I hope you learn from this and grow instead of lashing out as a child. 🙏🏼💙✨
helped me better understand my biology class, thanks!
My brother has dmd.he is in a hospice :'(
my brother has dmd too 😢😢😢
Hello,
My son just turned 8 years old. He has a symptom of the Duchenne types. He is tiptoeing still. He falls very easily. Lately we noticed he is falling more often for no reason.
His doctor referred him to Stanford and they're planning to do a DNA (gene) test.
Please advise if there is anything else we should do. We are really confused.
Dude Dude hello,im BMD sufferier,add my whats app:+8618983211644 or Facebook:juniorliao1985@gmail.com
شرح مفيد ورائع يوضح مرض ضمور العضلات عند الاطفال
Sir my diagnosis is going on still but according to my history doctors are saying about mitochondrial myopathy because some of symptoms of this disease is showing in my body. My treatment is going on from AIIMS New Delhi India.
How are you now please contact me on WhatsApp 91 9322303271
thank you for making these videos I appreciate it. Is very helpful and you make it so easy to understand with those drawings, cheers from Panamá.
Super lecture thanks and love you sir
I'm the MD Survivor
I need objective physical muscle tone visual description of these conditions
Oh my gawsh. Your last name is so beautifull! What is its origin!?
the video helped me understand the disease process while studying forr my exam.
Ur life saver thank u
Armando, could you do a video on FSHD muscular dystrophy?
Sir I am suffering from mitochondrial myopathy I want to know is any effective treatment of this disease. I am from India.
Read bible please
what is becker muscular dystrophy
But if the carrier has married to an affected one (male) we have then a possibility to get an affected girl !!! That's what I didn't understand
Contact doctor Akhigbe for your cure with his herbal medicine
Email him now
Am permanently cured with Dr iyaremoses herbal medicine#driyaremoses channel
on your own? just for yourself? why you didnt go to medical faculty?
I am sick with muscular dystrophy and I want you to help me, thank you
Contact doctor Akhigbe for your cure with his herbal medicine
Email him now
appreciated 🖤
Thank you I have Beckers Muscular Dystrophy and I just learned more
Carlo Basile I have Becker Muscular Dystrophy too
Interesting information ,Thank you .
my problem muscular diseases plz do you help me sir...?
Thank you so much 😊
Why there is no cure for MD ? 😅
True
thank you , my husband has duchenes m.d. very informative
💎💎👍👍👍👍👌
I will never forget the day I came across dr igho channel on RUclips , I will always keep it memorable, thank you doctor for helping me cure my muscle dystrophy & pain completely , and putting a smile on my face , you made me feel more alive like never before , Thank you Dr igho
ruclips.net/video/PEGmhxAIODQ/видео.html
so like.. a titan?
It was great helpful to do my homework :-)
great video! only thing is that it's pronounced like "ducane"
+Cassie Vega "Du-shen"
Neurology exam tomorrow, and I'm watching all of your videos, they are awesome!! Thank you so much!
Dmd recover how?
Thank You for this information. #Gratitude #ArtistReach
Thank you bhaiya
Nice description