Duchenne & Becker muscular dystrophy - causes, symptoms, treatment & pathology

[@millieg.47]

shout out to my dad who has MD. he's the strongest man i know and i love him with all mt heart, and am so happy that he is still here, although walking is hard for him.

[@anjlisharma2409]

All I have to say is may God bless him with all the kindness and love present in the world

[@WhatAmIBrewing]

How old is he now?

[@codeyhorn2406]

I have Becker muscular dystrophy an crebel Paulsy Iam age 22 hopefully I live a long life

[@dougscustomcargarage3434]

Codey Horn I have Becker's MD and I'm a male age 47 live in Portland, Oregon

[@andrewsomebody844]

How old where you when it was disgnosed?

[@Skxll_YT]

Codey Horn me too

[@anthonylucas81]

Codey Horn hey I have the same thing

[@adityapatil2047]

Live long I have BMD i am 17 now with basic symptoms ☺️ But i use to live my life normal without taking burden 😊

[@modii8168]

I am a 4th-year medical student and today I made a friend in the hospital with Becker muscular dystrophy. He is 40 years old and has been living in the hospital for many years because of the complications and need for monitoring. Anyway, I just wanted to say that he has literally the best personality, polite, and funny. I really admire him for educating himself and becoming the person he is now, also his the kind of person that you would never get bored while talking to him. Words wouldn't be enough to describe him. God bless him. Just wanted to say have some faith, it is the beginning of a long journey be strong.

[@osmosis]

We've updated this video! The previous version spelled scoliosis wrong.

[@pomboe]

Wow you re uploaded the whole thing for one misspelled word. Thank you so much Osmosis. Please never get tire of making videos like this. It would really help students studying in medical field so much

[@osmosis]

We take accuracy really seriously and do our best to help student learn this information in a fun and easy way. =) Glad you found it helpful.

[@briantracy271]

+Osmosis This channel is the best! Amazing work guys !

[@courtney.22]

+Osmosis How did you spell it before?

[@mansiudayjoshi]

I have excelled in all my path papers on the basis of your videos ❤️. Thanks . You are a gift from God .🤩

[@fernity2]

Just lost a family friend with DMD. He was 36 years old. Rest in heaven, Jose, where there will be no more suffering ❤ we miss you

[@syedjibran4792]

Same I Lost A Friend On June 3rd 2024

[@WhatAmIBrewing]

Just know you were lucky he lived that long, so sorry for your loss. I’ve got beckers, I hope I live a somewhat full life

[@adityaanurag4385]

For all of you guys out there with functioning muscles... you are very, very, very lucky. I have DMD, and it is the worst thing you can think of. I wouldn't wish this on my worst enemy.

[@foodiepanda7430]

Minion12 GT No, my brother has DMD and he hasn't taken a step in past 6-7 years. He'll be 20 soon. We are doing everything we can for him. Not everyone with this condition can walk! Most of them don't live past their mid 20's so STFU!

[@R1IY2N]

Usually can walk before age 9

[@docantle3410]

Sneak Nation Official Please research Dr. Robert Morse on KZbin🍇💕I wish you luck on your healing journey!

[@_AbhiRam_]

I hope you are doing well

[@farihachoudhury861]

Hello. Can I interview you for my research paper? I think you're currently in Singapore.

[@muhammadhussainmir7784]

You guys have a knack for making complex concepts palatable ! Keep up the good work ! (y)

[@osmosis]

Will do - thanks Muhammad! =)

[@SuinegNet]

I have Becker's and just wanted to say thank you for this. It's quite difficult to find good information that easily describes what is going on. This is imo, the very best resource I've seen in 30 years!

[@brahimazzaf9376]

Hey I have DMB too how you spend u'r life with it

[@SuinegNet]

@@brahimazzaf9376 that's a long answer. But to sum it up in a few words. I'm 34, finally on disability, and am trying to teach myself to program. I sleep a lot, sometimes up to 14hr, and am overweight. Most days I get nothing done from lack of energy and depression. Watch a lot of TV. And desperately want my life to change, but zero energy to do so. So... Take from that what you will, lol. Everyone will experience life differently and will get done what they can. It's taken my 30 years to finally accept and be okay with my failures. It's a hard, tiring disease, and we do the best we can. That's all we can do right :) I take 700mg carbamazapine daily... Which of course makes me drowsy all the time with little interest to do much. But it helps with the stiffness so I can actually move without the fear of falling each and every step. Anyhow, hope this helped in some small way :P

[@hammondsmucker]

@@SuinegNet I just wanna be normal I hope I don't have this shit and I won't even be able to get disability I'll be slaved till my skin starts rotting off by my parents

[@oladayoidowu226]

I will never forget the day I came across dr igho channel on KZbin , 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

[@jaysimoes3705]

@@oladayoidowu226 Yeah he helped me getting my grandparents who were burried for at least four decades out of the grave and back to life! I am so thankful too.

[@sukhmanikaur6429]

I'm on my third pathophysiology course of my nursing program because of you, you've carried me through these courses ❤❤❤

[@osmosis]

Thanks for making us part of your medical studies, Sukhmani! 🥰❤️🙏🏼

[@Nerdnp22]

Im a 3rd year medical student. I met a little 7y/o boy in the hospital yesterday who has DMD. Such a happy and spirited child. May God protect him and his parents. Thanks for the video!❤

[@carrollcarpenter-he4ch]

I am a teen with Beckers and I love how informative this video was

[@Heart2016Sim]

I love my brother and he's my world and I can't imagine life without him in it. I've noticed my brother sleeping more but that's about it.

[@juliadanielle6882]

have been dealing with muscular dystrophy for the past 7 years until i got review online about Dr Isibor on KZbin about his healing abilities through herbs and body cleanser and I contacted him after 14 days of treatment I felt better and completely cured!

[@lyefwwswq]

@@juliadanielle6882can u send me his account?

[@PL-oz8ci]

Fallen in love with such a kind of easily understandable description of diseases in a short span of time.....Thanks a lot OSMOSIS

[@fastfatty7785]

I think i have the rarest

[@fastfatty7785]

Because i am 13 and can still walk but barely

[@WhatAmIBrewing]

@@fastfatty7785barely? Wow that’s serious if you are only 13

[@ArshdeepSingh-pv7lf]

This give me 90% of the answers need for my 150 point project

[@shwepyisoe3030]

I am 53 year old male with DMD. Keep fighting.

[@smart13091]

Thank you so much you literally explained an entire lecture in just 7 minutes 👏🏼👏🏼👏🏼

[@osmosis]

You're very welcome! 🥰

[@ishasheikh8182]

The perfect explanation... You don't need to watch any other video for DMD after this one

[@dougscustomcargarage3434]

I have BMD I'm 47 a male. I'm Still walking but with a cane and walk very slow I'm still driving a car too I was diagnosis with Becker's muscular dystrophy at age 29 I'll be honest I'm having a real hard time mentally dealing with muscular dystrophy at 47 I like to stay busy doing stuff but I can't bend down pick stuff up that I drop alot because my right arm has gotten very weak in the 2 years

[@xSuperQx]

Stay strong, sending you love

[@badruddinhasansaky5881]

Bro, please seek physiotherapy. It will improve ur life condition. It's the mainstay of treatment.

[@dayeongE]

See @I feel good's comment above she talks about FDA study really hope that will help you..

[@cozgiy9716]

really hope your still doing well

[@Kiki-nm8uu]

Hey, If you want to talk about it I‘m here..

[@kylevanhouten4560]

I learned so much from this video. I'm 21 years old with Becker MD and yet have never learned this much about the disease. Thanks

[@juliadanielle6882]

have been dealing with muscular dystrophy for the past 7 years until i got review online about Dr Isibor on KZbin about his healing abilities through herbs and body cleanser and I contacted him after 14 days of treatment I felt better and completely cured!

[@yousefalslamain3278]

Thanks for all your videos , I will make sure that if I became a doctor I will donate for you All.

[@sahbabiiluvrx]

may god bless and have mercy upon anyone with this

[@nefimagana3283]

I have this and I've lived a more than gloriousll life... Trust me it only makes you stronger....... We stand because we were meant to stand out😊

[@monjier]

Need me some muscular dystrophy in my cheeks. Finna get that hollow cheek

[@familyislife36]

Fuck God, why would this even be a condition. Why would God put an innocent child through this!

[@zahidmiah5437]

Thank you I have Becker’s but at least It has not affected me so much yet

[@familyislife36]

@@jankjason omg you really are delusional

[@hawwaahmed772]

My dad had Becker's muscular dystrophy, he was the best person I ever knew. He died at 41.

[@sayblood8238]

Rest In Peace ❤️

[@Kiki-nm8uu]

Hello, my father has the same illness could I talk to you? Do you use instagram?

[@Kiki-nm8uu]

May allah grant him jannah ❤️

[@viraj9931]

I also BMD .most people dont care us😪😪😪

[@laleshahqeldiyeva9343]

​@@viraj9931Do you walk? How old are you?

[@shbh806]

i really love watching these videos. its educational and not boring at all.

[@napoh.5888]

This video has helped me a lot with my human growth and development class! Thanks a ton. ✨☺

[@osmosis]

Glad it helped, Janae! 💖

[@madisonswartz2571]

my little brother is leaning towards a diagnosis of muscular dystrophy and my whole family is terrified. we want him to live a happy healthy long life so i’m studying up and planning on becoming a doctor or scientist, and planning on studying for a cure.

[@voxtek]

Does anyone else in your family have it, as its passed on from the mother the son(s). And daughters become the carriers.

[@madisonswartz2571]

@@voxtek no, its either started at my mother or him himself. We’re pretty sure he has Duchenne but we believe it’s going to be a slow journey to a point where he even just needs a wheelchair, but as of now we’re taking it one step at a time.

[@juliadanielle6882]

@@madisonswartz2571 have been dealing with muscular dystrophy for the past 7 years until i got review online about Dr Isibor on KZbin about his healing abilities through herbs and body cleanser and I contacted him after 14 days of treatment I felt better and completely cured!

[@nursing7420]

@@juliadanielle6882 we need more people like you ❤️❤️❤️ thank you for sharing

[@dreamcatcher4820]

What was the symptoms.. can you pls mention?

[@dulminweerakkody7820]

Your channel is very helpful to study this diseases. Thank you

[@cliffordprasad8466]

became an instant fan of your videos

[@isaacjones748]

There's a special place in Heaven for people that make high quality, easily accessible educational resources

[@thethreesusketeers8038]

My little sister has a best friend who has DMD. He’s so sweet and it’s so horrible. His condition is getting worse, he’s repeatedly told her she needs to get ready to move on because he’s gonna die. She won’t accept it.

[@r.j.9822]

thats me with my family, they keep saying if i hold on theyll find a cure, ive been knowing it wasnt going to happen in my lifetime. i get so mad when they say " its ok we can try it again later"....i cant, i dont have that time. They are so focused on making sure i think im alive that i cant live a normal life...im 22 living with my parents and even when im working they have to check in to see how im doing because theres been times i was going to pass out and she had to pick me up while yelling at my boss, i feel bad but it was my fault for passing out but i still try to see the good things in life

[@ursheet2986]

@@r.j.9822 i wish you all the best🙏 may Allah help you live your life as you want it

[@ritikaarora6644]

Please help me with the cure, if there is any

[@squishymallow851]

@@r.j.9822I am sorry God bless you ,life is pain but it’s just a trial ,reward with God is better ,just do try to do good to please God so you have the best life in this world and afterlife ❤

[@WhatAmIBrewing]

@@ritikaarora6644there are ways to delay or slow it down but there is no cure and it’s very expensive

[@myriamschalk2649]

Would like to know if there are more cases like my father. He is 66yo and just found out that he has Becker dystrophy. He is healthy and doesn’t show any symptoms. He did the test because I was diagnosed carrier of the disease when I was pregnant. The geneticist ask automatically my mother to do the test but she is not a carrier that’s why they wanted to test my father as well. What a surprise for everybody when we found out.

[@juliadanielle6882]

have been dealing with muscular dystrophy for the past 7 years until i got review online about Dr Isibor on KZbin about his healing abilities through herbs and body cleanser and I contacted him after 14 days of treatment I felt better and completely cured!

[@BelieveInTheShi3ld]

Just for some more info, I'm an interesting case. Diagnosed at 5 (DMD), symptoms at this age, but did well past wheelchair stage, diagnosed changed to (severe BMD), nonsense mutation determined, now 26, still fully mobile, driving with no mods, but still progressing. Waiting for Translarna to be approved in Canada.

[@osmosis]

We're sorry to hear that BelieveInTheShi3ld. Good luck, and take care!

[@BelieveInTheShi3ld]

Just a question, the video states that if a mother is a carrier 50% chance her boys WILL have it or could? I am the youngest of 3 boys and was the only one affected. Could it have been possible if none of us had it? 2 of us had it? All 3 of us had it?

[@southwalesuk8765]

What’s translarna? My nephew has just been diagnosed with dmd he’s only 6.. 🥺

[@epicfox6825]

the pain of beckers is ungodly. It feels like something is eating you on the inside of the muscle and believe me when I say I would give this to my worst enemy.

[@miguellopezperez1687]

True..

[@kapilagrawal]

@Hey Boss 1987 my brother's 6 and he has identified with DMD ....can u pls tell what is your age and what condition do you suffer?😢

[@AyeshMedic]

Just the Perfect Cute Videos for my Medical Studies!!! It's my Third year and still tagging along with you. Thankss. Keep them coming. ☺️✨

[@osmosis]

Wow! Thanks for making us part of your medical education! ❤️

[@AyeshMedic]

@@osmosis I'm glad to be a part of Osmosis fam.

[@spynxz-_-8398]

Lost my little brother because of DMD.. back then there was'nt any cure for this.. i hope everyone that has it have a long life because now they finally have a way to cure this.

[@nursing7420]

I'm sorry for your loss, did he play any sports? I'm still trying to understand this.

[@spynxz-_-8398]

@@nursing7420 no, it just started to happen at around age 7 for my brother.. i noticed he would just fall down while walking for no reason.. as years go by it became more frequent as if he was loosing strenght in his legs everytime he falls down.. eventually he could'nt walk anymore and had to be bedridden until he died after one day he went to a coma and died the very next day at the age of 22.

[@nursing7420]

@@spynxz-_-8398 thank you for that. I’m a nursing student and want to do research yo one day find a cause and cute. Thank you again 🤍🙏

[@mauriciojones5043]

hi.the last I've heard is that there are no cure for it, can you kindly correct me.

[@mauriciojones5043]

@Spynxz

[@motogte]

The enlarged calf muscles with BMD are maybe one of the biggest hinderences as the quad muscle has to work even harder as there is definetly alot more more weight due to the fatty tissue if only there was a way of gaining lean muscle in the calf or even reducing the fatty tissue it may help quality of life. Personally ive tried quite a few supplements like aloe vera and creatine but little results now im trying testosterone booster few weeks in there could be some extra strength overall and with your core, i will report back if anything more dramatic. I know they have done testosterone therapy for DMD and there have been benefits but that is pure form of testosterone perscripted by a doctor unsure if it would help BMD also. Stay strong folks there has been breakthroughs so hopefully in the not to distance future we could have something. Im 32 btw with BMD and im doing fairly well still able to walk good distances and get up stairs slowly and at times disguise my condition altogether.

[@jaysimoes3705]

Some supplements that have encouriging data behind them: Liposomal Curcumin or CUrcumin with piperine. See: pubmed. Resveratrol 3 x day 500 mg, NAC ( N acetyl cystein) got very good results in mice but has side effects. Co Q10 (again would try the liposomal form). Green Tea estract (Epigallocatechin) seems to be promissing too, like epicatechin (some brands of dark chocolate have it in them). And while no tested for Duchenne nor beckers but in other muscular diseases: astaxanthin (again best in liposomal form) seems to be a good candidate. None of these will reduce whatever damage there has been caused already. But some, like resveratrol and epicatechin seem to have especially merit in people with BMD. Epicatechin because it acts on a substance that curbs down muscle formation. For Duchenne this is less interesting since that substance is already very low. But in most Becker patients it is pretty normal hence it getting cirbed down means (at lest intheory) muscle formation. Resveratrol showed very significant drops in CK levels in people with duchenne and becker nd that is the sign that muscle damage is significantly curbed down. A very encouriging one but also in its infancy when it comes to research is N Acetyl glucosamine. In DMD mice the muscles got 50% stronger (which I have never seen in any mouse model). If I were you and money permitting I would combine these after a good read of the literature that is available online. Most of these substances have been used by many people in large quantities without side effects so it seems to me they are worth a try. Good luck!

[@Thetoxicpeaceful1]

How are you now, how did everything work out

[@AdnanKhan-kg6ek]

can u please elaborate how ur symptoms started and progressed over the years in detail? I'm suffering from severe weakness and exhaustion and want to know about bmd. Please help.

[@mylifeinsweden575]

Thank you so much! i needed to repeat watching the video so i can understand the cellular and the genetic level. Thank you very very much.

[@komaldiptianandmaisuriya4301]

Love osmosis, for giving me all I need to know about topic in short time . ❤️

[@osmosis]

Happy to help, Komal! 🙏🏼

[@chloebreagan5193]

My friend has this and she’s in hospital her chest is really weak :(

[@taslucky1439]

such a nice short video that states all points without beating around the bush :) thank you so much this helped me understand it easily

[@salam7905]

thanks alooooot .. plz keep going you're doing a great job !!!

[@osmosis]

Thank you! 💕

[@Immolator772]

I just hope they find a cure soon or something to slow the process, i'm 26 now and i'm really scared, they say those with the disease die a slow and painful death and which is what i'm terrified by the most.

[@WhatAmIBrewing]

Me too. The thought of being so weak you can’t breath is terrifying

[@potatochipblueberry]

My younger brother has MD and I have no idea what it is. I had to look it up because I have never heard of it. I’m worried about him but I know he’s strong and he can get through it

[@osmosis]

Rooting for your brother as well! Hope our video was able to help. 🙏🏼

[@alexdiggs8566]

What a helpful video! thank you for helping me pass my exam :)

[@sadiahomyra9255]

excellent presentation...so far the best

[@asadaziz9]

I am so mesmerized by the website which I have purchased for my Step 1!! It's amazing. Got a question based on spaced repetition, should these videos be watched randomly or subject by subject? Do all 93 videos of Pathophysiology contain all of the organs on that page (especially Cardio)?

[@mar7956]

What!!!!! This is very useful, thank you I appreciate your effort💗💗💗

[@osmosis]

Glad it was helpful, Mar! ☀️

[@kiratpreetdhillon]

You may like to put this video under the Musculoskeletal Pathology playlist as well.

[@osmosis]

Thanks for the suggestion!

[@julieconmigo7443]

Your explanation is awesome!

[@osmosis]

Thanks, Julie! 😃

[@abuturab8778]

I am suffering from it but don't know which type of it I am 23 now and wheelchaired I am graduate now and want to live long and become a teacher of history

[@WhatAmIBrewing]

If you are wheelchaired you probably have DMD

[@abuturab8778]

@WhatAmIBrewing is there any treatment or medicine for it?

[@WhatAmIBrewing]

@ well there is creatine but that’s more of a supplement you take with exercise. But other than that there is no treatment that reverses it, but there is ways to slow it down

[@WhatAmIBrewing]

@ I really hope they come up with something. Unlikely though

[@abuturab8778]

@WhatAmIBrewing can u name it?

[@Leewoo77]

Eu sou brasileira, e meu inglês é básico do básico ahahahah,mas o vídeo estava muito bom que me forcei a ver ,e por incrível que pareça eu consegui entender as coisas escritas ,thank you 🙏

[@osmosis]

You're welcome! ❤️

[@DrSanjayNatarajan]

Gowers sign animated drawing was exceptional!! Osmosis is amazing.

[@osmosis]

Thank you so much, Sanjay! Did you know that if you like & review us on Facebook then you’ll get access to our videos a day before they’re published on KZbin? Check it out here: bit.ly/2u35D6J

[@n1n0azul1]

I just loved this explanation. Thanks a lot.

[@saalehamoorad2542]

Please make one for Osteogenesis imperfecta :)

[@epicfox6825]

I think I got the speratic mutation for beckers becuase none of my late family has it. But at the same time my brother has it and it affects him differently than me. While I have the worst of it my brother has less of an effect. Apparently its rare, like 1% rare to have two brothers with different mutations of the same genetic disease.

[@Deraspot]

I'm 23 with Beckers MD I'm just struggling to find my way through life and survive, it's really not easy

[@pennydeavin8448]

Great video and very clearly explained. I wonder about the inheritance description though. If mum is a carrier you say, "50% will end up having the mutation". Not necessarily so. Instead, there is a 50% chance of inheritance with each new pregnancy.

[@Stacie0725]

I was gonna comment the same thing. 50% chance of inheriting not 50% inheritance rate. Subtle but important difference

[@basmawahab879]

That was excellent! Thank you for your efforts

[@gothafloxacin]

I have a severe muscle disease that affects both my peripheral and visceral muscles. I'm going to see a neuromuscular specialist to figure out whether or not I have myopathy or adult onset muscular dystrophy (although I've had symptoms and issues with my muscles my entire life) Edit: I'm 23

[@sunilgajjarrajkot8911]

Any treatment available for DMD ?

[@NOIZEECONCEPTZ]

I got diagnosed yesterday...

Im so sorry. Hiw are you doing now?

[@felixhenrico]

You guys are just so perfect! thank you for teaching us in this very nice way! Greetings from Argentina! =)

[@osmosis]

Our pleasure! 🥰❤️🙏🏼

[@ahmedtarek3782]

thank u a lot for explaining the disease ... i love your channel. god bless u🤗😆

[@SENTINELV2-f7g]

DMD here genetic mutation 13 years old pretty healthy and I understand all of you 😊

[@fry6344]

Excellent explanation!

[@teenachoudhary1571]

Can u plz make a video on Erb's muscular dystropy...???

[@dr.vikramchoudhary3270]

Keep creating more such videos love your channel

[@osmosis]

Thanks, Dr. Vikram!

[@abradford222]

You're explanations are terrific.

[@hassansharifmohamed7935]

We are three brothers having muscular dystrophy, I'm the oldest and I'm 25years old. We live in Somalia 🇸🇴. Our mother has daughters who are healthy and our father has other healthy children (sons & daughters) from other wives. The symptoms appeared from everyone of us in his childhood. we have been walking on toes since our childhood and our arms have been gradually thickening, now we cannot fully straighten our arms. In the Beginning of 2016 i went to a doctor. He performed a surgery on my foot to make it put on the ground completely but failed. Now i eat food with spoon since my right arm doesn't fully straighten and i always pick up things from the ground with my left arm. We need consult, are there any ways that we can make our arms straight?

[@luchi4361]

Hope you are still persevering. Prayers to you and your family.

[@Oneaboveall653]

Come to india....u may get some help here

[@amikhakha1354]

@@Oneaboveall653 excuse me, but what kind of treatment in India, if there is any treatment in India for Duchenne muscular dystrophy?? ((

[@hassansharifmohamed7935]

​@@luchi4361yes Alhamdulillah ❤

[@cxunchuah405]

Very detailed explanation, thank you so much!

[@osmosis]

You're welcome! 💕

[@augustmiller6339]

Amazing video, keep it up!

[@aleenaantony9815]

Very nicely explained

[@solunox1150]

thanks man. I had a hard time figuring out the overall importance of dystrophin, before this video.

[@mimimez9591]

thank you guys!!! really this is amazing great job !

[@shihankhan3973]

superb explanation... thanx..

[@brendenvarty3266]

Very informative video! 🎉

[@osmosis]

Thanks, Brenden! 😊

[@h.q.1736]

Fantastic demonstration 👍🏻

[@osmosis]

Thanks, Helen!

[@MohamedHussein-lb5kr]

PERFECT EXPLANATION-REALLY THX

[@osmosis]

You're welcome, Mohamed! 🥰

[@Darkoxbrain3696]

Very informative, thank you.

[@mafuyu79]

THANK YOU OSMOSIS VERY HELPFUL 💗👏

[@mehrmaa6066]

Awesome work!! that complex disease is soo simple now! :-)

[@amerhallak5968]

excellent video well done 👍🏼👍🏼👍🏼

[@tunerd1921]

If anyone wanted to know what it is called when more of one X chromosome than the other is expressed by X-inactivation it is called skewed X inactivation

[@uzmakhan9264]

Thanks for helping at end moments.... m abt 2 write exms .... thanks for awesome explanation...😊

[@ansen6754]

I'm Jericho, 16 years old, And i have Duchenne Muscular, When i was a child i still able to walk but i often stumble and run slowly then when i become 13 years old i started to feel that my walk is disfigured and as i grow bigger and bigger, my muscle get weaker and weaker.

[@NnnHyyu]

I hope you get better and may God help you

[@r.j.9822]

i have beckers, i cant run anymore at 21 if u see this plz respond and let me know where u are at in this experience, ive never met someone with the same condition

[@M_0M]

​@@r.j.9822I also have Becker's. I was diagnosed when I was eighteen, and now a year and a half has passed and I cannot run or jump, only walk, and now I feel like I walk in a strange way, my backbone is curved, and there is swelling in my legs.

[@M_0M]

​@@r.j.9822The doctor says that maybe I will be sitting in a wheelchair in two years. The situation is very difficult. Can you tell me when you were diagnosed and how you are now?

[@r.j.9822]

@@M_0M diagnosed finally in middle school when I finally had it and hit a student because the teacher said I was just complaining and he said I was faking. I had this pain since 5th grade, I’d finish p.e. Physically shaking everywhere and not being able to talk because I’d feel zaps of pain going through my body. They initially said the only thing that MIGHT work was breaking my legs and letting them reset🤦‍♂️this is how little information we had. My parents clearly said no but I would come home crying that I didn’t care just do it. I’m glad they ended up not doing it, but now It’s 7 years later and I have to use a cane to get around, a wheelchair if I want to go to any place you have to walk a lot(like an amusement park), I legit can’t run without fallin after a few feet. The hardest part is the stairs, I have to pull my self up the steps with my hands, and use my hand strength to take most of the impact going down stairs. You won’t need a wheelchair if you do exercises and stretch regularly, (and I by exercises I don’t mean the normal running and lifting) you just have to make sure your muscles are always metaphorically lubed up . In the meantime try to enjoy some physical activities even if you can’t play them long, trust me.

[@tusharmane1262]

Sir, Can you tell about genetic inheritance/transfer of father affected with Beckers Muscular Dystrophy? Does it also equally affects as carrier mother?

[@مسلسلواديب]

I have been suffering from this disease since I was 15 years old and I am currently 27 years old. Is there a treatment? Please reply

[@dangooooo769]

Very helpful thank you!

[@Zahraa-vw7zj]

Osmosis always amazing 👏👏👏👏❤️

[@osmosis]

Thank you! 💕

[@xanderbraviant820]

What your solution to solve this

[@holyquran3285]

I am sick with muscular dystrophy and I want you to help me, thank you

[@osmosis]

We care for you, Ahmed. But unfortunately we don’t provide medical advice through this channel. We’d recommend reaching out to a local health professional for any consultation and diagnosis of your condition.

[@holyquran3285]

Thank you, brother, for this wonderful comment

[@holyquran3285]

Is there a cure for it?

[@zakkuto]

@@holyquran3285 no

[@DwuTom]

How to create the presentation like this one?

[@osmosis]

We have a video on how we make our videos. Check it out! kzbin.info/www/bejne/qHKvgHatr9tnsLM

[@DwuTom]

THANKS!

[@seansimonde9931]

i'm kindly asking for the pathophysiology

[@rehababdelbagi]

thank u soo much , that was an epic explanation

[@osmosis]

Glad you liked it! 😊

[@raeeszohaib8731]

I am suffered from muscle distrophy miyopathy please help me with suggestions

[@MN-iu9pd]

Your videos are amazing. Congratulations to the team :)

[@flamegamingx4717]

hopefully I can live my life very greatly before I become too old, and ride all of the roller coasters that I can because that is my favorite activity....

[@juliadanielle6882]

have been dealing with muscular dystrophy for the past 7 years until i got review online about Dr Isibor on KZbin about his healing abilities through herbs and body cleanser and I contacted him after 14 days of treatment I felt better and completely cured!

[@kellyaviguetero5876]

Can hemopexin measurement aids in diagnosis of muscular dystropies

[@seiyuokamihimura5082]

Would gene editing therapy have any effect on this hellish disease? I know one person who i went to school with whom had it, died halfway through the year. I never forget his face, even though he was a jerk i understand now that he must have been going through a tremendous torture.

[@zannatul23]

love every video!

[@مسلسلواديب]

I have been suffering from this disease since I was 15 years old and I am currently 27 years old. Is there a treatment? Please reply

[@cellhealing6756]

We have

[@Von715]

I had this at age of 7 to 11 occur periodically and since then never again! 25 now

[@nursing7420]

What did you do to reverse it?? Thank you for any feedback. Blessings

[@r.j.9822]

theres no cure XD bruh if you are going to lie, might wanna get the facts first