Im from Srilanka .My son also suffering from DMD.now he's 8years old.still he is working slowly .please please help me if there is any possibility .thank tou .

"Promo SM"

Your explanation is too fast for non native speaker

Schade daß alles nur in englisch ist😢

Can't see what you're doing... no contrast

Thanks for this video. I'm so glad I can do most of these exercises now after fracturing my ankle 5 months ago.

Hi I'm edrian from Philippines my brother suffere DMD since 7yr.old please help my brother

Successful Hope

I’m celiac disease but my husband buys gluten bread and cereal

❤😂😢😅so many emotional things going on in the Golden Hour. ❤

What is the difference between a vertical and horizontal mattress suture?

It's easy to forget that every single day babies, parents, and families experience the highest care possible while we go about living our ordinary lives. Thank you for all that you do!

A baby's life is a god gift from heaven be glad that you make your children

Please help my son is suffering ducchne muscular dystrophy since 8 years please help 😭😭 I am from India

I am from China. My son is DMD patient. He is 5 years old. Is it possible to cure? And how much would be the cost?❤

I'm from India am DMD patient I'm 21years old help me to cure 😢

Amazingly Educational video on a topic that is severely missing modern content.

My son is ten year old with DMD I am from Mauritius .He stop walking since last year please help if there is any treatment let me know.

my son is 9 years old he is DMD patient (7 exon is deletion) in genetic report im in pakistan please help me 😢

Yes great and all. I want to see results, of course I can find some results but I would like to see much more results and since what I have seen (have been shown?) are results within months we should be able to see these in more kids. Not just a few.

I wish older children could get it I would give anything to stop my sons rate of progression I hate this disease so much

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Æ😢😢😢😢😢😢😢😞😞😞😞😞😞😞😞😭😭😭😭

Thank you. Really nice to the point explanation

Hi. I have two years old daughter She is Juene Syndrome Patient She is dependent on oxygen concentrator She is in very very trouble But we have no source of income for her treatment and Pakistan Doctors told us that her treatment is not possible in Pakistan. Pls do something for us

Iam from Guyana my grandson is 10 years old he have dmd he is not walking we need help for him

My son 2years 11month old affect in DMD (14 exon is deletion or duplication) in gentic report. Please help me what is suitable treatment for my baby ( i am in India) please..... share me

Wow good news

Suggest any physical exercises which helps to overcome the low cardiac output and high pressure after fonton surgery

Waw am very encouraged and happy to hear about this new therapy for sickle cell disease. I believe it will reach us soon.

So u guys reading people's brain waves remotely

Hows this going?

Does it matter which you start with?

Great hope. Well done breakthrough makers

DEAR CASH & EVERYONE AT CHILDREN'S HOSPITAL OF PHILADELPHIA, GOD BLESS YOU MY FRIENDS. I AM VERY PROUD OF YOU AND VERY HAPPY FOR YOU. I HOPE ALL OF YOUR DREAMS COME TRUE. 🙏 I LOVE YOU SO VERY MUCH. 🙏 GOD BLESS YOU SO VERY MUCH CASH. 🙏 I LOVE CHILDREN'S HOSPITAL OF PHILADELPHIA SO VERY MUCH. 🙏 SINCERELY PETER

DEAR DR. COHEN, DR. MINTURN, DR. PERMAN, DR. PIPAN & EVERYONE AT THE CHILDREN'S HOSPITAL OF PHILADELPHIA, GOD BLESS YOU MY FRIENDS. I AM VERY PROUD OF YOU AND VERY HAPPY FOR YOU. I HOPE ALL OF YOUR DREAMS COME TRUE. 🙏 I LOVE YOU SO VERY MUCH. 🙏 CONGRATULATIONS DR. MINTURN. WOW! WOW! WOW! IT IS ABSOLUTELY BEAUTIFUL AND ABSOLUTELY INCREDIBLE. 🙏 I LOVE THE CHILDREN'S HOSPITAL OF PHILADELPHIA SO VERY MUCH. 🙏 SINCERELY PETER

Great presentation

Two years later ...... nothing has changed

Hydrocephalus Epilepsy Occipital Neuralgia Chronic migraines General Dystonia .... yes

हाईटेक सर हिंदी बोल कर बताओ

Scary that an exposure to Cipro can lead to an onset of Mitochondrial DNA depletion.

Everyone's doing studies based on diet, but is anyone doing studies on what mother's AREN'T eating? Doctors already say that diets rich in omega-3 foods from animal and plant sources can prevent children with food allergies. Has anyone compared the diets of the mothers with kids with allergies to see what they have in common? Could it be possible that this is being caused by veganism? I ask this because I'm black, grew up in black-only areas. We don't HAVE this food allergy stuff, as far as I know, and if we DO it's extremely rare. Quite possibly because black women for the most part don't engage in fad dieting, unlike their caucasian counterparts. You eat what's available. We generally don't engage in some fantasy of saving the world by eating like a prey animal. EVERY kid I ever met that had a food allergy was caucasian. I only went to school with them so I have no idea about their home life, but I'm betting there's more of a commonality with their mothers than just race. If your kids aren't exposed to certain proteins in the womb, studies show they will have an allergy to them after birth. Vegans exclude a LOT of healthy proteins from their diets. Have any doctors or dieticians examined this potential?

What can be done prenatal to support or in efforts to prevent this?

DEAR EVERYONE AT THE CHILDREN'S HOSPITAL OF PHILADELPHIA, GOD BLESS YOU MY FRIENDS. I AM VERY PROUD OF YOU AND VERY HAPPY FOR YOU. I HOPE ALL OF YOUR DREAMS COME TRUE. 🙏 I LOVE YOU SO VERY MUCH. 🙏 I LOVE THE CHILDREN'S HOSPITAL OF PHILADELPHIA SO VERY MUCH. 🙏 SINCERELY PETER

all fishermen know how to tie a square knot...lmfao!!!!!!!!!!

👏🏿

Shit video

The suture thread is very hard to see against the background color.