India need you sir 🌸🙏🌸

Thanks alot , this video is very helpful

Sir price pls

Sir price please.....

Titment

Тутера у вас какой фирмы???

Iam DMD . May I do cycle ? . I cannot walk.. pls tell me

Ami Bangladesh

Bangla hola volo hoto

I need help I am muscular dystrophy patient my name harikrish

Hi

Good video. The sound is too loud though. Sounds like you are shouting even after I turned the volume down.

Excelente! Precisamos de mais videos como esse. Sou Brasileiro resisdente no Brasil, com filho de 5 anos na DMD. Obrigado Great! We need more videos like this. I am Brazilian resident in Brazil, with 5 year old son in DMD. Thanks

Пожалуйста переведите на русском языке пожалуйста

how do we get our right to try??

Our government needs to hurry the hell up with this crispr cas9. We're losing beautiful young men to this wicked condition. The human race is better than this.

Sir where is the best treatment available for DMD patients in Karnataka or in India.

is it also useable for other muscular dystrophy forms?

Thanks. Seeing more helpful options takes some of the anxiety out.

Help me

 My name is henry donato I have muscular dystrophy I inherited from my mother of 4 children she had only me that I am the oldest of them inherit the disease, she died because of the disease they began to fail their organ died at 42 years of age 11/19/07 and three of his brothers also died in the same way

futurenet.club/fanpage/Myopathie/invite هدا رابط صفحتي علي موقع التواصل الاجتماعي فوترنت.المرجو دعمها ولكم مني كل الشكر والتقدير اخواني

futurenet.club/fanpage/Myopathie/invite هدا رابط صفحتي علي موقع التواصل الاجتماعي فوترنت.المرجو دعمها ولكم مني كل الشكر والتقدير اخواني

I m suffering lgmd muscular dystrophy..I am 25 years old and The disease has become 10 years old. please help me..🙏🙏🙏🙏

Is it possible to change skin color genetically?

Time is muscle. We need a treatment already hurry up.

For foot support, we added a couple of foam yoga blocks, attached by heavy-duty velcro strips.

😍

With all the respect for all researchers, you're moving very slow and many of us will die before having any chance to use this brilliant results!

😀

This infotmation though excellent is all about children. What about adults with any tupe of Muscular Dystrophy. Have you any advise for us. Thanks

So not excessive calcium.

So water and fibre

Fruit and vegs are key

Thanks for the advice about potatoes.

No fried foods for me!

I do not ever add salt or sugar

Oranges are good though or some type of fruit!

Vitamin D is very important. I hate my breakfast though except for a yogurt and lots of water.

Good advice, except I am an adult with a mild form of Becker Limb Carrier Muscular Dystrophy and thankfully NOT on steroids.

He appears very fit to me!

Does this model patient in this video have Muscular Dystrophy?

I have Beckers Muscular Limb Girdle Carrier Dystrophy only diagnosed finally in 2010 when I was 42 and am female.

Wow incredible I will be your first test subject.

Excellent video! Very powerful!

thank you soo much for all this videos. they really help.

When are they gonna start using it to cure H.I.V

Which oil using

Hello My name is Emi. I'm 21 years old. I live in Albania. I suffer from duchenne muscular dystrophy. Recently, I have a lot of difficulty walking. Please help me with any information.

Powerfull technique indeed!