Beating the Odds of Muscular Dystrophy: Julia's Story
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- Опубликовано: 10 ноя 2016
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Meet Julia, an energetic, fun-loving girl who is thriving despite her muscular dystrophy. She goes to therapy regularly at Nationwide Children's, which keeps her strong and mobile. With your support, we will continue making great strides in our muscular dystrophy research and treatment. Someday, kids like Julia won't need a wheelchair.
" i was born ready" oh my goodness amazing and so deep when you think about it<3
She's gorgeous 💗
she is so cute! full of life
She is adorable !
This video really caught my eye and made me feel some type of way..
May God bless all sick children in the world! Ameen!
Plz help my son has muscle dystrophy 🙏🙏🙏
I pray she is doing well today...
My five years and 8 months daughter and 3 years and 5 months son.... Both are recently diagnosed with muscular dystrophy.... My son actually starting walking at the age 2.8 years he has delayed milestones.... Can someone guide me about the symptoms and for what extreme should I be prepared for...
My son has muscle dystrophy plz help my son 🙏🙏🙏🙏🙏
Did anybody found out why this happened? Why a girl as a carrier is getting acutely sick with all DMD symptoms?
Oh angels may 😇
My gf has dmd she can't able to walk properly please anyone tell she can be ok any treatment available for that 😢 please i love my girl so much
I have congenital muscular dystrophy
I don't know if I'm suffering from muscular dystrophy or myositis
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.
I have muscular dystrophy
She is pretty baby . Actuly🙂 and she will fine sone😎
its a selenium deficiency i take my selenium every day!! but you do what you want!
Fake world with false hope, damn