My little sister had DMD. She was part of the 1% of girls with this disease, caused by a genetic mutation. I am not a carrier. She passed away 1 year ago today from cardiac arrest caused by Duchenne muscular dystrophy. I miss her so much.
There have been many cancer cures and cures to many different illness, but they all have been systematically suppressed by the cancer establishment, because they can't make much money off them.
Nutrition can cure cancer and loads of other illnesses like Muscular Dystrophy.
Look up some cancer cure documentaries for more info on this stuff. A nice one is "The Beautiful Truth".
Wow, what a touching video, we too are trying our hardest to help rare disease researchers find cures for DMD and many other rare diseases. In conjunction with the Children's Rare Disease Network we are giving away a $50,000 rare disease research system to the winner of a video contest and the organization of their choice. You should enter your video. For more info, visit RemedyMD's website and click on the "About" section then look under "Press Releases".
My little sister had DMD. She was part of the 1% of girls with this disease, caused by a genetic mutation. I am not a carrier. She passed away 1 year ago today from cardiac arrest caused by Duchenne muscular dystrophy. I miss her so much.
xxxgirlswithguns 2 weeks ago
There have been many cancer cures and cures to many different illness, but they all have been systematically suppressed by the cancer establishment, because they can't make much money off them.
Nutrition can cure cancer and loads of other illnesses like Muscular Dystrophy.
Look up some cancer cure documentaries for more info on this stuff. A nice one is "The Beautiful Truth".
watch?v=wvzDHGLEUyw
God Bless, Jesus is Lord!
retr0llz 6 months ago
@jubinjibin yes
Rasverix82 8 months ago
@Rasverix82 BUT ITS VERY RARE FOR GIRLS RIGHT
jubinjibin 8 months ago
@jubinjibin it does if a girl inherits 2 copies of the diseased chromosome but this is rare only 1% are female
Rasverix82 8 months ago
Wow, what a touching video, we too are trying our hardest to help rare disease researchers find cures for DMD and many other rare diseases. In conjunction with the Children's Rare Disease Network we are giving away a $50,000 rare disease research system to the winner of a video contest and the organization of their choice. You should enter your video. For more info, visit RemedyMD's website and click on the "About" section then look under "Press Releases".
RemedyMD 11 months ago
My sons best friend since they were 7 has this. He never walked. To see what he goes thru kills me. God bless us all.
jerzeytpke 1 year ago