The parents of a seriously ill boy say that Government plans to fast-track new drugs are offering them some badly needed hope for the future.
Jack Johnson, from Orrell near Wigan, has the incurable muscle wasting disease Duchenne Muscular Dystrophy.
Today, the Government said they would allow new medicines to be tried out on patients years earlier than normal.
the prosensa families are also sending videos to the fda
& their kids were doing great
pray the wet noodle doesn't blow this like everything else he touches
her dislike for the parents we treasure has no bounds
her ego is so inflated.
all things must be approved by this one
i like to think of her as the BELL of BALL