Parents of a baby boy with a rare muscle-wasting disease are desperately fighting to raise money for a miracle drug to keep their son alive.
Ted Chadwick, now eight months old, had trouble sleeping and feeding shortly after he was born.
Then, when he was just six weeks old, his parents learnt these were symptoms of condition called spinal muscular atrophy type one (SMA1).
This is the most severe form of a neuromuscular condition which sees the spinal cord motor