B2 Genetic Factors

Duchenne Muscular Dystrophy is a inherited genetic conditions that gradually cause the muscles to weaken. Different symptoms of DMD include: frequent falls, trouble running and jumping, walking on toes, large calf muscles, muscle pain and stiffness,
delayed growth. Treatments: mobility and breathing assistance (swimming, physiotherapy, occupational therapy), steroid medicine (strengthen muscles). Support: The DFSG is a national charity run for families affected by Duchenne muscular dystrophy. It provides support for parents and people suffering with the condition. Throughout life DMD gets worse for a child and they will need an increase in support when reaching adolescence and adulthood as it would be harder to move/walk themselves. The life expectancy for someone with Duchenne Muscular Dystrophy is 27 years
PIES
P - muscle weakening, unable to stand/walk
I - weakness in cognitive skills
E - depression, hypochondriac fears
S - inability to walk leads to inability to go out and socialise with friends