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muskeldystrofi

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English info
19.7 YEARS IS TOO SHORT A LIFE

Duchenne muscular dystrophy is a genetic muscle disorder that causes the loss of muscle function in all muscles throughout the body.  Most children are diagnosed in early childhood after living relatively normal lives the first 4-7 years.  The progressive disease confine these children to a wheelchair from age 8-12 years, and in their mid-teens most children depend on respiration assistance to live.  Without treatment the young men will die in their late teens or early 20s.

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SUPPORT AND DONATE

Time for Life is a true non-profit organization using 100% of the collected funds in the fight for finding efficient medication and a cure for the children and young men with the terrible disease Duchenne.  We highly appreciate the help to the boys.
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BOARD OF TIME FOR LIFE

Time for Life is a true non-profit organization to accelerate the research for finding efficient medication and a cure for Duchenne.  There are none in the organization who receives salaries or compensations for the work for Time for Life.  Decisions about which research programs to direct funds to are taken by the Board with input from the Advisory Board and other cooperating parent organizations world-wide.
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