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New Documentary Follows Family After Sons' Muscular Dystrophy Diagnosis

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What happened: A rare form of muscular dystrophy is chronicled in a new documentary where director and father Nick Taussig navigates the family’s life after his two sons are diagnosed with the condition. The boys, Theo and Oskar, have Duchenne muscular dystrophy. The film, “A Space in Time,” follows the boys as their condition progresses and reduces their mobility. The documentary includes perspective from the parents as well as a first-person account from the boys on adjusting to life with a disability.

Disability is often poorly portrayed or misrepresented, its depiction seeking to elicit sympathy, a sense of tragedy, or worse still, pity, which helps neither someone living with disability nor someone living without it. Why are the able-bodied so often unable to see beyond the disability … and witness instead an individual who leads a rich and varied life, their disability just one aspect of them? — Nick Taussig

The Frontlines: Duchenne muscular dystrophy is a genetic condition that causes muscles to atrophy over time. It’s a progressive disease and eventually leads to death. Symptoms usually present for the first time between ages 1 and 6 and symptoms typically include muscle weakness and missed developmental milestones.

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A Mighty Voice: Our contributor Michael Schiavo, who has Duchenne muscular dystrophy, shared what having a progressive disease has taught him about grief. “In time, I learned how to grieve and let go. The most important thing I learned about grieving is that you have to go through it. There is no way around it and no shortcuts to take. You must feel the pain and sorrow and express it in the company of those who love you. In the face of loss, no one can move on in an instant.” You can submit your first-person story, too.

From Our Community:

Duchenne Muscular Dystrophy and Mental Health

Other things to know: Duchenne muscular dystrophy occurs in about 1 in 3,500 male births. But the impacts of the disease are felt not only by those who go through it, but the families who love those with the diagnosis. Here is what Mighty contributors are saying about the condition:

How to take action: You can learn more about the documentary set to release in 2021 here and learn more about the condition and awareness efforts by visiting 

Header image via Twitter

Originally published: October 8, 2020
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