CANADIAN FAMILIES ARE FIGHTING
FOR THEIR CHILDREN’S LIFE

Our web documentary series
“Portrait of Duchenne”
is presenting their story.

Watch the Vlog

CYCLING ACROSS CANADA
TO CURE DMD

In July 2018, Bruce will take
on the challenge is goal raise
awareness and funds
for research about DMD

Watch the Vlog

Duchenne muscular dystrophy (DMD)

Children with DMD will experience a loss of muscle strength
and face premature death in their early twenties.

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Towards a cure with La Force

Strength in unity

There is hope. Promising new treatments are
in development and actually in clinical trials.

La Force informs you about new treatments

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Strength in unity

We unite the DMD community to raise awareness about
the disease and speed access to new treatments.

Take action with La Force

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RESEARCH NEWS

Each year at La Force Foundation, we select the most promising research for Duchenne muscular dystrophy (DMD) to support.

We live in an era of ultrafast change, where science and technology are working together more than ever. This is especially true for DMD.

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TREATMENT

Few treatments for Duchenne muscular dystrophy (DMD) are available. They may help to slow muscle weakening and loss of motor function, but there is no cure.

Yet, hope is on the horizon. International health authorities are currently evaluating two new therapies and many other therapies are now in development.

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DMD QUICK GUIDE

Duchenne muscular dystrophy (DMD) is a rare disease, for which there is no cure. To ensure that a young patient receives treatment to relieve symptoms and delay the progression of DMD, it’s important to have the right diagnosis and obtain a genetic profile.

The following information will direct you to clinical trials that may help your child and describe new experimental treatments.

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TAKE ACTION!

If you have Duchenne muscular dystrophy (DMD) or you’re a parent, family member or friend of someone who has DMD, can you do anything to help speed the approval process for new treatments?

The answer is yes, and you can start right here.

Vlog La Force

PORTRAIT OF DUCHENNE

Our new web documentary series has one objective: spreading the words about the brave families who take matter’s in their hand. We meet five families who became their own hero. We want to raise awareness about their story so we can closer to a cure for DMD.

SHARING THE STORIES IS BECOMING PART OF THE ANSWER.

VISIT OUR VLOG, HERE.

DMD Highlights

Browse through the topics below to get
a quick overview of the disease and its effects…

What is Duchenne Muscular Dystrophy?

Duchenne muscular dystrophy (DMD) is a rare genetic disease affecting 1 boy in 3600 and 1 girl in 50 million. It occurs in all ethnic groups and nationalities. DMD is a type of muscular dystrophy that causes a weakening of the muscles due to the absence of dystrophin.

What are the early symptoms?

Persons afflicted with the disease seem generally healthy at birth, but experience difficulties in achieving the important milestones of normal development. They have trouble running, jumping and climbing stairs in comparison to healthy children, and they fall frequently.

The evolution of DMD between 8 and 12 years of age

The ability to walk is usually lost between the ages of 8 and 12; in rare cases, it happens that some children with DMD never get to walk or are able to walk much longer. The disease evolves in different ways depending on individuals; this is only an average.

The evolution of DMD between 10 and 16 years of age

In general, there is a marked drop in the strength and mobility of the arms between the ages of 10 and 16 years. It is at this time that they lose the ability to feed themselves and hug family members.

The evolution of DMD after age 16

By the end of adolescence, it is usually necessary to rely on a breathing assistance apparatus. It is unusual for people with Duchenne live beyond their thirtieth year.

Treatment options

There are currently very few treatment options and no cure. Duchenne muscular dystrophy is 100% FATAL.

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