P L E A S E  S U P P O R T  U S  T O O

NOW is the time to act to give the people affected by LAMA2 a future worth living.

The mission we want to convey with the name of this association is that we must ACT NOW.

The future of Emily and all other children and adults with Merosin-LAMA2 muscular dystrophy must be secured as soon as possible.

If it takes 5 or 10 years to begin to understand this disease in depth, it will already be too late for Emily and children like her to ever walk; as the contractures in her legs, arms, wrists, ankles and the inevitable scoliosis in her spine will be too severe to treat and future walking will never be possible.

For these reasons, we emphasise once again the importance of timing treatment.

NOW is the time to act.

We want to give everyone with LAMA2 a future.

We want to make their dream of recovery a reality.

LET’S MAKE IT HAPPEN.

Now is the time to act – the future is now

P L E A S E  D O N A T E  N O W

CH93 8080 8003 7819 8177 3

Emily‘s future is now

c/o Contrada Maggiore 12

CH-6616 Losone

emilysfuture@bluewin.ch