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Watsu for Health, z.s.


People with disabilities Health

Watsu® Day for Muscular Dystrophy 6.9.2020

Duchenne muscular dystrophy is one of the most serious neuromuscular diseases. Patients lose strength and are already in a wheelchair around the age of ten. The Watsu® water rehabilitation method is very beneficial for these patients for many reasons.

we started on 2020-08-07

Watsu® Day for Muscular Dystrophy 6.9.2020

As part of World Duchenne Muscular Dystrophy Day, which falls on September 7 every year, we are preparing a Watsu® workshop for patients with muscular dystrophy and other neuromuscular diseases. The event is intended for this patients and caring family members. The benefit is a deep physical and mental regeneration. You can support us with any amount to our transparent account: 1122339939/5500 or simply by online paying method below:
€185
raised 22 % out of  €823

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11 people
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Participants can spend this day in a playful and relaxing way in the water and get acquainted with the Watsu®  rehabilitation method and experience it on their own body. The event is intended for caregivers and patients with dystrophies, atrophies and other NSOs.

The caring parent and child (or adult patient) will have the opportunity to experience 30 minutes of effective and deep relaxation, muscle stretching and gentle mobilization in warm water. The work takes place individually and each participant will be in the care of a professionally trained therapist from the Watsu for Health team.

During the group workshop, participants will be introduced to the basic theory of Watsu®  and practical training, in which parents will work with their own child under the guidance of a certified lecturer and professionally trained practitioners / therapists from the Watsu for Health team. They will learn the basic methodical movements of Watsu®  and a gentle relaxing massage. The workshop will be a playful way and parents will have space for questions.

Watsu®  is an amazing form of relaxation and rehabilitation for these patients.

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One in 5,000 newborn boys in the world has a rare and fatal disease: Duchenne Muscular Dystrophy (DMD).
It looks like a small group, but 250,000 patients worldwide go on and have big dreams of diagnosis despite it.
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