ALAN - Maladies Rares Luxembourg
What is ALAN - Maladies Rares Luxembourg?
Founded in 1998, “ALAN - Maladies Rares Luxembourg” is a non-profit association aiming to support people concerned by neuromuscular diseases and their families. In 2005, ALAN - Maladies Rares Luxembourg began to help people with rare diseases. The main aim of ALAN is to enhance the quality of life of their members.
Offer in the way of physical activity
ALAN - Maladies Rares Luxembourg has offered weekly aquatic physical activities (group called Zesummen an d’Schwemm) and soft gym which are adapted to the fitness of the participants. The sessions aim to decrease muscle stiffness and to improve balance, fitness and well-being by using adapted exercises.
Types of exercises offered
A session of aquaerobics is proposed for adults. The intensity of the exercises and the conditions of their completion are adapted to each person’s capacity. The aquaerobics is supervised by a physiotherapist and/or certified athletic trainer. At the same time as the aquaerobics for adults, two physiotherapists work with children to decrease their joint and muscle stiffness and to relax them. For these sessions, the presence of at least one parent is mandatory. A lifeguard is present to ensure the security in the pool. Before and after the session, ALAN volunteers will help participants to undress and to dress in the changing-room. The volunteers may also help in the swimming-pool.
Who can participate?
Anyone afflicted with a rare disease can take part in this group.
What are the costs?
The yearly membership card costs 20 € per person or 30 € per family. Course registration fees are € 15 per quarter.
Where and when are the sessions held?
9.30am to 10.30am
5pm - 7pm