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                <p>La totalité du bénéfice récolté par le Téléthon reste en Suisse, pour soutenir les familles touchées par une maladie génétique rare et la recherche.</p>
<p>Grâce à l’action de tous les bénévoles et au soutien de nos partenaires, les frais de fonctionnement de la Fondation Téléthon Action Suisse sont réduits au strict minimum.</p>
<p>Le Téléthon 2026 aura lieu les 4 et 5 décembre prochains. Et si vous faisiez partie de l&rsquo;aventure ?</p>
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                <p>À 17 ans, Jeremy avance avec énergie. Passionné de sport depuis toujours, il a trouvé dans le Powerchair Hockey bien plus qu&rsquo;un simple loisir : un moyen de se dépasser en équipe. Aujourd&rsquo;hui, il rêve d&rsquo;intégrer l&rsquo;équipe suisse et s’entraîne avec le Rolling Thunder Bern pour atteindre cet objectif.</p>
<p>Jeremy vient de débuter une formation de commerce en sport-études à Berne, pour préparer son avenir tout en restant au plus près des athlètes de haut niveau.</p>
<p>Grâce aux témoignages de Jeremy et de sa maman Maryline en tant que famille ambassadrice 2026, nous pourrons aborder de nombreux thèmes : le handisport bien sûr, les défis et la motivation nécessaires pour construire son projet de formation professionnelle, mais aussi un retour sur sa scolarité obligatoire dans une structure accompagnant des personnes en situation de handicap physique.</p>
<p><strong>Nous nous réjouissons de partager cette édition du Téléthon avec Maryline et Jeremy ! </strong><strong>💛</strong></p>
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                <p>Le Téléthon soutient une recherche innovante au travers des bourses octroyées par la <a href="https://www.fsrmm.ch/fr/" target="_blank" rel="noopener">Fondation de Recherche sur les Maladies Musculaires (FSRMM)</a>.</p>
<p>Accédez à des ressources utiles : pour s’informer sur les maladies neuromusculaire, <a href="https://www.afm-telethon.fr/fr/vivre-avec-la-maladie/je-m-informe-sur-les-maladies/trouver-ma-maladie-neuromusculaire" target="_blank" rel="noopener">consultez les fiches pratiques de l’AFM-Téléthon</a> (France) et trouvez des  informations sur le soutien social de l’<a href="https://www.asrimm.ch/" target="_blank" rel="noopener">ASRIMM</a> (Suisse romande) et de la <a href="https://www.malattiegeneticherare.ch/" target="_blank" rel="noopener">MGR</a> (Tessin).</p>
<p>Découvrez la révolution de la thérapie génique et l&rsquo;histoire de Romain, notre ambassadeur, touché par une Amyotrophie spinale de type 2 (SMA).</p>
<p><a href="https://telethon.ch/la-recherche/"><strong>Toutes les infos</strong></a></p>
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                <p>Atteinte d’une drôle de maladie que personne ne connaît, Mia se déplace en fauteuil électrique. Elle adore cuisiner avec son super Papi Toni, refaire le monde avec ses amis Julie et Renaud et raconter tous ses secrets à son chien Hector.</p>
<p>Mia adore passer ses vacances à la ferme de Tonton Gabriel et Tata Annie. Là-bas, elle retrouve tous les animaux qu’elle aime, surtout Bijou, une vache au grand coeur avec qui elle se sent bien et qui la comprend.</p>
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                    <div class="padding-s d-md-block d-lg-none"></div>                  <a href="https://telethon.ch/le-livre-illustre-jeunesse/" class="btn-corpo btn-light"  >Plus d&rsquo;infos sur notre livre&#8230;</a>

                                  
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