<div>Hola, somos El Avión de los Sueños A.C., una asociación que apoya a niños con enfermedades complejas a acceder a oportunidades que pueden cambiar su vida.
</div>
<div><br />
</div>
<div>Hoy estamos recaudando fondos para apoyar a Marko (11 años) y María Roberta (5 años), ambos con diagnóstico de CTNNB1, una condición genética poco común que afecta su desarrollo neurológico y motor.
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<div><br />
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<div>En México existen solo 5 casos registrados, lo que hace que el acceso a especialistas y alternativas médicas sea muy limitado.
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<div><br />
</div>
<div>Ambos han sido considerados para asistir a una convención internacional en Barcelona, organizada por la CTNNB1 Foundation, donde médicos y especialistas evaluarán su caso y podrán determinar si son candidatos a una nueva alternativa basada en reemplazo genético, que ya ha sido aplicada en un paciente con resultados alentadores.
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<div><br />
</div>
<div>Este viaje no es turístico.
</div>
<div>Es una oportunidad real de acceder a algo que hoy no existe en México.
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<div>El objetivo es cubrir el traslado redondo CDMX – Barcelona – CDMX para 2 menores y sus acompañantes.
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<div><br />
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<div>El tiempo es clave, ya que las fechas son únicas y los costos de vuelo pueden aumentar conforme se acerque el viaje.
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<div><br />
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<div>Tu apoyo, sin importar el monto, puede acercarlos a esta oportunidad.
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<div>Hoy puedes ser parte de algo que puede cambiar su historia.
</div>
<div><br />
</div>
<div>️SI ELLOS NO SE RINDEN, NOSOTROS TAMPOCO️
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<div><br />
</div>
<div>FRANCÉS
</div>
<div>Bonjour, nous sommes El Avión de los Sueños A.C. (L'Avion des Rêves), une association qui soutient les enfants atteints de maladies complexes en leur offrant des opportunités qui changent leur vie.
</div>
<div><br />
</div>
<div>Aujourd'hui, nous collectons des fonds pour soutenir Marko (11 ans) et María Roberta (5 ans), tous deux atteints de CTNNB1, une maladie génétique rare qui affecte leur développement neurologique et moteur.
</div>
<div><br />
</div>
<div>Au Mexique, seuls 5 cas sont recensés, ce qui limite considérablement l'accès aux spécialistes et aux alternatives médicales.
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<div><br />
</div>
<div>Tous deux ont été sélectionnés pour participer à un congrès international à Barcelone, organisé par la Fondation CTNNB1. Des médecins et des spécialistes y évalueront leurs cas et détermineront s'ils sont éligibles à une nouvelle thérapie génique, qui a déjà été appliquée à un patient avec des résultats encourageants.
</div>
<div><br />
</div>
<div>Il ne s'agit pas d'un voyage touristique.
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<div><br />
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<div>C'est une véritable opportunité d'accéder à un traitement actuellement indisponible au Mexique.
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<div><br />
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<div>Notre objectif est de financer les billets d'avion aller-retour de Mexico à Barcelone pour les deux enfants et leurs accompagnateurs.
</div>
<div><br />
</div>
<div>Le temps presse, car les dates sont uniques et le prix des vols peut augmenter à mesure que le voyage approche.
</div>
<div><br />
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<div>Votre soutien, quel qu'en soit le montant, peut les rapprocher de cette opportunité.
</div>
<div><br />
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<div>Aujourd'hui, vous pouvez contribuer à changer leur vie.
</div>
<div><br />
</div>
<div>S'ils ne baissent pas les bras, nous non plus.
</div>
<div><br />
</div>
<div>INGLÉS 
</div>
<div><br />
</div>
<div>Hello, we are El Avión de los Sueños A.C. (The Plane of Dreams), an organization that supports children with complex illnesses by providing them with life-changing opportunities.
</div>
<div><br />
</div>
<div>Today we are raising funds to support Marko (11 years old) and María Roberta (5 years old), both diagnosed with CTNNB1, a rare genetic condition that affects their neurological and motor development. 
</div>
<div><br />
</div>
<div>In Mexico, there are only 5 registered cases, making access to specialists and medical alternatives very limited. 
</div>
<div><br />
</div>
<div>Both have been selected to attend an international convention in Barcelona, ​​organized by the CTNNB1 Foundation, where doctors and specialists will evaluate their cases and determine if they are candidates for a new alternative based on gene replacement therapy, which has already been applied to one patient with encouraging results. 
</div>
<div><br />
</div>
<div>This is not a tourist trip. It is a real opportunity to access something that is currently unavailable in Mexico. 
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<div>The goal is to cover round-trip airfare from Mexico City to Barcelona and back for two children and their companions.
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<div><br />
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<div>Time is of the essence, as the dates are unique and flight costs can increase as the trip approaches.
</div>
<div><br />
</div>
<div>Your support, no matter the amount, can bring them closer to this opportunity.
</div>
<div><br />
</div>
<div>Today you can be part of something that can change their story. 
</div>
<div><br />
</div>
<div>IF THEY DON'T GIVE UP, NEITHER WILL WE 
</div>

Mario Lazcano torres

Marianna Yanahel Jimenez Arana

Anonymous

Familia Alcala Vamos Robertita vamos mark

Benjamin Alonso Rascon

Francisco Onesimo

Ara E Martz

Maria del Rosario Ramirez Aguirre

Yza Herrera

Alfonso López Corral

INGRID MONTEJANO

Alicia Andares

Ivan Orozco

Vamos Roberta te queremos Alex y carmelita Se va a lograr

celern celerno

Fernando Robles Cordero

Vicente Elias  Solorio Lara

Erika Silva

Mario Aníbal Bravo Peregrina

Ayuda para viajar a Barcelona: oportunidad médica única

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