Collected
2.000€
To benefit
Help us turn €8,000 into memories that last a lifetime
#EscuadrónPúrpura in Girona – Verano Guerrero 2026
Cause lead by
Category
This June, 8 Guerreros Púrpura families will travel to the Costa Brava.
This is not just another trip.
It is a medically supported and fully accompanied journey for children living with neurological and metabolic diseases and severe epilepsy.
Families who organize every single day around medication, seizures, and constant care.
And who still want something very simple: to enjoy time together.
These are not holidays.
This is about creating memories with our children.
What makes this project special?
✔️ Adapted transportation
✔️ Accessible hotel
✔️ Trained volunteers
✔️ Medical support team
✔️ Continuous safety and supervision
✔️ Activities adapted to their needs
A prepared environment.
A team that knows how to respond.
A space where families can breathe.
It is community.
It is support.
It is Verano Guerrero.
Our goal: €8,000
The full project exceeds €41,000 and families cover a significant part of the cost.
To keep it accessible and sustainable, we need to raise €8,000.
This will help cover transportation, medical support, volunteers, insurance, and professional coordination.
We are not funding leisure.
We are making a safe journey possible — one that many families could not undertake on their own.
Every donation brings us closer to the sea
€10 brings us closer to Girona.
€25 supports an adapted activity.
€50 sustains the volunteers who accompany us.
€100 helps ensure no family is left behind.
At Guerreros Púrpura, we believe illness should not take away memories too.
💜 Donate. Share.
Help us reach €8,000.
Guerreros Púrpura es una asociación diferente, nos unimos para apoyar a los niños y familias con diferentes patologías, trastornos, enfermedades,… para juntos darnos el mayor apoyo, visibilidad y fortaleza.
Desde Guerreroas Púrpura luchamos por dar visibilidad a un grupo heterogéneo de condiciones, patologías y enfermedades neurológicas y metabólicas, prestando especial importancia a aquellos casos considerados como “enfermedad rara”, o que carecen de diagnóstico, llegando incluso a niños que se encuentran en cuidados paliativos pediátricos.
Dentro de esta diversidad de afectaciones, existen tratamientos y líneas de investigación comunes y de utilidad para un gran número de niños.
En concreto, desde Guerreros Púrpura apoyamos a las familias afectadas por:
•Enfermedades endocrinas, nutricionales y metabólicas.
•Daño cerebral (congénito o adquirido).
•Enfermedades del sistema nervioso.
•Malformaciones congénitas, deformidades y anomalías cromosómicas.
•Trastornos del movimiento, del desarrollo, de conducta, del lenguaje, cognitivos.
•Epilepsia y síndromes relacionados.
Donators (41)
Dolores
475€
131 days ago
Rocio
Hidden donation
139 days ago
Patricia
50€
172 days ago
Familia Blanco V
35€
174 days ago
Fernando
15€
175 days ago
Elena
200€
175 days ago
Blanca
5€
175 days ago
Inés GV
5€
176 days ago
Anonymous
Hidden donation
176 days ago
Olga Lopez
25€
176 days ago
Anonymous
20€
183 days ago
Paloma
20€
187 days ago
Carmen
50€
189 days ago
Beatriz
200€
194 days ago
Virginia
50€
198 days ago
Anonymous
100€
218 days ago
Ana Belén
20€
229 days ago
Anonymous
10€
229 days ago
Rocío
50€
232 days ago
Jesús
100€
239 days ago
Mari Carmen
50€
239 days ago
Carlos
5€
239 days ago
Lourdes
35€
240 days ago
Laura
20€
242 days ago
Ana Belén
20€
242 days ago
Carlos
20€
242 days ago
Anonymous
20€
242 days ago
Anonymous
Hidden donation
242 days ago
Anonymous
Hidden donation
243 days ago
Anonymous
Hidden donation
243 days ago
Isabel Arribas
35€
243 days ago
Anonymous
35€
243 days ago
Edu
20€
243 days ago
Mayte
50€
243 days ago
Anonymous
Hidden donation
243 days ago
Ines Sanchez
15€
243 days ago
ANTONIO CARMONA
20€
245 days ago
Ana María
10€
245 days ago
Susana
Hidden donation
245 days ago
Elena
10€
245 days ago
Miriam
5€
245 days ago
Comments (7)
Rocio
0
Familia Blanco V
Para Guerreros Púrpura
Elena
Os lo merecéis!!!!
Rocío
Ánimo guerreros, conseguimos el reto!
Jesús
Grano a grano les alegramos el verano
Carlos
A por todas!