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Fila 0 for the Piel de Mariposa 5K Race, Seville – 4 October 2026

Make a donation to support people living with Butterfly Skin Disease

Collected

3.070€

Goal

10.000€

Donations

173

Left

24 days

31%

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Your contribution has tax benefits of up to 80%

Category

Inserción social Discapacidad física Infancia Enfermedades raras

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Published: 22 Sep 2026

Next 4 October, runners in Seville will come together for a very special cause. As part of the 5K race taking place in the Nervión-San Pablo District, we want you to be part of this solidarity movement supporting Butterfly Skin Disease.

Butterfly Skin Disease (Epidermolysis bullosa) is a rare, genetic and very painful condition that currently has no cure. People living with it have extremely fragile skin, as delicate as a butterfly’s wings. Even the slightest friction, such as a hug, can cause wounds and blisters that may take even years to heal.

Your donation helps DEBRA Piel de Mariposa, an NGO dedicated to supporting people and families affected by the condition, to continue accompanying them throughout their journey with the disease.

Will you join us? 🦋💙

Your support gives us wings.

Imagina no poder abrazar a tu bebé por miedo a hacerle daño. La Piel de Mariposa es una enfermedad de tipo genético, rara e incurable que provoca una extrema fragilidad de la piel, causando heridas y ampollas por todo el cuerpo ante el más leve roce. Su piel es tan frágil como las alas de una mariposa

Una de cada 227 personas somos portadoras del gen defectuoso que provoca la enfermedad, por lo que esta puede irrumpir en cualquier familia de forma inesperada. La Asociación Piel de Mariposa (DEBRA España) es una organización sin ánimo de lucro que trabaja para mejorar la calidad de vida de los afectados y sus familias.  Tú también puedes aportar tu granito de arena. www.pieldemariposa.es

About DEBRA, the Butterfly Children Charity:

Imagine not being able to hug your baby because you are afraid of hurting it. Because it was born with a rare genetic condition called Epidermolysis bullosa (EB) also known as Butterfly Skin. An incurable condition that causes blisters and wounds with the slightest touch. The skin is as fragile as the wings of a butterfly. DEBRA, the Butterfly Children Charity is a non-profit organization that works to improve the quality of life of those affected and their families.

If you would like to know more about DEBRA, the Butterfly Children Charity and our work please visit www.butterflychildrencharity.com

Donators (173)

Leonor

5€

One day ago

Anonymous

Hidden donation

One day ago

EMV

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2 days ago

Anonymous

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2 days ago

Anonymous

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2 days ago

Isabel María

5€

2 days ago

Jesica

50€

2 days ago

Anonymous

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2 days ago

Vanessa Ruiz fernandez

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2 days ago

Anonymous

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2 days ago

Anonymous

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2 days ago

Anonymous

5€

2 days ago

Celina

20€

2 days ago

Anonymous

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2 days ago

Anonymous

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2 days ago

Eva

35€

2 days ago

Bea

10€

2 days ago

Anonymous

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2 days ago

Aimar

5€

2 days ago

Anonymous

20€

2 days ago

Ignacio Medina

10€

2 days ago

TERESA

35€

2 days ago

Anonymous

Hidden donation

2 days ago

Beatriz

20€

2 days ago

Anonymous

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2 days ago

Anonymous

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2 days ago

Inmaculada

10€

2 days ago

Mireia

35€

2 days ago

Anonymous

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2 days ago

Abian

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2 days ago

Elena

10€

2 days ago

Analu

10€

2 days ago

Álvaro

12€

2 days ago

Anonymous

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2 days ago

ManuelyNatalia

5€

3 days ago

Anonymous

10€

3 days ago

Anonymous

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3 days ago

Inés del Sol Martín

10€

3 days ago

Anonymous

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3 days ago

Macan

10€

3 days ago

Eduardo

10€

3 days ago

Anonymous

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3 days ago

Anonymous

5€

3 days ago

Héctor H.

20€

3 days ago

Pilar

50€

3 days ago

Pauca1316 Gestion S.l.

100€

3 days ago

Antonio

50€

3 days ago

Dolores

10€

3 days ago

Marta

5€

3 days ago

Rosa

3€

3 days ago

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Comments (28)

Jesica

2 days ago

Mucho ánimo, lo has hecho genial

TERESA

2 days ago

Muchísimo ánimo y muchísima suerte

Beatriz

2 days ago

Animo valientes 😌

Abian

2 days ago

Ánimo Leo y su mami

Álvaro

2 days ago

Nada como apoyar con lo que sea por una grandísima causa

ManuelyNatalia

3 days ago

Por Leo , Fuerza

Pauca1316 Gestion S.l.

3 days ago

De parte del club 365Training

Francisco Manuel

3 days ago

Sois unos grandes!!!

Teresa

3 days ago

DIOS LOS BENDIGA A TODOS LOS ENFERMITOS Y A TODOS LOS QUE LOS AYUDAN🙏🏻🙏🏻🙏🏻🙏🏻🙏🏻

Patri

3 days ago

Un abrazo enorme Leo!!!

Dolores

4 days ago

Para seguir investigando y dando calidad de vida a estas personas.

Pilar

4 days ago

Disfrutemos de la carrera y del evento

Adriana

6 days ago

Adriana

Juan

9 days ago

Lo vamos a conseguir!!!

María Esther

9 days ago

Porque se cumplan los sueños de los niños con piel de mariposa

AITHOR

10 days ago

Ánimo Leo!!Un fuerte abrazo de Djamel!

María Isabel

12 days ago

Un besazo Leo

Miguel Gallardo Galán

12 days ago

💪🏻💪🏻

Andrea brundin

14 days ago

Vamos Leo!

Susana Limon Rodriguez

14 days ago

Soy voluntaria de la tienda en calle feria Sevilla

Yuliana

14 days ago

Animo Leo! Te admiramos

Lui

14 days ago

No podré asistir físicamente pero me sentirás muy cerca. "Valençia amb tu", Valencia contigo.

Antonio

14 days ago

Por seguir avanzando y llegar a encontrar una cura 🦋❤️

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