OUR MISSION IS TO PROMOTE RESEARCH ON MUSCULAR DISTROPHIES AND RARE DISEASES WE CENTER ALL OUR EFFORTS IN FUNDRAISING RESEARCH PROJECTS DRIVING THE INVESTIGATION OF DM AND OTHER RARE DISEASES WE HELP TO KNOW THE REALITY OF THE AFFECTED AND THEIR FAMILIES AND WE TRY TO IMPROVE THEIR QUALITY OF LIFE

KNOW OUR OBJECTIVES

I WANT TO HELP

Presentation video

Vídeos

XIV Aniversario – ‘Noche mágica por la ciencia’

Balance – Research Projects

Photocall XIV Aniversario – ‘Noche mágica por la ciencia’

El CRISPR y las Enfermedades Raras | Lluís Montoliu (CNB-CSIC)

Evento por el Día Mundial de las Enfermedades Raras – Directo ZOOM

Trailer Documental “Jóvenes Invisibles”

Protagonistas del Día Mundial de las Enfermedades Raras

¿Cómo te sentirías tú?

News of the Foundation

New online meeting of the ERASMUS+ EDUCATIONAL AID KITS IN THE FIELD OF RARE DISEASES

March 17, 2025

On 14th March 2025, the partnership of the Erasmus+ project…

Barcelona hosts the second transnational meeting of ERASMUS+ EDUCATIONAL KITS IN THE FIELD OF RARE DISEASES

January 27, 2025

On 24 January 2025, the partnership of the Erasmus+ project…

Erasmus+ project ‘Quality Youth Mentoring for Inclusion’ showcases its results in Multiplier Events across Europe

December 20, 2024

In recent weeks, the partners of the Erasmus+ project ‘Quality…

NEW ONLINE MEETING OF THE ERASMUS+ EDUCATIONAL AID KITS IN THE FIELD OF RARE DISEASES

December 18, 2024

On December 12th, 2024, the partnership of the Erasmus+ project…

See more news

Events

We invite you to the launch of the You’re Not Alone network for rare diseases

November 29, 2024

Next Monday, 16 December, the Isabel Gemio Foundation will present…

VII Torneo de Golf Villa de San Javier (Murcia)para la investigación de enfermedades raras y distrofias musculares

July 19, 2024

El viernes 23 y el sábado 24 de agosto de 2024, Roda Golf organiza el VII Torneo de Golf Villa de San Javier (Murcia). Se trata de un torneo solidario que destinaría los fondos a la Fundación Isabel Gemio para la investigación de enfermedades raras y distrofias musculares. Puedes inscribirte en https://www.rodagolf.com/es/

Fundación Isabel Gemio holds new multiplier events of the Erasmus+ THE VALUE OF FACING SCHOOL

February 29, 2024

In recent days, Fundación Isabel Gemio has held new multiplier…

Fundación Isabel Gemio holds a new multiplier event in the Representation of the European Commission in Spain’s venue to present the Erasmus+ project THE VALUE OF FACING SCHOOL

January 31, 2024

Madrid, January 30th 2024. Fundación Isabel Gemio…

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Last news

NOTICIA DE ONDA REGIONAL: Encarna Guillén. “Queremos crear una plataforma federada de datos que esté disponible para trabajar con las enfermedades raras”

November 28, 2024

La Dra. Encarna Guillén, exjefa de la sección pediátrica…

IIS La Fe researcher, Javier Poyatos, defends his doctoral thesis and receives outstanding distinctions

March 3, 2023

Javier Poyatos, from the Neuromuscular Pathology and Ataxias…

Farmaindustria proposes twelve measures to improve access to new treatments for patients with rare diseases

February 3, 2023

Improving access to new treatments for Spanish patients with…

Scientists succeed in culturing mature neurons in laboratories to study neurodegenerative diseases

January 16, 2023

Scientists from Instituto de Bioingeniería de Cataluña (IBEC)…

See more news

Publications of our scientific committee

IIS La Fe researcher, Javier Poyatos, defends his doctoral thesis and receives outstanding distinctions

March 3, 2023

Javier Poyatos, from the Neuromuscular Pathology and Ataxias…

The scientific journal ‘Cells’ publishes a new study developed by Grupo Park with the collaboration of Fundación Isabel Gemio

October 19, 2022

The scientific journal 'Cells', with almost 7.7 impact factor,…

A new study co-funded by Fundación Isabel Gemio Foundation advances our knowledge of a mutation responsible for Duchenne and Becker muscular dystrophies

October 10, 2022

A Spanish multicentre study, co-funded by Fundación Isabel…

See more publications

Mecenas de Oro Awards

The Gold Awards of the Isabel Gemio Foundation are a recognition of the commitment to the Foundation and its primary purpose: the financing of research projects in less frequent diseases.

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Awards to the foundation

Premio Solidario a la Fundación Isabel Gemio (Espabrok-Asegurados solidarios) 2020

February 19, 2020

La Real Academia de Bellas Artes de San Fernando en Madrid ha…

Premio Augusto a la Entidad Social del Festival de Cine de Zaragoza a la Fundación Isabel Gemio

November 19, 2019

El Festival de Cine de Zaragoza (FCZ) ha hecho entrega este…

La Fundación recibe el Premio Investigación de Movistar Estudiantes

June 5, 2019

Todos Somos Estudiantes reconoce la innovación y los valores En…

See more awards

Send FUERZA to 28030

And you will be contributing € 1.20 to our projects for the investigation of less frequent diseases.

More information

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Friends of the Foundation

Eva Isanta

Rosa Montero

Víctor Palmero

Pablo Chiapella

Macarena Gómez

Jordi Sánchez

Know them all

Solidarity Restaurants

Do you have a restaurant or do you know one that would like to become a charity restaurant by donating one euro of one of its dishes?

These are the solidarity restaurants that are already collaborating in the fight against minority diseases through the Isabel Gemio Foundation:

Associates

THE FOUNDATION IS A MEMBER:

WE NEED YOUR DONATION NOW

Eradicating rare diseases is only possible with the funding of research projects.

Thanks to many people we have contributed € 1,793,700 to the research lines of the Isabel Gemio Foundation.
Help us and get a 75% discount on your donation.

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OUR MISSION IS TO PROMOTE RESEARCH ON MUSCULAR DISTROPHIES AND RARE DISEASES WE CENTER ALL OUR EFFORTS IN FUNDRAISING RESEARCH PROJECTS DRIVING THE INVESTIGATION OF DM AND OTHER RARE DISEASES WE HELP TO KNOW THE REALITY OF THE AFFECTED AND THEIR FAMILIES AND WE TRY TO IMPROVE THEIR QUALITY OF LIFE

Vídeos

News of the Foundation

New online meeting of the ERASMUS+ EDUCATIONAL AID KITS IN THE FIELD OF RARE DISEASES

Barcelona hosts the second transnational meeting of ERASMUS+ EDUCATIONAL KITS IN THE FIELD OF RARE DISEASES

Erasmus+ project ‘Quality Youth Mentoring for Inclusion’ showcases its results in Multiplier Events across Europe

NEW ONLINE MEETING OF THE ERASMUS+ EDUCATIONAL AID KITS IN THE FIELD OF RARE DISEASES

Events

We invite you to the launch of the You’re Not Alone network for rare diseases

VII Torneo de Golf Villa de San Javier (Murcia)para la investigación de enfermedades raras y distrofias musculares

Fundación Isabel Gemio holds new multiplier events of the Erasmus+ THE VALUE OF FACING SCHOOL

Fundación Isabel Gemio holds a new multiplier event in the Representation of the European Commission in Spain’s venue to present the Erasmus+ project THE VALUE OF FACING SCHOOL

Last news

NOTICIA DE ONDA REGIONAL: Encarna Guillén. “Queremos crear una plataforma federada de datos que esté disponible para trabajar con las enfermedades raras”

IIS La Fe researcher, Javier Poyatos, defends his doctoral thesis and receives outstanding distinctions

Farmaindustria proposes twelve measures to improve access to new treatments for patients with rare diseases

Scientists succeed in culturing mature neurons in laboratories to study neurodegenerative diseases

Publications of our scientific committee

IIS La Fe researcher, Javier Poyatos, defends his doctoral thesis and receives outstanding distinctions

The scientific journal ‘Cells’ publishes a new study developed by Grupo Park with the collaboration of Fundación Isabel Gemio

A new study co-funded by Fundación Isabel Gemio Foundation advances our knowledge of a mutation responsible for Duchenne and Becker muscular dystrophies

Mecenas de Oro Awards

Awards to the foundation

Premio Solidario a la Fundación Isabel Gemio (Espabrok-Asegurados solidarios) 2020

Premio Augusto a la Entidad Social del Festival de Cine de Zaragoza a la Fundación Isabel Gemio

La Fundación recibe el Premio Investigación de Movistar Estudiantes

Send FUERZA to 28030

Friends of the Foundation

Eva Isanta

Rosa Montero

Víctor Palmero

Pablo Chiapella

Macarena Gómez

Jordi Sánchez

Solidarity Restaurants

Associates

THE FOUNDATION IS A MEMBER:

Redes sociales

Ayúdanos

WE NEED YOUR DONATION NOW