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

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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

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News of the Foundation

Disponible la Memoria 2023 de la Fundación Isabel Gemio

June 28, 2024

Descubre la MEMORIA ANUAL 2023 de la Fundación Isabel…

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

June 28, 2024

The partnership of the Erasmus+ project EDUCATIONAL AID KITS…

New online meeting of the Erasmus+ QUALITY YOUTH MENTORING FOR INCLUSION

June 14, 2024

On Thursday, June 13th, the partnership of the Erasmus+ QUALITY…

The partnership of the Erasmus+ KITS EDUCATIVOS EN EL ÁMBITO DE LAS ENFERMEDADES RARAS meets in Madrid

June 5, 2024

The partnership of the Erasmus+ project EDUCATIONAL AID…

See more news

Events

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…

We organize the first multiplier events of the Erasmus+ THE VALUE OF FACING SCHOOL

December 5, 2023

On 29th and 30th November, we held the first multiplier events…

Fundación Isabel Gemio commemorates World Rare Disease Day together with young people affected and their families

March 1, 2023

On the occasion of World Rare Disease Day, the Isabel Gemio…

See more events

Last news

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)…

Ancestors of the 2.6 billion-year-old gene-editing tool CRISPR are resurrected

January 9, 2023

The prestigious scientific journal Nature Microbiology has published…

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.

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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:

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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.
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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

Disponible la Memoria 2023 de la Fundación Isabel Gemio

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

New online meeting of the Erasmus+ QUALITY YOUTH MENTORING FOR INCLUSION

The partnership of the Erasmus+ KITS EDUCATIVOS EN EL ÁMBITO DE LAS ENFERMEDADES RARAS meets in Madrid

Events

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

We organize the first multiplier events of the Erasmus+ THE VALUE OF FACING SCHOOL

Fundación Isabel Gemio commemorates World Rare Disease Day together with young people affected and their families

Last news

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

Ancestors of the 2.6 billion-year-old gene-editing tool CRISPR are resurrected

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