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We are a non-profit institution created in 2016 whose resources are entirely dedicated to the foundational purposes: Education, research and dissemination and social awareness related to children with special educational needs derived from their neurological diseases and who specifically suffer from Language Disorder such as consequence of their illnesses and / or disorders. The mission of the Querer Foundation is to promote the creation of multidisciplinary work groups that have the capacity to diagnose and investigate neurological disorders related to language from a clinical, pharmacological, neurological, and educational point of view. The Querer Foundation has an inclusive and disruptive vision. We want to bring together under the umbrella of Education, Research, and Communication all agents and institutions that have a genuine interest in researching the brain, rare neurological diseases, and epilepsy. The Querer Foundation is a non-profit institution that believes in equality and equity. Equal opportunity, fair treatment in life and diversity from difference. We believe in Different Education for different children.

1. To act as a leading organisation and a global voice for the rights of those who face discrimination on the grounds of sexual orientation, gender identity, gender expression and/or sex characteristics (SOGIESC). 2. To work towards achieving equality, freedom and justice for lesbian, gay, bisexual, trans and intersex people through advocacy, collaborative actions, and by educating and informing relevant international and regional institutions as well as governments, media and civil society. 3. To empower our members and other human rights organisations in promoting and protecting human rights, irrespective of people's sexual orientation, gender identity, gender expression and/or sex characteristics and to facilitate cooperation and solidarity among ILGA regions and members. 4. To promote the diversity and strengths of persons of diverse SOGIESC around the world.

Fundacion Corazonistas is the tool of the Institute of Brothers of the Sacred Heart in the Province of Spain for the promotion and participation of lay Corazonistas through social commitment. In 2021, Fundacion Corazonistas is the reference space for lay Corazonistas in educational works in Spain to get socially involved in building a more just world. Thus, it contributes to the development of committed personal and community vocations in Spain and to the development of projects of heart solidarity with impoverished people and peoples throughout the world.

The mission of FEBA consists in contributing to the reduction of hunger and malnutrition in Europe, through the fight against food waste and the call for solidarity, by supporting and developing Food Banks in coutries where they are most needed. FEBA bases its activity on these values: giving, sharing, European solidarity and fighting food waste.

Our goal is to promote the full cure of childhood leukemia. To fulfill this mission, we rely on scientific research projects that have an impact on clinical healing and differentiating projects that positively affect the healing of the emotional health of this disease, which not only affects the child, but also the entire family in different fronts. Our dream is that a doctor can one day say "don't worry, your son just has leukemia", can you imagine it? We do. Extraordinary solutions for known problems. Our purpose as a Foundation, focused on strengthening the third sector, promoting social action, or improving the welfare of the most disadvantaged, is to work on the development and support of innovative and different projects that seek to make a difference. And allocate all the benefits of our research projects. In these 10 years of growth, we have taken another step forward, with presence and reference at all levels of the disease: prevention, diagnosis, personalization, therapy, assistance...

Medicos del Mundo (MdM) is an independent international association that promotes solidarity and pursues the fulfilment of the fundamental right to health and the enjoyment of a dignified life for any person. Goals are: Help victims of human crises: wars or natural disasters and those living in the less developed areas of the planet. Attend people who live in our country and are in a vulnerable situation MdM has a firm commitment to the values of humanitarian medicine, as access to health is a right of all people, regardless of their place of birth, race, social or sexual estatus or religion.

Address the needs and improve the quality of life of groups in vulnerable situations

Empower unemployed people, especially women in risk of exclusion to achieve economic independence by providing them professional attire, training, and the development tools to give them self confidence, so that they can successfully pass their job interview and obtain a job.

Improve the quality of life of famiies with Butterfly skin.

Luchar por los Derechos de los afectados por la enfermedad del sindrome de Rett, Mejorar su calidad de Vida e impulsar decididamente la Investigacion del Sindrome de Rett para lograr su cura

The Ben Raemers Foundation aims to end the stigma and burden that so often clouds issues of mental health by bringing awareness of these issues and suicide to the forefront within the wider skateboarding community. The Ben Raemers Foundation aims to relieve the needs of people with mental health issues or those at risk of mental health issues, in particular but not exclusively those within the skateboarding community, in the UK by: (i) Providing educational resources to inform people about mental health issues (ii) Providing training schemes for volunteers, and the general public and service providing organisations, to raise awareness and increase the ability to assist those in need. (iii) Raising public awareness of mental health issues.

The AEetc association (known as ETC Association) is a non-profit organisation of parents of children with cancer. Its main objective is to improve the quality of life of children with cancer and adolescents both during treatment and after treatment, when most side-effects start to appear. The life expectancy of a child diagnosed with cancer a few years ago was quite low. However, today many children survive cancer (around 80%) thanks, among other things, to early diagnosis, more precise surgery, more technologically advanced instruments and more effective chemotherapy, radiotherapy and immunotherapy treatments. New treatments are more effective, but they are also more aggressive, and they leave a mark on children. As life expectancy of children diagnosed with cancer has increased, important long-term side effects have also been identified. They significantly limit children's quality of life: cognitive, physical, emotional and, consequently, social effects. The name ETC has a double meaning. On the one had, it is the acronym in Spanish for "cancer treatment side-effects" (Efectos del Tratamiento del Cancer). On the other hand, ETC means the fight against cancer does not finish when treatment comes to an end. Instead, there is a long "ETC" after treatment that negatively affect our children's quality of life. Side effects are not exclusive to childhood cancer, but children are the most vulnerable group, since they are in the process of intellectual, physical and emotional development. In the case of children diagnosed with brain tumors, mainly those that have been treated with radiotherapy, the consequences are lifelong and progressive.