Club de Malasmadres y Cinfa celebrates the IV edition of the solidarity action “Ellas Cuentan” with the recognition of four inspiring women.

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The initiative, launched in 2021 by many people, is intended for women who face major life challenges: the imprisonment or incapacity of a spouse, or the desperation to live with their property in imprisonment or functional diversity. This year, a total of 98 women from all over Spain were compared to our stories, adding to some of the 800 stories featured in previous editions.

Patricia Gonzalez Velasco.

Patricia Gonzalez Velasco.

Four women selected for this year’s recognition for Ellas Quenton and one of the films aimed at improving the quality of life for them and their families Patricia Gonzalez Velasco (Madrid) in Joanna Aramendia Duque (Estella, Navarra), recognized in the category “Madres cuidadoras de hijos e hijas con enfermedades o especiales necessidades”; in Angela Dominguez Dorada (Madrid) in Alba Saskia Rivas (Blanes, Girona), recognized in the category “Women living in confinement or functional diversity”.

Patricia Gonzalez Velasco (@patrimakeupmadrid) is the mother of a 17-month-old child diagnosed with “ultra-low information”, the only case in Spain. Patricia convivió desde la adolescencia con le cáncer de her mother et esa enfermedado la enfrentó en años recientes dos deaths very close: el de su mother y el de her mano. “This Christmas, the best thing is that my child is cured, and my mother and my husband from heaven are my orgulosos for this recognition”Patricia confirmed. “Ayuda is intended for guests who support treatment, medication and hospital travel for a non-100% CUME autonomous mother”signal.

Joanna Aramendia Duque.

Joanna Aramendia Duque.

Joanna Aramendia Duque (@hodeilargicln6) are mothers of three who were diagnosed with Betten’s syndrome, a rare degenerative disorder. Jaana reveals that her participation in “Ellas Cuentan” has a side “The opportunity to learn about our new history and the Batten fence and with it to care, research and treat to improve the quality of life of people affected by it, like my little ones Hoday and Ilargi”. In a specific plan, the ayuda grant will be predestined “The investigation clearly suggests that clinical trials of gene therapy for the delivery of our children will begin this year in California, and everything will be necessary.” adds.

Angela Dominguez Dorada.

Angela Dominguez Dorada.

Angela Dominguez Dorada (@angela_paraciclista) was diagnosed with a spinal cord injury that the patient had been using for years of medical complications. In addition, I also faced the imprisonment of my husband and his wife. Angela is an example of superación and quiere que este reconocimiento serva para continuar concienciado sobre las enfermedades y demosare que su discapacidad no define quién es. “Para mí, ser una de las recencias means being able to continue to demonstrate that he may have a disability, but that does not allow me to take him from there. This advice will allow me to purchase a bike with the cushioning I need and need to deal with Tourette’s mid-to-mid winter as it has already happened.’.

Alba Saskia Rivas (@soyhope), diagnosed with Brown-Violet-Van Laer Syndrome, has a rare condition that affects hearing and movement. Para Alba, this recognition is an emotional impulse and a platform to make rare prisoners visible. “Ser una de las recognisas es dopamina en vena. It’s clear that my story relates to a lot of women, and we feel very comforted. Use the voice that a voice quebró me to shout: “No one is invisible””. Sobre el apoyo economico, este l’este destinará “my neurorehabilitation treatment that hacienda with my osteopathy. After 12 years of muscular dystrophy, this type of treatment is helping me recover my lower back muscles.confirmed.

Alba Saskia Rivas.

Alba Saskia Rivas.

Mission: To achieve functional diversity

A year later, in “Ellas Cuentan” we gathered the power of stories that made different realities visible and changed society. After the stories received in this fourth edition, women and mothers are seen and their stories are studied as mothers.

“Cada año, the project “Ellas Cuentan” our emotions because of the stories we learned during the four editions, the hay of the great women who inspired us with their resilience, his lucha and his compromise, and what just to be recognized. Alba, Angela, Patricia and Joanna are this year in the community of women “Ellas Cuentan”, but they are much more than that, thanks to this initiative they can tell their story and make it visible. Our compromise, the compromise of Malasmadres and Cinfa, is to build community ‘Ellas Cuentan’ para que no se sientan solas, porque el apoyo emocional es clave para alldas ellas”commented Laura Baena, founder of the Club de Malasmadres.

For his part, Enrique Ardiéres, president of Grupo Cinfa, claims this “From the beginning of this initiative, we have been able to know stories of overcoming and fortifying before very difficult situations. Testimony that we allow us to appreciate the importance of intense life every moment, weighing the adversities, and that we are convinced of the convenience of being able to live with both women and families who agree with confinement or disability in their lives today y nos sirven de example”.

Position December 11Madrid hosted a gala concert attended by these four women as well as the “Ellas Cuentan” community. In addition, the ambassadors of this publication will be present at this festive evening: Lucía Mi Pediatricraambassador of honor; Sarah Pereiramadre que lucha day a día con la enfermedad rara de sa hijo Mateo, y Marta Brulewho, like his wife, was diagnosed with cancer, is an example of super-activity and hope.

Stories that we simply reconocimiento

Along with the four women selected by the jury among the five stories most voted for by the Malasmadres community, we receive other testimonials that have also had a great social benefit. In the category “Madres cuidadoras de niños y niñas con enfermedades o necessidades especiales” están ambién las historias de Christina Arias Garciamother of a small number of years with a rare case to which nadie has a number sabido ponerle; Isabel MegraMateo’s mother, who suffers from the male llama BCAP31 mutation, untreated or untreated, and Tamara Blanco Polomother of a child diagnosed with Tay-Sachs as an infant, she has no treatment and expects to live 3 to 5 years.

In the category of Women Living in Imprisonment or Functional Diversity, we also recognize social stories such as Lydia Abispothat chronic fibromyalgia is irreversible in severe severity, chronic fatigue syndrome / chronic cephalomyelitis of serious and multiple chemical sensitivity, among other fecciones; Aroa Estevez Garciadiagnosed with autism, fibromyalgia and TEPT-C, Bruno Karominasdiagnosed with severe bilateral hypoacusis.

Collect all the life stories presented in the fourth edition of this solidarity initiative at ellascuentan2024.es

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