María José Castro Serrano

Group to raise funds for veterinary debts of cats positive for immunodeficiency and leukemia. If you can collaborate, with something else Paypal: contacto@soypositivo.es Openbank ES78 0073 0100 5305 0605 8386 Titular: Asociación Soy Positivo Bizum pago ONG a través del código 04641 Concepto: Ayuda Soy Positivo

Soy Miriam. Desde hace más de 10 años me encargo de alimentar y atender a los gatos de las colonias asentadas en las cocheras del metro de Canillejas, y en la zona universitaria de Madrid. Yo y Marisa atendemos actualmente a 55 gatitos, todos ellos castrados y esterilizados. Sólo alimentarles y proporcionarles atención veterinaria supone un gasto muy elevado que no podemos asumir solas, ¿nos echas una patita? Juntos podemos hacer que tengan una vida mejor. ¡Gracias de corazón por tu apoyo!

FAPAM rescues abandoned and mistreated animals that have been seized from illegal kennels and hunting dog rehalas in collaboration with the Community of Madrid and police forces. FAPAM has created a legal department to ensure that these cases are not shelved and that the abusers are tried and convicted. With your help of 1€, we will be able to continue rescuing animals, and very importantly, we will also be able, with our lawyers, to pursue and do justice for so many innocent victims.

ASPACE Soria is a non-profit association that aims to comprehensively cover the needs of people with cerebral palsy, related pathologies and other disabilities in the province of Soria. We provide specialised services and treatments. Our attention addresses problems of movement, learning, speech, swallowing, hearing, psycho-social and emotional development. Our aim is that both users and families have the best possible quality of life.

Somos un grupo de niños/as que tenemos el síndrome de duplicación mecp2, que nos produce retraso mental, psicomotor y de lenguaje, insomnio, infecciones respiratorias, esteriotipias… crisis epilépticas que nos producen regresión. En el hospital Sant Joan de Deu de Bcn se investiga gracias a las familias y a las donaciones privadas para encontrar un tratamiento o cura que mejore nuestra calidad de vida.Necesitamos tu ayuda! www.duplicacionmecp2.es

When Martina was 2 months old, she broke her two legs while into her mothers arms. Since then, she has suffered multiple fractures that prevent her from walking normally. Our daughter suffers from Osteogenesis Imperfecta, better known as brittle bone disease. 100% of the collected funds go to entities and projects committed to improving the quality of life of patients.

Yemen is living a brutal humanitarian emergency. The girls are married off in hopes that they will be fed. The boys are recruited as soldiers. Their lives are hell: rapes, pregnancies, violence. If the school provides food, families are more likely to bring them. We give milk, bread, egg/cheese/tuna and fruit to 2205 children in 4 schools and their lifes have changed!!. 1 breakfast =€0.59. 1month=€12,32. TOTAL 4 school/month= €27.165. Your € FEEDS, EDUCATES AND PROTECTS.

Kittens Shelter for Leukemic Cats. On April 9th, 2021, the 8 babies of Bombay were born, a kitten rescued 21 days earlier from the street. An angel suffering from 3 mastitis since giving birth, yet continuing to breastfeed her babies. Two months later, we find out that both the 8 babies and Bombay are positive for Leukemia, and today 'Bombay Family' begins to fulfill a dream and not abandon the weakest at the worst moment. Help with veterinary expenses, medicines, and food. www.familiabombay.com

Since the conflict began in 2022, we formed this group to support Ukrainians impacted by the war. Nearly three years later, they still need our help. Together with various organizations, including CEAR (the Spanish Commission for Refugee Aid), we remain committed to supporting those who have come to Spain to build a new life.

Soy Marco y Tay-Sachs ha marcado mi vida ya que mi hijo Liam la padecía. En España hay, en este momento, 13 niños y niñas afectados por las enfermedades de Tay-Sachs y Sandhoff. Madreperla recauda fondos para financiar la investigación y gracias a personas como tú hemos logrado que 2 universidades estudien Tay-Sachs y Sandhoff. Te necesitamos por todos los niños que padecen estas enfermedades, presentes y futuros. 12 Teamers= 1,5h de investigación.

The Galgos del Sur Association is a non-profit organization located in Córdoba. We fight against the abandonment and massive sacrifice of greyhounds and hunting dogs, to raise awareness and awareness in society about this problem and give a new life looking for good families. In this group you collaborate with the expenses we have every day: veterinarians, rent, cleaning, food, etc. Keep in mind that Galgos del Sur does not receive aid or subsidies, we only have you to go on.

GAB is an association that fights against the mistreatment and abandonment of the Ratonero Bodeguero Andaluz. This breed is used for hunting and when they are "no longer useful" they are abandoned. It is the same problem as with galgos and podencos, except that the bodegueros are not such a well known breed. The money raised goes directly to pay for the dogs' homes, which cost 100 euros per month per dog, plus countless veterinary expenses. Every euro counts to keep saving dogs.

Somos Galgos del Sur, una organización sin ánimo de lucro que lucha por el fin de la caza con perros y de todas las prácticas cruentas que provoca esa terrible actividad como es la caza. Entendemos que sólo recogiendo animales no solucionamos el problema, hay que luchar y hay que denunciar. Desgraciadamente esta lucha legal no es barata y necesitamos tu ayuda, son muchos los costes que hay que afrontar, abogados, costas, fianzas, procuradores, etc. Apoya esta lucha por los que no tienen voz!

Abril is a 9-year-old girl diagnosed with SPG52, with only 55 diagnoses in the world. SPG52 is an ultra-rare disease that causes very serious symptoms such as severe intellectual disability, epileptic seizures and very rapid muscle degradation in the lower body. Abril started walking when she was 3 years old and now at 9 she can hardly move anymore.

I'm Martin, they call me Tintin, I'm 4 years old. I was born with some malformations and one of them was a cleft lip, for which they operated on me when I was 3 months old. They had given my parents full assurance that it would be a simple operation, but something went wrong and I ended up in the Ucip with mechanical ventilation and deep sedation, and one day, they accidentally extubate me and I went into cardiorespiratory arrest for 15 min, and because of that accident I have cerebral palsy.

Somos un grupo de mujeres que estamos pasando por diferentes etapas de cáncer de mamá con un tumor clasificado como triple negativo y que tenemos un proyecto en común: Formar esta asociación para ayudar a recaudar fondos para proyectos de investigación específicos para el triple negativo y ayudar a la divulgación de este tumor con información actualizada.

Hola! me llamo Erick y nací con 28 semanas. Soy un Gran Prematuro, al que diagnosticaron PARÁLISIS CEREBRAL, por una lesión llamada LEUCOMALACIA PERIVENTRICULAR MODERADA. Esta lesión me genera Tetraparesia Espastica. El colegio se encarga de algunas terapias, las cuales no son suficientes y mis PAPÁS tienen que costearme las terapias complementarias, de Fisioterapia, Logopedia, Psicopedagogía, Hidroterapia, Equinoterapia y las Ortesis para mejorar mi calidad de vida.

Jimena es una niña de 2 añitos con una enfermedad rara, llamada síndrome de Angelman. Este síndrome afecta a 1 de cada 20.000 nacimientos. Su pronóstico es muy duro, con dificultad para caminar, ausencia del lenguaje, retraso metal, hiperactividad y epilepsia entre otros trastornos. A día de hoy no existe cura, y en el 95% de los casos la causa es puro azar. Para paliar todo esto se precisan costosas horas de rehabilitación y terapia, además de la adaptación de elementos utilizados a diario.

Ayuda a gatos callejeros y otros animales.

I'm Melani an animal lover who cares for more than 20 community cats living in a plastics recycling factory near Barcelona (Spain). I try to help every single cat I find, whether by feeding them, rescuing them, neutering them, or providing veterinary assistance. Unfortunately, I don't have any economic support to deal with all the expenses that helping stray cats means, so, if you wanna help me help them, please, join this team :) You can check my labour on insta: @todostenemoshuellas

Can you imagine being afraid to hug your child? This is how the parents of Butterfly Children feel. A rare and incurable condition, which causes the skin to break with the slightest touch. DEBRA-BUTTERFLY CHILDREN CHARITY works to improve their quality of life. By joining this group you are giving them wings.

1 in 5 children in Yemen suffer from acute malnutrition (2.3 million total). 500,000 are at risk of death. Families do not have money for the hospital or for necessary food. Under Yemeni pediatric supervision we take care of serious and difficult cases. We give milk, food, medicine, medical assistance, pay hospital admissions, etc., until their recovery or improvement. €1 pays for 1 day's worth of milk for 1 baby. Every €10 we buy 1 can of milk for 4 days.

We give DRINKING WATER to families in Yemen who were displaced from their homes by 10 years of war. Yemen is the biggest humanitarian emergency on the planet and is suffering from a cholera epidemic and shocking infant mortality. With your EURO we buy and refill WATER TANKS in IDP camps and schools. We have 50 in 4 camps and in 5 schools. More than 000 9people receive water (800 thousand litres/month). Yemen needs more water! 1€=101 litres in the north and 129 in the south. JOIN US!

CADASIL is a rare hereditary disease that affects arteries throughout the body, but its symptoms only occur in the brain, with recurrent strokes and dementia at an early age (around 45-50 years old) being characteristic. There is NO cure, but a research team at the Hospital de la Santa Creu i Sant Pau (Barcelona) is going to start a clinical trial to see if treatments already on the market can help to stop this incapacitating disease. We need you! Help us to cure!

El síndrome IRF2BPL (Nedamss) es una alteración en este gen, que con el paso de los años su cuerpo deja de producir una proteína esencial para el cerebro, como consecuencia van perdiendo poco a poco sus capacidades motoras como caminar, hablar, comer, incluso hasta dejan de respirara por si solos. La Asociación Española IRF2BPL nace para ayudar a estos niños, niñas y familiares con esta enfermedad minoritaria que afecta actualmente a 14 personas. Te necesitamos. Ayúdanos con 1€ al mes.