Robin Dragojevic

Daniela Knezevic and Nadine Bartel lead the Kitten Safe House. They usually take on injured street cats, kitten thrown into the trash or abandoned cats. Try to look after them well and give them in good hands. They also look after feeding sites and catches the cats for castration. There are at least 60 cats in her house, all of whom need food, medicines, cat litter and medical care. This all costs money, you can help us to support Daniela and her crew!

It all started with the street cat Maya, you can find her story on our Facebook page. The Mayacat Rescue team takes care of street cats on the island of Korcula with a lot of love and heart. Street cats will be treated and neutered with your donation. Street kittens come to care homes, are treated, chipped, tested, vaccinated, neutered and placed in a loving forever home. Let us fight together against the unbearable suffering of the street cats.

Wir kümmern uns um die Straßenkatzen auf Zypern. Die Population ist sehr hoch und wir versuchen durch Kastrationen dem Elend entgegen zu wirken. Außerdem betreiben wir Futterstellen und kümmern uns um kranke und verletze Tiere.

Wir sind eine private Organisation auf Mallorca und retten Katzen vor Ort | ausgesetzt - krank - von der Strasse - aus allen Notfallsituationen | Bei uns werden sie tierärztlich versorgt, kastriert, dürfen zu neuen Kräften kommen, sind in Sicherheit | sobald sie bereit & gesund sind, suchen sie einen Sofaplatz auf Lebenszeit. Aktuell versorgen wir täglich um die 150 Katzen - in unserem Katzen-Refugio, auf externen Pflegestellen und auf der Strasse.

Ajudamos mais de milhares de causas sociais a tornar os seus projetos possíveis todos os dias. Desde que lançámos o Teaming, já angariámos mais de 60 milhões de euros para as causas, totalmente livres de comissões. Criámos este Grupo Teaming para ajudar a Fundação Teaming a continuar a ajudar os outros com esta plataforma. Entre outros apoios, graças aos Teamers deste Grupo,o Teaming é totalmente gratuito. O nosso sonho: sermos autossustentáveis graças a este Grupo.

Somos la Asociación Niemann Pick de Fuenlabrada.Padres y amigos que luchan para acabar con ésta terrible enfermedad neurodegenerativa, genética y mortal. ¿Imagináis ver a vuestro hijo perder facultades día a día? Nuestra esperanza es la Terapia génica, la CURA de nuestros hijos, tenemos un equipo de investigación y necesitamos de vuestra ayuda, os estaremos eternamente agradecidos. Visítanos en Facebook y conócenos. ¿Nos ayudas? Asociación Niemann Pick Fuenlabrada Viviendo con Niemann pick

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 1747 children and their lifes have changed!!. 1 breakfast =€0.59. 1month=€13. TOTAL 3 school/month= €22.711. Your € FEEDS, EDUCATES AND PROTECTS.

Ayúdanos a recaudar fondos para la investigación y tratamiento de ésta enfermedad rara degenerativa y de carácter genético denominada Distrofia Muscular Facio Escapulo Humeral (FSHD) que se caracteriza por una marcada inexpresividad facial, debilidad muscular progresiva y que cuyos afectados se encuentran con una incapacidad muy variable llegando a perder la capacidad de caminar y la dependencia total de terceras personas durante gran parte de sus vidas. ww.fshd-spain.org

We are a group of people affected by multiple sclerosis, a neurodegenerative disease experienced by some 50,000 people in Spain. Two-thirds of the 1,800 people who each year learn they have MS are under the age of 40; three out of four of them are women. GAEM promotes research into treatments for this disease, and seeks to improve the quality of life of affected people and their families. We finance ourselves from the resources of conscious and generous people like you. Will you help us?

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.

The Dravet Syndrome Foundation transforms lives affected by this rare and severe childhood disease described in 1978. Dravet syndrome, a severe myoclonic epilepsy with mutations in the SCN1A gene, causes frequent seizures, developmental delays, orthopedic problems, speech difficulties, autism spectrum disorders, and growth and nutrition issues. We offer emotional support, research, and awareness efforts to bring hope. Join us and be the change!

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

A CADASIL é uma doença hereditária rara que provoca a oclusão das pequenas artérias cerebrais, com acidentes vasculares cerebrais recorrentes e demência numa idade precoce (por volta dos 50 anos). Não existe cura, mas uma equipa de investigação do Hospital de la Santa Creu i Sant Pau (Barcelona) vai iniciar um ensaio clínico para ver se os tratamentos já existentes no mercado podem ajudar a retardar esta doença incapacitante. Precisamos de si! Ajude-nos a curar!

El proyecto tiene como objetivo disminuir la mortalidad materno-infantil. Que no mueran más madres durante el embarazo y el parto por causas evitables. Para ser madre y poder vivirlo! Sensibilizar a la comunidad de la importancia de acudir a los controles prenatales y dar a luz en un centro sanitarios Formación de comadronas, dotación a los centros sanitarios rurales y hospital rural de Gambo del material necesario para atender un parto y sus complicaciones. Y transporte médico

La Fundación CRIS nace con un único objetivo: vencer al cáncer a través de la investigación. Un desafío enorme pero que justifica todo el esfuerzo, el talento y el compromiso necesario para conseguirlo, y que además, cada día, nos llena de esperanza y vida. Porque con CRIS, invertir en investigación es invertir en vida.

I'm Martin, they call me Tintin, I'm 3 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.