Pili Marzal palomera

Somos un grupo chicas que nos dedicados a la búsqueda y rescate de perros abandonados, heridos... no tenemos ningún tipo de ayuda ni financiación. Pedimos ayuda para poder pagar gastos veterinarios, guarderias y manutención de nuestros pequeños. Muchisimas gracias Con tu ayuda podemos hacerlo... Unete!

Gaia Sanctuary Foundation is a vegan rescue and recovery center for animals considered as farm, where those who have been exploited, mistreated or abandoned, receive the necessary care to have a decent life for the rest of their lives.   Located in Camprodon (Girona) in the Pyrenees, surrounded by forests, rivers and mountains.   You could meet the inhabitants of the Sanctuary here: http://www.fundacionsantuariogaia.org/population/

A Osteogénese Imperfeita (OI) é um grupo de doenças hereditárias responsáveis por graus variados de fragilidade óssea. Um traumatismo minor é suficiente para causar fracturas e deformações ósseas. Geralmente é utilizada uma classificação em 5 tipos. A OI é causada por mutações nos genes COL1A1 ou COL1A2. A terapia com Pamidronato na infância é o tratamento mais extensamente estudado, tendo-se provado benéfico.

The SJD Pediatric Center is the first monographic centre for paediatric oncology in Spain (2nd in Europe). 70% of the centre is devoted to care and 30% to research. It has the capacity to care for 400 children and youngsters. Its spaces are designed with the emotional well-being of the children and their families in mind. Our aim is that the children have more options to overcome cancer with less after-effects. Your euro helps to carry out the humanisation programmes and new treatments. Will you join 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.

Nuestro lema es Niños contra la Laminopatía, en concreto del tipo L-CMD. Recaudamos fondos para la investigación de esta grave enfermedad, rara entre las raras, con el sueño de encontrar curación a la misma. No se conocen más de 50 ó 60 casos registrados en el mundo, lo que hace que ni los laboratorios farmacéuticos ni los estados investiguen esta enfermedad, todo debemos conseguirlo los padres con fondos privados. Es una enfermedad degenerativa que en pocos años tiene un desenlace fatal.

Xènia is a pretty little girl became tetraplegic due the enterovirus outbreak happened in Spain on 2016. She had the most agressive strain, D68 that made several damages in her spinal chord. She's been in the PICU for 3 months having 3 heart attacks and 2 pneumonia, and she recovered succesfully. After that we'd been in Guttmann Institute, a recovery center for 6 months. We're fighting to keep her as healthy as possible Follow us in: https://www.facebook.com/helpxenia/ Thank you so much,

Hi! I'm Aitor and I'm almost 10 years old. When I was 2 years old, I choked on a sausage and got very sick. I went into cardiorespiratory arrest for more than 15 minutes and with a lack of oxygen to the brain. Now it's as if I had new one month, my little head has been damaged and I need help for everything, I can't see, talk, or move, I need a very expensive neurorehabilitation treatment and something else that I can't have, if you help me I promise to give you a smile.

12 years of war in Syria have left millions of victims and 5.5 million refugees. Since then, donations have been made in this group to assist them through harsh winters without heating or during the pandemic. Their situation is now even more critical after the earthquakes in February. UNHCR continues to support them with cash to cover basic needs, as well as their access to health, education, shelter and livelihoods. Photo ©UNHCR/S.Sawas

Claudia, con tan solo 4 años y medio, se encuentra afrontando mil batallas, las que le acompañan en esta enfermedad genética y muy rara denominada "MENKE-HENNEKAM", en la que apenas hay diagnosticados unos 50 casos en todo el mundo. Los problemas que le genera son tanto físicos como neurológicos. Así que lanzamos esta campaña para recaudar fondos y así aportarlos a la investigación de su enfermedad. @lasmilbatallasdeclaudia Mil gracias a todos♥️