Dominique Treiber

The refuge of Amance, it is neighborhood 60 dogs, and not less than 250 cats. But it is also and every month 20000 euros of freshly bound to the functioning of the establishment (salaries, welfare costs, expenses of veterinary care, maintenances of the places etc.), obviously it is also the management of all the emergency, unforeseen situations and of last minutes. But unfortunately, today still, we meet of great difficulties. It is necessary out of the question to give up.

Seul on va plus vite, mais à plusieurs on va plus loin. Notre objectif est de donner une vie la plus normale qui soit à notre petit Tom qui est condamné par une maladie rare et incurable : La maladie de pompe. Tom est soins palliatifs à la maison. Il nous est impossible de rajouter des jours à la vie de Tom, mais nous pouvons ajouter de la vie à ses jours. Pour cela nous avons besoin de vous. Aidez-nous à adoucir le quotidien de Tom ✿

Our NGO "Lueur d' espoir pour Ayden" needs funds to help the Laboratoire médicale de l'Université du Québec in Montréal research into Krabbe disease and other neurodegenerative diseases known as incurable (leucodystrophies), multiple sclerosis and so on. There is currently no treatment available to ensure that these diseases are no longer fatal, which would help saving the lives of babies and children whose life expectancy is too short.

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 "La Ninna" Hedgehogs Recovery Center is located in Piedmont in Novello, in the province of Cuneo in the Langhe and is a center specialized in curing the European hedgehog, in their preservation in order to reinsert them (when possible) in nature in their habitat. The idea of ​​creating a place to care for and assist the hedgehogs was born following the discovery of an orphaned hog of a few grams "Ninna", taken care of by the veterinarian Massimo Vacchetta.

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

More than 2,000 animals are admitted annually to the AMUS hospital; a team of professionals has been formed, which has revolutionized the way of treating injured wildlife with innovative medicine and excellence supported by cutting-edge techniques. The responsibility for each animal operated on, some of them highly endangered and returned to the wild, has made it an entity of excellence. aturaleza make it a decisive entity, with a real contribution to the conservation of biodiversity.

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 54 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.

We rescue abandoned and mistreated animals all around Spain. With your support, all of us together can make this possible! Just 1 euro a month can help us a lot to make these animals' dreams come true!

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!