Donation
For Simon

Help and give Simon a better quality of life

Simon is a bundle of energy. "He doesn't like sitting still at all," laughs his mom, Tamara. Things didn't look good for him at first. Four months of his life in the children's hospital - it was uncertain whether he would survive would survive was uncertain. But Simon is a fighter, has since survived two major heart Heart operations and is developing magnificently. Hippotherapy to support his development and at the same time give him carefree moments give him carefree moments.

Therapeutic riding for Simon

Already it was discovered in the 17th week of pregnancy that Simon was a "hypoblast" is a "hypoblast". "Hypoplastic left heart syndrome (HLHS) is one of the worst heart defects heart defects in children. Many of those affected die in the first few weeks of Weeks of life," says his mother. On the seventh day of life, the Newborn underwent heart surgery for the first time on the seventh day of life another major operation followed. "Since then, our son has been steadily improving and we sometimes forget that he has such a serious heart defect," says Tamara. If it weren't for the medication he has to take every day.

Simon's family thanks you for your donation

Simon loves animals more than anything and has two rabbits at home. To Support his development, they were recommended therapeutic riding (hippotherapy) was recommended. The aim of of this form of treatment is to loosen tense muscles, promote balance Balance and strengthen the core muscles. Hippotherapy Hippotherapy is not paid for by the IV and is not affordable for parents affordable for parents. Tamara: "On behalf of Simon, we would like to thank you very much for all the donations!"

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Support association for children with rare diseases
Around 350,000 children and young people in Switzerland are affected by a rare disease.

Everyday life for these families is characterized by uncertainty, especially when there is no diagnosis yet. The Support Association for Children with Rare Diseases has been committed to helping affected children and their families since 2014. We provide direct financial support, create free family events (more than 2,200 family members were able to take part in 2019) to connect affected families and raise awareness of rare diseases among the general public. We rely on donations, legacies and patronage contributions to make this possible in the future.

Link KMSK donation flyer