Donation
for Mina

Intensive therapy for Mina: better quality of life

Mina had a severe cerebral hemorrhage after birth. The cerebral palsy also causes recurrent seizures. Although Mina can walk and talk, she is restricted on the right side of her body. Her cheerful nature makes her the ray of sunshine in our family and in her environment. Thanks to her strong will, she has already achieved a great deal. With the two weeks of intensive therapy at the Adeli Center, we as parents are convinced that we can significantly improve her overall development and provide her with the best possible support.

Mina's life

Mina's start in life was turbulent and very emotional for us as a family. One day after her birth, she had a severe brain haemorrhage and spent the first month in the neonatal unit. There was a lot of uncertainty every day. But we also had a lot of confidence, hope and positive thoughts right from the start. Her older brother Fynn is very supportive and we are very grateful for that. As a family, we always manage to bring as much "normality" as possible into everyday life alongside all the therapies. However, this also requires a lot of creativity and flexibility. Mina's situation has worsened over the past year and she keeps complaining of pain when walking. Her pointed foot is getting worse and worse. We see therapy as a great opportunity to improve this. So that Mina can move without pain and doesn't lose the joy of movement.

Mina's illness

Hemiparesis is a paralysis of one half of the body in which residual activity may still be present. There is a reduction in strength in the face, arm and leg in one half of the body. In Mina's case, the hemiparesis was caused by a brain haemorrhage after birth.

Mina has the following symptoms:

SYMPTOMS

- impaired sense of balance

- Spasticity on the right side of the body (arm and leg)

- Dystonia (involuntary movement disorders)

- Seizures

- Visuomotor weakness

- Concentration and learning difficulties

Mina's family thanks for your donation

We hope that Mina will always remain so cheerful and positive. She wants to accept as little help as possible and continue to be independent. We became aware of the therapy through other affected families who have had positive experiences. This makes us feel very positive and we are convinced that it adds value for us as a family. The aim is to travel to Slovakia once a year.

On behalf of Mina, we would like to thank you for every donation!

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Would you like to start a crowdfunding project as an affected family?

Are you registered in our KMSK Family Network and would like to use crowdfunding to give your affected child (up to the age of 18) a better quality of life?

We are happy to support you and offer you our platform to realize your crowdfunding project in just a few steps.

There are no costs for you and we will cover the bank charges so that the target amount is paid out without any deductions. If the target amount is not reached, we will pay you the amount raised in the 100 days.

Are you interested? Write us an e-mail so that we can send you the registration form: info@kmsk.ch

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 affected families is characterized by uncertainty, especially when there is no diagnosis yet. The Support Association for Children with Rare Diseases has been working on behalf of affected children and their families since 2014. We provide direct financial aid (CHF 3 million has been paid out to families so far), organize free family events (more than 10,000 family members have taken part since 2014) to connect the 830 families in our KMSK network, and share knowledge about rare diseases with (newly) affected families, specialists and the media.

We rely on donations, legacies and patronage contributions to make this possible in the future.

Link KMSK donation flyer