Anika is a small and cheerful girl from Gornji Milanovac who in the earliest days of her life faced a big problem – a very rare disease called spinal muscular atrophy type 1. This disease leads to muscle atrophy because the body lacks the gene that produces the protein. It starts with large muscle groups such as the arms, legs, neck, but after a while the muscles for swallowing, coughing and breathing also atrophy.
Until now, Anika received Spinraza as a therapy to slow down the disease, but that is no longer enough. In order to solve the problem permanently, Anika must resort to the new genetic therapy Zolgensma.
Her parents firmly believe that all people with a big heart will join the action and help raise money for therapy, travel and treatment.
We responded with 50,000 din, and we invite you to pay as much as you can into their current account. Our little is a lot for someone!
Dinar account: 160-6000000732571-65
Foreign currency account: 160600000073290242