The municipality of Bitola has announced a public call for support for people with rare diseases. It is about financial support for people with rare diseases, who are in an unenviable position, and the Municipality will financially help them with travel expenses to hospitals outside Bitola. -During last year 2023, for the first time at the proposal of the mayor...
"Sloboden Pechat" has unofficially learned that a child who was in a private hospital ten days ago received medicine that cost over 100.000 euros, but the medicine was given by the Clinic for Children's Diseases in Skopje. In the show "Sloboden Pechat" on Slobodna TV, we asked Dr. Aspazija Sofianova if the information we received is correct. - I am no longer...
The latest report from the European Commission on the country's progress notes the problem with the lack of doctors in Macedonia, healthcare is identified as one of the most corrupt areas, cancer screening and support for patients with rare diseases are poor. Additionally, in Macedonia, according to the EC report, there is a shortage of certain medical specialties, and the ratio of doctors and...
The municipality of Bitola, at the proposal of the mayor Toni Konjanovski, will allocate one million denars (about 16.000 euros) to support people with rare diseases from the city at the next budget rebalancing session. This was announced today by Konjanovski at the working meeting with the members of the Association of People with Rare Diseases from Bitola, held with the aim of understanding...
The citizens' association for rare diseases "Life with challenges" today marked February 28 - the Day of Rare Diseases. The first lady Elizaebta Gjorgievska opened the exhibition dedicated to rare diseases and said that the goal of this month and of this day dedicated to rare diseases is to increase visibility before the entire Macedonian public, and at the same time...
Rare Disease Day: Disease cannot erase a person's inherent dignity Read More »
