On February 28, We Celebrate Rare Disease Day

February 28 marks Rare Disease Day—a day dedicated to raising awareness and supporting individuals affected by rare and often underrecognized health conditions. This day highlights the urgent need for better diagnosis, innovative treatments, and scientific research that can transform the lives of those living with rare diseases. Among these conditions, interstitial lung diseases (ILDs) deserve […]
Second Annual CILDAPANET Meeting

Second Annual Meeting of the project Central & Eastern European ILDs Patient Network – CILDAPANET (www.cildapanet.org) will take place on 14 December 2024 in Sofia, Bulagaria
World Lung Cancer Month

November is dedicated to raising awareness and providing support for lung cancer patients, the most commonly diagnosed cancer and the leading cause of cancer mortality worldwide. According to the latest data from the International Agency for Research on Cancer (IARC), nearly 2.5 million people were diagnosed with lung cancer in 2022, and over 1.8 million […]
CILDAPANET Final meeting for 2023

CILDAPANET Final meeting for 2023 will take place on 24/11/2023 at 17:00 CET.
Face2Face CILDAPANET Meeting

Face2Face CILDAPANET Meeting Idiopathic Pulmonary Fibrosis Association held from 01-03 September, 2023 in Roslyn Central Park Hotel Sofia the First Annual Meeting of the project Central & Eastern European ILDs Patient Network – CILDAPANET (www.cildapanet.org). Within two days, medical specialists from the country and abroad informed the Bulgarian and foreign participants – patients and […]
CILDAPANET Summer Virtual Meeting

CILDAPANET Summer Virtual Meeting will take place on 21 June 16:30-18:00 CET
CILDAPANET First meeting for 2023

CILDAPANET meeting – 30.03.2023- 16:30 h
Rare Disease Day 2023

What is rare disease day? Rare Disease Day is the official international awareness-raising campaign for rare diseases which takes place on the last day of February each year. The main objective of the campaign is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients’ lives. Rare Disease […]