In the Republic of Moldova, 2,500 patients are diagnosed with rare diseases, half of whom are children. Each confirmed diagnosis “represents an unseen story of a family and a continuous effort of a multidisciplinary team, which does not end their work once they leave home,” mentions parliamentarian and doctor Ana Oglinda.
On the occasion of the International Day of People with Rare Diseases, marked on the last day of February, the parliamentarian sent a message of solidarity, encouraging the community to show empathy and support for these families, notes IPN.
For many patients, the period until a diagnosis is confirmed can last months or even years, marking a long period of uncertainty and questions, some remaining unanswered. Sometimes, the diagnosis is delayed, which can affect the proper adjustment of treatments or necessary interventions.
“We encourage the support of these patients, who are facing not only the medical challenges of the disease, but also emotional difficulties and social inclusion issues, which require psychological support. Equally important are early diagnosis, innovative treatment, replacement therapy, and equitable access to orphan drugs,” emphasized Ana Oglinda.
The parliamentarian highlighted the progress made in the last ten years in the field of genetic and molecular mechanisms, which offer people with rare diseases more treatment opportunities and can contribute to improving their quality of life.
