Finally Free: Man’s Pain Relieved 32 Years After Diagnosis
Sibel Çakır, born in Denizli, had been struggling with severe abdominal pain since the age of 3. After multiple hospitalizations and interrupted education due to health issues, Çakır’s condition remained undiagnosed for years. It wasn’t until 2001, when Çakır became a faculty member at Ege University, that a breakthrough occurred.
After genetic testing, Çakır was finally diagnosed with “Hereditary Angioedema”, a rare hereditary disease. The treatment began, and Çakır’s symptoms started to improve after 32 long years of struggling with unknown health issues.
In an interview, Çakır expressed relief at finally receiving a diagnosis, stating that her life had gotten back on track. With proper medication, she was able to lead a more social and active life, putting an end to years of fear and uncertainty.
Dr. Nihal Mete Gökmen, President of the National Rare Diseases Association, emphasized the importance of early diagnosis for rare diseases like Hereditary Angioedema. Due to the confusion with allergies and other conditions, patients often face late diagnoses and unnecessary treatments.
Gökben Yurdakul, President of Hereditary Angioedema Patients Solidarity and Assistance Association, shared her own experience with the disease, highlighting the need for increased awareness and support for patients. With many undiagnosed individuals still suffering, the association works tirelessly to connect at-risk individuals with proper medical care.
Overall, Sibel Çakır’s journey serves as a reminder of the importance of timely and accurate diagnoses for rare diseases. With proper medical attention and support, patients like Çakır can finally find relief and reclaim their lives from years of uncertainty and pain.
