She went to "hell and back" for a diagnosis. Then her sister showed symptoms.
Megan Koverman's weight gain, fatigue, high blood pressure and other symptoms were dismissed for years before she was diagnosed with a rare heart disease.
Megan Koverman endured a harrowing journey to receive a diagnosis at the age of 18, experiencing weight gain and shortness of breath. Despite multiple doctor visits and emergency room visits, her concerns were dismissed. When she was 25, sudden severe fatigue and breathing difficulties led her to a rare genetic disorder called heritable pulmonary arterial hypertension.
She was determined to stay optimistic and found relief at the Cleveland Clinic, where she was able to return to daily life. Her sister, Katie Gusching, then 32, began showing similar symptoms after delivering her first child. After rigorous testing, Gusching was also diagnosed with heritable pulmonary arterial hypertension. Both sisters sought treatment at the Cleveland Clinic and participated in clinical trials to develop new care options.
Despite the challenges, they have found silver linings, such as being able to travel together and rekindle their shared experiences.
Written by urgent.news from CBS News's reporting — not their text. Machine-written — it may contain errors, so check the original before relying on it.
