Rare Condition Causes Mum’s Face to Swell up ‘Like a Puffer Fish’
Ashley Hoskins, a 36-year-old mum of four, has a rare condition causing her face to swell three times its size, resembling a puffer fish. Initially mistaken for allergies or infection, her diagnosis in 2019 revealed type III hereditary angioedema, which can be fatal if swelling occurs internally, like in the windpipe or lungs. Stress triggers her flare-ups, affecting her daily life and mobility. Despite finding relief through an expensive IV treatment, her struggle highlights the challenges of living with a little-known condition, advocating for awareness to prevent delayed diagnoses.
Living with Daily Challenges
Ashley’s condition, causing frequent facial and bodily swelling, impairs her ability to walk and function normally. Her supportive husband, Dustin, helps her navigate the physical and emotional toll of the disease. Constant hospital visits, misdiagnoses, and severe pain episodes, including the need for a hysterectomy, illustrate the debilitating impact on her life. Despite facing judgment and embarrassment due to her appearance, Ashley maintains a positive outlook and humour, trying to lighten the weight of her condition.
Raising Awareness for Type III Hereditary Angioedema
Ashley’s journey sheds light on the challenges faced by those with rare conditions like type III hereditary angioedema. Delayed diagnoses, lack of cure, and the need for expensive treatments pose significant obstacles. By sharing her story, Ashley hopes to educate others about the condition’s complexities, symptoms, and the importance of timely recognition. Her advocacy aims to empower patients, healthcare providers, and the community to improve understanding and support for those living with similar conditions.