Eosinophilic Granulomatosis with Polyangiitis Fund

Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare autoimmune disease that causes swelling and damage in small and medium-sized blood vessels. It happens when the immune system attacks the body’s own tissues, especially in the lungs, nerves, skin, and digestive organs. People with EGPA often have a history of severe asthma, chronic sinus infections, and high levels of eosinophils (a type of white blood cell). The symptoms can vary but may include numbness, fatigue, pain, rashes, and trouble breathing.

Over time, EGPA can lead to serious problems like heart inflammation, nerve damage, or organ failure if it’s not treated. Treatment usually includes medications to lower inflammation and control the immune system. Supportive therapies help with asthma symptoms, pain, or mobility issues. With early diagnosis and the right treatment, many people can manage their symptoms, but relapses and complications can still occur.