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Alpha-1 Antitrypsin Deficiency (Alpha-1) is an inherited genetic condition that affects the body's ability to produce alpha-1 antitrypsin, a protein that helps protect the lungs and, in some cases, the liver. Because it is passed down through families, there is nothing you did to cause it. Although Alpha-1 is considered a rare disease, it is often under-diagnosed, leaving many people unaware they have the condition for years.

A diagnosis provides answers and a path forward. While learning you have Alpha-1 can feel overwhelming, it is also the first step toward understanding your health and receiving the care you need. With regular monitoring, healthy lifestyle choices, and treatment when appropriate, many people with Alpha-1 are able to live active, fulfilling lives.

Treatment recommendations vary based on your specific diagnosis, symptoms, and lung function. Your physician will work with you to determine the most appropriate course of care and whether treatment is recommended at this time. For eligible patients, augmentation therapy is often administered as a weekly infusion and can frequently be received in the comfort of your home.

Yes. Because Alpha-1 is an inherited genetic condition, family members may also be at risk. If you have been diagnosed with Alpha-1, it's important to talk with your physician about whether your parents, siblings, and children should consider testing. Testing may be completed through a healthcare provider or with a confidential at-home testing kit. In many cases, a diagnosis in one family member leads to the identification of others who may benefit from early awareness and appropriate medical care. Tests can be done by doctor or at home with confidential self tested kits.

Concerns about the cost of treatment are common, and it's important to discuss them early. AvevoRx helps eligible patients explore and enroll in third-party financial assistance programs that may help reduce out-of-pocket expenses and make treatment more accessible.