Supporting Australian Alphas since 2002

Newly Diagonised Alphas

Welcome to the Alpha-1 Association.

You are probably here because you or a family member has just been diagnosed with Alpha-1. Perhaps your doctor didn't tell you much about it. Perhaps he or she told you he has never had a patient with Alpha-1. At this point you have more questions than you have information. The Association is here to help you understand the diagnosis and provide you with the education and support to empower you in coping with Alpha-1.

A serious genetic (inherited) diagnosis can leave you feeling afraid and unsure of what to do next. This can be a very difficult time for you and your family. It is often overwhelming to think about the care, the treatment options, possible lifestyle changes and the effects this will have not only on your life, but on your immediate family. A diagnosis of Alpha-1 could impact your family including brothers, sisters, children and grandchildren and possibly your extended family members.

You may be experiencing uncertainty, anger, fear, guilt, grief, and frustration. These are all normal feelings. Your next step is to learn how to cope with these feelings. You accomplish this through a step-by-step process of:

  • Education:
    Knowledge is the key to understanding the diagnosis of Alpha-1. The Alpha-1 Foundation (based in Florida, US) provides comprehensive information about treatement, diagnonsis, family inheritance/risk factors, testing options, health management and other resources.
  • Medical Care:
    The Alpha-1 Foundation has a network of Alpha-1 Clinical Resource Centers where you can find a specialist in the treatment of Alpha-1.
  • Support:
    We can support your endeavour in dealing with your recent diagnosis through our website, and by helping you to connect to other members. If you require any financial assistance, then please write to us at the following email - This email address is being protected from spambots. You need JavaScript enabled to view it.
  • Testing:
    For information on Alpha-1 testing, please click here to visit the Alpha-1 Foundation's webpage.

The most important message to share with you today is that you are not alone! The Association is here to help you—to answer your questions, refer you to physician specialists, provide you with literature, refer you to other resources, and, if you wish, to connect you with other Alphas who have faced this diagnosis and who are taking charge of their health and their life!


 The AAA has produced an information booklet which contains more detail about A1AD, and a poster for raising awareness. You can access the booklet and poster by clicking on the images below. The poster may be printed locally in A3 or A4 size. Please encourage your family doctor or respiratory physician to put a poster on display in the surgery or patient waiting area! For more information about A1AD, see our Links section.