Thank you for visiting my fundraising page!

Donating through this website is simple, fast and totally secure. It is also the most efficient way to support my fundraising efforts.

In 2005, after several years of respiratory infections and numerous doctor visits, I was diagnosed with a hereditary lung disorder called Alpha-1 Antitrypsin Deficiency (AAT Deficiency or Alpha-1). Alpha-1 is a genetic disorder that can cause liver and lung disease in children and adults.  Alpha-1 is the most common genetic risk factor for COPD.   My story is much like the average Alpha patient, who experiences symptoms for more than 8 years and sees 3 doctors before being correctly diagnosed with Alpha-1.  Alpha-1 is easily diagnosed with simple blood tests.  There is no cure at this time, although there is treatment to slow the progress of this genetic disorder.

Contributions to the Alpha-1 Association help provide funding for the many programs and services we provide to the Alpha-1 Community. These include our network of patient support groups, myriad of educational programs, grassroots advocacy efforts and other specialized services. We are committed to making a difference in the lives of Alphas and their families on a daily basis.
Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too!