Adrenal Alternatives Foundation Team represents the cortisol deficiency demographic directly in congress through the Rare Disease Legislative Caucus. Our team proudly serves on the COVID19 response, Public Policy and Healthcare Access congressional committees.
Currently we are supporting the following legislation.
We will be attending RARE DISEASE WEEK ON THE HILL in July of 2021.
You can watch our latest Townhall meeting at the video link below:
Adrenal Alternatives Foundation is a 5o1c3 nonprofit patient advocacy organization dedicated to education, advocacy and encouragement for all adrenal disease. EIN: 83-3629121.
We appreciate all contributions which allow us to further our mission, Education, Advocacy and Awareness for all adrenal disease. We also accept donated insulin pumps and supplies for our Pumps for Purpose Program.