My Nonprofit Reviews

I wish the Primary Aldosteronism Foundation existed when I was experiencing symptoms - when I was diagnosed the only place to find information was a Facebook page but imagine how many people are not on Facebook or don’t find that page- what if the page gets hacked or goes away? The Foundation is doing absolutely crucial, much needed work for PA and I am so grateful. I am luckily cured, but lived with excessive aldosterone in my system wreaking havoc for 15 years. I know because of the foundation, others like me, will not have to wait 15 years and will not have to do the amount of leg work I did to get proper care since so few doctors truly understand how to properly diagnose and treat PA. For new patients, they have amazing resources for you. For doctors, this will help them in properly diagnosing and treating this condition. Thank you Primary Aldosteronism Foundation!