My Nonprofit Reviews

kittyc
Review for Primary Aldosteronism Foundation, Phoenix, AZ, USA
I was recently diagnosed with PA, however have struggled with PA for over 10 years. Similar stories shared amongst people who have the disease are all too familiar with High blood pressure and struggles with low potassium. I had little to no knowledge of the disease. The PA Foundation has helped me better understand the intricacies of the disease. From Aldosterone, renin, cortisol, adrenals, to the where, how, what’s. I am able to understand and find what I’m looking for from the site. I also have the comfort of knowing that I can reach out to the founders and ask questions at any time. The information on the website is also a powerful tool armed with information, especially before I head to a doctor visit. It allows patients such as myself to be able to self advocate and fight for better care. The site also contains a vast data bank of drs and surgeons all qualified and vetted by patients who treat the disease. The Foundation offers me support that no others can compare to. Most importantly I know that I am not alone. Invaluable.