APS Foundation of America, Inc.
June 6, 2011
I was diagnosed with APS October 2010. When I first learned of my diagnosis I was scared and confused. The first thing that I did when I got home was throw myself into the internet to learn everything I could about APS. I came across APS foundation of America, and I have to say it was a sigh a relief. There is so much helpful information and it was written in a way that whoever was reading could understand it. I love the fact that they have a facebook, and on that facebook are so many people that have APS and can relate. I dont ever feel uncomfortable posting a quetstion because the people that are on there know what I am going thru and will not look down on me. I am greatful for a organization, it helps me in many ways understand my diagnosis and my family can go onto the site and get more of a insight of what I am going thru. In many ways it is my outlet when I am going thru my "down days". I am truely greatful.
I've personally experienced the results of this organization in...
I have met many people who are also diagnosed with APS, there is a sense of connection with people on there since they know what I am going thru.
Ways to make it better...
If I had to make changes to this organization, I would...
I wouldnt change a thing.
General Member of the Public & I have shared this website with numerous family and friends, in hope that they can have a better understanding of APS.