My Nonprofit Reviews
Review for APS Foundation of America, Inc., La Crosse, WI, USA
I was diagnosed with this rare blood disorder a little over 20 years ago. Because it is rare, it is difficult to easily find reliable information or to meet people who share this same diagnosis. Through this organization's online community, I have learned more about my illness and gained friends that are able to offer support/advice when I am having challenges.
I've personally experienced the results of this organization in...
In receiving a minimum of weekly postings from their Director, Tina Pohlman.
If I had to make changes to this organization, I would...
hope to see it continue to grow in staff and services.