The HEA Website Project
by Betty Engel, HEA Webmaster
Our newly-updated website went online in December, 2011. I'm still moving some of the old website content to this new site. Everything (stories, surgery blogs, newsletters in web format, etc.) should be moved over by the end of January, 2012.
This website contains more information than the old site. The content is being written by the members of the HEA community so that it is both accurate and written from an insider-perspective, from their own experiences and the experiences of other community members.
We don't have all the answers, and some of the content is controversial. But we can offer information that is relevant and based on real life experiences. We can't say we're a representative sample of all people with HS or ES or related conditions, but we can offer what researchers call the deep understanding not possible in statistically-based research, textbooks, or medically-based websites.
We are seeking help from any HEA website user who is willing to pitch in and write some of this new content. We'll help you if you need help, but only you can provide the deep understanding based on your own experiences that our website visitors need and can't find elsewhere. To participate, send email to the link below.
Can you improve on or add to the content on this page or other pages? Send email here.