Some of you may have seen the article referencing AboutBFS at Slate ().
Well, you may interested to know that I was not aware that article had been written - the editors / writer at Slate never contacted me! Be that as it may, I am grateful that the site got some coverage as a wider audience can only help to make people who are experiencing the kind of fear that many of us have had in past more aware of the forum.
Interestingly, I actually received word of the article from a reporter at The Independent - a national newspaper in the UK. He interviewed me yesterday about the site and about "Cyberchondria" in general for a feature hi is writing. Again, I am thankful that the site may receive some wider exposure so that more people can find support here and BFS will be more widely known. I will let you know if / when anything comes of that.
As I described to him, after I was diagnosed I saw the need to provide a dedicated space on the web for info and support for BFS sufferers and had the technical expertise and time to throw together this site. However it has been you, the forum participants that have been the lifeblood of this forum and have really made this a community that welcomes users to a place that people can "find support, get information, have your questions answered, and raise awareness about this illness".
As a commenter @ the Slate article mentioned - "I briefly perused aboutbfs.com. I was impressed by how supportive and reassuring the posters were." This is to your credit, not mine and this is what has allowed the site to fulfill that mission and grow beyond my original vision.
My thanks goes out to Aaron and garym who have helped me moderate the site over the years, and also to those regulars in the forums who have given so much of their time to be active in them as well.
I am always open to comments, ideas, and concerns about the site and forums, so please don’t hesitate to contact me.