.
Last Sunday's New York Times Magazine had an article
about the web site PatientsLikeMe.
This site has been mentioned on MSNews
before and is a community where you can share data about your disease and learn
from other people with similar experiences. The article talks about how people
are using the site to their benefit and features some users who have MS. It also
discusses broader issues relating to use of personal data and the Internet in
healthcare. Well-worth reading, particularly if you're curious to learn more
about PatientsLikeMe.
*Note:
I visited this site and it seems like a good tool for those of us
with MS. The article is more in depth and is an excellent
read.
MS_Kitty70
