Dear colleagues: Thanks to all those who sent me resources regarding congenital disorders so far. A few very good English-based websites have been added to my list. But I have not added any NON-ENGLISH resources, nor any non-Internet-based resources. Surely other countries have some version of the (US) March of Dimes Birth Defects Foundation or the (US) National Organization of Rare Disorders or the (UK) Birth Defects Foundation...! So, if you are lactnetting from Israel, Belgium, the Netherlands, Japan, Mexico, Egypt, Antarctica or anywhere outside the US (actually, I'm happy to get more US ideas, too), where do you refer mothers of nurslings with a congenital disorder when they need more information and support (which would be, in my rough estimate, 100% of the time!)? Please email me privately. (By the way, my spell-checker suggested I replace "lactnetting" above with "lactating." That would probably work well, too!) Anxiously awaiting some global assistance, Cynthia Good Mojab (Breastfeeding mother, advocate, independent [cross-cultural] researcher and author; LLL Leader and researcher in the LLLI Publications Department; and former psychotherapist currently busy nurturing her own little one.) Ammawell Email: [log in to unmask] Web site: http://ammawell.homepage.com *********************************************** The LACTNET mailing list is powered by L-Soft's renowned LISTSERV(R) list management software together with L-Soft's LSMTP(TM) mailer for lightning fast mail delivery. For more information, go to: http://www.lsoft.com/LISTSERV-powered.html