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

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