What are some organizations that can help a family cope with a child's hemophilia?

Hemophilia groups: The hemophilia websites i find most valuable (and accurate) belong to the national hemophilia foundation and world federation of hemophilia.

Hemophilia foundatio: Your best bet would be to call your local hemophilia foundation, or hemophilia treatment center. You can google it, obtain the telephone number and location. Once you do that, i bet that you find abundance of resources. Hemophilia support group, hemophilia camp, and other patients' and parent's organizations have very good educational and support activities.