Resources are invaluable tools when searching for knowledge, information, answers, options or strategies.
When newly diagnosed or moving to another state, the first thing to do is reach out to the local association or National Hemophilia Foundation Chapter. They will be able to immediately connect you with the nearest Hemophilia Treatment Center, other families to network with, and other necessary social services you may be entitled to. They may also be very helpful to guide you through the insurance maze that lies ahead.
Networking and resources are both opportunistic keys that open the doors to access of quality, experienced care and the means to pay for those treatment services.
Please e-mail us if you want to add to our list.