We are here to help. When you are newly diagnosed or have relocated to a new state, the first thing to do is reach out to your local association or National Hemophilia Foundation Chapter. They will be able to immediately connect you with the nearest Hemophilia Treatment Center, families to meet, and necessary social services.

Networking and resources are keys that open the door to quality, experienced care, help with the means to pay for those treatment services, and an improved quality of life.

These resources are a starting point – please reach out if you need additional questions.

• Treatment centers
• Mental health resources
• Nonprofit and government organizations
• Pharma resources
• Camps and family weekends