The Hemophilia Association of New Jersey is committed to serving the needs of our patients and their families in the bleeding disorder community; providing the most up-to-date information to the community. Please do not hesitate to contact us with any questions or concerns you may have.

  • Assist with insurance premium payments if financially eligible.
  • Assist with medical co-pays and deductibles if financially eligible.
  • Monitor insurance companies to see if they comply with hemophilia homecare standards law.
  • Advocate with insurance companies on behalf of members.
  • Review insurance policies if companies switch policies or during open enrollment.

**Please see Services Tab for more information about the Medical Insurance Grant Program.

  • Direct financial assistance, access to insurance coverage and help with getting grants for the services described here.
  • Professional counseling referrals.
  • Development of outreach and peer networking programs.
  • Campership programs for children with hemophilia.
  • Scholarships for persons with bleeding disorders.
  • Homecare delivery program monitoring.
  • Advocate for our members.
  • Literature concerning hemophilia, von Willebrand disease and HIV free of charge.
  • Public education.
  • Quarterly newsletter.
  • Website.
  • Annual meeting held in May (open to all members).
  • Educational mailings, bulletins and advisories, etc.
  • Seminars.
  • Provide information and guidelines to state/federal legislators regarding issues of importance to persons with hemophilia.
  • Monitor all newly introduced legislation pertaining to healthcare, medical insurance and blood safety.
  • Secure laws which preserve policies and programs required by the bleeding disorder community.
  • Advocate.

Click here for what’s important in new legislation