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