MISSION

Programs

  • HCC Future Leaders

    Each year young men and women ages 14-22 come together in spring from all over California to Sacramento for a unique learning experience with HCC's (Hemophilia Council of California). Teen and young adults learn how California government works and the programs that support people with bleeding disorders throughout the state.

    Learn how to tell your story to legislators about living with a bleeding disorder and how to be an advocate for yourself and others.

     

    Future Leaders also learn about career choices, and challenges for people with bleeding disorders, and meet other young people from across the state who want their voices heard. If you would like to receive more information about this program please contact HCC: phone: (916) 498-3780 or email: hccassist@aol.com

  • Asian Infusion

  • B Leaders

  •  Blood Brotherhood

    HFNC is partnering with the Hemophilia Federation of

    America's Blood Brotherhood Program.

     

    The Blood Brotherhood is the HFA’s flagship program for adult men with hemophilia and von Willebrand.  Designed to be a multi-avenue outreach to provide education, social support and a sense of community, the program reaches men with in three ways.

     

    • Online forum:  Join to register and get connected! http://hemophiliafed.net/hfabb/
    • Face-to-face local BB Meetings on our pilot site: http://programs@hemophiliafed.org
    • National Blood Brotherhood Call/Webinars see:
    • site: http://programs@hemophiliafed.org

     

    Check our Events page for updates and flyers.

  • Family Education Day

    Our annual Family Education Day provides comprehensive learning by

    keynote speakers who are experts in the medical community.

    Past year’s program have included topics such as:

     

    • Emotional Health
    • Women’s Support Group
    • Building Great Relationships
    • vWD Understanding
    • Affordable Care Act Update
    • Vendor’s Booths

     

    Check our Events page for updates and flyers.

     

  • Camp Hemotion

    In 2017 Camp Hemotion will be celebrating its 40th year!

     

    Camp Hemotion is a week-long outdoor camp for kids and teens with bleeding disorders to play, bond, and learn. See Camp page for information and applications.

    If you would be interested in volunteering please contact Patrick.

  • The Female Factor

    We are a large group of women in the bleeding disorders community that have come together to form The Female Factor. We invite and provide outreach, leadership guidance, advocacy opportunities, networking, education and support to any and all women in the bleeding disorders community. Many mothers, daughters, sisters etc. are undiagnosed with our own bleeding disorders. We are working tirelessly to affect change for proper diagnosis and treatment for all women affected.

     

    Check our Events page for updates and flyers.

  • Legislation Day

    HCC’s annual Legislative Day is a chance for members of the bleeding disorders community to come together and meet with key members of the Senate and Assembly to educate them about hemophilia, other co-diagnoses, and issues of concern to the bleeding disorders community.

     

    Because of the ongoing budget crisis this is a crucial time for the bleeding disorders community to come to the capitol to advocate for protection of programs and services used by people with bleeding disorders. HCC is also enforcing the Standards of Service legislation for home healthcare providers that we passed, and community support is vital to the success of the bill.  Come to the State Capitol this spring and make your voice heard in support of programs and services crucial to the bleeding disorders community!

    For more information, please contact Heidi Scanlan at hccassist@aol.com or

     (916) 498-3780.

     

  • Hispanic Heritage

     

    Each year the symposium

    celebrates Hispanic culture, and provides health

    information and education for our Spanish speaking

    families and the community at large.

     

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THIS SITE IS DONATED AND MAINTAINED BY A PARENT AND DESIGNER MICHELLE HIGGINS

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