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Supports medical research into the causes, treatment, and prevention of diseases of the bones, muscles, joints, and skin. Provides free printed educational materials as well as referrals to major professional and voluntary health organizations.

(E-Kokua Club) The Epilepsy Foundation of Hawaii (EFH) offers a free membership to the E-Kokua Club to children, teens, adults, and caregivers. Through monthly cultural healing activities (hula, lei-making, ukulele, art therapy), peer support groups, and seizure first aid education, the E-Kokua Club provides a welcoming, stigma-free community where families can learn, connect, and thrive. In addition, EFH is the local manager of the National Epilepsy Helpline for Hawaii. This means families calling for seizure support, education, or resources speak directly to persons in the islands who understand our communities. Visit the website for more information.

(Alzheimers Association - Hawaii) Care services for family caregivers and persons living with Alzheimer's disease include educational workshops and classes, care consultations and supportive counseling, neighborhood support groups, and information and referral services to community resources. Offers a 24-hour Helpline, 1-800-272-3900, and the MedicAlert+Safe Return™ program to help reunite wanderers with their caregivers. Creates public awareness about Alzheimer's disease, conducts advocacy efforts at the local and national level, and supports research efforts to find a cure or prevention for Alzheimer's disease.

From humble beginnings, the American Heart Association has grown into the nation’s oldest and largest voluntary organization dedicated to fighting heart disease and stroke. A shared focus on cardiovascular health unites our more than 33 million volunteers and supporters as well as our more than 3,400 employees. Learn more about our impact over time. Heart disease is the No. 1 killer worldwide, and stroke ranks second globally. Even when those conditions don’t result in death, they cause disability and diminish quality of life. We want to see a world free of cardiovascular diseases and stroke. From pioneering precision cardiovascular medicine to accelerating drug discovery, we’re leading bold innovations to improve health and wellbeing worldwide. In short, we provide vital tools and information to help people make lifestyle choices that lead to longer, healthier lives. We also advocate for stronger policies that protect and improve the health of our communities by educating lawmakers, policymakers and th

NIH Osteoporosis and Related Bone Diseases National Resource Center is a service provided by the National Institutes of Health. Provides written material on osteoporosis to patients, health professionals and the public in English, Spanish and selected Asian languages (Vietnamese, Chinese & Korean). Also carries materials on other metabolic bone diseases such as Paget's Disease and Osteogenesis Imperfecta. Does not provide counseling over the phone.

The HBF, founded in 1991, is a national nonprofit organization dedicated solely to those affected by hepatitis B. The foundation accomplishes its work with a dedicated staff of researchers, educators, and outreach experts working with physicians, scientists, academic institutions, corporations, governmental agencies, and others to raise awareness and search for a cure to hepatitis B.

Hep Free Hawai'i (HFH) is a coalition of local, national, and global partners dedicated to increasing awareness of and access to viral hepatitis and harm reduction services throughout the state of Hawaii. Born out of a partnership between the Hawaii Department of Health, the CHOW Project (now the Hawai'i Health & Harm Reduction Center), and other community agencies, Hep Free Hawai'i has been successful by connecting with communities across the islands to make Hawai'i truly “Hep Free.” Use the form on the website.

(Epilepsy and Seizures 24 Hours Helpline, Epilepsy and Seizure Helpline, Epilepsy Foundation) The Epilepsy and Seizures Helpline has trained information specialists to answer your questions about epilepsy and seizures and provide you with help, hope, support, guidance, and access to national and local resources.

The American Diabetes Association (ADA) provides trusted resources such as the annually updated Standards of Care in Diabetes, advances research and education through initiatives like Scientific Sessions, and supports youth and families through programs like Camp He Ola Ke Keiki and the upcoming Project Power Youth. We also advocate for safe and inclusive schools through the Safe at School program, engage the public through events such as the Step Out Walk to Stop Diabetes and the State of Diabetes Hawaii. We connect local communities to culturally relevant resources like the ADA Food Hub.

(Jdrf International - Hawaii Chapter) Juvenile Diabetes Research Foundation Southern California and Hawaii Chapter provides an outreach program - adult to adult mentorship that runs by volunteers, provides educational materials and information about diabetes, strives to alert the general public about the seriousness of diabetes, raises money to fund diabetes research, and has an advocacy program where they visit senators, etc. regarding diabetes government funding, children gets to travel to Washington DC to meet senators, etc. and talk about diabetes.

(National Alliance on Mental Illness - Hawaii) NAMI Hawaii provides free mental health support groups and classes for people in recovery and the families that support them. Connection Recovery Support Group -Family Support Group -Family to Family Education -Peer to Peer Education -Family and Friends -Hearts and Minds -Ending the Silence Youth Presentations -NAMI on Campus Youth Clubs -Information and Support -NAMIWalks on Kauai, Oahu, Lanai, Maui, Hilo -Speakers Bureau -Crisis Intervention Team Training for Law Enforcement -Conferences and Workshops NAMI website updated weekly.

Provides case management, counseling, hospital visitation, and support programs. Provides food pantry to clients only. Offers support groups. Conducts outreach to youth, women and high risk populations in the community and work place. Advocates for progressive public policy and effective service systems. Provides free Hepatitis C testing, free HIV testing and free Syphilis testing.

Maintains a national information center for those affected by anxiety disorders, including Panic Disorder, Obsessive-Compulsive Disorder, Post Traumatic Stress Disorder, Generalized Anxiety Disorder, Social anxiety Disorder, and specific phobias. Provides referrals to local treatment providers and local support groups, and provides information on these and related disorders. Publishes an E-Newsletter, Triumph, and detailed pamphlets. Promotes public awareness and education with media campaigns and events. Sponsors an annual conference to encourage researchers in the field of anxiety disorders to share their findings, and funds research.

(St Francis Healthcare Foundation of Hawaii) The role of St. Francis Healthcare Foundation of Hawaii, established in 1984 as an entity of St. Francis Healthcare System of Hawaii, is to raise funds, acquire and hold assets, and provide community education that enhance and support the activities of the healthcare system and our entities.Accepts gifts made by cash, check or credit card is the easiest way to give and provides a tax deduction for the full amount of your gift. Also accepts other types of donations such as cars, please call or write to us for more information on ways to give.

MISSION: The urgent mission of The Foundation Fighting Blindness is to drive the research that will provide preventions, treatments, and cures for people affected by retinitis pigmentosa, macular degeneration, Usher syndrome and the entire spectrum of retinal degenerative diseases. SERVICES: For a $25.00 annual membership fee, FFB offers information and referral services for affected individuals and their families as well as for doctors and eye care professionals. The Foundation also provides comprehensive information kits on retinitis pigmentosa, macular degeneration, and usher syndrome. Our newsletter, InFocus, and our e-newsletter, InFocus online, present articles on coping, research updates, and Foundation news. InFocus is published 3 times per year; InFocus online is sent approximately 3 times per year. Our national conference is usually held every year.

The National Resource Center is SBA's information and connection hub. It links people with Spina Bifida to healthcare providers, local Chapters and support groups, and provides information about a range of topics related to Spina Bifida. Read about SBA's programs and activities at www.spinabifidaassociation.org, and check the Facebook page at https://facebook.com/spina.bifida.learn/

Supports advancements in CF (cystic fibrosis) research by funding its own network of research centers throughout the United States. Accredits and supports 115 CF care centers nationwide to provide high-quality, specialized care for those with CF. Provides referrals and information regarding CF to the general public. Supports extensive clinical trials to test new drug therapies for people with CF. Provides a variety of grants to scientists to conduct CF research.

The Friends' mission is to generate community support for cancer research and education to prevent and reduce cancer-related deaths as well as improve the quality of life of those diagnosed with cancer. The Friends organization was established to support the Cancer Center in their quest to prevent and find cures for cancer in Hawaii. This includes the Center’s education and outreach programs for those battling cancer, and family and friends who care or are caregivers. The Friends respond to and fulfill the UH Cancer Center's need for private funds to supplement federal and state resources by coordinating fundraising events and conducting an annual friendship drive to give people like you the opportunity to play a vital role in the fight against cancer. Donations: [email protected] or [email protected]

Non-profit breast cancer organization working to save lives and end breast cancer forever. We advocate for patients, drive research breakthroughs, improve access to high-quality care, offer direct patient support and empower people with trustworthy information.

Operates a variety of programs to prevent cancer or assist persons with cancer or persons who want information on cancer. Cancer Specialists: On duty with science-based, trusted information 24 hours a day by calling 1-800-227-2345 or you can visit www.cancer.org. Each office is stocked with up-to-date free brochures, books and videos you or your caregiver can borrow. For your convenience, many items can be mailed to you. Patient Services Navigators: Through our Division's Patient Services Center, specialists connect patients with information, resources and support, and help eliminate barriers to needed care. Financial Assistance: A limited amount of indirect assistance is available to any cancer patient in Hawaii for patient services not covered by insurance such as transportation for medical appointments and treatment, breast prostheses, wigs and hats. Referrals to local resources as well as mainland resources too.

(Information and Educational Programs) MS Navigators help connect individuals to the information, resources and support needed to move their lives with multiple sclerosis (MS) forward. These trusted supportive partners help individuals navigate life with MS. Visit the website for more information.

Founded by a group of people with OCD in 1986, the International OCD Foundation (IOCDF) is an international not-for-profit organization made up of people with Obsessive Compulsive Disorder (OCD) and related disorders, as well as their families, friends, professionals and others. The mission and goals of the IOCDF are to:

• Educate the public and professionals about OCD in order to raise awareness and improve the quality of treatment provided;
• Support research into the cause of, and effective treatments for, OCD and related disorders;
• Improve access to resources for those with OCD and their families;
• Advocate and lobby for the OCD community.

Provides information and referral on treatment or support groups for those with obsessive-compulsive disorders (OCD). Publishes newsletter and other materials. Funds research and holds annual conference.

The American Lung Association works to save lives by improving lung health and preventing lung disease, through research, education and advocacy.

HAF partners with various community organizations to assist families with autism access evidenced-based treatment, family support, and other needed resources.

Designed to reduce the incidence of undetected glaucoma, educate primary care physicians and the public about risk factors for glaucoma, offers a glaucoma examination at no cost to uninsured individuals determined to be at increased risk for glaucoma.