The Hepatitis Foundation International (HFI) is a voluntary health organization focusing on increasing support for research to find effective treatments and cures for viral hepatitis while promoting liver wellness and the adoption of healthy lifestyle behaviors to prevent hepatitis and substance abuse. HFI's Foundation for Decision Making Train the Trainer programs include effective communication techniques for skills building, videos and print materials for healthcare professionals, teachers, counselors, and patients. Training has been conducted for health departments, Centers for Substance Abuse Prevention and Treatment, for drug rehabilitation counselors, clinical, occupational and school nurses, physician's assistants and mental health professionals, and other private and public organzations.

The MAGIC Foundation (MAGIC) is a national non-profit tax exempt organization focusing on growth related issues in children and adult related disorders. With over 600 disorders affecting growth, MAGIC assists with networking and education on a multitude of disorders, including, but not limited to, Growth Hormone Deficiency and all disorders related to growth hormone therapy; renal deficiencies such as CRI; tumors that now require replacement hormone therapy; many syndromes such as Turner Syndrome; Russell Silver Syndrome; McCune-Albright Syndrome; Panhypopituitarism; Congenital Adrenal Hyperplasia (CAH); and many more. Our annual educational program in July of each year consists of numerous distinguished and recognized speakers in the field of endocrinology and other related fields. MAGIC's educational and supportive services are recognized worldwide as a leader in family support. Contact MAGIC to learn more or with any questions related to a growth disorder.

NPF is the only national not-for-profit group dedicated to scientific research in all forms of pancreatic disease - both pancreatitis and pancreatic cancer. Over the past 6 years, we have funded 32 research projects. We also support patients and doctors through our website, literature, patient education nights, workshops for scientists, support groups, and advocacy efforts.