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To serve, educate and fund research for families coping with the effects of SYNGAP mutations.

Our primary goal is to help underwrite life-saving medical treatment and research throughout the United States for catastrophically and terminally ill children (and adults) battling, but not solely limited to, cancer and aids. Further, to underwrite aid to women battling breast cancer, as well as purchasing respite homes throughout the United States for families supporting loved ones undergoing treatment at various speciality treatment centers. Likewise, to advocate against health insurance companies and any other organization and/or firm that would deny any claim filed by an individual who is disabled and requires benefits, help and/or assistance. The success of our organization over the last thirty-five (35) years is due substantially to the generous help and support of retired judges, attorneys at law, congressmen and senators and a host of other individuals throughout the United States. Altruistic by nature, these individuals have provided invaluable assistance –– often at no cost –– to help us safeguard the rights of catastrophically and terminally ill children (and adults) to life-saving medical care throughout the United States.

DEAAF, Deaf Education & Arts for African Families, is a not-for-profit organization committed to providing much needed schooling to deaf children within the African continent. Our goal is to provide education, assist in poverty and hunger alleviation, and encourage the local community and government to become actively involved to ensure deaf children have an educational future that is often taken for granted in more well developed countries.

Improve the spiritual and social well-being of young people in poor communities by means of education and personal support. To give underprivileged children and young people the chance to develop themselves intellectually, emotionally, psychologically, and spiritually by means of education and personal coaching. The organization wants to see young people developing their (hidden) talents and gifting and in doing so escape the vicious circle of poverty.

The core activities of the Foundation include supporting education, research, and missionary medical aid to those who need health care within the United States and abroad.

The National Fibromyalgia & Chronic Pain Association unites patients, policy makers, and healthcare, medical and scientific communities to transform lives through visionary support, advocacy, research and education of fibromyalgia and chronic pain illnesses.