The Cure ALD Foundation, a public non-profit organization, provides support and education to those suffering from ALD or AMN, as well as to their families, friends, caretakers and doctors and funds research in complementary medicine to find a cure.
The problem with the current Western Medical Treatments as well as the future treatments Scientists are working toward is that none of them follow their own creed of “First do no harm.” We are only interested in funding medicine that follows this creed.
We are a non-profit, 501(c)(3) organization, whose mission is to orchestrate cutting-edge, collaborative research with the goal of expediting the creation of effective treatments and therapies for children with ALD and Adults with AMN, and related problems.
In addition, it's our goal to provide families and health care providers with user-friendly access to state-of-the-art information and education supporting their decision-making processes and:
a) To help educate patients inflicted with ALD/AMN on alternative therapies and assist them financially to pay for those therapies
b) To educate the public, bringing awareness to the disease and earlier diagnoses through Lectures at schools, Newspaper articles, Television, Radio, and our Website
c) To educate doctors, and students in medical and science fields through our School Lectures, Mailings to doctors and hospitals, Lectures at hospitals, as well as our Website so that we might fund medical research in areas not typically addressed by the science community because it is not profit driven. These areas would include any alternative medicine that may give hope to a cure for ALD/AMN and are not limited to, but may include Acupuncture, Homeopathy, and other energy medicines, Aromatherapy, Herbs, Vitamins and other natural supplements.