The Cure ALD Foundation is a public non-profit organization founded in 2003 by Diane Suchomel after her son, Wyatt, was diagnosed with Adrenoleukodystrophy or ALD. The Cure ALD foundation seeks to 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. Please feel free to search our site to learn more about ALD, our family, and how you can help.