Progress in rare disease research depends on sustained financial support. Funding allows Team ALD to make advancements in several areas: developing cutting-edge diagnostics, investigating disease mechanisms through lipidomics and cellular studies, documenting the natural history of the disease through our Dutch ALD cohort and biobank, conducting clinical trials, and expanding newborn screening programs worldwide. Every contribution, whether from foundations, patient organizations, or research grants, accelerates our ability to provide answers to families facing uncertainty and brings us closer to effective treatments for all forms of X-linked adrenoleukodystrophy. Below are organizations that support our mission.
