United Leukodystrophy Foundation
About United Leukodystrophy Foundation
The United Leukodystrophy Foundation (ULF) is a voluntary, non-profit organization dedicated to helping children and adults with leukodystrophy and assisting the family members, caregivers, and professionals who serve them. Leukodystrophy is a group of rare, progressive diseases that affect the white matter of the brain. Established in 1982, the United Leukodystrophy Foundation is committed to the identification, treatment, and cure of all leukodystrophies through programs of education, advocacy, research, and service. The foundation also provides appropriate referrals, including support groups; promotes professional and patient education; and offers a variety of educational and support materials. These include a regular newsletter, brochures, and audiovisual aids.
Related Rare Diseases:
- Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
- Cerebral Folate Deficiency
- Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation
- Acute Disseminated Encephalomyelitis
- CARASIL
- Cerebrotendinous Xanthomatosis
- PMM2-CDG
- Leukodystrophy
- PLA2G6-Associated Neurodegeneration
- Zellweger Spectrum Disorders
- Refsum Disease
- Metachromatic Leukodystrophy
- Pelizaeus-Merzbacher Disease
- Canavan Disease
- Alexander Disease
- X-Linked Adrenoleukodystrophy
- Aicardi-Goutières Syndrome
- Síndrome de Aicardi-Goutieres
- Leucodistrofia
- Encefalomielitis aguda diseminada
- Leucoencefalopatía de inicio en el adulto con esferoides axonales y células gliales pigmentadas
- Krabbe Disease
- Enfermedad de Krabbe