Metachromatic leukodystrophy

Support Type
Support Services
  • MLD Foundation

    We C.A.R.E.™ – The MLD Foundation’s global mission is reflected in four areas of purpose that start with people and families … facilitating Compassion, increasing Awareness, influencing Research, and promoting Education for metachromatic leukodystrophy.

    We are active in rare disease advocacy, newborn screening, registries, FDA policy, and “educate” regularly on Capitol Hill.

    The MLD Foundation collaborates with other leukodystrophy and lysosomal disease organizations globally. We are also quite active in global rare disease issues.

    Disease Support Organization Last Updated: 30 Jan 2019
  • The Stennis Foundation

    Raising awareness of the Leukodystrophies, and raising funds for Leukodystrophies research.

    Disease Support Organization Last Updated: 30 Jan 2019
  • Contact a Family

    Contact a Family improves the lives of all families with disabled children. With them, we transform their lives, break down barriers and tackle disadvantage through ambitious, collaborative and innovative work. We make a real and lasting impact and are a force for positive change.

    General Support Organization Last Updated: 13 Nov 2018
  • Advocacy for Patients with Chronic Illness, Inc.

    To provide free information, advice and advocacy services to patients with chronic illnesses, in areas including health and disability insurance, Social Security disability, employment discrimination, school-based accommodations, and resource location.

    General Support Organization Last Updated: 13 Nov 2018
  • Any Baby Can, Inc.

    Any Baby Can serves families that have a child under the age of 13 with a chronic illnes, developmental delay or health risk, through case management and other support services.

    General Support Organization Last Updated: 13 Nov 2018

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