COMMUNITY
European Resources
The following websites have been provided as a source of information, directing you to other resources and services specific to LAL-D.
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This link will take you to a website with a different privacy notice and terms of use. The links are provided as a courtesy for informational purposes only. We do not make or imply any endorsement of external websites.Hosted by trusted patient advocates, RareConnect is a place where rare disease patients can connect with others globally. Patient organisations partner with RareConnect, itself an international patient organisation, to create communities and provide moderators from within their network.
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LAL-D your way
This link will take you to a website with a different privacy notice and terms of use.
The links are provided as a courtesy for informational purposes only.
We do not make or imply any endorsement of external websites.
EURORDIS is a non-governmental patient-driven alliance of patient organisations representing 962 rare disease patient organisations in 73 countries.
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This link will take you to a website with a different privacy notice and terms of use. The links are provided as a courtesy for informational purposes only. We do not make or imply any endorsement of external websites.Metabolic Support UK is a leading patient organisation for Inherited Metabolic Disorders, supporting thousands of families worldwide that have no other support.
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This link will take you to a website with a different privacy notice and terms of use. The links are provided as a courtesy for informational purposes only. We do not make or imply any endorsement of external websites.Orphanet is a unique resource, gathering and improving knowledge on rare diseases so as to improve the diagnosis, care and treatment of patients with rare diseases.