The LPL Deficiency Association™ is the first nonprofit organization in the United States who mission is to provide support, education, awareness, and access to services to patients with lipoprotein lipase deficiency (LPLD), their families, caregivers, and medical professionals.

Are you or someone you know living with lipoprotein lipase deficiency (LPLD)?

People living with rare diseases can feel isolated as they struggle to find information and connect with others like themselves.

The LPL Deficiency Association™ is a new organization that provides support, education, awareness and access to services for patients, their families, caregivers and medical professionals of LPLD.

With the new LPL Deficiency Association™, you’ll never again have to face this disease alone.

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Do you know the symptoms that might indicate your patient has LPLD?

Would you be able to help him or her?

The LPL Deficiency Association™ helps support medical professionals with online and downloadable resources and materials including our physician guide, informational handouts, medical articles and information on diagnostic testing.

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You can improve a life.

Help a patient and their family by raising awareness.

Volunteer.
Donate.
Spread the Word.

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