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Scientists are finally close to understanding what causes Warburg Micro,  a Hereditary Spastic Paraplegia called SPG69. By acting now, you can help complete these discoveries and change children’s lives.

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Rare disorders

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People with WMS

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To Fund Drug Discovery

The Warburg Micro Research Foundation announces

the 2022 Patient Registry

If your loved one has been diagnosed with Warburg Micro please complete the patient registry survey. Click here for more info.

Are you a scientist or researcher?

Research = Hope
It's our mission to improve lives.

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Warburg Micro is a complicated form of hereditary spastic paraplegia.

Researchers are closer than ever to understanding what causes WMS and how to treat it.

Newly Diagnosed?

You are not alone.

Find resources for your family.
Check out our list of clinicians and therapy centers and connect with others fighting this disorder.