Petition Increase funding for research into and treatment of STXBP1 encephalopathy

STXBP1 encephalopathy is a rare genetic condition characterized by abnormal brain function (encephalopathy) and intellectual disability.

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We want the Government to increase funding for research into and treatment of STXBP1 encephalopathy, to help sufferers and their families.

We believe the NHS is far behind other countries in their knowledge of and treatment available for this terrible condition. Additional funding could held address this gap, and identify new treatments.

This petition is closed This petition ran for 6 months

111 signatures

Progress of the petition towards its next target: 111 of 10,000 signatures required to get a government response

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10,000 signatures required to get a government response

Date closed 11 January 2024
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