News & Annual Reports

The ALSP patient registry pre-study survey is LIVE!

Completing this is the first step for patients who want to participate in the Vigil Neuroscience global digital ALSP patient...
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Kim’s ALSP Story

Kim’s ALSP Story

“In July, I had a genetics test done to see if I carry the CSF1R gene variant the same variant...
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Vigil Neuroscience Enrolls First Subject in ALSP Study

Vigil Neuroscience Enrolls First Subject in ALSP Study

Vigil Neuroscience, a biotechnology company harnessing the power of microglia for the treatment of neurodegenerative diseases, announced today the enrollment...
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Vigil Neuroscience hopes to eventually target ALSP

Vigil Neuroscience hopes to eventually target ALSP

Vigil Neuroscience has revealed the first condition that it will target: a rare, genetic neurodegenerative disorder called ALSP, or adult-onset...
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Vigil Neuro Announces It Is Launching ALSP Programs

Vigil Neuro Announces It Is Launching ALSP Programs

Vigil is conducting an observational natural history study with ALSP patients to better understand the disease and help us inform...
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Bone Marrow Transplant Study on Treatment of CSF1R-Related Leukoencephalopathy

Bone Marrow Transplant Study on Treatment of CSF1R-Related Leukoencephalopathy

This is the largest series of patients with CSF1R-related leukoencephalopathy receiving HSCT. The study concludes that HSCT can stabilize the...
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How To Host a Pink Lemonade Fundraiser for Sisters’ Hope Foundation

How To Host a Pink Lemonade Fundraiser for Sisters’ Hope Foundation

A lemonade stand fundraiser works best during the summer months. Hot days equals lots of thirsty supporters! What you’ll need...
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Heidi Edwards’ Story

Heidi Edwards’ Story

I’m Heidi Edwards, President and founder of Sisters Hope Foundation, a non-profit organization supporting families struggling with Hereditary Diffuse leukodystrophy...
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