Rarebase News

Read our latest updates.

Video: Drug discovery for rare diseases

Rarebase Team | Aug 15, 2022

Celebrating Our Second Anniversary

Rarebase Team | Jul 23, 2022

Fundraising best practices for rare disease foundations

Brittany Anderton, PhD | Jul 20, 2022

Using mathematics to provide a rare disease roadmap

Brittany Anderton, PhD | Jun 27, 2022

Rarebase Remarks Episode #2 - Chris Moxham: Drug hunting for rare disease

Rarebase Team | Mar 16, 2022

A path forward, for one or for many

Onno Faber | Feb 28, 2022

Rarebase Remarks Episode #1 – Lynsey Chediak: Never give up

Rarebase Team | Jan 24, 2022

Photograph by Winnie Wintermeyer

The Champion for Rare Disease Cures (neo.life)

Neo.life | Sep 27, 2021

Mariah Gillaspie, the Founder and CEO of the Lightning and Love Foundation, reads a book to her daughter Emma who is affected by THAP12 epileptic encephalopathy.

Rarebase launches a neuroscience drug discovery platform collaborating with 15 rare disease patient organizations

Rarebase Team | Sep 14, 2021

MRI Scan of one of my brain tumors in 2015

What does it mean to find a “cure” for a disease?

Onno Faber | Aug 03, 2021

It’s Monday. It’s still Rare Disease Day.

Onno Faber | Feb 26, 2021

Translating science into therapies, for one or for many.

Onno Faber | Nov 19, 2020