A rare disease research charity, Finland



We fund the research that will treat and one day cure SLC35A2-CDG, so that our children get to dream about their own lives.


Cure SLC35A2 funds the next step. The science on this mutation exists, built by researchers over years; what it lacks is money to carry it forward. We fund laboratories to do that work, each project with a result we can name and a date we can point to.


Started by one family in Helsinki. Built for every child with this gene.
Fewer than 100 published cases · No approved treatment