Background on the condition, and on what we're trying to do here.
[ Add a plain-language explanation here: what the FARS2 gene does, what goes wrong when it's mutated, and how the condition typically presents. ]
[ Add background on who's behind FARS2.org, how the research is being funded, and how the site will be kept up to date. ]
[ Add guidance here for families who just received a FARS2 diagnosis — what to expect, who to talk to, and how to get in touch with this project. ]