Cure Kcnh1 Foundation

Cure KCNH1 was formed out of desperation – our children are very sick, and there are currently no treatments available.  Families are faced with a ticking clock; every day that goes by without a treatment causes additional damage to our children’s developing brains and bodies.  Our goal is to fight for a better future where one randomly-mutated nucleotide doesn’t define their entire lives.  Life-altering gene therapies and drug treatments have been approved for other severe genetic disorders, the technology exists, but as far as traditional drug development companies are concerned, KCNH1 is “too rare to care.”  That’s why it is up to us to make this happen.  Our foundation must raise the necessary funds to develop treatments and cure KCNH1.