Genetic Testing:
Because every patient deserves a diagnosis
Because every patient deserves a diagnosis
Genetic conditions affect millions, yet most people wait years for an answer, cycling through wrong treatments, unnecessary procedures, and missed opportunities. A single diagnosis can unlock the right treatment, open doors to clinical trials, and identify risk in family members before symptoms ever appear. Knowing your genetic makeup isn't just useful - it's the starting point for everything that follows.
Consider genetic testing if you or a family member:
for these conditions
ADH1 is a common form of genetic hypoparathyroidism caused by gain-of-function variants in the calcium-sensing receptor gene (CASR).
Hereditary transthyretin amyloidosis (ATTRv) is a type of amyloidosis that is caused by a change in the transthyretin (TTR) gene.
Limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9) is a rare, neuromuscular condition caused by variants in the fukutin-related protein (FKRP) gene.
to fit your needs
Order a no-cost test kit to your location; return by mail after completion.
Request no-cost, on demand genetic testing and sample collection.
Genetic Testing Tour Summer ‘26
Because answers shouldn't depend on access, we will be coming to you, making stops all along the west coast. Washington. Oregon. California. Arizona.
Our tour will focus on ADH1 & Hypoparathyroidism.
Want us to come to your community? We will be adding stops along the way, so don’t hesitate to let us know.
Arielle, Living with ADH1
Explore the websites of the NSGC, CDC & NIH for general information and genetic testing resources.