GA1 Glutaric Acidemia Guard

Built for parents and caregivers of infants and children with glutaric acidemia type 1 — GA1, also written glutaric aciduria type I, caused by glutaryl-CoA dehydrogenase (GCDH) deficiency. You track on your child's behalf, and the app is designed around the two jobs that matter: everyday metabolic tracking and being ready when illness strikes. Everyday mode: • Food log with lysine tracking — recent foods refill name, portion and lysine mg in one tap • Daily lysine intake bar against your dietitian's plan • Medication doses, including acute/crisis medications, and caregiver notes Crisis mode, one tap away: • Your emergency protocol and contacts, front and center • Illness checklist designed for stressed 3am use — large targets, clear text • One-tap event logging: fluids, urine output, nausea, diarrhea, weight — with the last weight shown for comparison • Everything time-stamped so the metabolic team can reconstruct the day Insights and PDF reports give your metabolic clinic a clean history of intake, meds and events. Log from your wrist: an Apple Watch companion app is included for quick one-tap entries that sync to your phone. Your data stays on your device — no account, no sign-up, and your health information is never uploaded to our servers. Export everything anytime as CSV or a PDF report. This app is a tracking and preparedness journal for caregivers. It is not a medical device and does not provide medical advice, diagnosis, or treatment. In any suspected metabolic crisis, follow your emergency protocol and seek medical care immediately.