The parts nobody else sees
Sickle cell disease is invisible work: pain that arrives without warning, blood counts that move with your medicine, water and warmth to plan around, and emergency rooms where the story has to be explained from the start. Healya is built by people who know what that load feels like.
A pain crisis can start without warning and keep you in bed or in the emergency room for days.
Your hemoglobin runs below the lab's normal range, and your care team watches it against your own baseline.
With sickle cell disease a fever is an emergency, and it often means the emergency room that day.
Your numbers already tell a story
Healya connects your blood counts, your pain days, your fluids, your medicines and what your watch sees so the story is visible, to you and to your hematologist.
Your hemoglobin at each three-month draw over two years, eight draws, with the draw where your hydroxyurea dose was raised marked. It climbed from 8.1 to the low nines, held between 9.0 and 9.3 for a year, then came back at 7.6 on Oct 14.
Your neutrophil count (ANC) at the same eight draws, with the draw where your hydroxyurea dose was raised marked. A lower count is expected on hydroxyurea, which is why it is drawn every time: yours came down from 4.6 and has held near 2.7 for the last year, inside the range on your report.
Pain days you logged in each of the last twelve months, as bars and as a line, with the month you went to six-day weeks marked. Two to four a month before it, then five in that month and six, seven and nine in the three months after.
Diagnosed at birth, years into treatment, or just starting to count your pain days: your counts and your pain days are data, and Healya can keep the story.
How Healya helps with sickle cell disease
A record that catches a run of pain days
A thirty-second check-in of pain, fluids, temperature, sleep and what changed that day, so a run of pain days that builds over a month is visible to you and your hematologist instead of lost between blood draws.
Labs explained in plain words
Your hemoglobin, neutrophil count, platelets and the yearly urine albumin check that watches for kidney strain: what each one measures in plain words, which way it moved since last time, and what is worth asking about at the next visit.
Check-ins that pair the numbers with the day
Pain score, fluids, temperature, medicines taken, hours slept, steps from your watch and what changed that day, side by side, so a pain day sits next to the cold snap, the long day and the short sleep around it.
A summary your hematologist can scan
A year of blood counts, pain days, emergency room visits, hospital stays and medications on one page, with the questions worth asking. Fifteen-minute visits go further when the story is already organized.
No wearable required. A thirty-second daily check-in is enough.
Reports written for sickle cell disease
Three kinds, each built from your own record. A summary before every hematology visit. A report on how your counts and pain days are actually moving. And a plain-language digest of new sickle cell research, on a schedule you choose.
Questions people with sickle cell disease ask us
Clear answers about what Healya does with your data, and what stays between you and your care team.
Bring your story together
Your blood counts, pain days, fluids and medicines in one place before your next appointment. Free for a week, no card required.