We’re creating the world’s smartest doctors, including yours.
Albright™ brings experts and AI together to solve your mystery illness.
Your doctor may not recognize obscure conditions. It’s our job to help them.
Did you know?
1 out of 10 people has a rare disease, many of which are triggered by infection, nutrient deficiencies, or other environmental factors.
45 million Americans go on a diet each year, which means that millions of people are experimenting on themselves with diet and supplements.
Restrictive diets often lead to nutritional deficiencies that can exacerbate an underlying medical condition.
There are common environmental hazards that can affect anybody, but are especially harmful to people with rare diseases.
Albright™ uses artificial intelligence to predict and prevent illness.
When something goes wrong with your health, it creates a molecular signature in different types of biomedical data. Our patented diagnostic algorithms help us pinpoint the origin of a disease. With this level of resolution, we can quickly resolve an obscure condition and help match patients with the right specialists and therapies.
If you are struggling with an unresolved medical issue, it’s hard to know where to turn for help.
What We Do
Albright™ is a personal health advisor
Albright™ is designed to connect the dots between your genetics, your environment, and your health. As you build your personal health profile, Albright™ asks questions and offers feedback about how to navigate life’s everyday choices.
You make the observations, Albright™ provides the oversight
Our tracker apps help you visualize your health story. By helping you monitor yourself and your environment, Albright™ helps identify potential triggers and risk factors. Over time, our algorithms grow more predictive as we match your distinct symptoms to our catalog of solved cases.
Albright™ helps you dive deeper
When chronic health problems arise, it’s often difficult to pin down the cause. Albright™ helps you get access to genetic testing and novel laboratory-derived diagnostic tests for a deeper investigation of your underlying medical concerns.
Albright™ gets smarter every day
Albright™ features a team of biomedical experts and researchers that work together to solve mysterious illnesses. When the team solves an obscure case, the solution becomes part of our extensive medical library that we share with clinicians. Our resolution gets better with every user, which means that Albright™ will eventually solve anything and everything.
We are currently signing up participants through research studies at Stanford University. Follow the link below to learn more about the study and to get on the waiting list.
What People Are Saying
“I kept getting spells that felt like low blood sugar when I exercised. I would also get symptoms like muscle cramps and a woozy feeling in my brain when I tried intermittent fasting. Doctors kept checking me for diabetes, but my blood tests were always normal. Albright figured out that I have rare genetic variants that affect how I use fats for fuel. I’m 50 years old— doctors never considered looking at my genetics before. Now I avoid fasting and I keep snacks in my purse for emergencies. I also shared my information with my regular doctors so that it’s part of my medical records.
DC from California
“I have a problem with common food additives like baking soda and citric acid. They affect my kidney so that I can’t concentrate urine— the condition is called “diabetes insipidus.” No one has ever reported this particular reaction to baking soda before, and it’s not in any scientific literature. I’m helping Albright experts study this rare phenomenon, and they connected me with researchers in the UK and Australia. I guess I’m one in a million. :-) The good thing is that the condition is easy to manage if you know what to look for, and I’m happy to teach other doctors and other rare disease patients about it.”
RO from California
“I was a high performance athlete before I got sick with Chronic Fatigue Syndrome. I used to load up on lean protein at every meal. I didn’t know that eating fish every day would expose me to toxic levels of mercury. I guess pregnant women are told to avoid fish because of the health risks, but nobody ever told me (a 29 year old man).”
ME/CFS Case from California
After learning about the dangers of mercury in fish using Albright, it reminded me that I broke a mercury thermometer in my college backpack. I was exposed to toxic vapor in my bedroom for months! Mercury intoxication is such a rare problem that doctors probably wouldn’t even recognize it. Fortunately, my doctor heard about it from the Albright experts and connected me with a neurologist and a toxicologist for follow-up.
ME/CFS Case from Europe
“I got diagnosed with Chronic Fatigue Syndrome several years ago. I have all of the classic symptoms like fatigue, brain fog, sleeping problems, and post-exertional malaise, and I’ve seen several ME/CFS specialists. Albright showed me that I have a rare genetic condition that affects my immune cells, and they measured a whole set of cytokines and inflammatory markers that proved that I had active but low-simmering disease. Now I’m working with a new specialist and I’m finally getting answers.”
ME/CFS Case from California
“I went to the emergency room with symptoms of extreme muscle stiffness and a racing heartbeat. The doctors checked me for a heart attack and told me nothing was wrong. They didn’t notice that I was thirsty, had no urge to breathe at all, and had to go to the bathroom several times during my visit. It’s frustrating and scary when doctors don’t have answers. Albright™ showed me that I’m a carrier of a rare genetic condition that affects my kidney function. I was actually causing the symptoms with one of my dietary supplements!
XC from California
“I did my own genetic testing with 23andMe and I found something that said I was low in tetrahydrobiopterin (BH4). There are no commercial tests for BH4 unless I get a spinal tap done, and I’ve never been sick enough to need one. But low BH4 explains why I get a tremor sometimes and it potentially explains why my father has Parkinson’s Disease. I am part of a discussion board of other people with these BH4 mutations, and we worked with Albright to set up a research study to measure BH4 in plasma. It’s been great to work with scientists who listen to us".”
Patient advocate in California
