Your (or your loved one’s) medical records contain clues that can lead to new treatments.
AllStripes researchers learn from patient records what would truly improve quality of life.
Using cutting-edge tech we analyze your community’s data to improve trial design and chances of success.
Your community’s de-identified records can advance multiple treatment studies.
We do the work to collect all your records, at no cost, in your secure account. Access doctors’ notes you’ve never seen.
See how your rare disease journey compares to others with your condition, and what’s helping.
We’ll send you exclusive updates on the studies you’re contributing to and how you’re driving forward research.
Sickle cell disease is a group of blood disorders that affects the red blood cells, which are important for moving oxygen throughout the body. People with sickle cell disease have abnormal hemoglobin, which is the protein in red blood cells that carries oxygen. In sickle cell disease, a difference in the HBB gene leads to an abnormal form of hemoglobin called hemoglobin S. Some people with sickle cell disease have two copies of HBB with the difference causing hemoglobin S, one inherited from each of their two parents. This is called sickle cell anemia. Others have one HBB gene causing hemoglobin S and another copy causing another form of abnormal hemoglobin.
Hemoglobin S causes "sickling" of the red blood cell, in which the red blood cell is shaped like a C-shaped farm tool called a sickle. These sickle cells break down too early, leading to anemia, and may also get stuck in small blood vessels, blocking blood flow and causing pain, infections, organ damage and stroke.
Treatments that may help mitigate symptoms of sickle cell disease include medications such as hydroxyurea and red blood cell transfusions. Stem cell therapies can be curative but also present risks and are not an option for many patients.
The latest on our research: We are jumpstarting our sickle cell disease program to accelerate research on the disorder to ultimately improve treatment options. We welcome all parents and caregivers interested in participating and spreading the word to the sickle cell community.
1. Sign up
Create your private account and review our research consent (takes about 10 minutes)
2. We get to work
We do all the behind-the-scenes work to retrieve and process your records
3. Impact research
Power multiple research projects at once by contributing your de-identified data
We believe that the only way to keep data accessible to the researchers who need it is by enabling patients to own and control their own data. Patients decide for themselves whether they want to privately and securely contribute to research, rather than having the decision made on their behalf.
We aim to make useful data accessible to all researchers who have legitimate research questions or research programs. For academic research, we offer access without charge. We take research ethics seriously, and we have policies in place to ensure that research is conducted with integrity.
We don’t like to take sides—we give all members of the community the option to get involved. Success in rare disease research takes a village and we always welcome additional collaborators who can advance and benefit from the mission.
Our primary mission is to accelerate drug development, so we prioritize generating insights specifically relevant to therapeutic research. We invest deeply in quality, security, and compliance to make this a reality.