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.
Warm autoimmune hemolytic anemia (wAIHA) is an autoimmune condition that causes a person’s immune system to create antibodies that attack red blood cells. This leads to anemia, which is a shortage of red blood cells carrying oxygen throughout the body. Anemia can cause symptoms such as fatigue, muscle weakness, shortness of breath while exercising, abnormal paleness of the skin, palpitations and dizziness. Some patients have more severe symptoms, including loss of consciousness due to a sudden fall in blood pressure, chest pain, abnormally fast heartbeat and heart failure. wAIHA can onset at any age but is most commonly diagnosed between 50 and 70. Current treatments are supportive and include corticosteroids, artificial antibodies, removal of the spleen, blood transfusions and immunosuppressive therapies.
The latest on our research: We are jumpstarting our wAIHA program in collaboration with the wAIHA Warriors to accelerate research for this condition. We welcome all patients, caregivers and researchers interested in participating and spreading the word to the wAIHA 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.