Helping you improve your health and wellbeing.
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Request admission into the programme through your Physician or download the app and request admission.
We will connect with you, your GP, your physician and treatment centre to ensure you get all the information you need.
We enrol you into the programme and start improving the quality of life and outcomes for you.
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Health should never come at the expense of your privacy. Your records are encrypted, protected and under your control. You decide what you want to share.
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At Project Eleven, we run focus groups with the purpose incorporating the patient voice directly into the development of the unified Sickle Cell Disease data platform. The goal of this is to assess how patients feel in the context: psychological wellbeing, wearables. By gaining a deep level of insight around the specific needs of the patient, the aim is to fully incorporate the patient voice into future developments, ensuring all features are aligned to what will benefit patients day-to-day. Please email us if you want to join our next focus group.
Much of the current system for monitoring Sickle Cell Disease rely on scheduled blood tests and diaries for self-reporting, which can in many cases show a low adherence rate long-term. We believe that, automated monitoring and tracking of vital metrics via wearable devices will reduce the need for patients to have to actively record these themselves, making life easier for people living with SCD, while also providing higher quality and more in-depth data to clinicians to improve quality of care.
Help us revolutionise Sickle Cell Disease health outcomes & research
We are always exploring more ways we can support patients, if you have any ideas we would love explore your ideas!