Be a part of a digital memorial booklet. Warriors, we have had our hearts broken. We have lost many amazing warrior friends, families, and brothers and sisters-in-blood. We wept, we suffered, we mourned, but we are not defeated. Still we rise. Join us and the entire sickle cell warrior family as we celebrate and honor […]
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pre-register and watch the sickle cell disease therapeutics conference here live sickle cell disease awareness month warriors
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A Virtual Symposium Hosted by the HHS Office of Minority Health Advancing the Response to Covid-19 September 17, 2020 | 12:00 PM to 6:00 PM ET The Response to Covid-19 meeting features several things. Firstly, promising practices, programs, and strategies for combatting the pandemic in order to achieve health equity in communities of color. In
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Blueprint for Action – Report Release Webinar Addressing Sickle Cell Disease through a Strategic Plan How are we addressing sickle cell disease? On September 10, 2020, from 2:00 PM to 3:00 PM ET, join the National Academies of Sciences, Engineering, and Medicine for a webinar. They are releasing a new report on SCD in the
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Register here for the new Mental Health Initiative, a free benefit provided by the Sickle Cell Warriors, Inc., community. The program details are below. This program is for warriors, by warriors, to warriors and funded with donations from the SCW community.
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Learn more about the sickle cell scholarship sickle cell disease. This education scholarship is for sickle cell warriors scholarship whoo are pursuing higher education. Will help with tuition for school.
Tuition Scholarship: First Annual Read More »
Ready to join us for the sickle cell disease Livestream? Join here for the sickle cell conference disease therapeutics conference sickle cell disease pre register for livestream here at sickle cell warriors
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Increasing Appointment Attendance: A Vital Opportunity to Improve Health Outcomes for Those Living with Sickle Cell Diseases August 10, 2020, 3:30 – 4:30 p.m. ET To make health outcomes better, national rules for routine follow-up appointment every six months. More often for patients on specific drugs or having probelms. Yet, a 2019 national study showed that
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Sickle Cell Data Collection Program “Unite Sickle Cell: Collaboration and Community in Sickle Cell” Wednesday, September 18, 2019 1:30 – 3:00 PM PDT Register now: https://attendee.gotowebinar.com/register/2843093377260613389 Presented by Dr. Nik Rashid and Ms. Linetta Barnes from Nevada and Ms. Mary Brown and Ms. Jennifer Fields from the Sickle Cell Disease Foundation of California. Tracking California’s
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WEBINAR SERIES Sickle Cell Science: Path to Progress To commemorate Sickle Cell Awareness Month 2019, this September the National Heart, Lung, and Blood Institute (NHLBI) and partner agencies and institutions will host Sickle Cell Science: Path to Progress, a four-part webinar series that will discuss genetic therapies, progress in pain management, bone marrow transplants and other therapies, and
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