SCW Video: Pain From A Shower
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Living with Sickle Cell
ASGCT Patient Education on Blood Disorders
What is this? The American Society of Gene & Cell Therapy (ASGCT) is proud to announce the first release of the Society’s Patient Education program, a new initiative for 2019. The new patient-centered portal is designed by ASGCT committee volunteers in coordination with patient advocacy groups to educate and inform patients, families, and the general
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Manual For Life by Paulo Andre Chenso
PAULO ANDRÉ CHENSO is a doctor and professor in London. He created a “MANUAL FOR LIFE”. IT’S WORTH A READ AND TO PUT IN PRACTICE. IN THE HEALTH: 01. Drink a lot of water. 02. Eat more what is born in trees and plants. 03. Live with the 3 E’s Energy. Enthusiasm and Empathy 04.
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Warrior University Online Series
Dear Sickle Cell Community, Join a 5-week webinar series on the topic “Blood Transfusions: What You Need to Know and Do”. The interactive series will include in-depth information on blood matching, iron overload, blood donations, and patient-provider communication techniques/skills. Register here for the educational series: https://ghpc.wufoo.com/forms/the-warrior-university-online-series/ *Registry and Education for Hemoglobinopathies and Hemovigilance/Transfusion Therapy in Georgia
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Holistic Health and Sickle Cell Disease Webinar
Holistic Health and Sickle Cell Disease: A focus on Mental and Behavioral Health Thursday, February 28, 2019 1:00 – 2:15 pm EST Register Here Sickle cell disease (SCD) affects millions globally, disproportionately impacting certain racial and ethnic minority populations, including African Americans, Latinos and people of Middle Eastern, Indian, Asian and Mediterranean descent. According to
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Heart’s Truth Facebook Live 2/26
Join The Heart Truth’s Facebook Live at noon EST on Tuesday, February 26 to see how heart healthy cooking can be fun, especially when you do it together! We’re over halfway through American Heart Month 2019! This month, we have been focusing on how #OurHearts stay heart healthy at work, with our friends and family, and in
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Rare Disease Day Countdown!
Hello warriors! We have just over a week until February 28th, which is Rare Disease Day! In the US, a rare disease is defined as one that affects a minor population of less than 200,000 people. Sickle cell disease falls under the collective umbrella of Rare Diseases, so its another great opportunity to spread the
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Water is Life
Water is a very powerful thing. Cultures as old as time have worshiped it. It flows throughout all the lands, connecting the entire world, teeming with life, feeding the entire population of living things. Our bodies are made up of 80% water. Planet Earth has more than 70% made up of water. Water is life.
SCW Video: Flying Across the World with Sickle Cell
Have you ever taken a cross country or international trip with sickle cell? How was your experience? Have you ever wanted to take an international trip but didn’t know where to begin? Come on a journey with Tosin as she sojourns to her homeland of Nigeria. Sickle cell came too…of course! Share your international or
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