Doctors and nurses, even our friends and family often see us as “the sickler” Hard Global Launch September 2019 . We will have a story featured every day (or several features every week) on the website and on all our social media. #SCWLiveBig
The #ShowYourRare campaign was launched in 2018. The campaign has inspired the Rare Disease Day 2019 poster and videos. Rare diseases affect an estimated 300 million people around the world. There are over 6000 different diseases. So rare’s not so rare after all. Support the rare disease community by showing your rare. With your help, we can raise awareness
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
Rare Disease Day Countdown! Read More »
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.
[vc_row][vc_column][vc_column_text custom_title=”USING THE INTERNET TO FIND HEALTH INFO” header_color=”#dd3333″] The pros and cons of finding information on the Internet The Internet (Web) can be a good source of sickle cell disease information. Within a few minutes, you can learn about the latest sickle cell disease research, find a clinical trial or confirm a hematologist is
Using the Internet to find Health Info Read More »
Sickle Cell Warriors, Inc. is a non-profit charitable organization dedicated to elevating education, empowerment, advocacy, and awareness about sickle cell disease. Our mission is to inspire those affected by sickle cell. As of this minute, you are no longer alone. You have us—and we have you. Welcome to the Warrior family. WHO WE ARE The
Did you know that your #SickleCell Birthday is around the corner? SCW shares her personalized letter to friends.
It’s Your #SickleCell Birthday!!! Read More »
What are your plans to celebrate World Sickle Cell Day? I hope you have some…if not…get some!
June 19th is World Sickle Cell Day! Read More »
Registration Hello Warrior Family, Registration is now open for the 2018 Annual Sickle Cell Patient & Family Educational Symposium. To learn more visit www.sicklecellconvention.com. In conclusion, this is the same one that we have done for the past 3 years. It will be in Los Angeles, CA from July 28-31. Above all, hope to see
Registration Open for Sickle Cell Patient & Family Convention 2018 Read More »
If you have an e-reader or an iPad or tablet, then you want to get some free ebooks! When I don’t feel well, sometimes all I do is read or study. I have always loved to read, since I was a child. Almost from the beginning, I have had an e-reader. I recently underwent surgery
Free and Almost Free Ebooks by April Farrell-Hasty Read More »
