Sickle Cell AF
@SickleCellAF
Life is good but we can make it better.|| Its all about the awareness of the world we are living. || Living at large
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Happy #WorldSickleCellDay! In collaboration w/@sicklecellmattrs we are posting important #sicklecell facts. We encourage you to repost these facts and other content under the hashtag #RepostForSickleCell. Let's combine our efforts and raise awareness on a large scale.
We have to preserve ourselves for the cure! Listen to our first episode today, #WorldSickleCellDay. We are talking about the current state of #sicklecell. Listen to The Sickle Cell Podcast on iTunes, Google Play, and other podcast platforms. Let us know what you think!
On Dec 22, 2008 the General Assembly of the UN recognized #sicklecell disease as a global public health concern. This resolution encouraged raising awareness at an international level on June 19 annually. The first #WorldSickleCellDay was celebrated in 2009. #RepostForSickleCell
Over 2.5 million people do not know that they have sickle cell trait. Often times they discover their trait status when they have a baby born with #sicklecell disease. Knowing your sickle cell status is important. #RepostForSickleCell #SickleCell101 #WorldSickleCellDay
When I lived w/#sicklecell disease I remember my first day of kindergarten — closing my eyes to check if I was feeling pain anywhere in my body. I didn’t. I felt completely normal. That would be the last time I would feel normal for a long time. #BoneMarrowTransplant @BeTheMatch
In a study conducted by evolutionary biologist, Fred Piel and his colleagues, they estimated a 30% increase of sickle cell disease births, primarily in #Nigeria and Democratic Republic of #Congo. Sickle cell education on screening for trait is needed. #RepostForSickleCell
Sickle cell is not witchcraft! There are places that still think it is. Listen to our 1st episode launched today. We're talking about the current state of #sicklecell. You can listen to The Sickle Cell Podcast on iTunes and Google Play (in bio). Let us know what you think!
More than half of the world’s sickle cell population live in #Nigeria, #Congo, and #India. Nigeria leads with anywhere from 90,000 to 150,000 babies born with sickle cell disease each year. #RepostForSickleCell
These influencers used their platform to raise awareness, support our #repostforsicklecell campaign and/or #WorldSickleCellDay. Huge thank you to @uamshealth @WHURfm @GBT_news. The #repostforsicklecell campaign received over 10.5k likes, comments, and shares. Thank you!
We are warriors #inobewaste @SAMIupdate @TVCconnect @iamtoyinadesola @SickleCellAF @sicklecellngos @CrimsonBowSCI @tmospeaks @LadyOMary @chyzandy @moakabash
#SickleCellTheTeacher #YourFellowSickler #FIGHTdontGiveUP SPRINKLING A LITTLE POSITIVITY AND UNDERSTANDING. #THANKSSICKLECELL
#honour @ Oranfe instagram.com/p/BegeWOqh9pj/
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the365HUB (@the365hub) • Instagram photo
the365HUB (@the365hub) • Instagram photo
Tonight at 7pm est in the Bold Lips For Sickle Cell Group Page on FB with SCCA Clayton Andrews talking about Sickle Cell & Mental Health
Check this out...very informative! #YouAreWhatYouEat #BeHealthy #EatHealthy #SickleSmart fb.me/7wRvjosVv
Boy With Rare Genetic Disorder in Desperate Need of Bone Marrow Transplant ms.spr.ly/6016rL8Xy via @nbc6
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