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#Repost @sicklecellga
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They want to know if we exist , They want to see us in action. The Day at the Capitol is the Most important day of the year. A day for us to show how important we are. The day for Sicklecell families not just warriors ,to show up and be heard.
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Thanks to @eastlondonlines for their article about the #SouthLondonLink project and the need for more blood donors: eastlondonlines.co.uk/2020/0… @GiveBloodNHS #SickleCell #BloodDonation #GiveBlood
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Kobe was a legend on the court and just getting started in what would have been just as meaningful a second act. To lose Gianna is even more heartbreaking to us as parents. Michelle and I send love and prayers to Vanessa and the entire Bryant family on an unthinkable day.
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The Colour of Pain is a brand new multi-media exhibition exploring the experience of sickle cell. Open from 1st November to the 12th December at Imperial College London. Find out more here: ow.ly/tQty50x3oX0 #ColourOfPain #SickleCell #Exhibition
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Please follow @dralexkumar on @Novartis_NSB as he is sharing stories from patients with #sicklecell disease in Ghana as part of our #takeoverweek series:
1/ "There is misunderstanding combined with stigma and discrimination about #sicklecell disease (SCD)." @DrAlexKumar #takeoverweek #AccessStories #AccessinAction
Novartis Social Business | Sickle Cell Disease in Ghana
Alex Kumar, a medical doctor and photographer, is travelling in Ghana and collecting stories from patients with sickle cell disease (SCD).
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A little inspiration for today.
You are not your age,
Nor the size of clothes you wear,
You are not a weight,... fb.me/1U0cCGBUt
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Pregnancy & Sickle Cell Anemia; What you need to know -> scdjournal.com/files/37.pdf
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Thanks to a clinical trial, some are being completely cured of their sickle cell disease. abc7.ws/2gHCYNX
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#DYK January is National Blood Donor Month? Learn more about the importance of blood donation: ow.ly/iFld3087V5h #texaschildrens
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Working with our partners TANSCDA during the launch of Sickle Scan fb.me/8le5cmQOh
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Thank you for everything. My last ask is the same as my first. I'm asking you to believe—not in my ability to create change, but in yours.
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"The power of hope"
First Lady Michelle Obama brings it back to the Obamas' enduring message in her final official remarks.
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Yes we are... SickleCell Miracles! Knowing how this illness works and the fact of us still… instagram.com/p/BKtMnkhgyf2/
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It's not too late to join our team. Come out and support Sickle Cell Disease Awarness Walk in Central Park. Click... fb.me/1denmnNZT
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#SickleCellAwarenessMonth Day 11. Hydroxyurea is a drug widely prescribed to Sickle Cell… instagram.com/p/BKONcCnBoug/
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September is National Sickle Cell Awareness Month!
We are ready for the Sickle Cell Dance Party Fashion Show! Great job Verlinda Allen!!!
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Check out this article for tips on how to keep those Living Well with Sickle Cell and their families healthy! #SMASH ow.ly/zZHt302xudQ























