so as some of you know sickle cell can be real unpredictable. so I now have one ticket available! Looking for someone with sickle cell who is feeling up for coming to Wireless today! 18-25.
Drop myself or @hersickledj a message. First come, first serve basis. Share pls.
Sickle cell disease is a lifelong blood disorder causing severe pain.
Many people like Tito need regular blood transfusions from closely matched donors to help manage symptoms.
Your donation is a lifeline.
Visit https://t.co/oxdR1nKDQK to donate today. 🩸
#WorldSickleCellDay
What do you do if you find out your baby has sickle cell?
Here are some tips for what is often a very stressful time in the life of a family ♥️ #sicklecell#family
wow. Haven’t promoted on here. But I brought back my show. But with a twist. Had a talk with some friends @hersickledj@AstarMusicUK@IbeBellah 🥳
"SOME PEOPLE DRINK BATTERY ACID" | Mistar & Mates - The Roundtable Editi... https://t.co/UUMOaFbCm7 via @YouTube
VOXELOTOR WITHDRAWN FROM NHS. We are deeply shocked and extremely disappointed by Pfizer’s sudden decision to withdraw Voxelotor (OXBRYTA®) from the NHS in the UK, and across the world. We were given no warning. Read our full statement here https://t.co/UisEb60s8X
Swimming is a crucial skill, but with #sicklecell, it’s can easily trigger a crisis & land me in the hospital 😭 Still, I’ve decided to take on the challenge (with great caution) & learn. Wish me luck & drop your tips below! ♥️🙏🏽🏊🏽♀️
#HerSickledJourney#SickleCellAwarenessMonth
🚨🩸URGENT. BLOOD NEEDED. PLEASE SHARE 🩸🚨
There is currently a shortage of blood in the UK and people like myself cannot receive our regular treatment because of it. If you can, PLEASE sign up and donate blood!!!
—> https://t.co/C5SprpjWaE <—
RT 🙏🏾