Joined February 2021
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SC RED is more than an organization — it’s a bridge between patients, people, and providers. These testimonies reflect why this work matters and how creating space for honest conversations can change care, outcomes, and lives.
At SC RED, we’re addressing the challenges individuals with sickle cell disease face in reproductive and maternal health care. Through advocacy, research, and lived experiences, we empower individuals with the knowledge and support they need for their health and future. 🌟
Still processing the beauty of last night’s fireside chat. So grateful for every person who showed up, shared their truth, and created space for real, raw, and honest conversations. These stories matter. You matter. Thank you for trusting this space 🤍✨ #sicklecellawareness
Here at SC RED, we never get tired of talking about sickle cell and reproductive health — because every conversation brings us closer to awareness, access, and change. ❤️🩹 #SCRED #SickleCellAwareness #ReproductiveHealthMatters
💭 Living with sickle cell (or supporting someone who does) comes with so many ups and downs—physically, mentally, and emotionally. Your mental health matters just as much as your physical health.
💜 Drop the heart that matches how you’re feeling today. #SickleCell #MentalHealth
✨ “Having sickle cell doesn’t mean you can’t have kids. 💕 It just means planning, support, and the right care are key. Talk with your hematologist + OB team early, know the risks, and make a plan for a healthy pregnancy. 🍼❤️ #SickleCellStrong #ReproductiveHealth #YouCan
💔 Did you know sickle cell can impact fertility in both men and women? From low testosterone and priapism in men, to diminished ovarian reserve and chemotherapy effects in women — warriors face unique challenges when it comes to reproductive health.
🌹 It’s more than physical.
Let’s raise our voices, spread awareness, and uplift our community.
Together, we are stronger. 💪🏽❤️
#SickleCell #Awareness #SCRED
🚨Clinical Trial Update🚨
We remain committed to advocating for research that centers the needs, perspectives, and voices of the sickle cell community—and we’re deeply grateful to every participant whose involvement strengthens the future of SCD treatments. ❤️
#SickleCell
Dinner, discussions, and reproductive health across every stage of life 🌸✨ Join us at 6:30 PM! #SCRED #SickleCell #HealthAcrossTheLifespan
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Share & repost please 🥰🙏🏽
Now who said that?! 👀🤭
With that being said, You don’t want to miss our
✨CRITICAL CONVERSATIONS DINNER✨
📆 SEPTEMBER 6th, 2025
📍 The Arena Stage in Washington D.C
⏰ 6pm
Get your tickets now, link in our bio 🎟️
#sicklecellawareness #scred #reproductivejustice
🩸✨ DINNER WITH PURPOSE ✨🩸
We’re gathering the community for a night of powerful conversation, good food, and real solutions. Let’s talk about Maternal Mortality & Morbidity in the Sickle Cell Community.
📍 DC | 🗓️ Sept 6 | 🕕 6–10PM
🎟️ Limited seats —register now! Link in bio
Today is #WorldSickleCellDay ❤️🩹
Sickle cell is more than pain. It’s a fight for our lives, our futures, and our voices.
I live it. I raise awareness for it. I’m surviving it.
🎗️Support sickle cell warriors.
🎗️Learn the facts.
🎗️Speak up for health equity.
#SickleCellAwareness
Please be mindful of your responses if someone brings up infertility. It can be a very difficult topic for some🩵 If you are living with sickle cell and dealing with infertility, Sickle Red is here for you. We have many resources for you. Visit our website sicklecellred.org
SickleRED retweeted
Sickle Cell Reproductive Health Education Directive is having another Critical Conversation:Contraception in Sickle Cell Disease - More Than Just Depo! Webinar Series. @SickleRED20
Register here, streamyard.com/watch/hKhXBqV…
Mark your Calendars, LIVE on Streamyard, October 16th
Good morning good people! Today we wanted to send a bit of motivation your way.
This too shall pass.
#thistooshallpass #scred #sicklecellred
Our Critical Conversations Webinar Series has been incredibly informative. Register to join the next one where we will hear from the man behind the science of gene therapy, Dr. John Tisdale.
Register here: eventleaf.com/e/gene
Hey @nbcsnl We have a gene and cell therapy education day at our conference in April 🩷 #SickleCellAwareness
