Sickle Cell Community Consortium

Sickle Cell Community Consortium There are over 200 non-profit Community-Based Organizations (CBOs) for sickle cell disease in the U.S. The Consortium exists to address the needs of the CBOs.

The Consortium was founded in February of 2014 to provide a platform to unify, strengthen and increase the visibility of SCD community-based organizations


https://linktr.ee/sicklecellconsoritum The Sickle Cell Community Consortium (SCCC) was founded in Februrary of 2014 to provide a platform to unify, strengthen and increase the visibility of sickle cell community-based organizations (CBOs) thro

ughout the country. This Consortium is founded on the belief that a "house divided against itself cannot stand" and a commitment to create an outstanding model of commUNITY and patient engagement. We have developed a unified entity, modeled after the U.N. where the individual needs of each CBO can be identified and addressed as a unit, while maintaining the autonomy of each individual organization. SCCC is not a CBO, nor does it seek to replace the actions or activities of existing CBOs. Sickle cell disease CBOs exist to address the needs of the sickle cell community. Our mission is to assist the CBOs in identifying the needs of their patient population, to aggressively seek funding to address those needs, provide infrastructure support and a platform for collaboration and cooperation between individual CBOs, governmental agencies and pharmaceutical and corporate stakeholders. Our CBO partners span across the country and are actively involved in direct patient services, support services, education, awareness and advocacy. These CBOs collaborate with the Consortium and with each
other on a wide range of projects to benefit the sickle cell community. These projects include, but are not limited to, the development of educational materials and sickle cell toolkits, transition services geared towards the teen
market, bereavement services and funeral cost assistance, medical accountability, legislative calls to action, and the creation of a platform to assist data collection and analysis for patient-reported outcomes and research. With strong commitment to fund-raising, charitable donations and grants, we have built, and will continue to strengthen and grow, a network of patient and advocate-powered community non-profit organizations dedicated to redefining what it means to live with, conquer and overcome sickle cell disease.

🚨 SC3 Public Office Hours are happening NOW! 🚨Have questions about SC3, partnerships, your upcoming events, or the 13th ...
06/17/2026

🚨 SC3 Public Office Hours are happening NOW! 🚨

Have questions about SC3, partnerships, your upcoming events, or the 13th Annual Warrior Convention? Join us now on Zoom and let’s chat!

Many exciting Warrior Con updates and details will begin dropping TONIGHT at 6 PM, so now is the perfect time to get your questions answered. 👀🔥

Interested in joining?

Comment below and we’ll send the link directly to your DMs. ❤️🩸

06/17/2026

🚨 SOMETHING HUGE IS COMING… 🚨

The biggest Warrior Con announcement of the summer drops TONIGHT at 6 PM EST. 👀🔥

Trust us. You do NOT want to miss this one.

🔔 Turn your post notifications ON now so you’re the first to know when registration officially opens!

Who’s ready for Warrior Con 2026? 🌴☀️✈️

📣 SC3 PUBLIC OFFICE HOURS ARE TODAY! 📣Do you have questions about becoming a partner, SC3 programs, or the upcoming 13th...
06/17/2026

📣 SC3 PUBLIC OFFICE HOURS ARE TODAY! 📣

Do you have questions about becoming a partner, SC3 programs, or the upcoming 13th Annual Warrior Convention in Los Angeles? This is your opportunity to connect directly with the SC3 team and get your questions answered.

🕒 Today | 3:00 PM – 6:00 PM

Our office hours are open to anyone interested in learning more about SC3, upcoming opportunities, and Warrior Con 2026.

If you would like to join us for questions and discussion, simply COMMENT BELOW and we will send the meeting link directly to you via DM.

We look forward to connecting with you! ❤️🩸

WarriorConvention SickleCellWarriors

❤️🩸 Sickle Cell Community, Let’s Show Up for One of Our Own! 🩸❤️Our fellow Warrior, Ayana Johnson, is competing for the ...
06/16/2026

❤️🩸 Sickle Cell Community, Let’s Show Up for One of Our Own! 🩸❤️

Our fellow Warrior, Ayana Johnson, is competing for the People’s Choice Award and needs our support!

As a community, we understand the importance of uplifting and celebrating one another. Ayana has proudly represented both her state and the sickle cell community with grace, resilience, and determination. Now it’s our turn to help her shine!

✨ Voting is only $1 per vote
✨ Unlimited voting
✨ Every vote helps secure her place in the finals

Let’s come together and show Ayana the strength of the sickle cell community. Whether you cast one vote or many, your support matters!

📲 Scan the QR code or visit:
americashighschoolpageant.com

Drop a ❤️ in the comments once you’ve voted and help us spread the word by sharing this post!

This is soooo cool!
06/15/2026

This is soooo cool!

Keep up the Great work!
06/15/2026

Keep up the Great work!

06/12/2026

👋🏾 This is Theo – he spent this Thursday of National Blood Week having a blood exchange.

For Theo, this isn't a one-off.

It's part of his regular treatment for sickle cell.

The 14 year old was diagnosed with the genetic condition at birth. He needs blood exchanges at Birmingham Children’s Hospital to ease his painful symptoms.

In 2017, Theo had a sickle cell crisis that put him in intensive care and needing every drop of his blood replaced with healthy donor blood.

Mum Sylviann says the hardest part isn't all the hospital visits — it's watching Theo experience extreme pain and having to explain why the everyday things other children do freely aren't always possible for him.

"Nothing prepares you for watching your child go through extreme pain," she says.

“Recovering from painful episodes can last from just a few hours to weeks.”

But blood donation changes the story.

When Theo has an exchange, Sylviann says the improvement can be almost immediate. It gives him more energy to do the things he loves like playing the violin, recorder and guitar, and playing football and rugby. 🎻🏉

For sickle cell patients, well-matched blood is vital. The Ro subtype is more commonly found in people of Black African and Black Caribbean descent, and many sickle cell patients need this specific type.

More Black donors mean better, more effective matches - for Theo and the thousands of others living with the condition.

🩸 If you're of Black heritage and haven't donated before, your blood could be the match someone is waiting for.

Something special is coming to Crescent Commons (our new flagship property). 👀On June 19, we’ll gather to celebrate June...
06/12/2026

Something special is coming to Crescent Commons (our new flagship property). 👀

On June 19, we’ll gather to celebrate Juneteenth and World Sickle Cell Day through community, culture, wellness, connection, and joy.

Save the date | Register via link in bio 💃🏾🪩🎉



https://www.facebook.com/crescentfoundationscd

Events in the community 📢 ATTENTION ALL SICKLE CELL MOMS & CAREGIVERS ❤️Being a parent of a sickle cell warrior is not e...
06/12/2026

Events in the community

📢 ATTENTION ALL SICKLE CELL MOMS & CAREGIVERS ❤️

Being a parent of a sickle cell warrior is not easy.

The sleepless nights.
The hospital visits.
The emotional stress.
The constant worry.

While we often focus on the warriors, we sometimes forget the incredible mothers and caregivers who fight alongside them every day.

That's why I'm sharing this special opportunity from the No One Behind (NOB) Foundation.

💜 WARRIOR MOM EMPOWERMENT WEBINAR

This webinar is designed to support, encourage, and empower mothers and caregivers of children living with sickle cell disease.

If you're a warrior mom, this is for YOU.

📝 Register here:
https://luma.com/b39wzj8o

Tag a sickle cell mom who needs to see this. ❤️👇

Let's continue supporting the people who never stop supporting our warriors.

🤝 Community Partnership Notice

BROS ME is committed to supporting initiatives that improve the lives of sickle cell warriors and their families.

For awareness campaigns, health advocacy projects, community outreach programs, webinars, events, and partnership opportunities, feel free to send a DM.

Together, we can reach more people and make a greater impact. ❤️🩸



Fasan Oluwatosin
Sickle Cell Advocate || BROS ME
Founder A Warrior with Purpose

Address

P. O. Box 1195
Atlanta, GA
30028

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