Cayenne Wellness Center and Children's Foundation

Cayenne Wellness Center and Children's Foundation We are dedicated to health promotion & disease prevention with a focus on Sickle Cell.

🚨 DEADLINE APPROACHING! 🚨Register today in order to qualify for designated hotel and free parking to attend Advocacy Day...
03/23/2026

🚨 DEADLINE APPROACHING! 🚨

Register today in order to qualify for designated hotel and free parking to attend Advocacy Day - April 20th, 2026, 9am - 1pm PST - at the California State Capitol. Link in bio/comments.

Leebo’s Sickle Cell Support Group is launching a four-part virtual cooking class series for warriors, caregivers, famili...
03/20/2026

Leebo’s Sickle Cell Support Group is launching a four-part virtual cooking class series for warriors, caregivers, families, and medical professionals.

The monthly series will feature easy, healthy meals, practical cooking tips, grocery lists kept to about $20, limited grocery scholarships, and additional recipe support from Dr. Rowley for those who need more healthy options.

Thursday, March 26th at 3pm PST / 6pm EST.
Register via link below.

Navigating the healthcare system during a Sickle Cell crisis is an immense challenge. When pain is at its peak, clear co...
03/20/2026

Navigating the healthcare system during a Sickle Cell crisis is an immense challenge. When pain is at its peak, clear communication with medical staff becomes difficult, making preparation essential.

Self-advocacy is about ensuring your medical history is respected and your pain is treated with urgency. These steps are designed to help patients and caregivers navigate the ER with more confidence and better outcomes.

Swipe through for a guide on how to prepare for your next hospital visit. Sharing this can help a fellow Warrior get the care they deserve.

San Diego warriors, it's time to advocate 💜Join guest speaker Selemani Zimbo for CA SCD Advocacy Day preparation. Learn ...
03/18/2026

San Diego warriors, it's time to advocate 💜

Join guest speaker Selemani Zimbo for CA SCD Advocacy Day preparation. Learn how to be an effective voice for the Sickle Cell community in California.

📅 Tuesday, March 24, 2026
⏰ 6:00-8:00 PM PST
💻 Virtual

Contact Ayanna Hatton for the link.

Forever in our hearts. 💔Today, we honor the life and legacy of our dear friend and cherished partner, KiKi Shepard.KiKi ...
03/17/2026

Forever in our hearts. 💔

Today, we honor the life and legacy of our dear friend and cherished partner, KiKi Shepard.

KiKi was more than a remarkable talent—she was a radiant light. A woman who commanded every stage she stepped on, from television screens to Broadway theaters, and into the hearts of audiences around the world. For over 30 years, she graced American television with elegance, charisma, and undeniable presence.

Many knew and loved her as the iconic “Apollo Queen of Fashion,” dazzling us for 15 unforgettable years as co-host of It’s Showtime at the Apollo. But beyond the spotlight, KiKi was a woman of purpose.

She was a storyteller.
A trailblazer.
A woman of grace, faith, and fierce compassion.

Through her work on shows like Grey’s Anatomy, Mind Your Business, and Highly Favored, she continued to shine—proving that her gift knew no bounds.

But perhaps her most powerful role was as an advocate.

In 2006, KiKi founded The KIS Foundation, Inc., turning her compassion into action. She fought tirelessly to raise awareness for Sickle Cell Disease—uplifting families, mentoring youth, and creating programs that brought real support and real change. Her impact will continue to ripple through countless lives.

She believed deeply in education, in family, and in God.
She lived with intention.
And she loved with her whole heart.

We are grateful for every moment, every collaboration, every laugh, and every lesson shared.

KiKi, your legacy is not just what you did—it's how you made people feel. Seen. Inspired. Empowered.

You will be deeply missed.
And forever remembered.

Please join us in celebrating her life and legacy by sharing your memories, sending love to her family, and continuing the work she cared so deeply about.

Rest beautifully, KiKi. 🕊️

Ready to advocate? Let's do this together 💜This Thursday, join guest speaker Nevaeh Gutierrez for CA SCD Advocacy Day pr...
03/16/2026

Ready to advocate? Let's do this together 💜

This Thursday, join guest speaker Nevaeh Gutierrez for CA SCD Advocacy Day prep. Learn the tools and strategies to effectively advocate for the Sickle Cell community in California.

📅 Thursday, March 19, 2026
⏰ 6:00-8:00 PM PST
💻 Virtual

Contact Shantijh or Terrina for the link.

Sick Cells is thrilled to present an amazing lineup of speakers for the 2026 SCD Policy Forum!Prepare to be inspired by ...
03/14/2026

Sick Cells is thrilled to present an amazing lineup of speakers for the 2026 SCD Policy Forum!

Prepare to be inspired by passionate SCD Warriors, researchers, thought leaders, fellow advocates, and changemakers.

"Voices to Action" is not just this year's theme—it's a call to arms.

This event is your chance to transform lived experiences, research, and policy into meaningful change. Ensure your voice is part of the conversation—there's still time to join us!

📆 March 17-18, 2026 | Virtual
🔗 Don’t miss your last chance to register at http://www.sickcells.org/policy-forum?utm_source=facebook&utm_medium=social&utm_content=ap_dsbngr9qfw

Sickle Cell Disease is often called an invisible illness. A person can look perfectly healthy while their body is naviga...
03/14/2026

Sickle Cell Disease is often called an invisible illness. A person can look perfectly healthy while their body is navigating a severe lack of oxygen.

Living with this diagnosis means managing a constant risk of a pain crisis. These episodes are sudden and require immediate medical attention, yet the resilience shown by this community is unmatched.

Swipe through for a look at the daily reality of SCD. Awareness starts with listening to the people who live it.

Most people know the name Sickle Cell but cannot explain what actually happens to the blood. It is a mechanical issue wh...
03/13/2026

Most people know the name Sickle Cell but cannot explain what actually happens to the blood. It is a mechanical issue where cells change from flexible circles into stiff crescents.

When these cells lose their shape, they create blockages in the vessels. This stops oxygen from reaching the rest of the body and causes the intense pain known as a crisis.

Swipe through for a quick breakdown of the science. Understanding the biology is the first step toward being a better advocate.

Be the change our community needs 💜Join us for CA SCD Advocacy Day preparation - together we'll learn how to effectively...
03/11/2026

Be the change our community needs 💜

Join us for CA SCD Advocacy Day preparation - together we'll learn how to effectively advocate for Sickle Cell Disease awareness, research, and resources in California.

📅 Wednesday, March 18, 2026
⏰ 6:30-8:30 PM PST
📍 Comprehensive Blood Cancer Center, 6501 Truxton Ave., Bakersfield, CA 93309

Contact Shantijh for details.

Mental health is health. Let's talk about it 💜Join our Men's Conversation focused on mental health and wellness for men ...
03/10/2026

Mental health is health. Let's talk about it 💜

Join our Men's Conversation focused on mental health and wellness for men living with Sickle Cell Disease. A safe space for real talk and genuine support.

📅 Tuesday, March 17, 2026
⏰ 6:00-8:00 PM PST
💻 Virtual

Contact Dorian Archie for the link.

Address

PO Box 3856
Glendale, CA
91221

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