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Dima Hendricks

@dimahendricks

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📖Author | Coach | Advocate
👑 Helping people @unleashingroyalty #ThroughThePain

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You’ve seen the moments. Now experience the stories.

Thriving #ThroughThePain brought together people living with sickle cell disease, caregivers, and advocates to have honest conversations about pain, resilience, healthcare decisions, self-advocacy, and what it truly means to thrive while living with SCD.

Every voice brought something different to the conversation. Every story reminded us that there is no single way to live with sickle cell disease.

If you missed any of the series, now is the perfect time to catch up.

🎥 Watch ALL of the Thriving #ThroughThePain videos on our Instagram page.

Then come back and tell us what you think.

Save this Reel. Share it with someone in the sickle cell community. And most importantly, keep the conversation going.

#ThrivingThroughThePain #ThroughThePain SickleCellDisease taken in Alan Lux Studios, LLC by @dimahendricks

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9 days ago

A Message from the CEO:

September was Sickle Cell Awareness Month, and while it was a meaningful month for visibility, education, and advocacy. Last month was also incredibly hard for me personally and physically.
#ThroughThePain was able to roll out a powerful campaign with the support of amazing warriors who trusted us with their stories, time, and truth. I am deeply grateful to everyone who participated in the Thriving #ThroughThePain project and helped bring this vision to life.
From the outside, it may have looked like I was up, traveling, promoting the campaign, and moving from one thing to the next.
The truth is, I wasn’t.

I began the month recovering from surgery and trying to give my body the care it needed. Then came another unexpected turn: discovering that I have a blood clot.
And still, life continued to life.
Between appointments, pain, recovery, uncertainty, school, leadership, family, advocacy, and the responsibility of keeping an organization moving forward, I have been trying my best to 𝐃𝐎 all the things.
But I am beginning to consider that maybe my best, in this season, is simply to 𝐁𝐄.
To be present. To be still. To be honest about what my body needs. To be okay with not carrying everything at once.
There were moments this month when I genuinely asked myself, “Should I keep going?”
Not because I stopped believing in the mission. I believe in it deeply. But leadership during a difficult personal season requires honesty. Sometimes strength looks like moving forward. Other times, it looks like slowing down, asking for help, and recognizing that rest does not erase your purpose.
I am still here. Still healing. Still leading. Still learning what moving forward looks like for me now.
To every warrior who participated in Thriving #ThroughThePain, thank you. You helped carry this campaign during a time when I could not carry everything myself.
As I rest, recover, and reflect, I will also be considering what comes next for #ThroughThePain Inc.
For now, maybe my best is not to do.
Maybe my best is simply to be.

With gratitude,
Dima by @dimahendricks

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16 days ago

In this final Thriving #ThroughThePain conversation, our featured warriors and caregivers answer one powerful question:

“How are you thriving #ThroughThePain today?”

Thriving does not always look like having everything together. Sometimes it looks like choosing rest. Sometimes it looks like speaking up at a medical appointment, setting a boundary, finding joy in the middle of uncertainty, asking for help, or simply making it through the day.
For people living with sickle cell disease and chronic illness, thriving can be deeply personal. It can mean reclaiming your voice, protecting your mental health, advocating for your care, and creating a life that is bigger than a diagnosis.
This series has always been about more than pain. It is about lived experience, resilience, patient advocacy, community healing, and the many ways people continue to choose hope and purpose.

Now we want to hear from you.

How are YOU thriving #ThroughThePain today? (You don't have to be a warrior to answer the question).

Share your answer in the comments, tag someone whose story inspires you, and help us close this series by reminding our community that there is no single way to thrive. by @dimahendricks

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19 days ago

Up next for Day 24 of Sickle Cell Awareness Month, as we continue SC3’s 10 Days of Sickle Cell Celebs, we’re celebrating the incredible Dima Hendricks! 👑❤️🩸🌟

Dima is a wife, mother, Sickle Cell Warrior, advocate, mentor, beauty queen, and a valued partner of the Sickle Cell Community Consortium.

Whether she’s conquering the pageant stage, mentoring and pouring into others, or advocating for fellow Warriors, Dima continues to turn her lived experience into purpose. Through her nonprofit, Through the Pain, she provides patient-centered services and support to the sickle cell community.

Her crown may shine, but the impact she makes in the lives of others shines even brighter. 👑❤️

Today, we celebrate YOU, Dima!

THIS is a Sickle Cell Celeb. Because impact deserves the spotlight. 🌟

#chronicillness #SickleCellAwarenessMonth #SickleCell #SickleCellWarrior #celebrity by @dimahendricks

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24 days ago

What does taking control of your health look like when you live with sickle cell disease?
In our next Thriving #ThroughThePain video, all of our featured participants come together to answer: “How are you taking control of your condition?”

Each person’s experience with sickle cell disease is different, and so is the way they make decisions about their care and their lives. Hear their perspectives in this next conversation, then tell us: What does taking control look like for you?

#ThrivingThroughThePain #ThroughThePain by @dimahendricks

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24 days ago

Meet Dima Hendricks. 👑

She is more than a sickle cell warrior. She is an ADVOCATE, AUTHOR, PAGEANT QUEEN, and CO-FOUNDER of #ThroughThePain Inc.

Throughout her journey, Dima has faced many challenges, but her faith and spirit remain unbroken. Sickle cell has sometimes limited her ability to participate in physical activities and required her to carefully manage her time, energy, and health. Yet, those limitations have never determined the purpose of her life.

Instead of allowing sickle cell to define her, Dima has transformed her pain into purpose, using her experiences to advocate for others and expand what people believe is possible.

As part of the Thriving #ThroughThePain series, listen as Dima answers the question:

“What limitations were placed on you because of sickle cell?”

If you’re a warrior, join the conversation: What limitations have been placed on you, and how have you moved beyond them?

#ThrivingThroughThePain #ThroughThePain #SickleCellWarrior taken in Alan Lux Studios, LLC by @dimahendricks

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a month ago

The visionary of #ThroughThePain is stepping in front of the camera to share her own story.

Meet Dima Hendricks, founder, advocate, author, mother, pageant titleholder, and sickle cell warrior.
Long before #ThroughThePain came into existence , Dima was learning how to navigate a life shaped by sickle cell disease, grief, survival, faith, and purpose. Through pageantry, she stepped onto stages that were not always designed with women living with chronic illness in mind and used her platform to challenge narrow ideas about beauty, strength, and possibility.

Her story is not only about what she has survived. It is about the woman she has become and the life she continues to build beyond her diagnosis.
Dima is next in the Thriving #ThroughThePain lineup.

#ThrivingThroughThePain #ThroughThePain #SickleCellAdvocacy #SickleCellWarrior #PatientLedStorytelling #PageantryWithPurpose by @dimahendricks

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a month ago

September is Sickle Cell Awareness Month. 🗓️
This month, #ThroughThePain Inc. is making room for a fuller story of life with sickle cell disease, a story that acknowledges the pain without allowing it to define the person.
Thriving #ThroughThePain was a warrior-led project, produced by warriors and featuring warriors. Created in partnership with Pfizer, the project introduces five warriors through a collection of intimate visual stories. They are artists, advocates, entrepreneurs, leaders, creators, and community builders. Each one reminds us that living with sickle cell is only one part of who they are.
Throughout September, we will share their stories, candid behind-the-scenes moments, educational content, and voices from across the sickle cell community.
Because there is life beyond the hospital room.
There is purpose. There is creativity. There is leadership. There is love. There is joy. There is thriving.
We invite healthcare organizations, educators, community partners, advocates, and allies to follow the series, share these stories, and help expand the way the world sees people living with sickle cell disease.
The pain is real, but it is not the whole story.

#ThrivingThroughThePain #ThroughThePain #SickleCellAwarenessMonth #SickleCellAwareness #SickleCellAdvocacy #PatientVoices #HealthEquity by @dimahendricks

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2 months ago

July came and went!

🙌🏽 Officially joined the worship team
💍 @realbigruckus and I celebrated our wedding anniversary
✈️Traveled to California for Warrior Con
📸 Supported two of my friends at their exhibit openings

So grateful for the lessons we learned and the amazing memories we made. Next month we’re walking into new beginnings!

Congratulations @heath_avant and @chellypicphotography. So proud of you both. 🤗

#julydump by @dimahendricks

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3 months ago

The countdown is on! 🎉❤️🩸

Join us for the 13th Annual Warrior Convention, July 22–26, 2026, in Los Angeles, California! This is more than a conference, it’s a family reunion for the sickle cell community. Warriors, caregivers, advocates, healthcare professionals, and supporters from across the country will come together to learn, connect, celebrate, and create unforgettable memories.

There’s still time to register and apply for lodging scholarships!

🔗 Register & Scholarship Information:
https://sicklecellconvention.org

Whether you’re attending for the education, community, special events, entertainment, or lifelong connections, Warrior Con is where the sickle cell community comes together as one.

We can’t wait to see you in Los Angeles! ✈️☀️

#WarriorCon2026 #SickleCellWarrior #SickleCellCommunity #WarriorConvention #SickleCellAwareness by @dimahendricks

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4 months ago

Happy Birthday 🎁 to my Son! Mikey, continue to be the joy that people need in this world. Mom and I are grateful that God blessed us with you! Stay close to God and He will never fail you! #happybirthday🎂 by @dimahendricks

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4 months ago

I have officially been working day and night on the marketing for the 7th Annual World Sickle Cell Day Marathon… and when I say day and night, I mean I’m pretty sure my laptop and I are now in a committed relationship. 😂💻
But it was worth it.
The marathon was a SUCCESS! We surpassed our registration goal, and people from all over the world were able to attend, connect, learn, and be part of this powerful global conversation around sickle cell disease.
I am so proud of what we accomplished… but BABY, I am TIRED.
A huge thank you to the incredible teams at Cayenne Wellness Center, Global Alliance of Sickle Cell Disease Organizations, and Major Effects. This collaboration was truly epic, and I’m grateful to everyone who helped bring this vision to life.
Now excuse me while I go recap the recap… from my bed. ❤️🩸
See y’all at @sccconsortium convention!

#WorldSickleCellDay #CayenneWellnessCenter #GASCDO #throughthepain by @dimahendricks

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4 months ago