From D1 Athlete to Autoimmune Warrior: Misty’s Journey of Resilience and Redefining Strength

From D1 Athlete to Autoimmune Warrior: Misty’s Journey of Resilience and Redefining Strength

Karin W

August 18, 2025

When you’ve trained your whole life to push your body to the limit, listening when it says “stop” doesn’t come naturally. 

For Misty, a former Division 1 field hockey player turned elite coach, the journey from peak performance to living with lupus and rheumatoid arthritis has been one of resilience, self-discovery, and redefining what strength really means.

Ignoring the Red Flags

Looking back, Misty admits her body was signaling trouble long before her diagnosis.

Hair loss at 20, unexplained fatigue, and repeated “mono” misdiagnoses were dismissed as normal stressors of college athletics and academics.

Like many athletes, she rationalized every symptom—until her body forced her to stop.

“I was training for a marathon when everything went sideways. My body just quit,” she recalls. “I thought I was having an allergic reaction. My throat closed, my legs gave out. It was terrifying.”

Takeaways:

  • Don’t dismiss unusual symptoms as “just stress.”
  • Track patterns—energy dips, flares, recurring illnesses.
  • Advocate for yourself in medical appointments. If you don’t feel heard, push back or seek another doctor.
A female field hockey coach in a black jacket, looking focused while observing a training session at night.

The Betrayal of the Body

For an athlete whose identity was built on physical ability, losing control of her legs was devastating.

“Field hockey was my craft. To suddenly not be able to demonstrate skills for my players—it felt like my body betrayed me.”

And yet, that sense of betrayal eventually transformed into gratitude.

Misty vividly remembers sobbing on the side of the road one Halloween, convinced she’d never walk through a pumpkin patch with her son.

Today, even on difficult days, she grounds herself in gratitude: “If I can laugh with my kids at night, that’s a successful day.”

A coach in a white hooded sweatshirt with 'LOYOLA FIELD HOCKEY' printed on it, wearing sunglasses and smiling while walking on a sports field, with a quote about strength in adapting over overcoming displayed on the image.

Redefining Success

For Misty, success used to mean winning, medals, and relentless drive. Now, it means balance, boundaries, and perspective.

“I sprint, then I rest. I force breaks into my day. I’d rather have giggles with my kids than a clean house or a perfect dinner.”

She applies the same philosophy in her coaching.

While she still pushes her athletes to sharpen their skills, she also emphasizes mental health and perspective:

“I wish someone had told me it was okay to just take up space without the medals and the crowns. That’s the message I want to give my players: your worth isn’t tied to performance.”

Takeaways:

  • Create flexible definitions of success (e.g., finishing a light workout, enjoying practice, being present with loved ones).
  • Recognize that rest is a form of training.
  • Celebrate consistency, not just peak performance.
A group of enthusiastic female athletes celebrating together on a dirt field, showcasing joy and camaraderie after a game.

Breaking the Myths of Autoimmune Disease

One of the biggest lessons Misty wants other athletes to know is that appearance doesn’t equal health.

At her sickest, weighing just 102 pounds, people told her she looked “great.” In reality, her body was eating itself.

“Weight has nothing to do with performance. Your body is a gift, no matter what it looks like. What matters is how you manage your energy—your spoons—and whether your goals are worth the risk.”

Takeaways:

  • Health is not defined by weight or appearance.
  • Focus on function: energy levels, recovery, and performance—not aesthetics.
  • Strength is about resilience, not body type.

👉 “Your body is a gift. It doesn’t need to look a certain way to perform.”

A family of four poses together outdoors, smiling. The father stands on the left wearing a black t-shirt and dark pants, while the mother, on the right, wears a striped blue and white sweater. The son, in a blue shirt and beige shorts, stands in front of them, and the daughter, dressed in a yellow outfit, is held by the mother.

Finding Invisible Strength

Through setbacks, diagnoses, and loss, Misty has found strength not in powering through but in adapting, slowing down, and embracing gratitude.

“My oldest sister passed away. My younger sister is battling cancer. I live with lupus and RA. But I wake up knowing how lucky I am. I’ve been through hell and I’m still here—and that perspective changes everything.”

Her story is a powerful reminder that invisible strength isn’t about doing it all—it’s about knowing when to rest, when to fight, and how to find joy in the small moments.

Dance on, friends,
Karin

P.S. If you live with an autoimmune condition or love someone who does, know this: You’re not alone.

P.S.S. Subscribe to our blog and podcast for more inspiring stories and practical strategies from real warriors like Misty.

Disclaimer: These tools do not replace the advice of a health care professional; if you have concerns about your health, please consult a health care professional.

This page may contain affiliate links that won’t change your price but will share some commission. As an Amazon Associate, we earn from qualifying purchases.

🧠 Turn Down Brain Fog: A Focus Game-Changer for Autoimmune Warriors

🧠 Turn Down Brain Fog: A Focus Game-Changer for Autoimmune Warriors

Karin W

August 14, 2025

Brain fog—difficulty concentrating, remembering, or staying alert—is one of the most common and frustrating symptoms for people with autoimmune diseases. But there are practical, science-backed ways to fight it.

🔊 Binaural Beats: 40 Hz for Focus

Binaural beats are an auditory illusion created when two slightly different frequencies are played in each ear, producing a perceived third tone.

Research shows that 40 Hz gamma-frequency beats can improve focus and cognitive clarity.

Tips to use binaural beats effectively:

  • Use quality headphones.
  • Listen for 20–30 minutes before deep work.
  • Experiment with consistency—daily use primes your brain for better attention.
  • White noise can also help if silence is distracting, but silence is often best for focus.

🖥️ Optimize Your Workspace

According to Andrew Huberman:

  • Position your computer screen at eye level or slightly above—this prevents drowsiness and promotes alertness.
  • Ensure good lighting and maintain upright posture to support mental energy.

⏰ Time Your Deep Work

Your brain has natural windows for optimal cognitive performance:

  • 1–4 hours after waking is ideal for challenging mental tasks.
  • Schedule lighter tasks during afternoon energy dips.

🏃‍♀️ Move to Improve Focus

Moderate-intensity exercise before deep work boosts blood flow to the brain and improves attention and productivity:

  • 20–30 minutes of walking, yoga, or light cardio before mentally demanding tasks.
  • Aim for consistency to maintain cognitive health.

💧 Hydrate Your Brain

Dehydration worsens brain fog. Both water and electrolytes are crucial:

  • Start your day with water.
  • Sip consistently throughout the day.
  • Include electrolyte beverages if active.

🧘‍♀️ Sound vs. Silence

Your auditory environment impacts focus:

  • Silence often works best for concentration.
  • Binaural beats or white noise can improve focus if silence is difficult.

🌟 Putting It All Together

  • Listen to 40 Hz binaural beats or use white noise before deep work.
  • Elevate your screen to eye level.
  • Do mentally demanding work 1–4 hours after waking.
  • Include moderate exercise before tasks.
  • Stay hydrated.
  • Experiment with your sound environment to find what works for you.

Consistency is key. These habits can help reduce brain fog, improve focus, and boost your productivity—despite the challenges of autoimmune disease.

Dance on, friends,
Karin

P.S. If you live with an autoimmune condition or love someone who does, know this: You’re not alone.

P.S.S. Subscribe to our blog and podcast for more inspiring stories and practical strategies from real warriors like Courtney.

Disclaimer: These tools do not replace the advice of a health care professional; if you have concerns about your health, please consult a health care professional.

This page may contain affiliate links that won’t change your price but will share some commission. As an Amazon Associate, we earn from qualifying purchases.

Maya Rogers: Turning Lupus Battles into Beauty, Purpose, and Power

Maya Rogers: Turning Lupus Battles into Beauty, Purpose, and Power

Karin W

August 11, 2025

When you first meet Maya Rogers, you notice her energy — the kind that says “I’ve been through it, but I’m still here shining.”

She’s a former standout softball player at Harris-Stowe State University, now coaching high school athletes.

She’s earning her master’s at Morehouse School of Medicine.

She’s the founder of Mocha Beauty, a brand specializing in organic wigs, facials, and hair products designed with chronic illness warriors in mind.

And through it all, she’s navigating life with lupus — an unpredictable, invisible autoimmune disease that took six years to diagnose.

From “Allergic to the City” to an Actual Diagnosis

At 16, Maya started noticing strange symptoms: painful rashes on her elbows during volleyball, unexplained swelling, and flare-ups that got worse in the sun.

In college, her skin would break out, her hair would fall out, and fatigue hit hard.

“I honestly thought I was allergic to the city I was in,” she laughs now. “But it was lupus all along.”

-Maya Rogers, Lupus Warrior

It wasn’t until after graduation that a rheumatologist finally confirmed the diagnosis: systemic lupus — a disease that attacks healthy tissues and organs.

Finding Purpose in the Middle of Pain

Like many of us in Gen Z and Millennial circles who juggle side hustles, school, and dreams, Maya didn’t wait for perfect circumstances to take action.

During COVID shutdowns, she turned her passion for hair and skincare into Mocha Beauty.

Every product is organic, inspired by her own battles with hair loss and skin issues caused by lupus and psoriasis.

“It was slow, jobs were closed, and I had to make money somehow,” she says. “I started braiding hair, taking lash courses, and creating products that actually work for people like me.”

Redefining Success — One Small Win at a Time

For Maya, success isn’t about massive milestones anymore.

“Now, success is the little things,” she says. “Like when my softball players finally get a drill right, or when I knock out my school lectures before the deadline. I give myself grace. I get things done when I can — and that’s enough.”

The Everyday Habits That Keep Her Thriving

Maya’s daily health playbook is simple but powerful:

  • Fruits first – “Fruit takes my flares from 100 to 15%. It’s my go-to.”
  • Hydration always – Water before bed, water upon waking.
  • Organic living – From apple cider vinegar shots to ginger root and Epsom salt baths.
  • Trigger awareness – No red meat or pork, minimal dairy.

And maybe the most important? Protecting her energy. “I used to be hot-tempered. Now I live calmer. Junk food and stress make me feel worse, so I let both go.”

Her Advice for Young Chronic Illness Warriors

“Live like it’s not there,” Maya says. “We know we have a condition that may never go away, but don’t let it take away your life. Do as much as you were doing before you knew you had it.”

Her biggest wish? That people would extend more grace to those with invisible illnesses.

“You might see me looking fine today, but tomorrow I could be in bed, and I can’t even tell you why. This is a physical, mental, and spiritual battle.”

Big Dreams on the Horizon

Maya plans to apply to medical school, with her sights set on dermatology or cardiology, and a vision to build a three-story Mocha Beauty Dream Lounge — a place where she can see patients upstairs, run a salon downstairs, and offer a cozy community space in between.

She’ll keep coaching, keep building, and keep proving that unseen doesn’t mean unstoppable.

If you’re navigating chronic illness, Maya’s story is a reminder:

✅Your condition doesn’t define you.
✅Your dreams are still valid.
✅And your invisible strength might just inspire the world.

🔔 Listen to Maya’s Full Story

🎧 Invisible Strength Podcast — 🎙️Living with Lupus & Chasing Dreams: Maya Rogers’ Inspiring Story (Athlete to Entrepreneur)

📌 Chapters Include:

  • 0:00 Introduction to Maya Rogers and Her Journey
  • 2:31 Living with Lupus: Diagnosis and Challenges
  • 4:57 Redefining Success: Small Wins Matter
  • 7:19 Faith and Support: Overcoming Tough Times
  • 9:59 Healthy Habits: Diet and Lifestyle Changes
  • 12:11 Advice for Young Athletes: Living Beyond Illness
  • 14:13 Mocha Beauty: Turning Pain into Purpose
  • 15:28 Future Aspirations: Medical School and Community Impact
  • 18:03 Closing Thoughts and Community Support

🎧 Listen now on Apple Podcasts: Invisible Strength Podcast

📺 Watch on YouTube: 🎙️Living with Lupus & Chasing Dreams: Maya Rogers’ Inspiring Story (Athlete to Entrepreneur)

👉 Or search “Invisible Strength Podcast” on your favorite platform!

Dance on, friends,
Karin

P.S. If you live with an autoimmune condition or love someone who does, know this: You’re not alone.

Subscribe to our blog and podcast for more inspiring stories and practical strategies from real warriors like Courtney.

Disclaimer: These tools do not replace the advice of a health care professional; if you have concerns about your health, please consult a health care professional.

This page may contain affiliate links that won’t change your price but will share some commission. As an Amazon Associate, we earn from qualifying purchases.