Living With MS: After being dismissed for months, Destiny’s Multiple Sclerosis (MS) journey led to vision loss, a life-changing diagnosis at age 22, and years of resilience. Her story highlights the challenges of living with MS, the power of self-advocacy, and finding strength through motherhood, family support, and perseverance.

Living With MS: After being diagnosed with multiple sclerosis, Selena turned fear into purpose. Through advocacy, family support, and the creation of the MSwired Podcast, she shares how living with MS has shaped her resilience, strengthened her voice, and inspired others to find hope and strength in their own journey.

Living With MS: Rosie shares how she navigated her diagnosis, managed her symptoms, and drew strength from her family.

In this quarterly newsletter from The New Face of MS, we go beyond the diagnosis to explore the invisible realities of life with MS — from caregiver love to shifting relationships, emotional labor, and the strength found in community. Our stories highlight resilience and connection, inviting readers to walk this journey together.

When Alex was first diagnosed with Multiple Sclerosis, confusion and frustration set in after a discouraging first doctor visit. But instead of giving up, he chose resilience. Through daily physical therapy, natural pain management, and an unbreakable spirit, Alex transformed his journey from struggle to strength. Today, he walks miles every morning, proving that with determination and faith, life with MS can still be powerful and fulfilling.

Diagnosed with Relapsing-Remitting MS, Delonda turned fear into faith and resilience. Despite relapses, pain, and fatigue, she became her own advocate—relocating, finding new doctors, and using her faith to thrive. Today, she’s a district activist leader with the MS Society and an ambassador for marriage and MS, inspiring others to fight back and live thieir lives to the fulliest.

In this edition, we embrace gratitude, purpose, and community. Discover how to thrive through change, reflect on the power of thankfulness, and join us as we spread cheer through our Tree of Hope holiday drawing. Every act of kindness helps light the way for someone in need.

STOP and BREATHE! Getting overwhelmed only makes things worse.Try not to rush into decisions, and set clear boundaries about what you need.

My advice to anyone just starting their MS journey is to stay prayed up and surround yourself with a great support system.

God is my foundation. Life could be worse, so I continue to push forward. Although this is my new “normal,” I am still incredibly blessed.

Stay true to yourself. Surround yourself with positive people and things. Your journey is unique. Don’t compare your MS to anyone else’s.

MS became my catalyst for self-empowerment, showing me that I could take control of my life and break through the limitations.

Educate yourself about the disease, work with your doctor to find the best treatment plan, and rally your support system.

I believe sharing our stories is crucial in breaking the stigma around chronic conditions.

Keep things in perspective. Even if you think you can handle it alone, opening up to others will help you navigate your journey better.

To anyone on their own MS journey, I want to say this. You are not alone. Don’t lose hope! You are stronger than you think.

Get a relationship with your higher power. I truly believe we need that to thrive with confidence in spite of our diagnoses.

Take it one day at a time. Grieving the old you is a process, and there’s no set timeline for it. Always remember...You are not alone!

SPEAK MS is a virtual support group that meets every Monday. If you’re looking for a supportive, fun community, you’re welcome to join us!

Words of encouragement...This journey is yours to own. Your story is still being written, and you hold the pen!