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Meet - Alex Ramirez Jr.
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.
The New Face of MS
Oct 270 min read


Meet - DeLonda Owens-Tucker
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.
The New Face of MS
Oct 200 min read


The New Face of MS Quarterly Newsletter
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.
The New Face of MS
Oct 161 min read


Meet - Virginia Moore
STOP and BREATHE! Getting overwhelmed only makes things worse.Try not to rush into decisions, and set clear boundaries about what you need.
The New Face of MS
Mar 270 min read


Meet - Angela Harris
My advice to anyone just starting their MS journey is to stay prayed up and surround yourself with a great support system.
The New Face of MS
Mar 250 min read


Meet - Nana Opong-Owusu
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.
The New Face of MS
Mar 240 min read


Meet - Tasha Andrews
Stay true to yourself. Surround yourself with positive people and things. Your journey is unique. Don’t compare your MS to anyone else’s.
The New Face of MS
Mar 220 min read


Meet - Angie Gensler
MS became my catalyst for self-empowerment, showing me that I could take control of my life and break through the limitations.
The New Face of MS
Mar 200 min read


Meet - Zenovia Wright
Educate yourself about the disease, work with your doctor to find the best treatment plan, and rally your support system.
The New Face of MS
Mar 180 min read


Meet - Cynthia Allen
I believe sharing our stories is crucial in breaking the stigma around chronic conditions.
The New Face of MS
Mar 170 min read


Meet - Heather Nodeland
Keep things in perspective. Even if you think you can handle it alone, opening up to others will help you navigate your journey better.
The New Face of MS
Mar 140 min read


Meet - Ronald Harris
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.
The New Face of MS
Mar 130 min read


Meet - Tina Robinson
Get a relationship with your higher power. I truly believe we need that to thrive with confidence in spite of our diagnoses.
The New Face of MS
Mar 120 min read


Meet - Stephanie Doctor
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!
The New Face of MS
Mar 110 min read


Meet - Monica Proctor Wilson
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!
The New Face of MS
Mar 100 min read


Meet - Anita Monique
Words of encouragement...This journey is yours to own. Your story is still being written, and you hold the pen!
The New Face of MS
Mar 50 min read


Meet - Nick G.
Words of Encouragement...Focus on what you can do rather than what you can’t, and don’t be afraid to lean on others for help.
The New Face of MS
Mar 30 min read


Meet - Ashley Graves
Words of encouragement...Your life may look different now, but it is still meaningful, beautiful, and full of possibility.
The New Face of MS
Jan 160 min read


**NEW**The New Face of MS Quarterly Newsletter
Manage MS in summer heat, back-to-school tips for MS parents, accessible activities guide, MS warrior stories, recipes, remote ops and more!
The New Face of MS
Aug 12, 20241 min read


Meet - Karen Matingou
Explore Karen's inspiring journey with Primary-Progressive Multiple Sclerosis (PPMS).
The New Face of MS
Aug 12, 20240 min read
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