Resources

Welcome to our comprehensive resource center, designed to support individuals and families affected by neurological conditions, particularly multiple sclerosis and brain health challenges. These carefully curated resources provide education, community connection, and empowerment tools for your wellness journey.

Dr. Mitzi's Published Works

You Can Live Well With Multiple Sclerosis: A Guidebook for Navigating Life After MS Diagnosis

A step-by-step empowerment guide for those living with MS. This quick read is packed with practical tips and tools to help you partner with your doctor and healthcare team to navigate your “new normal.” Dr. Mitzi provides clear, concise guidance to help readers avoid overwhelming online searches and instead rely on trusted, expert information for decision-making about their care.

You Can Live Well With Multiple Sclerosis Guided Journal and Health Tracker empowers and equips you with the guidance to own your journey and stay organized.

Every MS diagnosis is different, and this guided journal invites you to capture your story and reflect on your unique experiences.

Digital Resources

BrainChat Podcast

Our flagship podcast featuring Dr. Mitzi Joi Williams and leading experts in neurology, brain health, and wellness. BrainChat delivers insightful conversations about multiple sclerosis, neurological conditions, health equity, and empowerment strategies for patients and families. New episodes prov

Listen on: Apple Podcasts | Spotify | Google Podcasts | All major podcast platforms

Digital Resources

Coming Soon
BiCOMS (Black International Coalition on MS Research) (formerly NAAMSR)

Dedicated to advancing research participation and improving outcomes for African Americans living with multiple sclerosis. NAAMSR works to bridge gaps in healthcare access, increase diversity in clinical trials, and provide culturally relevant resources for the Black MS community.

Minority Research Partnership Engagement Network

A collaborative initiative focused on increasing diversity in neurological research and clinical trials. This network connects patients from underrepresented communities with research opportunities while ensuring culturally competent care and communication throughout the research process.

Educational Materials

Brain Health & Wellness Guides

Webinar Series Archives

Access recordings of our educational webinars featuring:

Community Support

Support Groups

Virtual Events

Clinical Resources

Finding Specialized Care

Treatment Information

Advocacy & Policy

Legislative Updates

Stay informed about policies affecting neurological care, research funding, and patient rights.

Advocacy Training

Resources to help you become an effective advocate for yourself, your family, and the broader neurological community.

Professional Resources

Healthcare Provider Education

Research Collaboration

Information for researchers interested in partnering with our foundation on studies focused on health equity and neurological conditions in underrepresented populations.

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