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Up until recently, MS was treated like a “white woman’s disease” – often making Black people feel isolated, or worse, undiagnosed and unheard. Today, we know that Black populations have an increased risk for earlier and greater disability from MS. It can feel like the healthcare system is set up against you, representation is lacking, and the search for people you can relate to is an ongoing struggle. The resources below were created for you to educate yourself on your disease and learn tips on receiving the best care so you can live well with MS.
Understand the basics of multiple sclerosis and what you can expect living with this disease.
Featuring: Mitzi Joi Williams, Neurologist
In this video you’ll learn:
Why multiple sclerosis is different in the Black community and what you can do about it.
Featuring: Mitzi Joi Williams, Neurologist
In this video you’ll learn:
Different treatment options, symptom management strategies, and healthcare professionals who can help.
Featuring: Paula Hardeman, Physician’s Assitant
In this video you’ll learn:
Learn ways to feel empowered as a patient and take ownership of your health.
Featuring: Victoria Reese, Patient Advocate
This video covers:
Victoria shares her tips for being open and honest with her doctors and when to know if it’s time for a second opinion.
Featuring: Victoria Reese, Patient Advocate
In this video she covers:
The importance of being involved in your own care.
Featuring: Paula Hardeman, Physician’s Assistant
In this video you’ll learn: