Welcome to Episode 2 of MS In Colour, where we dive into how multiple sclerosis (MS) affects individuals of black heritage. In this episode, our host Natalie Busari interviews Dr IIya Kister, a renowned neurologist and clinical researcher at NYU Grossman School of Medicine. Dr Kister has been working at the NYU Multiple Sclerosis Center for over 20 years, with a focus on studying MS patients from diverse ethnic backgrounds.

Natalie and Dr Kister discuss the challenges and implications of MS research on black people, as historically, MS has been predominantly seen as a disease affecting white individuals. They explore the reasons behind the underrepresentation of black people in MS research and the potential cultural barriers that may contribute to this phenomenon.

The conversation delves into Dr Kister's study on black Americans with MS, specifically focusing on the re-emergence of B cells in patients using certain therapies. They examine the differences in response to treatments between African Americans and individuals of non-African descent, shedding light on the importance of understanding how MS manifests in different ethnic groups.

Additionally, Natalie shares her personal experiences and observations about MS in Africa and the need for more research to understand the prevalence and impact of the disease in the region. They explore the potential future directions of MS research, including the possibility of preventing the disease or finding more effective treatments.

Join us in this thought-provoking episode as we explore the intersection of MS and black heritage, uncovering new insights and understanding about this complex disease. Stay tuned for an enlightening conversation with Dr IIya Kister.

**Disclaimer: The conversation in this episode is based on the views, experiences, and opinions of the host, Natalie Busari, and her guest, Dr IIya Kister. It is important to note that I am not a qualified medical professional, and any knowledge or experience that I discuss is based on my own understanding. Therefore, it is crucial to seek advice from qualified medical professionals for accurate and personalised healthcare information.**

Contact Natalie Busari at: natalie@thenerveofmyms.org.uk

Follow the Podcast's Instagram: @MSINCOLOUR

Follow the US on social media: @thenerveofmyms

In this episode of MS In Colour titled "Two of a Kind," host Natalie Busari sits down with her guests Carly and Ekow to discuss their experiences living with multiple sclerosis (MS). 

Please note that a lot of the conversation in this episode is based on personal opinions and experiences, and any listeners seeking medical advice should consult with a healthcare professional. 

Carly and Ekow share their unique perspectives on living with MS, including the challenges they have faced and the support they have found through their journey. 

For black individuals living with MS in the UK, there is a patient organization available for support. Follow @thenerveofmymultiplesclerosis on Instagram for more information and resources. 

As Natalie and her guests continue to produce the podcast independently, the team apologizes for any audio issues encountered. Rest assured, they are working to improve the quality with each passing week. 

Tune in to MS In Colour to gain insight and connect with others in the MS community, as Natalie, Carly, and Ekow share their stories and discuss various aspects of life with MS. 

Guest Instagram Profiles:

GO AND SAY HI

Carly - @carlylhouston (https://instagram.com/carlylhouston?igshid=OGQ5ZDc2ODk2ZA==)

Ekow - @ekow.e.otoo (https://instagram.com/ekow.e.otoo?igshid=OGQ5ZDc2ODk2ZA==)

Email Natalie Busari for any inquires at : natalie@thenerveofmyms.org.uk

Welcome to MS in Colour, the groundbreaking podcast where we discuss the realities and experiences of living with multiple sclerosis (MS) within the black community. I’m your host, Natalie Busari, and in this episode, we’ll be diving into the trailer of our podcast. We’ll explore the basics of MS, its impact on the central nervous system, and the unique challenges faced by black individuals with the disease. Join us as we break down barriers within the healthcare system, shed light on the latest treatments and research, and give voice to the lived experiences of black individuals living with MS. Get ready to raise awareness and break the silence surrounding this often misunderstood disease. Let’s get started!