Shattering stigmas: 'The Nerve of My Multiple Sclerosis'

[@monicabarnes5091]

I am a black female and I was diagnosed with MS in 2021. My symptoms started in 2017 and I had no clue what was happening to me. I told my GP that I thought that MS was my problem but they dismissed it until I demanded to see a Neurologist. This is definitely an isolating condition. We definitely don't talk about illness in the black community.

[@mstrust]

Thank you so much for watching and sharing your experiences. Natalie's foundation is really inspiring and we hope that it helps people feel empowered to talk about MS in their communities 💙

[@victoriajohnston3219]

Bless you , fantastic advice 🙂

[@mstrust]

Thank you so much for watching - really powerful message from Natalie in this one!