A Day in the Life of a Neurosarcoidosis Patient

As part of Rare Disease Day 2023, our Charity Ambassador Kemi Sulola filmed a video showing a day in her life living with neurosarcoidosis!
Sarcoidosis affects everyone differently and the experiences of one person are not applicable to all. The views shared in this video and ways of living with neurosarcoidosis are individual to Kemi.
We'd love to hear from you! If you'd like to share your story of living with sarcoidosis, please get in touch with us or if you need any support with your sarcoidosis email us on [e-mail]