Kim Dumais, a patient partner and active member of the Lupus Quebec Foundation, was recently highlighted in an article in Le Soleil. 👏
In this article, she shares her personal journey living with lupus and her commitment to raising awareness about this disease. It is invaluable to hear directly from patients like Kim, and we express our gratitude to her for her contributions. Take a moment to read the article, as it offers valuable insights! 💜 🦋