Hey Shift.ms community 👋 We'd love to hear from you about how you identify with multiple sclerosis. Do you consider yourself a "person with MS," or do you prefer terms like "MS warrior" or "MS survivor?" How do these labels make you feel, and do you feel like they accurately represent your experience with the disease? We're always looking for ways to better understand and support our community, and your thoughts on this topic would be greatly appreciated. Please share your experiences and feelings in the comments below 👇 Thanks for your participation - Shift.ms 💚