When it comes to multiple sclerosis, being able to cut through the medical jargon and disease pathology is not just helpful, it’s crucial. That’s why this site strives to create an ongoing narrative of MS experiences from those living with the disease.
It’s also a resource for the newly diagnosed. While information on the web has improved in the years since I was diagnosed, there is still a need for candid and personal stories, a human connection.
It’s empowering to talk about MS – by naming it, calling it out, slamming it, confronting it, we are taking charge of this disease in a way that is proactive (and cathartic).
One, Wild & Precious 