Well, hello, hello

I’m Ashley, The MS Muse, a chronically-ill, disabilababe with relapsing-remitting multiple sclerosis (MS) as of 2017. This blog is my therapy of sorts. These stories are of my life with MS, an autoimmune disease that has attempted to take my independence, my life, and self-worth.

Unfortunately, this blog is about the real ass life of a woman attempting to find herself, her worthwhile fighting a debilitating disability. Though every day is a testament to what has and continues to keep me motivated.

I dedicate this open space, publicly, for my honest thoughts, ideas, and to those sporadic good and bad days, because I have decided MS is what I have, not who I am.