I cried when I read this. At last, someone gets it. It's been 2 years since the completion of my treatment and when I tell my oncologist that my CIPN continues to worsen, she looks at me like I'm nuts. My neurologist pats my shoulder and tells me it will get better. Someday. My family and friends are loving and supportive and remind me that "it beats the alternative." At last, a ray of hope. Someone is paying attention to this debilitating side effect. Thank you!