The Struggle to Accept the Diagnosis of FND
Way back in 2000 when my neurological problems began, I was shocked when the horrible, exhausting, uncontrollable seizures I was experiencing were written off as a psychological problem. The first time a neurologist tried to explain the diagnosis, he was kind, but his words didn’t make sense to me and I couldn’t overcome the thoughts in my head of “They think I’m making this up! They don’t believe me! What am I going to do? How am I supposed to convince them that this is real?”. Later that night in the hospital when I was having a prolonged seizure, a nurse trying to administer medication through my IV screamed at me, “Just stop it! How are we supposed to help you if you won’t stop shaking?”. I felt devastated. Here I was, going through the worst health crisis I had ever faced, and the medical professionals that I had trusted to help me were accusing me of faking my symptoms! At that point in my life, I was honest to a fault, and to be accused of making up something so horrifying felt like a slap in the face on top of the terror I was experiencing from the seizures.