This is the start of bringing awareness of blepharospasm and other types of dystonia and the effects that it has on me and everyone that is affected. There are only treatments and no cures at this time. Awareness is the only way progress can be made. I am treated with Botox B injections every 3 months. My end of it causes functional blindness where my eyes can spasm shut at anytime for any amounts of time which varies. Also hemofacial spasms.