My name is Valerie Windsor and I have lumbar arachnoiditis and cervical neuropathy as well as hyperrflexia my pain is horrible. My nerve conduction study showed how much pain I'm living in, but still denied enough opioids to allow me a quality of life. I have been told that my condition was caused by a medical procedure gone wrong, and I know which procedures caused this. It was the spinal nerve block injections, yet I was forced to have them or my insurance would not authorize my prescription for oxymorphone; as well as the doctor would not write the prescription. I told my insurance and the doctors the injections were making me worse, yet I had to submit to them. My last nerve block injection was in January, right after I felt tingling on the top of my left foot and shortly after extreme pain in my left leg and now it's going on 6 months of horrible pain. Before that spinal injection in January my left leg had no pain. Before the spinal injections and after my spinal surgeries I only had pain in my right hip, after the injections my knees, right calf, bottom of my right foot, left hip, left knee, left thigh...I know there's something in that medication because there's no way every doctor is incompetent. I also was told of any possible adverse reaction to these spinal injections, I was only told I had to submit to them.
I have actually tried everything to combat the pain from, massage/physical therapy, tens-unit, acupuncture, surgery, spinal cord stimulation, ultrasound treatment, the horrible spinal injections, and all forms of non-opioid medication. The only relief I get is from opioids. The attack on opioids is bs, and never have I heard anyone defend them, for opioids are the only form of relief for most chronic pain patients
I can't keep living in this pain.
Since these opioid laws have now denied chronic pain patients Human Rights, Civil Rights, and taken away our HIPPA protection.

Chronic Pain Patients are the new Lepors (Leporsy) That is who we now identify with.
Valerie Windsor

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