Nicole Jane Miller – Pfizer First Dose 22nd Dec 2020 & Second Dose 12th January 2021
Severe Ongoing Adverse Reactions
Nicole telling her story:
I am a Covid PCU nurse. I volunteered to work the ICU/PCU July 2020, and continue to treat Covid patients now. I wanted the Vaccine. I believed it would end this.
The first dose made me very sick and fatigued. At first it was some heart rate increase and facial flushing that I ignored. Then I spent Christmas Eve feeling like I was hit by a train. It took five days of feeling run down and aches and pains until I felt better. From that point on I had joint pain more than I had before.
The second dose made my face feel numb and tingly. I did get this same feeling with my migraines occasionally.
That day I Face-Timed with my mother who’s also a nurse. She was convinced I had Bell’s Palsy. I dismissed her.
Two days later these symptoms came back with a vengeance and never went away. I started getting electric shocks in my left temple radiating behind my eye. I would get headaches that would not go away with any treatment. I took pain medicine that was OTC or prescribed and it wouldn’t touch it. The burning in my face was insane.
My symptoms kept snowballing. I went to the ER for treatment and was told I probably had shingles in my eye. Lol!
I Went to an eye doctor who quickly dismissed that and said no you have Trigeminal Neuralgia. I had to wait for an appointment. My first appointment I was prescribed Topamax and Gabapentin.
A MRI was scheduled. The meds were not good for me. Topamax knocked me for a loop! The MRI discovered Intracranial Hypertension. Whoa!!! Where’d that come from??? I was scared!
While waiting to see the neurologist the Gabapentin caused a kidney infection and made me extremely ill. My symptoms got so bad with being dizzy, nauseous and blurry vision I had to take FMLA that extended 3 months.
Since seeing the neurologist I’ve been put on Diamox that has been increased to 1000 mg, Lasix, several migraine meds. Although I can function better than when I had to take FMLA,
I still have constant headaches, funky vision and sometimes fuzzy cognition. I am waiting to see a new Neurologist to try for better treatment and hopefully a better outlook.
I want something closer to my old life back.
Elizabethton, Tennessee, USA