top of page

Amy McCain-Davis, Registered Nurse

First Dose of Moderna on 12/30/20 Lot #039k20a

Second Dose of Moderna on 01/27/21 Lot #013L20a

Oregon

40 yrs old


Q: What was your life like before you got the vaccine?

I was active and loved life. Just starting to enjoy the empty nester part of life. I was one term away from my master's degree in nursing when I got my second vaccine. A new grandmother to the most beautiful little girl EVER. I have a hobby farm that truly was my happy place and sharing it with my soul mate.


Q: Would you like to share your reasons for getting vaccinated?

I was informed by a nurse manager that they were going to be mandated very soon so I figured I'd get my appointment set up with employee health while they were still readily available.


Q: What was your reaction, symptoms, & timeline?

After the first shot I just felt achy for a couple of days then I was fine. After my second shot at aprox 1pm on the 27, I started to feel really run down and sore by 4 pm. Felt like I was hardly able to move. I went to bed at 6:30pm as I just could not stay awake. I woke up at 4am and feeling even worse, only having extreme dizzy spells. The whole room would spin and almost fell. I shook it off and drove into work. As I started to walk up the sidewalk to work I really started spinning, blacked out, almost fell, extreme leg weakness and losing function. Co-workers were going to call an ambulance but i said NO (nurses are the worst patients). Had my spouse take me to ER. I was admitted for 4 days. Diagnosis: Possible reaction to covid vaccine and labrynthitis. I spent the next 2 months in my bed not able to move or control my bladder or bowels. Extremely light and sound sensitive my room had to be completely blacked out. After the 2 months I was slowly able to start getting up to the bathroom, (in a wheelchair) and on meclizine and promethazine every 6 hours around the clock, as well as prednisone. I was slowly able to get around more and using a walker for the next couple of months. May 2021 I felt like i was having a stroke and went to ER. I was admitted for 2 days and eventually stroke was ruled out. The Dr. literally said "I'll give my left nut if this is not the diagnosis" of Hemiplegic Migraine. The first neurologist I saw refused to acknowledge anything about the vaccine and said I had migraines and conversion disorder. Saw psych, ruled out conversion disorder. Saw a second neurologist that confirmed the shot "set this off" but it should be long out of your system by now (around 7 months later).


Q: What is your life like now, after getting the vaccine?

I've lived the last 14 months in the dark. I have days I literally can't even move. I spend most of the time in bed or on the couch (still in the dark). I had to get prescription sunglasses. If I remotely exert myself on a day I feel slightly better, I end up spending the next couple of days completely down. I still use a walker and a wheelchair to get around. I haven't driven a car or even able to hold my new granddaughter without sitting down first. I had to drop out of my nursing master's program.


Q: Share your experience with any medical care and any diagnoses you have received:

Medical care has been CRAP. The first neurologist I saw pretty much wrote me off with migraines & psych issues. My PCP is a NP and didn't believe that for a second. This has pretty much set the tone for all future neurology referrals, as every single one in my state has been denied. I can't get in to see a neurologist for anything. I see cardiology soon and hope they are able to see through this nonsense as I was healthy before the vaccine. I have also seen rheumatology for high ANA but because the specific markers are negative, he says it is not autoimmune despite consistent high ANA's.


Q: Was your reaction reported, and what was the response?

It was reported to VAERS by my employee health department. There was no response to me. I was able to apply for work comp for my reaction and it was approved. Finding an MD that will write the magic words is a different story.


Q: Is there anything that has helped, and have your symptoms improved?

The only thing that seems to help has been steroids. I was on them initially for a few months. I am currently on them, which is going on 8 weeks. As soon as a taper or stop of prednisone I decline back to how I was at first


Q: Have you had Covid before?

No, I have never been diagnosed with Covid.


Q: What do you wish others knew?

PLEASE, do not give up. This is REAL. Keep on fighting and searching for providers that will believe you. They do exist.




REAL NOT RARE DISCLAIMER:

Real Not Rare does not diagnose medical conditions, offer treatment advice, treat illnesses, or prescribe medicine or drugs. Anything contained on this website or conveyed in the blog stories or groups, is not substitute for adequate medical care, diagnosis, and/or treatment from a medical doctor. It is strongly recommended that prior to acting upon any information gleaned via Real Not Rare or their representatives, you at all times first consult a physician. The views and opinions expressed are those of the individual being interviewed in each story, and do not necessarily reflect the position of Real, Not Rare as a whole.

5,368 views
bottom of page