PD and COVID-19 Vaccine

I have to start with, "I'm not a doctor and any mention of medical or science is my opinion"

About 4 weeks ago I received the second COVID-19 vaccination. My memory of events may be a bit hazy, but it seems like the effectiveness of my Parkinson's medications changed shortly after the vaccine.  

This is my personal opinion and others will confirm I have been complaining about off times and dose failures for a long time. Can you tell I am emphasizing this is a personal opinion of a lay person, not the results of medical science.

Pfizer 💉💉

First shot -

2:00 PM - First dose of the vaccine had.a brief warm/burning sensation.

7:00 PM - The arm which got the vaccine was very week a few hours after the vaccination. 

Day 2 - 9:00 AM - The next day I could barely lift the arm.  This only lasted about a day and a half. 

Day 2 - 2:00 PM - 24 hours after injection, I felt slightly sick, like a mild flu.

Pfizer 💉💉

2nd shot - 

4:00 PM - 2 hours after fell asleep sitting upright for a few hours.

Day 2 - 7 PM - 27 hours after had a throbbing headache followed by aching legs and arms

Day 2 - 10 PM - 30 hours in, fluish. Funny he doesn’t look fluish. 

Day 2 - 11 PM - After a brief battle headache and flu stopped. 

Day 2 - 11 PM - Arm pain. This may just be my regular day to day pain. 

Day 3 - 1 PM - approaching the 48 hour mark and eyelids feel very heavy. 

Strength in arm is okay with 2nd.  No extreme weakness like first dose.

A day after the vaccine I was definitely falling asleep during the daytime more frequently.  The off times were more pronounced, 30 to 60 minutes after taking PD med, it hit me like a boomerang. The stiffness and freezing was extreme. I tried reducing the medication and it seems to have helped the extreme off times for a while.  

Since my experience, I have read stories of others with a similar response to the vaccine. Any PD experts tracking this data to see if there are side effects from COVID-19 vaccine that changes effectiveness of levadopa/carbadopa?  It would be a nice project for a medical professional to start.

Since March, when I got the vaccine, I've also been having extreme anxiety, mostly when I wake up but also associated with the mediation off times and my vision is blurred.


Comments

Post a Comment

Popular posts from this blog

When the Phone Stops Ringing

Image
At first, I didn’t want to tell anyone. When I was diagnosed with Parkinson’s disease, it felt like a private earthquake—my world shifted, but from the outside, everything looked the same. I thought if I just carried on as usual, maybe people wouldn’t notice. But Parkinson’s has a way of showing itself. The the frozen face, the slow movements, the voice that gets softer without me realizing it—it all adds up. Eventually, people began to ask if I was okay. That’s when I started telling the truth, at least privately to closer friends and family. I’d try to sound calm, even casual. “Yeah, I’ve got Parkinson’s,” I’d say, “but I’m doing all right.” I didn’t want sympathy or a sad look. I just wanted people to understand. Most of them reacted kindly. They said things like, “You’re strong.” “You’ll beat this.” “Let me know if you need anything.” And they meant it—at least in that moment. But as time went on, the calls slowed down. The texts got shorter. Invitations stopped coming. It’s not th...
Read More »

Medical bill decoded by ChatGPT

Image
Forget 8 minute doc appointments-for around $20 out of pocket, you can get a more detailed appointment. My movement disorder specialist checkup usually involves multiple doctors that are thinking, exchanging ideas, and keeping me in the loop. My input is heard. The appointment can last over an hour, could be 90 minutes sometimes. Maybe I just never noticed it before but code G2211 changes my appointment from a quick hello you look great, see you in six months to an actual doctor exam. Have you seen a billing code of G2211 on any of your bills? A simple explanation of the medical billing code from ChatGPT: The code G2211 is used by doctors when they believe your visit involved extra time, effort, or complexity beyond a standard appointment — usually because of your overall health situation or ongoing treatment needs. Here’s a breakdown in plain language: "E/Ms" stands for Evaluation and Management services — basically, your regular checkups or doctor visits. "G2211"...
Read More »

The Job No One Sees: Life as a Parkinson’s Caregiver

Image
Trying to explain to someone how much my spouse does for me is not easy. When they ask how my spouse is doing, my jaw tightens, my heart races and I want to disappear. But I calmly and politely say "she's fine."   So I asked ChatGPT to help me out and describe the life a caregiver.  Life of a Caregiver, described by Chat GPT (AI) There’s a job out there more demanding than most people can imagine. It’s 24 hours a day, 7 days a week. No salary. No sick days. No weekends off. No benefits package. It comes with high emotional stress, physical exhaustion, and a level of responsibility that never lets up. It’s called being a caregiver. Specifically, a caregiver to someone with Parkinson’s disease. When people think of Parkinson’s, they picture the tremors. The slowness. Maybe they’ve seen someone shuffle or freeze mid-step. But what they don’t see is the person behind the scenes—the one making sure medications are taken on time, adjusting the daily routine around unpredictable...
Read More »