First Dose of Pfizer on 07/02/21
United Kingdom
22 yrs old
Q: What was your life like before you got the vaccine?
We were in lockdown off and on for a while, but I was living at my mum's with my sister. We would go on walks, and I would go skateboarding most days. We also went on holiday to Cornwall. I was pretty happy.
Q: Would you like to share your reasons for getting vaccinated?
I felt pressured a lot by society in general. I wanted to be able to travel, go out clubbing at university, and be allowed to do other things. I did also want to protect myself, and I definitely wasn't against it at all. I was a bit hesitant. My mum made me an appointment, and I put off having it done. She ended up calling me anti-vax, which made me feel a bit stupid, so I decided to go ahead and get it. I definitely regret my choice now.
Q: What was your reaction, symptoms, & timeline?
It started 2 weeks after my first dose. I felt extremely dizzy and unwell. Then my arms and legs went numb, starting in my hands and spreading upwards. I still had some feeling but barely 30% of normal. I also had vertigo, rapid heart, chest pains, tremors, dizziness, dissociative, seizures, extreme anxiety, fatigue, confusion. I basically thought I'd had some sort of stroke. My symptoms have varied over the course of 8 months now. I also developed some vision issues, including blurry vision, and seeing flashing green dots and flashes of white. At the moment, I am having heart issues. My heart races whenever I do any small activity, and I have shortness of breath.
Q: What is your life like now, after getting the vaccine?
I wake up most days at 1pm. I have really bad insomnia, and I usually finally fall asleep at 5am. I am mainly in bed at the moment. My mum works, so I am alone in the flat all day. I try and get up and do yoga or go for a walk, if my symptoms aren't too bad. I am mainly lying down, because I have really bad chest pains and shortness of breath, if I try to do anything too physical. I am constantly stressing out, because I develop new symptoms all the time and some of them feel really worrying.
Q: Share your experience with any medical care and any diagnoses you have received:
I have seen a private neurologist, a cardiologist, and a functional doctor. The neurologist diagnosed me with FND, and the cardiologist has diagnosed me with POTS. I have been to A and E about 5 times. Every time I go there, I just get told that I have anxiety, and doctors don't listen to any of my symptoms.
Q: Was your reaction reported, and what was the response?
I reported to the yellow card reporting system in the UK, and I had no response.
Q: Is there anything that has helped, and have your symptoms improved?
For me, nothing I have tried has really helped. I think getting a good amount of sleep makes a difference, and any time I can do exercise, it helps. The only thing that has really helped is time. It seems like there is a timeline of different symptoms. Some symptoms improve, and others change over time. I think in general, I have improved slightly over the 8 months.
Q: Have you had Covid before? What was your experience if so?
I haven't had covid before. I tested myself when my symptoms started, and I have never tested positive or had any symptoms.
Q: What do you wish others knew?
That you are not alone. There are a lot of people like us who, for whatever reason, these shots did not agree with in the slightest. If it gives you any hope, I thought I would never see any improvement, but these last couple weeks, I feel like I am getting better. Still nowhere near normal, but definitely better.
Tell Your Story: www.realnotrare.com/submityourstory
Subscribe: www.realnotrare.com/contact
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.