First Dose of Moderna on 07/24/2021
Second Dose of Moderna on 08/21/2021
North Carolina
47 yrs old
Q: What was your life like before you got the vaccine?
My name is Martese Gee. I’m a 48 year old, single parent to four children, ages 9, 12, 21, 27 and my whole heart is my grandson, who will be 3 yrs old in November. I was a busy mom with a busy life, supporting my children in cheer and basketball and enjoying exercising and staying in shape before this. I was completely healthy!
Q: Would you like to share your reason(s) for getting the vaccine?
Mandated by my employer
Q: What was your reaction, symptoms, & timeline?
After the 2nd dose of the vaccine in August, I started having jaw and hand cramping, difficulty swallowing certain foods, and muscle twitching.
I was seen by the neurologist and had an MRI, a CT Scan, Ultrasound and EMG, which brought about being diagnosed with ALS on March 15, 2022. On that day, my world was shattered.
Since diagnosis, I have been to several doctors for testing and treatment, but nothing has proven effective at reversing my symptoms. I’m in the early stages of the disease, and I literally feel as if I am fighting for my life. I am currently experiencing slurred speech, difficulty swallowing, weakness in my left hand, and muscle twitching. I know God is my Healer, but everyday is a real struggle. My children are the reason that I get up and continue to fight. I want to live to see my youngest children graduate high school and live out their dreams. To be completely honest, I’m angry.
Q: Have you had Covid before?
Yes, had Covid in Jan 2022, was sick for about 1 month.
Q: What do you wish others knew?
I wish I would not have taken the vaccine.
Please share our stories!
Check out more stories at www.realnotrare.com and www.canwetalkaboutit.org
Story Submissions can be submitted here:
Subscribe Here: 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.