I cleaned this up a bit to avoid doxxing myself, but here's the copy pasta:

Before I can commit to an experimental mRNA injection, I have a several questions that do not fit into the two accommodation categories provided by corporate.

1.) Can corporate provide information stating how the mandate is a legally binding law?

a. Is corporate certain that a medication which is available only under EUA (Emergency Use Authorization) will not cause myself and family harm in the future?

b. The CDC and VAERS.hhs.gov (Vaccine Adverse Event Reporting System) has records of 48,000+ people dying due to complication of the injections.

i. Suspiciously, individuals that receive the injection are not considered fully vaccinated until 14 days after the second dose. The vast majority of those deaths occur between 1-3 days after the second dose.

c. Who will be responsible if I suffer any of the known side effects such as Myocarditis, Blood Clots, Guillain-Barre Syndrome, Sarcoidosis, Autoimmune Disorders, Cognitive Disorders, and many others?

d. Will my family or I have any legal recourse or financial compensation if incapacitated?

2.) Can corporate explain how I, who work from home all but 3 – 4 days per month could potentially infect someone working on a government contract with a virus that is 99.97% survivable?

3.) Can corporate explain why I can’t use drugs prophylactically that are already approved and have been in use for several decades in place of mRNA? Approved drugs like:

a. Ivermecten – Merck has provided 250 million doses in pill form annually to combat viral illnesses worldwide.

i. Awarded Nobel Prize in Medicine in 2015 - https://pubmed.ncbi.nlm.nih.gov/34466270/

ii. Been prescribed to humans for 20+ years.

iii. Little to no side effects.

b. Hydroxychloroquine – Developed in 1934 and has high success rates of eliminating COVID viral symptoms and promoting a quick recovery.

4.) Can corporate explain why mRNA treatments (Messenger Ribonucleic Acid) are better than traditional flu-virus treatments?

a. Early treatment protocols (Vitamin C, Tamiflu, Zithromax, etc) for past flu outbreaks have suddenly and suspiciously been abandoned in favor of experimental mRNA treatment.

b. Why did all the animals subjected to mRNA testing die and how may this be related to any detrimental effects from mRNA therapy?

c. Which injections contain fetal tissues and what why are they included in the injections? Ref HEK293

5.) Breakthrough infections

a. Why are break through COVID infections increasing especially in countries (Israel & UK) with high vaccination rates?

b. What is the benefit of receiving the experimental injection if I can still contract and spread the virus?

I look forward to a reassuring response or formal exemption. Please let me know if you have any questions.