Anytime!

Thank youuuuuuuu 🥺❤️

Yes it is! Thank you so much for initiating it! ❤️

Anytime! I really appreciate your discussion as well.

We didn’t get super deep, so if you have any lingering questions, I’m always happy to discuss further.

Would you mind if I share this thread to my page?

There is the Emergency Use Authorization process that we saw for the Covid vaccine that everyone was wary of. I will simply link this for further reading: www.fda.gov/vaccines-blo...

Drug companies (the sponsor) want their drug to be approved, but then you have clinical personnel (medical doctors, nurses, etc) carrying out the study at multiple sites, and then the third party Institutional Review Board (IRB) checks *everything* to ensure the processes are honest and ethical.

I wholeheartedly agree.

I’ve worked in clinical drug research for several years. While it is by no means perfect, I do have respect for the approval process.

I’m very glad you took the time to take care of yourself.

That’s awful. I’m very sorry.

My kids and I experienced a drop in our immune systems like that when we moved across the country to a dry climate from a sub-tropical one.

There are a large number of environmental factors that play into our immune response.

Long-term drug and vaccine studies are often needed to show that many seemingly random occurrences of a symptom that are deemed “just one of those things” by someone’s doctor are actually a qualifiable subset of symptoms from a certain source.

All of this being said, the FDA is responsible for drug and vaccine approval. Their job is to make sure dangerous products don’t go into market. Things go to market is they are “safe enough.”

They do not do much in the way of optimizing these drugs/vaccines for least harm.

Here’s a study I found looking for viable alternatives to aluminum adjuvants. www.sciencedirect.com/science/arti...

There appear to be viable alternatives. I’m sure cost, ease of access/availability, etc are barriers to switching over.