Thanks.
Sounds like you have answered your own question then. Qualifications are always a plus. I gave mine and now you gave yours. It's obvious nothing I say will be good enough, but my medical team ran into a brick wall and these tests showed irregularities along with tests and labs i received from researchers I've already discussed. I can't make people here believe me and have stopped trying and why i wanted to drop this and continue to have the conversation here, but from a little farther out. Lots of smart people here and I'm learning a lot.
And again I had a novel disease (reaction to spike protein), not totally unlike Lyme or ME/CFS. As you know in your training (or maybe not, I'm making an assumption) the symptoms to these diseases are real, but the diagnostics are still unclear as to why the body reacts how it does and what drives the long term symptoms. The standard bloods are clear for most people with the above diseases and long covid is no different. Now if you don't believe in Lyme, ME/CFS, and long covid then we have to be done here because we're not even in the same universe.
Is it really so hard to believe a team of medical professionals could think outside the box to try and help a patient that's suffering? I mean my doctors found a clinical use for the tests in my case and I'll only speak for myself, maybe for other people and in your opinion they are of no consequence. I can accept that. Second opinions exist for a reason.
Let me ask you this. Do you think the research you're aware of into long covid is sufficient? Do you have other tests you'd recommend (d-dimer was in range)? What was i supposed to do, lay on the floor in the fetal position waiting for a phone call with the answers to my problems?
I won't go back into the treatment (just quickly, i was on the treatment for 5 months total, weaned off, and have been completely off any medications for the last 1.5 years), which did work, but it wasn't something i took lightly and took 3 months to get the courage to try it. I worked with researchers at a prestigious institution aswell as my doctors locally. It was a team effort with professionals and i was monitored closely. These tests weren't the determining factor, but they were clues.
That's as much as i want to talk about that here and i hope this is good enough for you. I really don't want to have this conversation. It became clear i was triggering people with my story and i just wanted to leave a couple very easy tests as an idea for anyone struggling to find answers if they find themselves in the same situation. Sorry if you think I've harmed anyone in suggesting a painless blood test their doctors would interpret. I have stopped giving that kind of advice and will keep personal details private. Best i can do at this point. I have good intentions as someone that lived it and i really do understand the apprehension, especially from heathcare professionals but i needed to get better and i took a risk. It's easy to be critical from the outside looking in. We can re-litigate this again tomorrow morning if you'd like, but this is the best answer I'm comfortable giving.
I believe you mean well, but you're not a long covid researcher and I'm presuming you have no experience treating patients that are suffering from it. I'll defer to my team over internet advice with all due respect.
Edit to ask a question: I'll ask a question about my personal experience since you're insisting I expand and my TAT test in particular since this is your area of expertise. What do you make of my TAT score being >60 on a quest lab diagnostic test when the reference range ends at 60. My use of the therapy that will not be mentioned (Eloquis in particular was explained to me. I only say this one drug to help you give a better informed answer) lowered this (along with other markers they identified) and at the same time i began to heal.
Edit 2 electric boogaloo. As a show of good faith if you (or anyone else here for that matter) can identify posts i made that i didn't sufficiently source, didn't make clear were my opinion, or you feel is dangerous misinformation make a list of the post numbers and report them.
@Joe Bryant or moderation can delete them, or ask me to do it and I will. No questions asked, no complaining on my end. I'm telling my story as it happened and what i experienced finding treatment. It's pretty upsetting to quite a few people here and it's the same irl, so nothing new. I won't fight it. I didn't personally work with Dr David Putrino at Mt Sinai, but he may have the clout and answers for you if you were to email him (or his team) if you would truly like to learn more about what I'm talking about from a medical researcher looking into the clotting irregularities with long covid. If he refutes that microclotting is something they've found and that a d-dimer is sufficient in their research I will stand corrected, accept my beatdown and highly appreciate the correction.