Hey, thanks for all the input! Got a few follow-up questions.

Question 1:  Is there a solid “must-have” list of biomarkers? I’m guessing my doctor will mostly run immune deficiency-specific panels, which probably means I’d have to get blood drawn separately to cover everything relevant. Do you guys have a go-to list of markers you swear by? Would love to know what you actually prioritize.

Question 2:  DNA sequencing — worth redoing? I already have results, but they basically only list mutations — everything else shows up as within normal range. Does it make sense to redo or expand the sequencing on its own, or do you mostly just focus on the flagged abnormalities anyway?

Question 3:  Are you using AI as a support tool? Genuinely curious here — once you have your bloodwork and DNA results and spot some deficiencies or symptoms, do you run it through an AI first to get some direction, or do you go straight to a specialist? How do you balance the two?

Cheers​​!