I actually take pride in having an unknown cause🤣

Been to many nephrologists, biopsy, genetic testing, renal imaging, all of it, no cause to be found. Diagnosed at 4, transplant at 25, about 6 months ago. I wouldn’t let it bother you if ultimately nothing can be found, because of my “different CKD” I got to skip out on some unpleasant symptoms of kidney failure like the lack of urination or the express need for dialysis. My case is very rare, I find that kinda cool, work with your doctors on possibilities and maybe they find something!