We have ruled out all of the major kidney and immunity diseases so that is good news. What jack possibly has is called Minimal Change disease ( http://en.wikipedia.org/wiki/Minimal_change_disease ) and I say possibly because we still aren't 100% sure he has this because he isn't showing one of the key symptoms which is Edema. When the pathologists blew up the cells in his kidney, they could actually see where the protein is leaking and it does in fact look like its minimal change disease. Hence the possible diagnosis. We will start a dose of steroids and see if he responds, if he does then we know that he does have this disease. If he doesn't respond then we go forward with genetics testing (blood tests) to see what else it could be. We see the doc on Monday afternoon to get the prescriptions and testing strips to test his urine. This is how we will see if the meds are working - checking the protein in his urine. We should know if he is responding to the meds in about two weeks but it could take 3-4 months to see the proteins in his urine return to normal.
2 comments:
what a relief to know that it is something treatable and not something really horrible! Love you guys and glad you are beginning to have answers.
Is this something that he would have to always take medication for or that would be able to resolve itself with these steroids? What are his sypmtoms right now? I know you must feel relieved to be able to atleast be able to do something to try and help him! It sounds like you have some great doctors. We love you guys!
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