Response from Dr. Sherer

The good news in your story is that you feel great, and your T cells have climbed steadily on your regimen.
All available evidence suggests that drug resistance is more likely in patients who have detectable virus, even at the low levels you have described, than in those patients who consistently have viral loads below 50 copies/ml. Note that this process may take a long time to develop, i.e. months or even years.
Your regimen may be one that can withstand the added pressure for drug resistance to develop. In general, boosted PIs, and lopinavir/r (Kaletra or LPV/r) specifically, have a lesser risk of drug resistance than other agents. Indeed, in patients started on LPV/r as their first PI, as in your case, have shown a remarkable tendency to NOT develop protease inhibitor (PI) resistance mutations, particularly when they succeed in achieving excellent adherence.
Your physician has taken the step of adding a 3d NRTI - didanosine (or DDI) - in order to strengthen the regimen. Although the attempt to reduce the viral load to below detection failed, there may still be added value with this regimen. As long as you are tolerating the regimen, I would advise you to maintain your excellent adherence, and rely on your physician's judgments.
Unfortunately, I can't advise you not to worry at all. Having HIV demands a certain amount of vigilance. I would advise you not to worry too much, or unduly, and not to forget the benefits of ART that you have already experienced, as in the first paragraph above. I would also advise you not to let the possibility that drug resistance is developing overwhelm you. There are options for you in the event that resistance does develop.
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