I feel your pain (literally). I have had both strains for a total of 20 years now. After the horrific first outbreak, I rarely ever had outbreaks and if I did, it was a single bump that looked like a zit.
I was exposed to mold for several years and then after a particularly bad basement flood at my job, I started to have back to back outbreaks (still mild in severity), but still annoying nonetheless. It has now been a few years since that flood and I have never been in worse health than I am in now. The nerve pain is debilitating; it has robbed me of my short term memory, my cognitive and Comprehensive abilities have been severely diminished; I’m exhausted all the time and every time I orgasm it makes all my symptoms worse. It is absolute, pure hell. A lesion is now the least of my worries/problems. I am on a rapid decline that I am afraid will lead to cancer, Alzheimer’s or both. I have been to tons of different specialists and have gotten many second opinions and no one can find any other causes for all of my physical symptoms and cognitive decline. I am only 39 and yet, I feel like an old, tired, (and sometimes, bitter) woman.
I feel the same way as you in regards to my mate. He is 50, neither of us have been married and we don’t have kids. He knows I have herpes and has chosen to continue to date me. (We’ve been exclusively dating almost 3 years). We are both somewhat religious and haven’t had sex yet (with each other, I mean). It doesn’t bother me because we have other forms of intimacy. We are getting closer and closer to an engagement, but if he knew the true extent of what this disease has done to me, he would freak the f**k out and I couldn’t blame him. When I initially revealed my status to him three years ago, I didn’t connect all of my nerve pain and cognitive decline, etc. to this disease. I know more now than I did then and I’m conflicted as to how to continue our relationship. So, I can relate to where you are coming from and I empathize with you.