I’m going to be very brief about this; otherwise, I could write a book.
I was a single, sexually-active gay man, living in NYC when the epidemic began. I remember when there were merely a handful of men who were dying of a mysterious illness. I immediately joined GMHC (Gay Men’s Health Crisis) as a counselor and “buddy”. When ACT-UP began, I joined that too.
For the next 15 years, I watched almost all my friends, lovers and acquaintances drop like flies. The exception was my now-husband, whom I met in 1987. I held people’s hands while they were dying; I administered meds; I emptied bedpans; I attended countless funerals and memorial services.
After we relocated out of NYC, the numbers slowed down, but haven’t stopped. We attended our last funeral last year.
I hate referring to ourselves as “survivors”. With the death of each loved one, a little of our own lives is gone, and less remains. In moments of optimism, we think that it gives our own lives purpose, that we have a mission to continue the work of those whose lives have been shortened. But in moments of pessimism, we realize that this is too much of a burden, a weight to heavy to bear.
That’s all I can say, for now.