Dealing with Molluscum Contagiosum.
MCV is a pesky skin virus common among children but also increasingly prevalent among adults, and treatment is not always trivial. How do you deal with being contagious?
I have grown exceedingly cautious of physical contact (even with myself, since MCV is auto-inoculating: imagine not be able to touch your face without washing your hands afterwards!), and now I'm entering a relationship with a girl where physical contact is necessary; in fact, we are already at the kissing/cuddling stage, and I have slept next to her on two occasions. I'm frozen up with the fear that I may have already infected her, and obviously feel like a real bastard for not having told her yet. It's hard to confront someone with this information: not only because I'm ashamed of my condition, but also she would really have to choose between risking infection, and not getting involved with me. While I don't want to lose her, I truly don't want to inflict this condition on anyone else, and the thought that I might have infected people in the past (which, to my knowledge, I have not) disturbs and saddens me immensely.
How do you deal with the social aspect of this disease? When, if at all, do you tell a person that you're contagious? I'm so psychologically disturbed and ashamed by the condition that rather than explaining beforehand, I would rather not say anything and then afterward explain that "I
thought I was no longer contagious but apparently had a flare-up"; even though this is in violent disagreement with my principles.
To add some background, I was infected 2.5 years ago, and while it's been a long time since any true lesions broke out, I still have symptoms, and presumably I'm still contagious. At this point, the lesions that break out are not itchy, and they are either indistinct red spots that fade away quickly, or they look exactly like pimples -- red, volcano-shaped, white pus-filled tip, no central dimple as typical of true lesions -- and which break and fade relatively quickly. In other words I seem to be at the end of the disease's cycle. I'm otherwise healthy, but I do suffer from psoriasis, which was probably a factor in my initial infection and might explain why the infection has persisted for so long.
According to medical literature, MCV can last anything from 2 months to 5 years, with a mean of 2 years. During this time, it infects both through direct physical contact, and indirectly such as through bedding or towels. According to some sources,
most people are immune because of childhood exposure, but this fact is not widely reported. Mainstream treatement involve surgery, and while there are some recently-discovered treatments that seem promising, the rates of success seem low, success stories are
largely anecdotal, and nobody really seems to know much about MCV; it's not a popular disease to cure. (There also seem to be a lot of snake oil out there, eg. based on
silver.)
Back when I had the full-blown lesions, I had a few surgically removed; after that, I started used topical echinacea and comfrey creams, combined with anti-acne soap, and reached the stage where I'm nearly well. I'm almost certain that the echinacea works, less so about the comfrey. I would love to hear about other possible treatments, though I suspect most people just go for curettage or cryosurgery.
posted by mcwetboy at 2:24 PM on June 1, 2005