Hi there, my name is Anne and I’ve had
herpes since roughly 1987. Guess that makes me somewhat of
a veteran, but I can still clearly remember the fear and
devastation that went with the diagnosis. The first few
years I didn’t handle it so well – resources were very
limited back then. I avoided relationships and shared my
secret only with my sister (a nurse) until one day I met my
subsequent husband. Basically – if he survived "the talk",
that qualified him as "a keeper" for life! I never wanted to
go through that again…
For the first 10 years or so, I kept a
very close record of my outbreaks so I would be fine tuned
with my body. I used to have 5-8 a year and was able to
recognize when they were coming and what the triggers were.
In the mid 90’s all those doggone Valtrex commercials
finally sunk in – I wanted to toss my records, go kayaking
and have no worries! So, in 1999, I started on Acyclovir and
have been relatively outbreak free since.
In 2001 my 10 year marriage ended in
divorce (talk about stress – double up on the meds!!). I had
been living quite reclusively, so my social circle was
nonexistent. In the lots of spare time I had, I began
researching herpes online to see what
the latest scoop was.
I was amazed at all the resources available! In addition to
all the facts, which gave me much better insight, there were
Social Groups,
Singles Sites,
Support Groups – Oh MY!
By this time, I was beginning to
realize that I needed to meet people and even thought about
dating again, although I was frightened to death about "the
H factor". I decided I would start by dating within the
circle, so signed up on one of the H sites. I also met a few
people on-line through a herpes related chat room (something
I was completely new to as well). It was so easy to
"blindly" talk to strangers about herpes – I finally felt
like I really belonged! These people knew what it was like!
It was through one of my on-line pals
that I found out about a local social group, so I began
going to a few group functions as well. This was another
vital mechanism to opening up and becoming comfortable with
the fact that although herpes is part of who I am, it does
not define me. Life can still be good and fun and yes... I
even took up kayaking!
I assumed the role of "Social Queen"
for the local herpes social group
the Seattle H Scene in early 2003. I’ve met so many
wonderful people from all walks of life, veterans and
newbies alike. I have been inspired by many, which has led
me to explore additional involvement in the herpes
community.
My philosophy in this is to be
knowledgeable, be responsible, stay positive and don’t let
it take control. Having herpes, though challenging at times,
is manageable. Know that you are not alone in this. I
recognize that everyone copes in their own way, but having
someone to turn to can be a huge help. If you’d like to
talk, feel free to contact me any time! -
Anne