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First, I have been trying to get back in touch with the dr as I do not know what to do now. The pain has decreased during urination but only modestly, as I have this tingling sensation throughout the length of my urethra. Can feel it all the time. Lower back pain and pain in my legs. My Famciclovir runs out today and I am still waiting for the dr to call me back.
Also, I am frozen in fear, shame, and depression. I know what I did was stupid, but I am now here. I have been reading as much as I can but it only makes me more scared of the future. Having to live with this for the rest of my life.
If anyone can help me, I would appreciate. So scared that I have spent the last 3 days home from work because of my depression.View Thread

I have many questions and wonder if you could provide some help. First, I have read that some people prefer not to medicate at all as they want their body to build it's own 'fighters' for outbreaks. Is there any truth to this belief? Terri mentioned in her book that medicating outbreaks has no bearing on severity of future outbreaks. So curious if the opposite is true?
Also, in having HSV2, is it still possible to get HSV1?
Lastly, seems reoccurrence outbreaks vary widely for people both in severity, length, and number per year. I cannot find an average typical expecation of outbreaks. Any insights, and follow up to that would be given your long experience with H, how and what do you do to deal with outbreaks?
Thanks.View Thread

Still very scared and freaked out. Trying to find a therapist that I can talk with about the mental aspect of what I am going through.
I mentioned to my dr that he only tested me for herpes, gonnorhea, clamydia, and that he never tested for HIV. He made a comment that I may be getting ahead of myself and to be calm.
So freaked out.View Thread
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