That is certainly useful information that I will look into as soon as possible. Thanks!
I am so glad to hear that I am not the only one having this problem. I had began to worry that maybe my HIV test was incorrect because every time I type in joint pain and STD's only ghonorrhea (however it's spelled) and HIV come up. But anyway, I would like to see a specialist because like you, I never once had joint pain before until about a year after my diagnosis. When I was first informed of my HSV 1&2, my doctor told me that with the initial infection joint pain was common. I didn't think anything else about my herpes until so much later when unexplained joint pain began to occur and there was never another outbreak. I just don't get how the joint pain is EVERYWHERE! What does your doctor have you taking for the joint pain? Is it short or long term relief? and I definitely think you should mention the HSV to your doctor. Does he or she think that this sudden joint pain is completely unexplainable and what does the doctor say?
I agree about telling your doctor about herpes. There's no reason for them not to know, and on the very off chance that this is being caused by herpes, you aren't letting your doctor treat you the very best he can if he doesn't know.
Aj
I understand why it is important to tell Doctors the whole story,but my problem is I work in the hospital and know my Specialist,I also know many members of staff who work alongside him having worked there for over 17 years,I also know how staff talk amongst themselves regardless of patient Confidentiality rules,therefore I would not even consider this being documented on any medical history they would be liable to read,the Herpes is mine and not up for dicussion in the coffee room I would also then feel that everyone and their Granny knew my status whereby at the moment only myself and my Doctor ( outwith the hospital) knows and i'm happy to leave it that way,the Herpes doesn't bother me personally I am just not about to single handedly try to eraticate the stigma that has been impossible to do since Genital Herpes began,it has always been one of those conditions that those who don't have it love to talk about especially if they get wind of someone they know having it,we can talk about Patient Confidentaility till we are blue in the face it will never stop the chat that goes on among work collegues always adding "don't say anything about what I told you" I would then feel I was in a "nudge nudge" situation believing everyone knew,and I certainly don't need to add that to my problems right now .....
Besides it would make no difference if my Specialist knew or not they are two separate conditions and require different treatments,if i now have RA I have it there is nothing I can do about that either,I don't see that telling him I have Herpes is going to change things or make any difference to the way I would be treated if I didn't have it.
If having HSV2 wasn't such a taboo subject no one would need to hide it,but sadly society isn't going to change in the foreseeable future.
Daisy
To the original poster.....
there are many, many viruses out there that also cause all over joint pain. There is no reason at all to suspect your herpes has anything to do with this. See your provider for a further work up since you've felt so crappy for 2 weeks now.
grace
I do believe however that any infectious disease has the ability to trigger other conditions such as RA/ Fibromyalgia/Peripheral Neuropathy is some people ( not all ) ..... From what I have read about RA unless it is a genetic condition it can be triggered by other things,so it is very likely had I not got Herpes I wouldn't have got RA either but in saying that something else might have triggered it off like a bad flu or something.Our bodies are so complex :(
Daisy