Good Morning,
Last month I had the worse outbreak that I have had in the whole 9 years of having herpes. I can't remember ever having so much discomfort. My whole body felt like a severe sunburn. I don't know if anybody can relate to that sunburn feeling. My outbreak usually have the same MO travel across my shoulder down my back clear down to the bottom of my foot. I am aware that herpes are often on nerve endings. The lesion is the least of the problem for me. It is all the other discomfort that comes along with it. I get flu like symptoms. This last time I felt like I had the flu and a sunburn. Rarely do people understand that this disease is often very debilitating. An outbreak is a constant reminder that I am different and that I have to lead my life in a very self preservationary way. Has anybody had a drastic change in the occurence of their outbreaks. Any advice, suggestions or support would be appreciated.
Bright Blessings,
Tristan
Last month I had the worse outbreak that I have had in the whole 9 years of having herpes. I can't remember ever having so much discomfort. My whole body felt like a severe sunburn. I don't know if anybody can relate to that sunburn feeling. My outbreak usually have the same MO travel across my shoulder down my back clear down to the bottom of my foot. I am aware that herpes are often on nerve endings. The lesion is the least of the problem for me. It is all the other discomfort that comes along with it. I get flu like symptoms. This last time I felt like I had the flu and a sunburn. Rarely do people understand that this disease is often very debilitating. An outbreak is a constant reminder that I am different and that I have to lead my life in a very self preservationary way. Has anybody had a drastic change in the occurence of their outbreaks. Any advice, suggestions or support would be appreciated.
Bright Blessings,
Tristan
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Re: an outbreak
Mon, January 10, 2005 - 10:49 PMHi Tristan,
I can relate to the sunburn thing. My H is genital and causes deep muscular discomfort in my thighs and buttocks as an outbreak erupts. It feels like sunburn - I don't want anything touching it - I believe Shingles feels similar.
In my experience (I've had H for 10 years), outbreaks are usually caused by physical damage. If my now ex-partner was too "rough" with "certain parts of me" during sex then I would gradually develop (over the next 12 hours) the symptoms of sunburn, leading inevitably to lesions. I found that bathing them in salt water (ouch) would ease the lesions quicker than any fancy oitments - and much cheaper too!
The only other link I've found between general health and outbreaks is to do with stress. Too stressed or tired and the ourtbreaks come easier and are more diffcult to get rid of. I usually average about 2-4 a year, some pretty insignificant.
The flu thing I've also experienced, but not quite as bad as you. More a mild fever and feel rough for a day.
And by the way, you're not so different ;-) It is a cross spome of us have to bear - I'm newly separated after 11 years,and in a new country as well. I've still got a lot to be happy for, and although not relishing the day I have to tell a new partner, will forget about it until then. It doesn't matter whether it's H, or asthma, or hernias (!), everyone has something "different" about them. Try doing a search for H-dating or "437737" on Google to see just how many people are in the same boat. About 20% they reckon.
Celebrate your individuality!
Tim
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Re: an outbreak
Mon, January 10, 2005 - 11:12 PMTim,
Thank You so much for your support. It really is great to know that others have similiar symptoms and concerns. I also will develop an outbreak if sexual intercourse is too rough in a particular part of my body. I really thought that was only me. I guess I was wrong.
Bright Blessings to You Tim. And Thanks for sharing. It is great appreciated.
Tristan -
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Re: an outbreak
Thu, March 17, 2005 - 10:54 AMwow. sorry to hear y'all get the larger attacks. I knew a girl that got it on her lower back only.
I just get a bump or two in the nether regions. Of course I'm new, had my first outbreak in 03.
Is there evidence that the condition gets more extreme as years go by? And re colonization can give you even more possibilities of breakouts. I know about the stress thing and have altered my life accordingly. But does duration of infection have something to do withh severity?
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