Archive for May, 2008

L-Lysine Feedback

Posted in Health Buzz | 8 Comments »

I have been taking lysine for 3+ months now. I am truly a skeptic so my opinion is based on experience and not speculation.

Lysine has shown for me to reduce the length and severity of outbreaks dramatically. Normally 9-10 days from initial tingle to normal skin is my recovery rate.

I started with 1g per day and saw a noticeable decrease in outbreak severity. I upped it to 2g per day and reduced the recovery time from 9 days to 3-4 days.

Also the length of time from one out break to the next was increased from about every 30 days to every 45-50 days. I plan on upping the dose to 3g per day and seeing if there is any effect for the next 90 days.

As a side note, for years I was experiencing outbreaks maybe 3-4 times per year. I never treated or used suppressive therapy and just accepted it.

Over the last 2 years, I have seen increased outbreaks to every 30 days. I decided in Dec 07 to take a proactive stance and see if there was any change.

Lysine seems to work at reducing the recovery rate quite nicely but does not seem to reduce the frequency enough to stand on a mountain and claim victory. Maybe this is a cumulative thing so I will stay on the current regime for another 120 days and re-evaluate. – Joe

Read what others are saying about L-Lysine

HPV Linked to Oral Cancer in Men

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A recent study published in the Journal of Clinical Oncology highlights the link between human papilloma virus (HPV) and oral cancer in men.

The study examined data on more that 46,000 cases of oral cancer from the National Cancer Institute.

Researchers found that incidence rates for HPV-related oral cancers rose steadily in men from 1973 to 2004, with HPV causing nearly as many oral cancers as tobacco and alcohol.

Let’s talk about HPV

I tried Chemistry.com and I didn’t like it

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I tried Chemistry.com and based on my experience save your money. There really isn’t much to this site. I saw the tv ads too and gave it a shot.

I started with the trial that is advertised, filled the extensive personality test but didn’t get far before I got a page blocking me from fully using the site without subscribing. The site doesn’t let you see what you are getting until you subscribe.

So I did. I gave it a whirl and did the $99 three month membership. I was presented with 5 potential matches.

There is a slider bar where you indicate your level of interest for each match and then the site contacts them to see if the first impression is mutual to allow you to go to the questions phase or if the match should be archived.

So far this was all well and good except there was more than a little bs going on. According to “Dr Fisher” there are 4 personality categories. Each person has a major and minor personality category depending on your answers to the test. When a potential match is presented, you get a paragraph explaining why you match well with each of the other 15 possibilities (major/minor combinations). Except it becomes apparent it doesn’t really matter what that combination is. You get this vague paragraph in pyschobabblese supposedly from matchmaker Fisher selling you what actually is completely arbitrary.

So this was disappointing. But more I became annoyed when they wouldn’t accept one of my photos. It wasn’t pornographic or inappropriate. It was a facial shot with a blue graphic effect on it that I posted with my standard photos. I got an email saying it wasn’t acceptable because it was blurry even though I had standard photos that showed what I looked like. The point of this specific photo wasn’t to do that but to present myself in a more artistic light. The point of your profile is to present yourself for possible matches and yet Chemistry.com wanted to marshal how I was allowed to do that. Again, I would have understood if the photo was pornographic or something.

After the first couple days I only got 1 to 2 matches every other day or so many without photos and an underdeveloped profile page. This isn’t entirely the matches fault. The site only allows for a general paragraph and photos.

After deciding the service wasn’t worth the money I was paying I wrote them to asked for the prorated portion to be returned to my credit card and for my membership to be cancelled. I have written the site several times now and I only get a form letter telling me to call their CS line. I didn’t want to waste anymore time but eventually I did call, waited on hold and get the predictable nice girl on the phone hired to placate instead of solve any problems.

They refused to refund my money. After investing 30 to 45 minutes of my time she agreed to scale back my membership to 1 month for $50 instead of 3 months for $100 which wasn’t acceptable but I took only because it was all I could get. Again, the girl was pleasant enough but kept telling me it was detailed in the terms no refunds are returned for unused time when you cancel. Of course since I couldn’t see the product until I paid they had me.

It has been almost a week since that conversation and my subscription status page doesn’t even reflect the change they agreed to. I emailed them again about it and they told me to call the 800 number again. So far I haven’t which they are probably counting on.

My experience with Chemistry.com has just been a waste of time and money. They advertise, cast a wide net and once you pay they don’t care anymore. The service doesn’t give you anything you can’t get free at other sites. The psychological aspect of this site is a ruse. Every potential match combination comes with a form letter. Its all arbitrary. The site is very limited. And once they have your money they have no interest in keeping your business. Join a book club if you are sick of the bar. You won’t get your money’s worth here. – Tristram

Read more Match.com and Chemistry.com comments

Telling your Partner

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partners

1) Give them the chance to get to know YOU as a person and like everything about you. How long that takes is entirely up to you.

2) Do it BEFORE you get intimate. If you don’t (in the future), that tells a lot about your moral character.

3) Do it with your clothes ON. Once you’ve let it progress to ‘hot and heavy’, you’ve waited too long.

4) With regard to your depression, talk / talk / talk to anyone you can talk to. Psychologist, counselor, clergy, H-Pal, best friend, whoever.

5) Stay out of ANY potential relationships (even casual) until you’ve had a chance to get your head on straight!

Sounds like you need to be okay with you before you even think about bringing someone else into it.

The one constant thing that I’ve gotten from everyone that’s posted about stressing over telling is that they are not only letting herpes define them but they are letting the presence of another person define who they are as a person and that’s just CRAZY!!!!!

What’s so bad about being with only YOU for a while?????

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Imulux and Lectroject: Interesting Facts

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dumb

Imulux: Interesting Facts

Lectroject Product Analysis

Who do these people think they are fooling?

Imulux – What can it do?

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dynamiclear

People write to me all the time asking me about products and treatments they are finding on the internet. So, on things that I’m not sure of I will definitely ask you my readers about. I will also link the information to my herpes treatments pages so folks can find what they are looking for.

Please remember that if something on the Internet sounds too good to be true then it probably really is too good to be true. Do your homework and look up the research before you buy. Also, don’t ever forget to talk to your doctor first. Don’t let anybody try and diagnose you over the internet either. No matter how knowledgeable they might seem it just can NOT be done. Ok, here’s the latest I received on Imulux…

Angela,

Just wondering what Imulux really can do. I don’t know if you’ve seen the announcement, but I found it on XXX on the recent news page. Is this something that actually kills the virus off, or is it just something that clears up the symptoms, albeit possibly permanently, but the subject would still have herpes and be able to pass it on?

Leave a comment if you know something about Imulux. Feel free to leave a comment if you would like to respond in any way to this topic. For more products and treatments discussion please visit our STD Message Board where you can find a herpes treatment category.

Positive Feedback ROCKS

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happy

It’s so nice to get positive feedback from people. I recently received a note from a young lady that had this to say to me:

The page is great, one of the ones or the best that I have seen, very easy to travel, easy to read, and with a lot of help, topics, stories, and the Shut Up and Post is great! Thank you for all your work, and help… definitely God is with you, blessings to you, your husband, and the girls. ~ Glenda

If it wasn’t for people like Glenda encouraging me and letting me know the site is working I probably would have given up a very long time ago. Thanks so much for being so outspoken and positive!

Ongoing study in Sarasota Florida

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florida

We are looking for Positive Hsv-1, Hsv-2, And Zoster patients for a study on a patented protocol. The process does not involve drugs or pharmaceuticals.

We are examining the ability to diminish out breaks or alleviate them all together. The process has already gone through trails for expedited healing and will alleviate the symptoms at first visit in most cases.

The study is going on in Sarasota FL and the facility can be reached at (941) 706-3833 we have just been sponsor for a limited number of new patients so we are in active recruitment.

The study will include Md visits, treatment, labs, and follow up. We can be reached at Applied Medical Therapies (941) 706-3833. We will treat patients from out side areas but they may not qualify for the study if they cannot return on a regular basis.

We now have several patients with over 12 months and no out breaks. Although this info is only anecdotal. Any interested individuals can call for info.

Our mailing address is:

Applied Medical Therapies
1217 East Ave South
Sarasota Fl 34239
Midtown Medical Park
Necdet Orhon MD

Medical Director e-mail address:

appliedmedical1 [at] yahoo [dot] com

Just Ask Ang :)

Posted in Health Buzz | 2 Comments »

angela1 amj---1

Anonymous asked…
HI, I’ve had Herpes for 3 years now and lately I’ve wanted to have a baby but i cant seem to get pregnant, is the HSV2 interfering with me having a baby??

The HSV-2 has never kept me from getting pregnant and I am fertile myrtle who’s had genital herpes for 12 years now. Have you discussed any of this with your doctor? It might be that you need to see a specialist that will help you figure out why you are not getting pregnant. If you want to check out my pregnancy stuff I have information posted on my Herpes Biography and my Herpes Pregnancy pages.

Eman Cipate asked…
Have you heard of BHT and how it can be used to cure herpes? here is a book called “Wipe Out Herpes With BHT” by John A. Mann and Steven Wm. Fowkes. copyright 1983

Yes, I have heard of BHT. I have a BHT Feedback page set up just for people that are wondering about it like you. Don’t fall for the hype surrounding BHT. It’s all snake oil. As for that book, it’s hogwash. There is NO WAY to wipe out the herpes virus from your body.

She Sits in the Chair

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chair

I can tell she is trying to act as if being here at the std clinic isn’t a big deal.

As usual, I tell my patient that I will be good to her, take care to attempt to stick her only once to draw her blood and get her out of the chair as soon as possible with as little pain as possible.

She doesn’t respond. She is trying not to look at the needle, as do most of my patients. She is concentrating on the pictures and papers I have put on the wall to inspire my patients or to give them something “nice” to read while I am drawing their blood. For some of them it may be the only nice word they get all day. Who knows?

I make sure my words and touches are gentle and therapeutic for my patients. It may be the only “good” touch or word they get all day and I want to inspire them to give that good karma to someone else because they remember how reassuring it felt when they were uneasy and afraid. Still all of the goodness, reassurance and trust that I am attempting to pass on to this gal is hitting a brick wall. Her eyes are empty and I can tell she is asking herself all of the questions that we all ask ourselves when we are in trouble…. especially this sort of trouble… “What have I done now?, Why did I do that? Why didn’t he/she tell me?” and the all encompassing, mind boggling, “What now?”.

I ask her if she would like for me to count or just go for it? She doesn’t respond again.

She is still looking at the wall. I am hoping something has made some sense to her and she is feeling better by absorbing it a bit. I prepare the arm and begin to draw the blood. The moment the needle is inside the vein, the tears begin. Maybe the small pinch of the needle was simply the permission she needed to let go.

“May I have a tissue please?” she asks, embarrassed and sad faced, tears on their journey down her cheeks. I finish the draw, ask her to press on the cotton and reach for the paper towel dispenser telling her, “These aren’t exactly sandpaper but they also are not Puffs.” She buries her face. I do not want her to be embarrassed.

My compassion button has been pushed and activated. This is why I do this job, it is not glamorous, it does not use every skill I learned in school but having walked at least 5 miles in the shoes of every broken hearted person who sits in my chair I feel it does use the lessons – the very hard lessons – that life has taught me. One of those hard lessons is herpes. I work here for a reason. So I tell her, “I have sat in this very chair, please do not feel bad. Illness is not selective – if it is gonna get us – it is gonna get us. Illness does not care how much money we make or where we go to school or church or even what sort of car we drive.”

No response – only the constant flow of tears.

I know my patient is not going to leave the chair. She is curling up in a ball towards the wall. I grab more tissues and gently hand them to her. I push the door shut a bit.

I ask a difficult question. “Did someone hurt you? Do you need help?”

She erupts.

“YES!! He could have told me. He been my man for months and he couldn’t even tell me! His baby momma had to go and call me at 4 in the morning! I tried not to care about him having another girl; I cared about him…. he say he don’t love her but why he over there at 4 am? I tell you why….cause he already went and done this to her!

She already dead and now I’m gonna die too….he killed what I had left. Now I never gone have a baby, now no man gone want me! I’m messed up now.”

And more tears, more and more tears. I hand her more sandpaper Puffs.

I ask her “Why do you think you are messed up Boo? What did he not tell you?”

(I would like to thank whoEVER made the word “Boo” for friend. It is multi-purpose, comes off the end of your tongue, is recognized by most and sits well with my patients.)

She looks me straight in the eye for the first time since she has been in the room.

“His baby momma tol’ me! She tol’ me he has herpes and he give it to her and now she got to be careful when she has dis baby, maybe the baby will get it. I dunno if I care. I don’t wanna be hateful – I don’t want God to hate me cause I hate him but I hurt, an maybe dis isn’t all he give me. Di’we check me for hiv? Oh God! What if he gimme that too?” She is quietly breaking down in the chair. Her tears are racking her and still she tries to hold it together through this revolution – this sudden burst of painful “what ifs’.

I tell her that we have done an hiv test and it will be back before she leaves the clinic.

She is crying less now. She is trying to be big and brave again with little success.

I take her hand and look her straight in the eyes and tell her, “IF you really do have herpes – IF this is what is really happening – there is help for you. I have herpes. I am married. I have a wonderful life. This is not the end, maam; life begins over again so many times in our lives. We lose something and we gain something else.”

She looks at me as if I just told her the sky has fallen. “How do you gone stand there and tell me you have dis? You don’t act like it!” Not wanting to bring up that even a person with herpes doesn’t act a certain way, I remind her that I had told her I had sat in the same chair, felt the same way and admitted I had probably acted worse.

My patient takes her hand from mine, she stands up, I think she is going to leave the room. Have I upset her? She puts down her sandpaper Puffs – and she hugs me.

And cries a bit more. I tell her as she is hugging me that this is NOT the end and we really don’t even know if that is what it is yet. I tell her that I will be waiting when she comes out of the room with her clinician and I hope she will be smiling. In fact,

I am counting on it. I tell her if it is what the baby’s mother has told her it is – I will help her. But we will cross that bridge when we get there. I help her dry her eyes, give her one more little hug and tell her that after she gets her exam, I want her to come back and see me so I can know how she is.

There is a small light in her eyes that was not there before. She is just a tiny bit more alive than when I first saw her, a bit more hopeful perhaps. Again, she looks me straight in the eye and tells me “We gone figure dis out.” I tell her “Yes, we are.”

I believe she gave me the only small bit of a grin she had left in her. I gave her a wink and told her I would be here when her exam is done.

I am busy drawing more blood but I hear her called into a room. Her samples are taken and given to the lab. The patient is back in the waiting room nervously watching some television. In my heart I am praying the TV hasn’t been turned to Springer or some other nonsense show that might upset her. I try not to allow those types of shows in the clinic waiting room for a good reason. At the clinic we handle tough situations and on sensationalizing-type talk show, those tough situations are used as entertainment.

But she seems fine and is watching some old movie. Her Practitioner calls the patient back in. This is when they receive the results of their visit.

I am waiting.

I am stocking my room and sense someone is there, I look up, it is her…..and she is smiling! I put down my Sharps containers and she is coming into the room and she gives me another hug. NOT like the first one – no, this is so much different.

She has grabbed me and is holding me in a bear hug and patting me saying (nearly chanting!) “It izin’t herpes! It izin’t herpes! The doc say if dis is herpes he will eat his hat!” She is laughing, jovial and maybe a bit overly euphoric but hey! 20 minutes ago she said she was dead. The dead have suddenly come back to life with this bit of good news. I am elated for her.

She pulls back from our hug and pulls up her shirtsleeve, revealing a tattoo. It is a tattoo of a heart and it is made of bricks, only it is not finished. She says to me “I started this tattoo 3 years ago when my first ol’ man beat me and I ran away from him. When I get mad an’ sometime when I get hurts I go to the tattoo place and have another brick or two put in. This morning I told myself if I have the herpes I am filling it all in, ev’ry brick, and I am neva gone trust no one again, now I’m not gone do that today. I don’t have that herpes and I am happy. I am also happy not to have to go to the tattoo place cause it hurt when he does it.”

I am also very happy for my patient. She has been spared a life’s tragedy 1 in 4 of us live with every day. Many of us who are now reading this do have herpes and hopefully are making the most out of every day – despite this.

I tell her “I want you to think about not EVER having another brick tattooed onto that heart, not only because I hate to think that your young heart would be that hardened, but also because – doesn’t that mean they win? The person who hurt you and put another brink in your heart will be engraved on you and you cannot be rid of them. You will continue to carry them around with you brick by brick. Do not reward them with a permanent place on your body so that every time you see your tattoo – you remember they hurt you. Does that make any sense? Just think about it.”

I can tell that she is thinking about this. But I can also tell her little head is so full she will need time to digest all of this. She gives me a last little hug, says she has got to catch a bus, thanks me again and is gone. I think about how just 30 minutes ago she was thinking of being dead, of never trusting anyone again and of “marking herself” by her own sorrow.

I think of how much more damage she could have done to herself by possibly having a positive diagnosis of herpes – many have not survived well and did not even have a stranger to help them. These are the one’s that I worry about because that was once me. I was inconsolable when I received my diagnosis of herpes, I felt I had no one to turn to and if my furniture could talk, it would cuss me out for kicking it when I got home from the Dr’s. Appointment where I learned I have herpes. I may have damaged my furniture but I didn’t damage myself – not permanently anyway.

But I felt as if I had the word “Herpes” tattooed on my forehead. I felt as if anyone who looked at me would instantly know I have herpes. I felt “marked” by my life’s circumstance. I could not, in good conscience let this gal think that carving something so permanent and negative onto her skin was a good or productive thing. Life scars us as it is. We all have little battle scars just from living, life is hard sometimes and I felt in her case there was no extra need to advertise further.

I do not like to leave a job unfinished, but in this case, I would make an exception and not finish this heart tattoo made of bricks.

I am hoping she feels the same. I think she did when she left.

This story was written by my friend Amy.

If you’d like to be in touch with Amy her e-mail address is: amypb1129[AT]yahoo[DOT]com

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