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Heal World

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Heal World

Everyone knows that the Bill Gates Foundation has been committed to the development of HIV drugs, and has continued to study. Studies have now shown that HIV will be conquered soon. So, if this problem is solved successfully, Bill Gates Foundation, they will not invest in HSV research? I think we need to contact Alibaba Mayun of China, or contact the Bill Gates Foundation, hoping that they can pay attention to HSV and can overcome it as soon as possible.

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Waiting4newlife

I am writing to them everyday in gatesfoundation.org and also Billg@Microsoft.com. If thousands of us do it, it will definitely get their attention 

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Heal World
11 minutes ago, Waiting4newlife said:

我每天都在写信给gatesfoundation.org以及Billg@Microsoft.com。如果我们成千上万的人这样做,它肯定会引起他们的注意 

Everyone of us needs to do this, and hope that more capital investors can focus on conquering it, because it is really too painful. I hope everyone will advance the progress of this matter together.

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Heal World

I agree with you very much. This is positive and effective. I hope that everyone can actively write an e-mail to the investment agency after they see the post, and they are eager to get a positive answer from you.

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Waiting4newlife

They won't reply to us directly. If a tweet wants to get attention it should be retweeted Atleast 1000 times. Likewise everyone in this forum should write to them, then only it will reach management's ears. Else it will the be the administration responding. There are 65 k members in this forum, am asking only for a thousand email. 

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Heal World
1 hour ago, Waiting4newlife said:

他们不会直接回复我们。如果推文想要引起注意,它应该转推至少1000次。同样,这个论坛中的每个人都应该写信给他们,然后只有这样才能达到管理层的耳朵。否则,这将是行政部门的回应。这个论坛有65个成员,只要求一千封电子邮件。 

Do you have any good way? You can say it

 

How many investment institutions do you currently have? Please write down your institution's email address so that everyone can send emails together.

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Waiting4newlife

For now, I have already posted the gates email I'd which is Billg@Microsoft.com and you can write them at 

https://www.google.com/url?sa=t&source=web&rct=j&url=https://www.gatesfoundation.org/Who-We-Are/General-Information/Contact-Us/Write-to-Us&ved=0ahUKEwi-2--bjerbAhUYfysKHdtuD2wQFgglMAE&usg=AOvVaw3DHMk6Qlspbh3x0OZCO-vq

 

I will collect the email I'd of Congress, senate, NIH, CDC and post it sooner 

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lvlvlv4

The best bet for now is a Pritelivir/Vatrex cocktail style pill that will hopefully render most people symptom free with minimal shedding. This will hopefully be possible within 3 years. Then within 8-10 years I believe CRSPR technology will develop a functional cure

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JHenry
47 minutes ago, lvlvlv4 said:

The best bet for now is a Pritelivir/Vatrex cocktail style pill that will hopefully render most people symptom free with minimal shedding. This will hopefully be possible within 3 years. Then within 8-10 years I believe CRSPR technology will develop a functional cure

I love your optimism! Do you have a basis to support it – what do you know that we don’t?

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Heal World
6 hours ago, Waiting4newlife said:

现在,我已经发布了Billg@Microsoft.com的大门邮件,你可以在这里写下它们 

https://www.google.com/url?sa=t&source=web&rct=j&url=https://www.gatesfoundation.org/Who-We-Are/General-Information/Contact-Us/写到我们&安培; VED = 0ahUKEwi -2 - bjerbAhUYfysKHdtuD2wQFgglMAE&安培; USG = AOvVaw3DHMk6Qlspbh3x0OZCO-VQ

 

我会收集国会,参议院,NIH,CDC的电子邮件,并尽快发布 

thank you very much

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lvlvlv4
2 hours ago, JHenry said:

I love your optimism! Do you have a basis to support it – what do you know that we don’t?

Mostly the article referred to in the other post. Pritelivir has been around for a while now and seems to be well tolerated and anti-viral cocktails have been very successful in HIV treatment, as well as big money makers for the drug companies. As I said, this is a best bet. Definitely not a sure bet. 

https://www.acsh.org/news/2018/06/12/herpes-vaccines-dont-work-what-about-drugs-pritelivir-page-aids-playbook-13074

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valleynovascotia
4 hours ago, lvlvlv4 said:

The best bet for now is a Pritelivir/Vatrex cocktail style pill that will hopefully render most people symptom free with minimal shedding. This will hopefully be possible within 3 years. Then within 8-10 years I believe CRSPR technology will develop a functional cure

If we used valtrex/pritelvir would that eliminate shedding cause if so then we wouldn't have too disclose and guys like me could date again.

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brookeb300
58 minutes ago, valleynovascotia said:

If we used valtrex/pritelvir would that eliminate shedding cause if so then we wouldn't have too disclose and guys like me could date again.

I wish this would happen and we could all date again

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valleynovascotia
2 minutes ago, brookeb300 said:

I wish this would happen and we could all date again

Yes we should all be able too date again although many on this site are in happy relationships wish my experience was the same.

 

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S.hall@gmail.com
1 hour ago, valleynovascotia said:

If we used valtrex/pritelvir would that eliminate shedding cause if so then we wouldn't have too disclose and guys like me could date again.

I believe so because the rate is 2.4 so with Valtrex it’ll go down to at least a solid 2% or more and with a condom then no more disclosure

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valleynovascotia
2 minutes ago, S.hall@gmail.com said:

I believe so because the rate is 2.4 so with Valtrex it’ll go down to at least a solid 2% or more and with a condom then no more disclosure

Will we be able to use pritelvir/valtrex together and would it actually reduce it by that much because if we use valtrex/acyclover together it doesn't reduce shedding anymore than using one alone and how many years until pritelir will be available as im already 33 id like too be able too date before im 40.

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valleynovascotia
12 minutes ago, S.hall@gmail.com said:

I believe so because the rate is 2.4 so with Valtrex it’ll go down to at least a solid 2% or more and with a condom then no more disclosure

Is this true that the rate of spreading is only 2.4 does that apply with guys too and this is with using condoms right?

 

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brookeb300
8 minutes ago, valleynovascotia said:

Will we be able to use pritelvir/valtrex together and would it actually reduce it by that much because if we use valtrex/acyclover together it doesn't reduce shedding anymore than using one alone and how many years until pritelir will be available as im already 33 id like too be able too date before im 40.

I hope so - no one really knows yet if we can get pritelivir or if it is just for aids people - I’m trying neem it just came in the mail.  

I’ve never even used a comd before so idol what to do.  I just want a cure too I can’t handle this.

 

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S.hall@gmail.com
10 minutes ago, valleynovascotia said:

Will we be able to use pritelvir/valtrex together and would it actually reduce it by that much because if we use valtrex/acyclover together it doesn't reduce shedding anymore than using one alone and how many years until pritelir will be available as im already 33 id like too be able too date before im 40.

I believe so because Pritelivir from what I read works on a opposite part than Valtrex and trust me you’ll be able too I have faith, the drug is fast tracked so in my best guess I’ll say maybe 2 years 

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valleynovascotia
1 minute ago, brookeb300 said:

I hope so - no one really knows yet if we can get pritelivir or if it is just for aids people - I’m trying neem it just came in the mail.  

I’ve never even used a comd before so idol what to do.  I just want a cure too I can’t handle this.

 

I know how you feel it's even worse where i live at least your in the states way more people there with itvand lots of guys will take the risk with females so maybe u should try too date.

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brookeb300
3 minutes ago, valleynovascotia said:

Is this true that the rate of spreading is only 2.4 does that apply with guys too and this is with using condoms right?

 

have The girl take a shower right after sex.  Guy who gave it to me kept me clean now condom for over a year.  Immediate shower. It had to sink in.  Watch Ella’s talk.

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brookeb300
1 minute ago, valleynovascotia said:

I know how you feel it's even worse where i live at least your in the states way more people there with itvand lots of guys will take the risk with females so maybe u should try too date.

No I’m ruined.  Guy knew he was ruining me.  Need a cure 

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valleynovascotia
Just now, brookeb300 said:

have The girl take a shower right after sex.  Guy who gave it to me kept me clean now condom for over a year.  Immediate shower. It had to sink in.  Watch Ella’s talk.

I don't think a shower would stop the transmission. Is that what you mean?

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brookeb300
1 minute ago, brookeb300 said:

have The girl take a shower right after sex.  Guy who gave it to me kept me clean now condom for over a year.  Immediate shower. It had to sink in.  Watch Ella’s talk.

No condom but immediate shower

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S.hall@gmail.com
6 minutes ago, valleynovascotia said:

Is this true that the rate of spreading is only 2.4 does that apply with guys too and this is with using condoms right?

 

2.4 is without condoms so with condoms no break out maybe 1% then if Valtrex works then the rate will be less than 1% 

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  • The Hive is Thriving!

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      I am 44 and I have active herpes in both of my eyes.Only Amenalief helps.
    • Jayne
      I know this thread is a couple of years old, but it’s been helpful to me, and I wanted to contribute as well. Back to Berliner’s original post, I’ve tested negative on several IGGs, with the latest ones being 1 yr and now almost 2 years past exposure.  Figuring out what was going on was the worst nightmare I’ve ever been through in my life. I made the mistake of drinking heavily a week after my father died of cancer, and I had unprotected AS with an ex, who happened to be poly and had some occasional unprotected M2M encounters.   Three days later I had a red line rash along my (sorry to get explicit) crack. This was followed by a rectal burning. Tested negative for G&C and related tests.  Over the next couple of weeks I had severe swelling and discomfort in my lower right quadrant and was told to go to the ER, where (I guess as a standard practice) they did a cat scan, which revealed nothing.  Also not a bacterial infection.  However the repeated manual examinations that occurred at urgent care and the ER seemed to relieve the abdominal pressure over the next few days.  I then had diarrhea for the next several weeks after.  I developed what felt like internal hemorrhoids, which were exacerbated by the diarrhea, and a gastro doctor confirmed via digital exam that there was indeed some sort of mass that felt like possible hemorrhoids. He ordered a sigmoidoscopy, but by the time it was undertaken, whatever was there was gone. After the procedure though, I felt much better for a while, possibly due to digestive issues clearing up after the colon “cleanse.” But this was concurrent with other issues.   About 3 weeks after the encounter I developed a large rash on my left thigh. Shortly thereafter I started having light sensitivity issues, culminating in a fever-like state after being outside in the sun only for 15 minutes after work. At work around that time for a couple days I felt like I was going through life encased in a gauzy gel- similar to being on laughing gas at the dentist, but not in a good way. I didn’t know what the hell was happening to me. I developed a severe case of canker sores for about a day. Later during a sunny drive, after getting back in the car at a gas station I noticed a red blotch below my lip. I tried to shrug it off but it happened again on the trip back.  So by about a month after the encounter I was having more anxiety. I spent the night at a friend’s house and woke up with a massive, swollen red eye and swollen lips. I got eye drops for bacterial conjunctivitis but that was wishful thinking.  A couple of weeks later, my lips were covered in sores. I smothered them with abreva. By the next day, they had mostly gone away. I tried to do a swab test at urgent care (I believe it was the next day), but there was not enough there to make any sort of positive diagnosis. Since then, I’ve had what you could call repeated aborted lesions and red blotches that appear around my mouth, particularly after stress and alcohol consumption. But even having peanut butter or chocolate would set it off for a long time. Fair skin doesn’t help- there was no hiding it. Two months after the encounter, I had my first vaginal burning- it was pretty intense and I had to use ice cubes because I didn’t know what else to do.   The worse feeling though was the periodic flare-ups of rectal itching/burning, often accompanied by another red line rash. It made sitting uncomfortable for about the next two months. I couldn’t wear pants at work- only skirts seemed to make things somewhat less irritated. And for the first three months, I was still testing for HIV along with HSV because of the overlapping symptoms (rash, diarrhea, neural pain, severe flu like symptoms without fever). I lost a lot of weight and had panic attacks. On top of all this I had just moved to a new city and started a new job and didn’t have a support network. And the sad thing is, I had to deal with all of this instead of being able to grieve for my father and being a better source of support to my mother. She had to support me without understanding what was happening.   Another bad thing through all of this was having both my ex and my current partner treat me like I’m crazy. That makes me feel alone and in the dark. Another “hysterical woman.” F*** that.  And while I felt grateful that my current was at the time still ready to be with me even if I had hsv, it’s a little discomfiting that he still doesn’t really believe me. But I’ve learned to live with ambiguity. And now I’m used to doctors as well as partners acting like this is nonexistent. Especially with negative IGG tests even 2 years later, which have left me without any answers.  I’m lucky in a way to be able to blend in because I don’t get obvious sores, genitally or orally (I can cover up the blotches with concealer, and they fortunately have lessened in frequency). But I still get the rectal itching/burning every six months or so (anthistamines seem to alleviate it a bit). And as more of a concern, I’ve had a cramp in my lower right quadrant ever since, which feels like it’s in my digestive tract. Since this has pretty much spread everywhere else in my body, intestinal involvement wouldn’t surprise me, and it isn’t unheard of anyways. I’ve tried to move past this and have since gotten married to my partner, who is a source of support (even if he doesn’t believe I’m having health problems. I know that’s a contradiction but occasionally I want to believe that too.).  I’m also newly pregnant, and symptoms have started to flare up again somewhat. I’m sure this will be an adventure. Hopefully more good than crazy. I know I’m going to struggle with the fear of passing this along but I’m trying to reconcile what doctors say (which is that it is extremely rare) with my own intuition about what I need to be careful of. Maybe I’ll repost with an update down the road. In short, there are people out there who test negative and have to live with loved ones and doctors thinking that a negative test closes the book on this. Again, learning to live with ambiguity is a real life lesson that I’m still coming to grips with. This forum and specifically this post have been a source of comfort that I haven’t been able to find elsewhere. Thanks everyone for the support for the community.     
    • Rockster
      You deepthroat so good that you get all kinds of mouth-to-skin-of-base contact? Kudos to you, but that is extremely rare. 
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