Jump to content

This and That and Other


Feeling Normal Again

Recommended Posts

****Note to newcomers at the bottom.

The feedback coming back from others, who've tried the neem capsules and neem oil or graviola tea and having as good of results as I did, makes me overjoyed.

I'm not the type of person who seeks support or companionship. I'm content with myself and always been happy in my own skin. 

Herpes and meningitis support groups never crossed my mind, until I "fixed" myself, found things that really worked for me (note not cured), and then thought, "I wonder if these things work for others?"

I jumped on the forums and not seeing others on neem capsules, neem oil, and/or graviola tea shocked me. I would read others' stories who are suffering with constant outbreaks or the atypical symptoms (nerves, joints, lymphnodes, headaches, stiff neck, light sensitivity, etc) that can lead to more serious issues. 

I only decided to join forums to share what I found that completely stopped my constant outbreaks (neem) and what stopped all the other mollarets meningitis symptoms (graviola tea). 

I never had any intentions on staying on forums this long, but I got caught up with the positive feedback of others' successes with neem and graviola. 

I'm in the process of moving across the country again (I move a lot). And I need to get off of here and get back to living, I think these forums are great for some, but for me the internet is just a big distraction from life and things I enjoy (exploring, adventures-a bit of an adrenaline junkie, traveling, hiking) and it becomes too consuming.

Taking an indefinite break, good luck to all the wonderful people I've chatted with. 

*********And to Newcomers *****     There is hope for living normal and love; don't sell yourself short because you've been dealt this! And don't seek diagnosis or diagnosis advice on a forum!!!! Go to a doctor; neurologists, internalists (who can usually be listed as your pcp and are great at listening), and infectious disease specialists are usually pretty good at getting to the bottom of things, not someone on a forum you don't know from Adam who could just be a narcissistic sociopath with a god-complex. You just never know who you're really talking to! 

***When someone gets the nerve up to post in newcomers section or newly diagnosed, the first response should be, "Welcome to the group, sorry you're here, it gets better." 

Remember support groups should not be a stressful environment, especially for a disease that is affected by stress.

My hubby of fifteen years died ten years ago at age 34 in a car crash, and it taught me life is too short. Life is definitely too short to waste time arguing online! ;)

So, see doctors, boost immune system, find suppressant, treat the symptoms.

Enjoy Life and Live!!

 

 

 

 

 

Edited by Feeling Normal Again
Grammar
  • Like 2
  • Thanks 1
Link to comment
Share on other sites

In the section:  Just Signed Up-Say Hello Here -- posted After Nightmare Finally Living Again-- it is a full detailed list of what I took that stopped outbreaks and miraculously stopped meningitis symptoms.

I've been told by others who've tried the tea, the tea is a miracle, it's allowing them to live a normal life with no more headaches and nerve problems! :D

In the section:  Herpes Treatment Zone - Managing Outbreaks and Pain Relief -- posted Links to Neem Studies-- 4 links to institutions and research centers (including John Hopkins) who've tested neem and found it highly effective treatment against all herpes viruses including hsv 1 and hsv 2.

Any questions on exact regimen are answered in the comments.

Might check in on private messages here and there, but not replying to any attacks or arguments! All negativity will be ignored! 

Edited by Feeling Normal Again
Added wording
Link to comment
Share on other sites

Been keeping some private conversations going, I still get messages with success and still getting messages with questions. 

I've posted my story in so many places, I'm not sure which are still getting views and bringing in new private messages.

All questions on what I took and how much can be answered in just signed up say hello here-after nightmare finally living again and in the comments following that post. Also in herpes treatment zone- managing outbreaks and pain relief, links to studies done on neem and also in following comments of that post.

If you read my story and try what worked for me, I hope they work as well for you. If you don't try them, I hope you find something that works for you. 

Over two years now, still no outbreaks, no side effects, and feeling pretty good.

Good luck to all, especially those suffering constant outbreaks and atypical symptoms like I was.

Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

  • Donate

    If Honeycomb has helped you, please help us by making a donation so we can provide you with even better features and services.

  • The Hive is Thriving!

    • Total Topics
      71.9k
    • Total Posts
      485.2k
  • Posts

    • CHT
      Hi "Jeremy"..... I agree, the topic of your HSV status does not need to be something you disclose too soon in a developing relationship..... get to know each other first....see how it's going and as it progresses, then the HSV issue will naturally need to be revealed.... it's my personal opinion though that before there is any sexual encounter you ought to disclose your HSV status.... I know some will disagree with me on this but, I think it is morally wrong not to disclose first.  This can be a make/break situation for most people but, again, I feel it is simply wrong not to give the other person the whole story since your decision not to disclose could put their health at risk.... that is simply not an option in my opinion.  Looking back to my "pre-HSV" life I most certainly would want my partner to disclose their HSV+ status before intimacy so that I could make my decision as to whether I want to take that risk or not.... 
    • Jeremy Spokein
      Thanks, CHT. I appreciate the feedback. The whole trauma of going through this has led me to figure out a lot about myself and my attachment wounds, so I'm taking courses to come out of this better. This girl really was my dream woman in so many ways, it's been the hardest heartbreak to deal with ever. I'm truly in a lot of pain, but using the pain as fuel to launch that new business and work with coaches. I also opened up to my family about HSV, so my parents and sister know now, and they were very loving and accepting of it. Since opening up about it, I feel way better around this thing. After opening up, I also found out that some mutual friends in our family have discordant couples who are married with children, so HSV hasn't stopped them from living a loving life. The thing is... all of these couples I mention did not disclose until 6-8 months into the relationship. So now I'm thinking it might be better not to disclose until I know things are very serious. I'll of course stay on the medication and use protection, but maybe this is a better route than disclosing upfront and scaring women off.
    • WilsoInAus
      Hey @Lcj987 and welcome to the website. You can be sure that isn't HSV-2, looks nothing like it. It is much more likely to be folliculitis or inflamed fordyce spots.
    • WilsoInAus
      Hey @JackThrowAway herpes causes an outbreak where it enters the body first and maybe a progressive spread. If it doesn't cause an outbreak at the entry site then it won't cause one elsewhere, it also won't 'jump' upon infection - it would be more likely that the lesions are continuous from the penis to the anus. Nevertheless, testing trumps symptoms or any interpretation of symptoms. The correct conclusive result arises when: you have a positive swab; or An IgG HSV-2 level over 3.5 (Herpeselect test).
    • Lcj987
      Slept with someone unprotected, roughly 2 weeks ago now. I felt generally unwell the couple of days after but I’d been drinking the whole weekend and didn’t have much sleep either of the days of that weekend so put it down to that. 6 days after I noticed these spots appear on the shaft of my penis. Along with symptoms of discomfort in my shaft in the couple of days prior to them appearing. No pain when urinating at all that I have noticed. They don’t hurt, itch or tingle and they don’t have fluid in from what I can see or feel if I squeeze them and have never burst? I went to a sexual health clinic to get checked up, they took bloods to do a full test and looked at the spots but said they saw nothing that concerned them but I’m not sure about that, any advice? The smaller spots under the shaft are just follicles I had diagnosed years ago and non-sti related.
×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.