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YogaJ12

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  1. Sounds like neuropathy. I've had severe neuropathy for over 7 months now. I experience shooting pains, burning, pins and needles. Temperature changes and crawling sensations. It has spread to my arms and legs now: I'm currently taking gabapentin but I still have bad days. I'm experimenting not taking valtrex as well to see if I'm better on or off it supressively. @janedoe
  2. This sounds very promising! I can't wait to hear more about this vaccine! Valtrex has done nothing for me and I hate the dependency on big pharma's "manageable" drug. There is far more to this virus then a blister 2-3 times a year. As a sufferer of neuropathy i am patiently waiting for something new and improved. @2legit2quit
  3. @2legit2quit no autoimmune disease that I know of. My nerves are just really sensitive to this virus. I hope one of the doctors I'm seeing will prescribe something to give me some relief
  4. I'm not happy. It's been a year and a half and I'm in constant pain with electric shocks, pins and needles, and burning sensations almost everyday. I feel like I've regressed. Instead of outbreaks all the time it's nerve pain almost everyday. I've made an appointment with a neurologist March 2nd and I have an appointment with my gynogoloist feb 22nd. I hope one of them can write me a prescription for this pain. I would have never imagined herpes included feeling like a burned victim. I'm tired and I'm exhausted. I believe I am having a outbreak right now, the sensations are so strong. My outbreaks yet so small. I don't understand. That is all.
  5. Plus I am pretty much paranoid on the thought of having unprotected sex. I haven't had unprotected sex in a year.
  6. It's been a year a 3 months since I've been diagnosed with herpes. I seem to get outbreaks every 3 months now but that's not the issue. I have severe nerve pain/shocks/burning on the left side sometimes ride side pretty much on a daily basis. This has progressed after my year anniversary. I don't really want to take more meds as I already do suppressive therapy. I've been doing a little research, has anyone tried St. John's wort oil? Any other recommendations are welcomed. It's just a big annoyance, wearing jeans are the worst lol.
  7. Thanks, I am currently on suppressive therapy. I double up if I'm having a bad day of tingling and sensations @whitedaisies
  8. So I made my year anniversary having herpes in September. I haven't really had a outbreak since August. But since September I've had like non stop pins and needles and random tingles in my legs and sometimes arms! What is going on? Is it my immune system just taking over? Again I haven't gotten any outbreaks but my random sensations are almost everyday.
  9. I just wanted to share what a guy who "likes me" said to me last night. 5 months ago I would of cried, last night I laughed and said to myself what a ignorant fuck and deleted him out my text messages. What are the most ignorant things that were said to you when you disclosed about your herpes status? If one thing I've acquired more of with this virus is strength and the ability to know my worth. Don't ever let someone try to make you feel less than or that your lucky for them to accept you. Tell them to kiss your ass and that you're the prize not them. They aren't worth your time. So this is what he said "You better than every n*gga you dealt with I guarantee you this I been around the block a few times and you're wifey material just its just been hard for me to overcome your std issue but I'm hoping tha I continue to mature about your situation cause I really like you " then he asked me for nudes to better accept me. Wtf ?!
  10. Yes Patience and Acceptance is key. I'm still working on patience but I have accepted that I have to live with it. @libra @2legit2quit
  11. Yes @2legit2quit the is the longest I ever had prodromes since my initial outbreak. I just want it to go away. This has been a stressful work week though and I am drained. I guess it has a way of telling us to slow the hell down. Going to rest this weekend and hope it goes away.
  12. I have had constant prodromes since Monday, tingling and shocks from my butt to my toes, with no outbreak but with swollen lymph nodes. It's a pain in the ass. I've just reached my one year mark.
  13. I get the tingly sensations and itchyness too without a visible outbreak. I am currently on day 3 of prodromes and no outbreak. It's a pain in the ass and Im a year in.
  14. Sounds like you may be ovulating I get itchy and tingly when I'm ovulating too. Your hormones fluctuate and may activate the virus without a outbreak
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