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  1. June 3rd I may of been exposed to Herpes. Performed oral and vaginal sex with a one night stand. A few days later, "felt off" and got tested on the 7th (negative for all stds, but not tested for herpes) Took a round of Doxycycline the following week around the 14th for a few days as I was feeling extremely Hot and urinating frequently. It seemed to help for an instant, however still feeling off. Tested again n the 28th - Negative for all stds including HSV igg however positive for HSV igm with an index of 1.14 (Positive being anything greater than 1.1) *approximately 26 days after suspected exposure Dr. prescribed Valacyclovir 2x day. Started taking medication July 2nd. Pain and discomfort in the penis continuing. With sensations in the pelvic area and kidneys. Tested again on July 20th - Negative for all stds and HSV igg/igm. Tested again August 6th - Negative for all stds and HSV igg/igm. I have been taking valacyclovir since July 2nd 2x daily. I have felt just not right since the possible exposure date (or shortly after). My penis has gone through feelings of tingling sensations, heat, pain but not to touch, pain in my pelvis. Things seemed to of started with a burning sensation in the inner thigh. I feel as I am having shooting sensation in my legs and occasionally have an itchy/tingle around where my pubic hair is from time to time. Hell, today and maybe yesterday I've noticed tingling in my scalp. I tried again today to not take the valacyclovir and lasted until about 11:30 am after waking up around 8 am. My lips and the skin around my face starts to burn and the tingling around the pubic hair area of my genitals increase in its sensations. It's almost as a sleeping demon is waking up when I don't take the meds. When I take it, it takes about a day or so for things to get back in control. My penis/genitals have also not smelled the same since. It seems my scent has changed. Today is day 68 - is this how it's going to be forever? I am worried I have this all over my face as the burning is in the corners of my mouth and down my chin, as well as my nose. I have not shown any sores however I do feel my penis and scrotum has felt hot and sometimes red, typically on the head of the penis at the urethra. Multiple dr's say it looks normal to them. I am so lost and feel like I am falling apart physically, mentally and emotionally. I guess I just wait until week 12 (in a few more weeks) to maybe test positive... but then what?
  2. anom1990

    Well… here I am.

    Hi everyone. I’m still trying to process this but I am a gay male in my late 20’s that was recently diagnosed with HSV-2 in October 2018. I haven’t been sexually active since 2015 and have only engaged in sexual activity with four people in my life. I’m feeling a lot of emotions because of this; sad, angry, confused, violated, ect. Thoughts like who would’ve thought someone like little ole me, compared to all of the VERY promiscuous people in the world, would end up with Genital Herpes ESPECIALLY when I’ve been abstinent and just focusing on myself for years. That was a gunshot to my soul. It’s crazy that I’ve ALWAYS done regular STD testing, thinking I was negative for everything only to find out that Herpes was never included in my testing because I never knew you had to literally ask for that until this year. The CDC and medical industry is so fucked up and wrong for that. I’ve always used protection, except with my first boyfriend but that was back in 2009-2010 and a condom broke with a sexual encounter I had back in 2011 and I remember immediately putting a new one on him. Unfortunately, all of the men I’ve dealt with sexually are questionable. Half of me wants to know who gave this to me but the other half is like what’s the point. I only have access to contact three of them (I don’t know where the other guy is) but I haven’t spoken to two of them in years, one of them in a whole decade and it would be pretty awkward for me years later to write them a message about herpes. My first boyfriend and I are cordial but he’s still immature so it would be very awkward with him. Anyways, as I’ve been thinking and backtracking my life, I would think I caught this back in 2011 because I remember my anus itching so badly but I thought it was just my hair growing back because I do recall shaving before having sex so I guess that was my first outbreak. Other times I would just get a minor itch in and on my buttocks but I never would’ve thought herpes. I’ve never got outbreaks on my penile area. This is all still confusing and baffling to me. I’m still sad and feeling like my future love life was taken from me. I feel like part of my confidence was taken from me. I don’t even feel comfortable flirting and finding people attractive right now. I’m just releasing my thoughts about my situation but I do have questions. My results also came back saying I had extremely low Vitamin D deficiency; does HSV-2 have something to do with that? Is there a test I could take to tell me exactly when I contracted this virus? This question may be TMI but I masturbate and I notice that a lot of sperm doesn’t cum out sometimes, does HSV-2 have something to do with that?
  3. cracked

    Neuralgia

    Hey everyone. I’ve read a lot of posts and have talked to some people from the forums who suffer in various ways from this virus. I’ve also heard the term ‘neuralgia’ being thrown around in posts, but have yet to figure out what kind of pain and its origin is for all the people that said they experience it. Please do me a favor and comment below about your experience with it and where it causes you problems and what kind of pain is it exactly? This might help some other newer members also understand. Thanks.
  4. I’m trying to get some answers from people who already have HSV (preferrably type 2) regarding my symptoms, but not a lot of people seem to be commenting. So i’m trying again with a more in depth explanation. PLEASE HELP ME understand. This all started when I visited India from June 20-July 22. I was completely fine and healthy prior to that. In the first few days after arriving I became very sick with bowel movements 5-6 times a day and lethargy and little appetite. I came back and was still suffering from this but my bowel movement I believe started getting better. I decided to have sex for the first time in my life with someone I casually know less than 2 weeks later on August 2 (without my parents knowing because they would highly be against it prior to marriage). The next day after sex I had UTI symptoms and what seemed like a rash at the tip of my penis which was very sensitive and the bottom of my penis felt weird as if it was more exposed now. I found out I really did have a UTI due to a bacteria found in soil and had to take a couple of antibiotics and felt better but then a week after it came back. This time on August 15 (less than 2 weeks after my encounter) they did a STD panel on me which included Chlamydia, Gonorrhoeae, HIV, Syphillis, and only HSV-2. Everything came back negative except HSV-2 with an igg value of 2.0 and my world turned upside down after finding out. I noticed what seemed like lesions a few days AFTER finding out my results but when I went back to the doctor they never swabbed them. I was just prescribed valtrex and zovirax topical and jusr told that it’s nothing serious but referred to a urologist for what the doctor thought was a chronic UTI. The urologist after finding out that I had HSV-2 and examining the rash told me the one thing I didn’t want to hear—post herpetic neuralgia, which only made me feel worse. But it didn’t make sense to me because I’ve had that rash much longer than before the assumed outbreak and according to what I’ve read on the forums here antibodies for HSV should not be present BEFORE my primary outbreak and especially with a igg reading of 2.0 in less than 13 days. The female I was with didn’t know she was positive for HSV-2 even though she was tested several times in the past (maybe not for hsv) but her recent result a few weeks after me showed an igg value of 16.4, but the few people she was in a relationship with before me never have told her they got anything from her. It has been 2 months now almost since the encounter and I still have: -no appetite -nausea with gagging -oral thrush that wont go away and dry mouth -fast heart rate for several weeks -UTI’s -chronic fatigue -itchy area on both sides of my inner thighs (which I was told is fungal infection) -inability to sleep for long periods of time I have not had what I’ve been reading most people go through during their promary outbreak such as swollen lymphs, constipation, headaches, and no lesions that people say are fluid filled andn then ooze and scab over that I’ve been able to notice. Please answer if you can: -Does my IGG value make any sense? I’m going to get retested, but is there a chance its a false positive? They never checked me for HSV-1. -Does most or any of this sound like it’s due to HSV? -Do I possibly have a systemic yeast or bacterial infection? PLEASE HELP ME. Every doctor and specialist I go to keep sending me in circles.
  5. My relationship with the person I gave herpes to ended about three months ago (his choice). I was pretty freaking scared to date, so I just hung with my friends and the people I trusted. About a month ago, the brother of a close friend of mine told me he "had a thing for me" and wanted to see if we could date. I was petrified. (One thing I should mention is that I trust this person. To me, anyone I disclose to I want to trust not to spread the word, and to be kind to me when I disclose). I told him sure, I wanted to see him, but I had a couple things to tell him in person. I went over to his place, sat him down, and told him the basics as follows: I have genital herpes simplex 2. I haven't had an outbreak since the first three months. I take antivirals daily. If we have sex we have to wear condoms. There will still be a small chance of transmission, no matter how careful we are. He was super nice, didn't react strongly at all, which made me not burst into tears, haha. He said he needed a few days, which I understood, but was also very terrifying. He talked to a doctor about it (his dad) and asked me a few more questions. We had the talk Sunday, and he contacted me the following Wednesday to tell me he was still interested. Best of all, he told me how brave and awesome I was for being honest right out of the gate. I felt/feel amazing about this, and firmly believe being straightforward is the best course of action.
  6. Does anyone know if systematic symptoms show up later after already having the primary infection? Diagnosed in August after losing my virginity and have had UTI’s nonstop, unable to sleep well, and feeling fatigued and overall crappy for 3 months now as you all know. No headaches, back pain, swollen lymphs, etc for this entire time, but now it seems like the various symptoms people point out about ghsv-2 are taking their turns on me. I had tender lymph nodes in my groin, under my armpit, and one in my neck last week. I got a colonoscopy/endoscopy last week as well for gastric issues I’ve never had and these 2 small blisters appeared on my lip that didn’t hurt but made my lip feel like it was swollen on both inside and out, itching on my arms and sometimes face. and my entire face has been flaking and feels really bumpy for the past several weeks (lots of bumps on forehead). Today I was feeling fine all day and now I started feeling like I have a bad UTI and started getting a headache for the first time since these months. Can anyone explain this or help? (I only took antivirals initially but not anymore because if I do have GHSV-2 then I want my body to mount a response).
  7. So I just watched this Sci-Show video on just how HIV crossed the species to species barrier, how incredibly quickly it spread, and how a cure is on the horizon. After watching and seeing that HIV came from SIV and crossed into human blood from chimpanzees after the first human was infected in 1908 to over 70 million people (just a little over 100 years) it really makes one think how widespread HSV must be since it’s millions of years old. Fascinating stuff:
  8. I’m really, really scared, freaking out, depressed right now, and need some help. A lot of you might already know my story, but herpes has me freaked the fuck out now. I’m 25 years old, have always been a highly active person all of my life, have always eaten right and healthy, and haven’t ever dealt with any major health issues. I’m assuming I do have GHSV-2, but don’t know for sure yet, but was diagnosed visually and with a igg of 2.0. Since 4 months now after coming back from being abroad I don’t have any appetite, feel like I have food in my stomach, pronounced heart rate, shortness of breath, and just overall feeling of being unwell. I was told by a forum member that my vagus nerve could have been affected by the virus or maybe some other virus and caused me to have gastroparesis, causing me to feel full really quickly because my stomach isnt able to empty itself, and it isn’t curable apparently when I googled it!!? How am I supposed to live my life with having this virus and also dealing with not being able to eat and supposed to not die from losing weight?! On top of this I read diabetes is frequently a cause for this? No one in my family that I know of has diabetes. What the fuck has my life turned into?!?! All because of wanting to have sex one time in my life?! I have never dealt with anything like this in my life.
  9. NanoViricides to Present Results On Successful Treatment Of Herpes-Induced Acute Retinal Necrosis at the Annual Meeting of the Ocular Microbiology and Immunology Group (OMIG) of the American... PR Newswire Oct. 17, 2017, 07:00 AM NanoViricides, Inc. (NYSE American: NNVC) (the "Company") will present the results of its anti-herpes nanoviricide treatment for Viral Acute Retinal Necrosis (vARN) at the 2017 Annual meeting of the Ocular Microbiology and Immunology Group (OMIG) of the American Academy of Ophthalmology to be held in New Orleans, LA. v-ARN is a disease of the retina of the eye caused by various herpes viruses that leads to severe loss of vision and blindness. The infecting agent in this study was herpes simplex virus-2 (HSV-2), the type of herpes virus that also causes genital herpes. The abstract of the study has been accepted for presentation at this OMIG meeting on November 10th, 2017. Dr. Vivien Boniuk, consultant in ophthalmology at NanoViricides, Inc. will make the scientific presentation. The presentation will cover both the inhibition of virus infection and prevention of ocular tissue damage following virus infection. Viral Acute Retinal Necrosis is characterized by severe ocular inflammation, retinal necrosis, and a high incidence of retinal detachment (RD) leading to visual loss and blindness. This disease is caused by members of the herpesvirus family, including, herpes simplex virus-2 (HSV-2), varicella zoster virus (VZV), and herpes simplex virus (HSV-1). An estimated 50,000 new and recurrent cases of viral ARN per year are reported in the United States alone. The study was performed in the laboratory of Professor Curtis Brandt, Collaborative Ophthalmic Research Laboratories, CORL, at the University of Wisconsin. Dr. Brandt is Professor in the Departments of Ophthalmology and Visual Sciences, Medical Microbiology and Immunology, and Director of the Vision Research Core at the University of Wisconsin. NanoViricides believes that its broad-spectrum anti-herpes drug candidates being developed in its HerpeCide™ program may be capable of attacking many different herpesviruses. The Company intends to maximize shareholder value from this asset by aggressively expanding its portfolio of herpesvirus indications. The Company is already developing drugs for at least four different indications based on these broad-spectrum anti-herpes drug candidates, namely: (i) skin cream for the treatment of shingles (VZV), (ii) skin cream for the treatment of herpes labialis (HSV-1), (iii) eye drops for the treatment of herpes keratitis, a disease of the external eye (HSV-1), and (iv) skin cream for the treatment of genital herpes (HSV-2). Successful studies on vARN would add a fifth indication to this growing portfolio, further expanding the potential market.
  10. cracked

    Is it just me?

    So is it just me or does anyone else notice we have an increasing number of people signing up each day on HC alone? Does this maybe suggest the rate of infections is increasing? Sucks to see more people being victims of this virus.
  11. Can someone please tell me what’s going on with me? I’m a guy and It’s been 2+ months since I was diagnosed, which i’m still not sure if it was a false positive or not and i’ve had what seemed like 4-5 UTI’s ever since. Had 4 urine cultures, 2 of the have been UTI’s with actual bacteria, 1 was contaminated, and 1 showed no growth. I’ve been on macrobid for the bacterial infection, but after finishing that i’ve been having severe UTI symptoms again. I can’t sleep, it hurts to pee, urine is cloudy, my head is hot (my temp shows to bee at 98F) each time I wake up, and now my body is aching. I’ve taken AZO pills to and ibuprofen to help but does anyone have any similar experience? Is it due to HSV? Am I gonna have UTI’s like this for the rest of my life? @WTHerp has tried to help me, but anyone else know? I don’t how much more of this my body can take. I’ve had just these 2 bumps near my corona for 2 months now and they sometimes reduce in size and other times increase, but nothing ever comes out of them and they don’t go away.
  12. Okay everyone this is a very SERIOUS question and one of my biggest worries and stress factors after being diagnosed with ghsv-2 45 days ago. Ever since I was exposed I noticed the next day that my urinary meatus (pee hole) didn’t feel or look normal. I’m not being paranoid either. It almost seems like the skin from underneath was somehow pulled back and I can see inside the meatus now, which I COULD NEVER do before. I also know it’s not normal because when my stream ends the droplets at the end are large (like pea sized), which just scares me because they were always the size of say bean bag pellets or smaller. I don’t want this to be a permanent thing because I can’t seem to run or be active whenever I feel it touching the inside of my pants. From what I’ve read on here I’m not the only one suffering from this symptom, but not many others are, so please if you do then please comment below and if it gets better or is surgery required to fix this. The urologist said it looks fine, but I KNOW my penis and it’s not. I apologize for posting this pic, but I’m worred what’s going on.
  13. Hey everyone, I’m still a bit new to the forums and a bit to having herpes as well (~1.5 months since diagnosis). Some of you may have seen a few of my posts already, but I guess as much as I’m trying to overcome the fact that I am positive for it (and I intend on getting retested in a couple of months), it’s pretty damn difficult because of several things. This was my first ever sexual experience as a guy and as someone whose family is very against sex before marriage I am feeling regret, guilt, what i consider depression, and if I’ll ever feel ‘normal’ again emotionally and psychologically about myself or about my passions and hobbies, despite my physical symptoms. I feel like I should’ve just abstained until I would get arrange married in a few years, but I guess I let pressure and lust get to me. I don’t know whether if it’s because of the time since my diagnosis and I never expected to ever have something ‘incurable’, but I’m just worried about that aspect of it most. Can someone else relate or anyone know if this is normal and gets better? I experience I guess mild penile neuralgia compared to a lot of people on here, but whenever I do it just hits me that this virus is probably what’s causing it.
  14. Hi guys!!! It's coming up to a year since I contracted HSV2 and what a terrific day that was... Things have come a long way since then and I've managed to keep my OB's under control etc., but tbh it's still a constant psychological battle everyday. However, this might be down to the fact that I'm only 22 and I haven't had a relationship since my diagnosis. Anyway, I come here to ask what oral HSV2 symptoms would be, if there are any? Since my diagnosis I have developed a clicky neck, crackling and clicky ears, tinnitus, dizziness and strange sensations that radiate from my ears out towards my neck, side of my face and the back of my head. All the symptoms are exacerbated when I drink alcohol (sometimes even one glass!) and I feel like I can't breathe due to my nose becoming stuffy and suddenly feel very heady and dizzy. I've seen a ear, throat and nose specialist who said I have no infection or fluid in my ears as well as no signs of sinus issues. So it must be more internal?! These symptoms have been ongoing for months now. I'm not stressed and everything par having herpes is amazing in my life! So I come to my own conclusion that it could be herpes related. Three months into my diagnosis I remember I accidentally scratched the inside of my nose after touching my sores down there. I also remember a huge spot appearing inside my ear not shortly after. I didn't think anything of this but now I'm questioning whether this has anything to the symptoms affecting my ears, nose, neck and head. I'm absolutely tired of these symptoms as they affect my concentration and focus at work, plus I can't enjoy a nice drink with my friends without feeling like I can't breathe. I really would appreciate any advice or hear of similar experiences you might of had. All the best, Jude
  15. james7green

    gHSV-2 Penis Scarring

    Hi Guys, I am sure that this has been covered somewhere in the forums but I can't seem to find an answer. I thought I'd reach out to you and ask about what's the best way of tackling gHSV-2 OBs that occur on your penis. My OBs occur just below the head of my penis near the foreskin. When I get an OB I immediately start to take Acyclovir . Other than that Epsom Salt baths seem to help relieve the symptoms. I have has 12-15 OBs in the last two years and some of them are beginning to leave scars on my penis. This is highly distressing as I am only 32 and when I begin to think about how my penis will look like in 20 years I get terrified. Is there anything I can do to minimise this while I get an OB? Is there anything that has helped you? Ointments? Tea Tree Oil? Post OB creams? I am a bit scared of experimenting with various products on such a sensitive area. Thank you in advance for your help - I truly truly appreciate it. James.
  16. EforEllie

    Having both GHSV1 and GHSV2

    For those who have been diagnosed with having both GHSV1 and GHSV2, what are your symptoms like? I have GHSV1, and may have been exposed to GHSV2. I have not yet taken a blood test to confirm, but I'm having small symptoms that I can't identify as an outbreak. Curious to know how your symptoms manifest with this rarer diagnosis.
  17. Hi guys, I've read that GHSV-2 is very unlikely to be passed to a persons mouth by oral sex as this type prefers the genitals. Quite a lot of medical sites say that people rarely get hsv2 on their mouth. does anyone know how true this is ? Im also on suppressive meds
  18. CasperTheGhost

    Self-esteem

    Hello. Just signed up today because I didn't know where else to turn, so here goes nothing. I had my first sexual partner in almost over a year a couple weeks ago and we irresponsibly had unprotected penetration. On Saturday morning I noticed something was wrong and began searching online for an answer. After some searching, I figured it was a yeast infection and treated it accordingly. It only took a day or two for me to come to terms with the fact that it wasn't a yeast infection but something worse and the Internet agreed with me. I have not officially been diagnosed but I'm not fooling myself here and have an appointment to confirm what I already know on Tuesday. I'm in quite a bit of pain but I'm sticking it out and doing home remedies to help speed up the healing of what I can only call my first OB.... I've told my partner who I clearly contracted it from and one close friend who is being supportive. But I can't help but feel disgusting and unattractive which I'm not used to because I am normally a very self assured and confident person. I'm just looking for someone with a similar experience. I'm 18 and feel like my life has come to a grinding halt.
  19. Hiya, I just wanted to firstly say how relieved I am that I found this community. The work you all have put in over the years is so impressive and you have collectively created an incredible resource. THANK YOU! I was wondering if I could reach out to all of you and ask for some help. I have been recently diagnosed with gHSV-2 but my first OB was two years ago. Each OB after the initial one took place while I was travelling and I could never get to a Dr in time for a definitive test. In a a way I am now relieved because at least I know with certainty what I have. In the last two years I have had at least 12-15 OBs. From what I have been reading on this forum my OBs are mild and not too painful. Having said that they are a major cause of stress for me. They usually occur between the head of my penis and the foreskin but recently I have started developing OBs on my upper thigh/below my butt. Now that you have read my longwinded backstory I will cut to the chase ;-) I am scheduled to see my Dr in London to talk about the choices I have going forward. I am seriously considering a suppression therapy because even though my OBs are "mild" and painless they do last for many weeks. With so many outbreaks a year I am hoping that a suppression therapy will minimise the stress I go through and make the OBs less frequent. What do you think is the "best" suppression therapy available out there? I usually take Acyclovir during OBs and that seems to be working well. I just wanted to hear your thoughts on a possible long term suppression therapy and the side effects it might have. Is there a preferred and proven medication I should discuss with my Dr? I apologise in advance for the probably redundant post and than you in advance for reading this and pointing me in the right direction on the forums. Cheers James.
  20. I was diagnosed with G-HSV1 in August of 2016. I received a blister culture swab that indicated I was positive for G-HSV1 and negative for G-HSV2. I have only had an initial outbreak, and I have not been on suppressive therapy since my diagnosis. I have recently learned that my only sex partner, who I had been with for 5 years, transmitted G-HSV2 to a woman in August 2016, around the same time of my G-HSV1 diagnosis. Realistically, my partner may have been infected with G-HSV2 several years ago and has never showed symptoms, or he contracted G-HSV2 just before August of 2016 through another infidelity. The woman whom he infected has experienced 3 outbreaks since her diagnosis in August 2016 and is taking suppressive therapy. With the frequency of our respective outbreaks, it would seem I have textbook G-HSV1 and she has textbook G-HSV2. Or so I would like to believe. For 2 of the last 5 years, the relationship had been long distance. During a full panel STI test in August 2016, I tested negative for all STIs, other than G-HSV1 via blister culture. At that time, I believed that neither he nor I would have G-HSV2. I assumed it would have presented itself in the blister culture. I now am shaken to know that I have been put at further risk, as the other woman informed my partner of his G-HSV2 status in August 2016. He had unprotected sex with me in October 2016, and knew he was infected with G-HSV2 without telling me. What a prick. In any of your experiences, is it possible to have been infected with G-HSV2 (at anytime) but only a newly transmitted G-HSV1 tested positive in a blister culture? Or would a blister culture identify the presence of both G-HSV1 and G-HSV2 at the same time? I will be completing a blood test for HSV1 and HSV2 in the coming days for more clarity on what I do actually have. I am wishfully hoping that my physical symptoms of only having 1 outbreak and original G-HSV1 infection point toward an absence of G-HSV2. Thank you in advance for your input!
  21. Numb22

    Another outbreak?

    I feel itchy and uncomfortable down there.. No bump/blister. Could I be having a outbreak?
  22. Mpj1307

    Cant take the itching!

    It has been almost a month probably longer and i am still experiencing symptoms from my initial outbreak of HSV2. I dont have any bumps, but the itching and skin irritation is so bad. My skin is also peeling near my bottom area and thatitches, sorry for the tmi...but have any of you experience anything like this?
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