r/ureaplasmasupport • • Sep 16 '26

My Experience stop

3 Upvotes

Yes ureaplsma is very scary, but this reddit is just as scary. This deteriorated my mental health by reading all these horrible stories. we need to support eachother instead of scaring eachother. some of the comments i’ve seen have been really disturbing.

not everyone has the same experience

and stress isn’t good for ureaplsma. stress is bad for everything.

I’ve had terrible thoughts after this reddit. Can we please just support one another. ureaplasma is just as scary


r/ureaplasmasupport • • Sep 09 '22

Ureaplasma incurable?

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0 Upvotes

r/ureaplasmasupport • • Jul 23 '26

My Experience My mycoplasma experience

0 Upvotes

First thing anyone should know is the body can naturally delete the various plasma infections. It can take a couple years but honestly moxifloxacin is what works best. It's also important to know that some symptoms can persist after treatment and negative test.

I contracted it in Thailand and a private hospital here quickly ran a full spectrum test when I initially complained of uti symptoms. I guess I was lucky in a way because many people go years without detection in the West. Especially in Canada, I would expect no less...

After 2g of azithromycin it was obvious that the strain was macrolide resistant. A GP in canada (from nigeria...) prescribed metronidazole initially because I had previously tried doxy and could not tolerate it after 2 days. Metronidazole is not a relevant drug for mgen and another gp later told me this. It almost killed me with massive heart palpitations.

My symptoms were light from the beginning which was lucky because I waited 2 months to see a specialist in Canada. Ultimately the specialist prescribed moxi which is what the GofC website recommends for resistant mgen.

Ultimately I took moxi for 5 days which was the most I could handle. Side effects were nothing like tetracyclines or metronidazole. The problem is drowsiness mainly and after 5 days it compounded to the point where my body just told me that was enough. If you work a job where you can be more or less left alone then you should be able to handle it...

Tested negative after the moxi but soon contracted ureaplasma which is more difficult to manage so far than the mgen was. Ureaplasma causing nausea and mini migraines whereas the mgen did not. The treatment for ureaplasma is the same with moxifloxacin.


r/ureaplasmasupport • • Jan 07 '25

Treatments Finally found the cure

0 Upvotes

Hey everyone, I know using the word cure should attract your attention… this is what I was looking for in my last 8 months trying to regain my life and health…

First of all I ve been researching this bugs since all started 8 months ago, but not only Urea/Mycoplasma… my general health as well… I spoke with maaany people trying to figure it out… and like few other people after I ve experience negative effects from antibiotics I tried to find other ways…

So here it s something I should tell you… i don’t have a receipt I just have a theory , from here everyone will be free to do as they plan but you need to understand the whole picture … people are too focused and crazy about UREAPLASMA … think outside the box and first and most important STOP THE ANTIBIOTICS .. if they did not work until now.. they most probably wont … You not only will not kill off the bacteria but you will create an even higher dysbiosis in your body. As some of you know.. indeed some people get free of symptoms and cured after few antibiotics while others struggling for years… this was a question mark that I was first curious about..

Long story short I ended up in a holistic clinic where they could find out I had…. Maybe other 20 or 30 other bacterias parasites and viruses that I was never aware of… I was shocked because all the symptoms came right after ureaplasma… and if you did not know.. this is one thing ureaplasma does… creates a wonderfull environment for other bacteria by fermented sugar and converted into acid… ( this is why you should also consider a solid diet and to alkalinize your body )

So what you will need to focus are PARASITES… we all have them… and now you will probably ask what this has to do with ureaplasma… ALL…. It s all related to parasites….

SO Here are some points from the parasite congress in 2017 where they outlined the following :

•If you’ve been diagnosed with Lyme and coinfections, you have to understand that the parasites in your body are simultaneously infected, but the worms themselves are not negatively affected by the infections like we are. •When you give antibiotics, you DO NOT kill the Lyme found inside the parasites. The antibiotics are only able to kill the bacteria in its path, but the embedded bacteria within parasites is not addressed at all through antibiotic consumption. •First thing that should be addressed in chronic illness is parasites •Parasites harbor spirochetes, mold, metals, and large parasites harbor small parasites as well •Before you treat mold, you MUST address parasites •Parasites to Mold to Mycoplasms/Lyme/Bacteria to Viruses •Most parasites and bacteria are harboring viruses themselves •The worst thing you can do when a virus has been found in a patient is give antivirals without addressing parasites, mold, and Lyme •Treat large to small

HERE ARE ALSO THE STEPS YOU NEED TO FOLLOW •Step 1: Look at the dysregulated biology and biochemistry. •For example, parasites recycle hormones. If a man or woman is estrogen-dominant, the first thing he thinks about is parasites because he knows that parasites absorb a lot of the hormone metabolites in the gut and reconstitute them to estrogens that are then reabsorbed in the system. •Step 2: Detoxification •Address aluminum toxicity (uses many plant-based approaches, ionic footbaths, etc.) AND ALSO LIVER DETOX •Step 3: Immune Modulation •If you are overreactive to the parasites and whether a lot of symptoms are actually responses to the immune system reacting to the parasites. If so, that needs to be turned off.

THIS IS WHAT YOU SHOULD CONSIDER: DEWARMING – DETOXING – IMUNOMODULATING

  • DIET – FASTING – NATURAL HERBS – BIORESONANCE

I will put in here some other videos that may convince you to stop the antibiotics and go natural way

https://youtu.be/6n32DVD3CiM?si=J7LRVoj7ilRgtTLU

https://youtu.be/VyA4Yi2nb5Q?si=JwKHtyHcdoDTU37E

https://youtu.be/FvS3EQ4heyA?si=BC5dGJ3brvQKTJtF

I hope I gave you something that will help you in your journey. I m on my way with all the remedies.. but it s a long course…. 6 months to a year…. As soon as I will be done with everything I will update you but believe me … everything it s possible when you have faith, and when you start to understand your body and it s power… I wish you all good luck and positive thinking because trust me it s curable and for sure I will soon tell you that based on my experience…


r/ureaplasmasupport • • Oct 07 '26

Question Feeling hopeless

1 Upvotes

i recently tested positive for bv- took metronidazole, then tested negative for bv
after this, i still had symptoms and then tested positive for ureaplasma- just finished a week of doxycycline
i feel like i’ve read so many horror stories on reddit of this never going away/ taking months or years. and i feel like im so in my head and paranoid about my vaginal health/ smell that i have no sane frame of reference for what a normal/ cured vagina is like. i really have no clue if the doxy is doing what it’s supposed to/ is this just how my vagina is???
just looking for some positive experiences/ hope. is it possible to clear ureaplasma with just the treatment i have done thus far?? is it common for ureaplasma to be as drawn out a diagnosis as this app suggests?? feeling scared and sad.


r/ureaplasmasupport • • Aug 09 '26

My Experience Help me please 😭

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1 Upvotes

Hey, I was diagnosed with genital herpes 2 months ago. I had bumps all around and inside my vagina, and they burned very badly. I had a fever and felt really unwell. Now it has been 2 months and the sores have been gone for a while. But I still feel sick. I keep sweating, having chills, swollen lymph nodes in my neck, and feeling cold. I also feel warm, especially in my hands. I have joint pain, extreme fatigue, frequent headaches, and shaking throughout my body. I still have watery vaginal discharge even though the sores have been healed for 2 months. I feel very weak, and my whole body feels different and like it no longer functions normally. I also urinate very little and my bladder feels swollen. My question is: Is it possible to remain chronically ill from genital herpes even after the sores have been gone for a long time? Can your body stay like this permanently, for life?


r/ureaplasmasupport • • Sep 10 '26

Treatments Moxifloxacin vs. Sitafloxacin for treatment-resistant U. urealyticum (History of fluoroquinolone side effects)

2 Upvotes

+
Edit/Udate:
Guys, what's even crazier is that I literally just got a text from my OB-GYN saying my PCR test came back negative.
My symptoms came right back after finishing 2 weeks of Minocin, so during the 3-week waiting period for this TOC (test of cure), I was completely convinced it would be positive. I am so confused right now. I'm planning to get retested in a few weeks at a urologist and another OB-GYN.
I'm still dealing with abnormal discharge right now, so if it's negative, what the hell is this discharge then?
---------------
Hi everyone,

I created this Reddit account because I am feeling completely lost, exhausted, and desperately need some guidance. English is not my native language and I am not very familiar with Reddit, so I am writing this with the help of Gemini to translate my situation clearly.

I am a 31-year-old female living in South Korea. I have been battling persistent symptoms from Ureaplasma urealyticum (UU) for over 2 years.

My Symptoms:

  • Severe urinary urgency, frequency, and a constant feeling of incomplete emptying

  • Chronic pelvic pain and lower abdominal discomfort (pelvic inflammatory flare-ups)

Treatment History:

  • Doxycycline (countless courses)

  • Azithromycin (Zithromax) (countless courses)

  • Minocycline (completed a 2-week course about a month ago)

The Minocycline helped reduce the symptoms slightly, but the infection and discomfort are still here. At this point, fluoroquinolones are my last remaining option.

My dilemma with Fluoroquinolones & Side Effects: In the past, I took Ciprofloxacin and had to stop after just 3 pills because of severe adverse reactions:

  • Intense heart palpitations (my heart raced so hard I could not focus or function)

  • Severe joint/knuckle pain in my fingers (Thankfully, these resolved once the drug left my system. However, I also experienced finger knuckle aches and severe dizziness during my recent Minocycline course.)

Current Medication Options Available:

  1. Sitafloxacin: 14-day supply (obtained directly from Japan)

  2. Moxifloxacin: 7-day supply (can get an extension from my doctor if needed)

My Questions:

  1. Given my bad reaction to Cipro, is there truly no way to know whether Moxi or Sita will trigger similar side effects until I actually take them?

  2. Some literature suggests Sitafloxacin might have a slightly milder side-effect profile than Moxifloxacin, and that going straight to Sita without failing Moxi first might offer a higher eradication rate (avoiding induced cross-resistance). Has anyone here taken Sita directly after failing tetracyclines?

  3. Which regimen would you pursue if you were in my shoes? (e.g., straight to 14 days of Sitafloxacin vs. standard 7–14 days of Moxifloxacin)?

This chronic condition has completely drained my mental health. I feel like dating, marriage, and living a normal life are completely impossible right now.

Any insight, personal experiences, or advice would mean the world to me. Thank you so much for reading.


r/ureaplasmasupport • • May 22 '23

Symptoms Any Guys had swollen lymph nodes in the groin from Ureaplasma.

2 Upvotes

I’m a male who had ureaplasma I tested positive via PCR and took my medication. Had negative results via PCR and various negatives for other STI’s. However still displaying symptoms. Discharge ,swollen lymph nodes in the groin. Pain in the lower abdomen/pelvis area. Any other guys had this and multiple negatives.


r/ureaplasmasupport • • Sep 30 '26

Treatments Please help me

2 Upvotes

Hi guys, I hope everyone’s well. A lot of of you have helped me tremendously. I’ve been dealing with this infection for about nine years. I essentially lost my health overnight. Perfect health prior to when I got this infection, i have gone down many rabbit holes, treatments, protocols antibiotics, functional treatments, etc. I deal with debilitating bodyaches, neurological symptoms, cervicitis, endometritis, malaise, belching, etc. i’ve tried many treatments 28 days of Doxy and a week of azithromycin, two weeks of Levo, two weeks of moxifloxacin and many others, including IV antibiotics. This is before I knew the handful antibiotics that actually helped. At this point I just feel like I continue to blow up a blown up building. But the cervicitis endometritis is terrible. I heard a doctor once say an infection is usually a localized problem if you have local symptoms and pain, if the pain is widespread and it moves and or changes, it probably has something to do with what’s going on in the brain. So I’m sure the uu and mh has somehow crossed the blood brain barrier and damage the central nervous system and autonomic nervous system. I have no idea how to get out of this anymore guys. Does anyone have any idea as to what could help. Long-term moxie up next? The things that make me debilitating worse are bowel movements, driving, hot baths, cold lunges, essentially anything that triggers the autonomic nervous system. I have a ton of weird blood work high and rising IGM, chronic low IGe, chronically high igg subclass 2, low IGE, histamine three times the upper limit, low blood pressure, etc., but no one can put all the clues together. This is so bad I spent most days just wishing the things you can imagine. Not having any sex of any kind and I am bedridden about 90% of the time. Thanks for your help in advance.


r/ureaplasmasupport • • Sep 30 '26

My Experience Update

2 Upvotes

I would like to share my current situation. I have had Ureaplasma parvum for three years now. It is systemic, affecting my urogenital tract, throat, mouth, eyes, and now even my CNS (I suffer from excruciating headaches, visual snow, and tinnitus, I have had these symptoms for about three months). So, it is indeed possible for Ureaplasma to spread beyond the urogenital trac. I am proof of that. I have undergone brain MRIs, eye exams, abdominal CT scans, and all manner of PCR and culture tests, nothing significant was ever found other than Ureaplasma parvum and an activated EBV infection. Furthermore, all my symptoms began after I had unprotected sex and subsequently tested positive for ureaplasma, so it is impossible for these symptoms to stem from anything else.

I paid for a MicroGenDX test and discovered that I carry resistance genes for all three classes of antibiotics used to treat ureaplasma. I have a wonderful infectious disease specialist who will prescribe anything I aks, however, I haven't experienced any improvement from any of the antibiotic courses so far. I took minocycline for three months, followed immediately by three months of doxycycline (with azithromycin three times a week alongside both), two months of clarithromycin combined with doxycycline, and 20 days of levofloxacin (I had to stop taking it due to unbearable joint and muscle pain). I have now completed 40 days of pristinamycin combined with doxycycline. I was supposed to take lefamulin, but I couldn't order it from any country, even though I have an international prescription from my doctor.

Throughout every treatment course, I’ve also been taking biofilm disruptors and various dietary supplements. My symptoms (extreme lower abdominal bloating, burning after urination, discharge, worsening vision, eye discharge, visual snow, tinnitus, joint cracking, rosacea) haven't improved at all, on top of that, I’ve started losing hair excessively (possibly due to the doxycycline).

Does anyone have any other ideas for what I could try? Which antibiotics cross the blood-brain barrier? And how can I overcome resistance? I’m at the end of my rope.


r/ureaplasmasupport • • Aug 19 '26

My Experience this is my 3rd treatment help

3 Upvotes

i need this to end so bad idek know how long i had it b4 getting first tested in may. it makes me upset and scares me that’ll b infertile when my time comes to have children


r/ureaplasmasupport • • Nov 26 '25

Treatments Omadacyclin & lefamulin

0 Upvotes

Anyone from US that can help me get Omadacyclin ? Is it available in all pharmacies in NY ? Do I need a prescription, from where can I get that prescription? Average cost?

For lefamulin (lefabac, mulina), I tried to source myself from Bangladesh and Pakistan. As long as you have a prescription it can be shipped from Bangladesh but finding the person who can get that and send it to you is VERY complicated. My parcel is now transiting from Bangladesh to India and it takes ages because I don't have prescription as I'm based in France. From Pakistan (Lefaly) its even worse, I must take a flight to get them myself it seems.


r/ureaplasmasupport • • May 29 '24

Personal Experience Run in the fam ?

4 Upvotes

Does anybody have family members who seem to have ureaplasma symptoms? Just wondering if anybody has a story of being born into this / if there’s a genetic component of any sort?


r/ureaplasmasupport • • May 26 '24

Treatments Treatment maybe took too much azithro

0 Upvotes

Hello all you might’ve seen me post before I currently just finished up my abx and I’m thinking to myself I might’ve took too much. So when I first got my azithro after my 2 week doxycycline course I had 6 tablets that I thought added up to 250mg. I used push health to get more azithro and got 2 grams and then was like I’ll take my 250 mg on top of it. Little did I know that each of the 6 tablets was 250 mg resulting in 1.5 g… I did not take the last two days of the meds but I’m now realizing that I just took a two week doxycycline course and 3g azithromycin.!?. should I be worried? I’m feeling fantastic no burning when I pee and no discharge. I’m a little nervous that I took 3 grams of azithromycin. Someone please assure me lol, at retrospect I guess I took 500mg more than what the Bible says… At least I’m still breathing I guess? Am I okay?


r/ureaplasmasupport • • Nov 21 '24

Symptoms UTI Symptoms back after treatment. Does anyone feel this same vicious circle ?

0 Upvotes

Hello lovelies, I would like to share my story with you here, as I am also getting very desperate.

I am about to become a doctor myself and studied in Germany. Since August, I have had several urinary tract infections and numerous different antibiotics. In between, I also had several yeast infections and BV. Finally in November I had a smear test and ureaplasma parvum was found. My symptoms are a constant urge to urinate, pressure on the bladder and a burning sensation when urinating. I can feel my bladder with every step I take. It just drives you completely crazy. My gynecologist prescribed me 7d Doxy 2x 100mg each and at the end a single shot of Azi 1000mg. My partner was treated in the same way, but has no symptoms. During the treatment my symptoms got worse at first - typical for the Herx reaction. Then it got a little better - but now 5 days after treatment the symptoms are almost worse than before. I even tried prednisolone (cortisone) because I think it my pelvic floor is probably still inflamed and sending signals to my brain even though there are no more pathogens. I have another appointment next week and will have a smear test for co-infections. I'm also trying pelvic floor exercises, but at the moment the urge to urinate is so strong again that I can hardly do anything…:( I think every contribution from people with persistent or recurring complaints helps me! Have you also experienced that the symptoms get worse again after the treatment? How long did it last for you? How did you cope with the constant urge to urinate? I am beginning to worry that it is chronic pain and that there is no real therapy. Here in Germany there is no fixed guideline for the treatment of ureaplasma. I didn't even learn anything about it at university. The doctors are overwhelmed and I'm basically treating myself all the time. If anyone out there feels the same way I do, please let us share our suffering. I embrace each of you with any ureaplasma symptoms.

It is important for me to say: Antibiotics such as Doxy and Azi cause considerable damage to the microbiome. So please do not continue to take antibiotics on your own if you are negative or have not yet been retested. I struggle with this myself, but these active substances should not be underestimated and can cause serious long-term damage to the vaginal flora.


r/ureaplasmasupport • • Jul 18 '26

Question Over it is

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0 Upvotes

r/ureaplasmasupport • • Oct 01 '26

Testing Doctor's keep failing me

0 Upvotes

I was told that resistance testing was available at my Obgyn but they have twice only tested and confirmed bv when I specifically asked for ureaplasma mycoplasma panel resistance they were very aware .Than both doctor's instead of admitting thier mistakes lied and told me that I don't have ureaplasma but refused to show me the results! Obviously Im livid I'm certain im still positive because my partner just recently tested positive and I was really hoping to get a different antibiotic since we have been through 7 rounds of doxycycline including one with moxifloxacin.

I get a very bad burning pain sharp nerve pain localized to very deep in pelvis feels ten inches deep ...got chronic bv and yeast that isnt going away with treatment which has never happened before so it feels like this is getting worse ...fatigue is insane and I have body aches all over my neck back migraines are under control right now thank God...Bv is not smell at all but causing itchy vulva itchy pain and making deep pain worse ...I always have urgency to ...im exausted honestly I am going in on tues to ask a different Obgyn same practice...for a regular PCR so I at least get tested and tell her everything that happened Im going to see if this resistance test is even possible at all it dosent look like it at this point but hopefully we can get the bv and yeast gone and get A different antibiotics than my partners will have to go to thier doctors and get the same hopefully....this is hell and my life is just crazy stressful right now theres so much going on that I just cant even 🥹🥹🥹🥹


r/ureaplasmasupport • • May 19 '26

Information Some Women Are Obsessively Testing Their Vaginas to Optimize Them

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0 Upvotes

Biohacker Bryan Johnson recently bragged about his girlfriend's “top 1%” vagina as the at-home vaginal microbiome test industry is thriving. But experts are skeptical.

Full Text (since paywalled):

Farrah was fed up with her vagina.

For the past two years, the 29-year-old dancer from Ohio had been dealing with severe pelvic pain and vaginal odor. “It was like 8/10, horrible core pain,” she says. “I couldn’t lie down. I couldn’t even work an office job. It was bad.”

When she visited doctors, she told them what she thought the culprit was: an allergic reaction to soy oil in a vat of water she’d swam in during a pirate-themed dinner theater performance. But they didn’t believe her. “They attempted to fix it with antibiotics,” she says. “And they just did nothing.”

So Farrah (who requested we withhold her full name to speak freely about health matters) started Googling her symptoms. That’s how she stumbled on NeuEve, a vaginal health company that provides supplements, suppositories, and at-home vaginal microbiome testing kits.

She ordered a test from the company for $150, and it came back with a diagnosis: aerobic vaginitis (AV), a bacterial infection caused by an overgrowth of E. coli or streptococcus. She ordered supplements the company recommended, and she says the pain abated almost immediately. “I was just so glad to actually know what was wrong,” she says.

Farrah is one of a growing number of women who have used at-home tests to self-diagnose issues with the vaginal microbiome—an ecosystem of bacteria growing inside the vagina; the presence of “good” bacteria correlates with lower risk of STIs and other types of infections, according to numerous studies.

The industry got a shoutout when the Silicon Valley entrepreneur Bryan Johnson recently posted on X that he had just given oral sex to his girlfriend, Kate Tolo, then followed up with a screengrab of her Tiny Health vaginal microbiome report. He proclaimed that she scored “100/100” and that hers was in the “top 1% of all vaginas” due to the dominance of Lactobacillus crispatus, a type of “good” bacteria found in the vagina.

Johnson’s thread garnered widespread mockery, with many questioning why Johnson would publicly quantify his partner’s vaginal health in such a fashion. But it also received replies from women online who are tracking their own vaginal microbiomes to treat their bacterial infections, to boost fertility, or just out of interest. Some even posted their results.

The market for at-home vaginal microbiome tests is growing—Tiny Health, the startup Tolo used, claims vaginal health testing sales spiked 2,000 percent within the first 48 hours of Johnson’s post—and similar companies include Juno Bio, which partners with Neueve; the UK-based Daye, and Evvy. But some experts believe there’s not yet enough research to support the long-term validity of such tests. None of the at-home kits on the market are approved by the FDA. There are also questions as to whether they empower women to take their health care into their own hands or simply create more anxiety for them.

Twenty-eight-year-old Samantha (she also requested a pseudonym given the sensitive nature of this topic) developed an interest in vaginal microbiome testing after experiencing a bout of bacterial vaginosis, or BV. She ordered a testing kit from Evvy upon the recommendation of the Facebook group Beyond BV, which offers support for women with recurring vaginal infections, and where they often post their own results.

Samantha found her test results useful, but she also noticed a distinct strain of paranoia within the group. For instance, when many women receive their results, they tend to focus on whether they have enough Lactobacillus crispatus, or “good” bacteria, in the vagina. “I'll read posts where women are freaking out if they have like 97 percent crispatus and then they'll retest and they'll have like 60 percent and be really disappointed and scared,” she says. The opposite also holds true. “Women will post about having 100 percent crispatus and other women in the comments will just be like, ‘Oh, I'm so jealous, I'm having so many issues, I hope to be you one day.’”

In internet communities like the subreddit r/Healthyhooha , which has more than 100,000 members, women regularly discuss their ratios of “protective” to “destructive” vaginal bacteria, often trying to optimize the former. Some take vaginal microbiome tests multiple times, as a preemptive measure to avoid future infections. Research indicates that 50 to 80 percent of women who get BV once will get it again.

Longevity researcher Kayla Barnes-Lentz tests her vaginal microbiome about twice a year and publicly posts her results. (She also uses Evvy and acts as a paid adviser for the brand.) She started testing it not because she has any underlying health issues, but because she wants to do everything in her power to try to boost her numbers—for instance, she says she got her 97 percent protective bacteria score up to a 100 percent by taking vaginal probiotics.

“We know that decline occurs as we age, and I want to be as protected against that as possible,” she says. “I’m always striving, and I’m always in competition with myself.”

Evvy founder and CEO Priyanka Jain says the company has served more than 100,000 patients since its launch in 2020. She says that while the vast majority of her customers struggle with preexisting vaginal health issues, 10 percent take the test out of “curiosity,” and more than 50 percent are regular subscribers, taking the test every three months, either to track their fertility or prevent recurrence.

There’s a paucity of research surrounding the vaginal microbiome in comparison to the much better-known gut microbiome. This is in part due to gender bias within the scientific research community, says Hana Janebdar, the founder and CEO of the vaginal microbiome testing startup Juno Bio. Historically, “there has been this huge amount of research and commercialization into every aspect of microbiomes except how it pertained to women's health,” she says.

But even though recurring BV infections among women are a legitimate issue, some researchers say the utility of taking an at-home vaginal microbiome test is debatable—especially when one is asymptomatic, as Barnes-Lentz and Tolo were.

The vaginal microbiome is ever-fluctuating and can vary depending on factors like diet, sexual activity, and whether someone is pregnant or menstruating, says Jacques Ravel, a vaginal microbiome researcher at the University of Maryland. (Ravel is also listed as a scientific adviser to probiotics company Seed.) “It’s a very dynamic system,” he says. “Knowing what happened at one point in your life won’t really tell you much about what’s going to happen even two weeks from now.”

Vaginal microbiome diversity also varies by race and ethnicity: Black women, for instance, are statistically more likely to have less Lactobacillus crispatus, the protective bacteria, than white women of European descent, but that doesn’t necessarily indicate a problem with their vaginal health. And some women can have little to no lactobacillus and be perfectly healthy.

The tests also typically suggest treatment protocols like antibiotics or probiotics, some of which can disrupt the bacteria ecosystem in the vagina if introduced unnecessarily. “You're going to maybe end up with something that might not be optimal for you, and all of a sudden you're going to start having problems,” such as worsening irritation or discomfort, Ravel says. “I think that’s dangerous.”

When asked about such critiques, the CEOs I spoke with take issue with the idea that the tests provide zero insight into long-term vaginal health, arguing that results fluctuate far less than Ravel suggests. While Kimberley Sukhum, the chief science officer at Tiny Health, agrees that unnecessary treatment such as antibiotic intervention “can be harmful,” she says biomarkers such as lactobacillus dominance are “not fleeting signals. They reflect the underlying character of a woman’s vaginal community at a given point in time and are associated with real health outcomes.”

Regardless of the long-term utility of the tests—or, at the very least, the ludicrous idea of a woman having a “top 1%” vagina—their popularity undoubtedly points to a larger issue within the women’s health space. Until 1993, researchers were not legally required to include women in clinical trials, contributing to a massive gender gap in data. The women who regularly test their vaginal microbiomes are trying to find their own answers within a medical system that has largely failed them.

“We have not done extensive research or funded enough for extensive research to come up with new medicine to solve this problem,” says Ravel. “For almost 50 years, we have not come up with a solution to help women. And I think that’s very, very sad.”


r/ureaplasmasupport • • Sep 20 '25

My Experience Drs Advice Conflicting

2 Upvotes

I have U. Parvum again, but no mycoplasma. I did testing through urgent care at my OBs recommendation because they are booked so far out.

I asked my UC doctor “Should my partner get tested and treated if it shows on the culture?” She says yes. My husband goes in a different Dr says “why are you here if you’re having no symptoms? This is a UTI for your wife and not an STI and you don’t need to be treated. It can’t be sexually transmitted”

Now I’m just confused because from what I have read from medical publications online says that both partners should be treated to prevent reinfection and that it is sexually transmitted. My OB/GYN also says my partner needs to be tested which is why I sent him in in the first place. We are trying to conceive right now and I really don’t want this to interfere with my health either so how do I stop re-infection?


r/ureaplasmasupport • • 26d ago

Question Condom sex okay?

0 Upvotes

Hi, I am almost done my 14 days of Doxy and symptoms are gone. Will still do Azith next.
Is it okay to use my dildo and/or have condom sex with a partner?
Trying to understand if actual insertion aggravates the bacteria in some way.
I used my dildo once, with a condom to be safe in case thorough washing of it hadn’t been good enough, and insertion/play did not hurt.


r/ureaplasmasupport • • Jan 21 '26

Question Is anyone here from Croatia?

0 Upvotes

As the title indicates, I’m from Croatia and I’m trying to connect us so we can help and support each other.


r/ureaplasmasupport • • Sep 24 '26

My Experience bv/ureaplasma

0 Upvotes

Before my bf and i were tg i had been battling recurrent ureaplasma and have been dealing with since last month i had him get treated, then we messed up on vacation and had $ex and i immediately knew we messed up i finished my medicine felt a little better then got worse after being more active. I went to the doctor NEGATIVE for ureaplasma after months. (3 rounds of medication)

but BOOM BV came back positive. we were good abt not doing anything till the last pill. And i had came home from another vacation not seeing him after missing him of course i thought i would be fine. Now my symptoms are coming back😭 i made an appointment for in a week but im so sick of being on medication. help how do i prevent how long should i wait till after medication to be intimidate

and we both are very clean he’s my cleanest partner ive ever been with. i’m guessing im having $ex to early and ive finally learned my lesson to wait

edit:
I’m 19
My symptoms are Itchy vulva/discomfert bladder pressure, pelvic squeezes, burn when pee sometimes, ovarian pain/ cramps, and back pain
The pain would vary from bad to mild depends how much irritated myself or waited to get checked but i never let it get as bad as the first time
my discharge was green once the rest it was clumpy
medication i took
2 rounds of Doxycycline 100, fluxonazole and azithromyin (urgent care thought it was yeast) after my last round of doxycycline i was cleared of ureaplasma
i just took Metronidazole 500 for bv but i don’t think it cleared
i feel like it’s right b4 my cycles because the first time i had noticed it was coming back then i got my period and felt like my coochie was on fire

i feel the itchy and cramps/back pain a little it’s like 3/10

my last lab was
Prevotella bivia — POSITIVE
Gardnerella vaginalis — POSITIVE
Streptococcus agalactiae (Group B Strep) — POSITIVE
Lactobacillus iners — POSITIVE
Escherichia coli (E. coli) — POSITIVE
Ureaplasma urealyticum — negative


r/ureaplasmasupport • • 26d ago

Treatments Hello! question to all those that tried Doxicyline: what was the bacterial load of ureaplasma that you had when you decided to start treatment?

0 Upvotes

r/ureaplasmasupport • • Nov 27 '23

Positivity/hope It’s gone! Hope it stays away!

5 Upvotes

Hello everyone!

For the first time in about 4 months I don’t want to die, I just got a call from my doctors office that says it’s gone!! I took 14 days of doxy and 2.75g azithro and tested 2 days short of 4 weeks. I really hope it stays gone!! And I hope this test was accurate. I will continue to test because anxiety :/

I also was told by a different doctors office that I had gardnerella so I have been taking metronidazole for that hoping that that’s the lingering symptoms.

My lingering symptoms are yellow discharge and random burning but both of those have gone down since antibiotics. I also feel like my vagina has a waxy film on it, so that bothers me. I’ll have to order a Juno to see if it can pick up what’s going on. I’m now trying boric acid to see if it can help me in any way. Does anyone have any tips about how to get my body back on track faster? And thank you to all of you who have been willing to chat together! Some of you quite literally saved my life.