I am merely an observer here. though I might occasionally offer a thought or two.
Personally speaking, Yasmin has elevated my quality of life to an entirely different stratosphere. I have never experienced such debilitating amounts of pain—going from roughly twenty intense flare-ups down to maybe ten manageable ones over a three-day period—nor have I dealt with cycles this long. Honestly, I’m feeling a bit apprehensive now, but I am certain things would be significantly more agonizing if I weren't taking them. My skin remains clear, my cellulite hasn't changed one bit, and my weight has stayed exactly the same since my high school days, even now that I am a junior in college. My hair is unremarkable, sex is completely stress-free, and as for my libido... well, we have transitioned into a BDSM phase and 🤷
everything is working perfectly for me. In two months, I will begin my fourth year of continuous use, and I have absolutely no intention of stopping until I have a baby, which implies at least another five or six years of this regimen (even though my endometriosis technically dictates otherwise, though I cannot fathom why I would stop if that weren't the case).
So, there you have it; I truly cannot say enough good things.
Good grief... I suppose it just occurred to me... but given the circumstances...are you seriously considering skipping the ER?! Your finger is turning a ghastly shade of red and gray!
The blood needs to clot on its own; if it fails to do so while your finger is visibly discoloring, there isn't a thing in this world that will stop it.
Angela Edwards76 said:I'm 20 years old, and my first period arrived when I was 12.
Honestly, I suspect we might be looking at a simple cyst here. In my own experience, my cycle started around ten or eleven, and by thirteen, the cramps were already becoming a regular burden. While you waited a bit longer than I did, that extended gap actually makes me lean more toward the theory of a cyst; such things tend to develop gradually over time. My personal logic dictates that if it were truly PCOS, the symptoms would likely manifest much sooner, perhaps within a year or two after the reproductive system fully kicks into gear.
So, you should probably go greet the doctor on my behalf and demand a referral for an ultrasound, or perhaps just head to a private clinic to get it handled—I suspect we are looking at something around $67. Then, if the endocrinologist confirms it, you’ll need to get those markers checked, or look into hormones if it turns out to be PCOS, assuming my memory serves me correctly. Honestly, doing both simultaneously would be the most prudent course of action. And do it immediately! Good grief, you are sitting there enduring such agonizing pain (and believe me, both Angela Wright and I know exactly what you're going through), yet you're being told this isn't necessary simply because some doctor holds the misguided opinion that suffering is perfectly normal. 🙄 Regarding the doctor,
By the way, how old are you exactly?
From my own experience—as someone who was popping Voltaren and Baralgin like they were Tic Tacs, only to end up facing days of vomiting, eventual respiratory distress, ER visits, and pure screaming matches... Ketonal is the heavy hitter here, and it will likely be your best bet. It should provide enough relief to keep you functional until you can start a proper regimen, which will most likely involve pills. As for Baralgin, I have read that they are incredibly harmful, so I would steer clear of them entirely.
Hold on, hold on, hold on... have you actually gone through the motions of getting an ultrasound, running those marker tests, checking your hormone levels, and all that other necessary diagnostic work?
It is only once you have exhausted those clinical avenues that we can even begin to entertain the notion of alternative methods. One cannot meaningfully discuss alternatives until they have confirmed that this pain is truly an enigma of unknown origin.
Edit: Your doctor is being completely dismissive; nothing about experiencing pain should ever be considered "normal."
feralraven4 said:I simply wanted to provide an update now that I have returned from my appointment. As I had already suspected, we are dealing with a vaginal infection that has spiraled out of control due to being left untreated for far too long. I was prescribed some vaginal suppositories and requested a bacterial culture to pinpoint the exact pathogen involved, and for the time being, I will decline using the Aldare cream since it is far too aggressive for my system; furthermore, I am absolutely firing my gynecologist immediately!!!!!!!!!
I am truly relieved to hear that you have finally addressed this matter! Go forth and good luck with everything else 👍 😉
On that little paperwork slip you carry when you're switching doctors, there is actually a specific section where you can check a box stating you are leaving due to "misunderstanding," "disagreement," or some other nonsense, which grants you the freedom to change providers whenever you please; absolutely no one has the authority to force you to remain under the care of someone who provides substandard treatment.
Stop using Aldara immediately. I mean it. Since I suspect you’ve only gone through two or three of those tiny tubes, the damage isn't irreversible. Condylomas can wait; they aren't going anywhere. It seems obvious to me that you are applying it topically rather than internally, but even then, the cream has a much broader systemic effect. If it weren't for my own experience—where my entire pelvic region was in agony—I wouldn't have suffered such an intense, near-allergic reaction after application. For instance, when I applied it, I didn't feel any burning initially; instead, the reaction hit me on the second day and persisted until the next application, eventually becoming a prolonged ordeal.
It is entirely possible that you will respond favorably to the cream—for example, I managed to get free topical treatments at the doctor's office even though Aldara failed me—but given the side effects you're describing... I honestly don't know; perhaps borrow some money from a friend, as I have no idea what the local clinic fees look like, but you should check the gynecologist recommendation threads on this forum for pricing. Once you have handled that infection, you can return to using the cream, but you must resolve that suppuration first.
Aldara? Hmm, I have heard conflicting reports about its efficacy... personally, I purchased it once and had such a violent reaction that I ended up tossing $400 right out the window. It honestly escapes my comprehension how that incompetent doctor of yours could possibly justify applying a cream as aggressive as Aldara to compromised tissue; you are essentially courting systemic toxicity at this point. The protocol should always be to address the inflammation first before even considering HPV treatment, as this cream is far too potent for such reckless experimentation. Those warts aren't going anywhere, so there was no need to rush. How long are you currently applying this stuff? Furthermore, you have every right to switch gynecologists well before your insurance cycle resets, and frankly, I strongly suggest you do so before things take a turn for the worse. Please, just give it some serious thought and take decisive action immediately. From what I understand, you cannot simply layer these different therapies on top of one another; combining Aldara with a vaginal suppository is asking for trouble. At the very least, try calling a different specialist to seek a second opinion and see if you can transfer your care. I am genuinely worried about your well-being right now...😢 Good luck.
Has the concept of switching gynecologists even crossed your mind? Who can say for certain how she actually manages your warts? Are you being treated with topical applications, or is she simply shoving pills down your throat? You really ought to be opting for topical treatments while simultaneously working on boosting your immune system. It is imperative that you find a new doctor immediately. If we are truly dealing with a pyogenic infection—and you claim the mucosa is swollen and producing pus—then the situation could have already escalated quite significantly. Cut ties with that incompetent hack, even if you have to transition to a new clinic privately, and get some swabs done. I haven't the slightest clue what this might be, but it sounds deeply concerning. I simply cannot fathom why you are still seeing her...😲
Just a small observation here—and please don't mistake this for any kind of endorsement of drug use, as I have no desire to catch the attention of a moderator—but there has been some recent research regarding the intersection of marijuana and Alzheimer's. http://www.webmd.com/alzheimers/news...low-alzheimers
While I am not entirely certain about the exact degree of correlation between Alzheimer's processes and brain atrophy, it certainly seems like a subject worth investigating, as it might actually offer some meaningful insights.
Back when I was just a young girl, I suffered through these excruciating pains centered around my right kidney that seemed to radiate through my entire torso and all over my body. I ended up being hospitalized twice, undergoing every conceivable renal test they could throw at me, yet they found absolutely nothing. It wasn't until years later that the realization finally hit me: during that first hospital visit, I had actually been experiencing my very first heavy period, and every subsequent cycle followed that same pattern. Only then did I understand that everything I had endured was actually the result of endometriosis, a condition that wasn't officially diagnosed until it had reached an advanced stage several years down the line.
Now, I am certainly not suggesting that you definitely have endometriosis, but I do want to point out that pain in the kidney area isn't always about the kidneys themselves. In my case, it wasn't, and despite spending countless days in hospitals, not a single doctor ever made the connection. Why? Because I was young, and because the pain would flare up up to two weeks before my period started, so nobody bothered to link the two. It is far easier for them to look for the obvious culprit rather than digging deeper.
You should really have your ovaries and other internal organs checked out. Please let me know how it goes; I am genuinely interested in what you find.
Kimberly Mitchell42 said:If anyone actually wants to figure out how to eat and live healthily, they should probably give this page a read:
And I don't mean just skimming a couple of sentences—read the whole thing first, then we can actually have a real discussion.
Honestly, whenever I encounter those delusions regarding Cassiopeians or third densities, I find myself unable to even move from the headline before I instinctively close the tab. I am convinced that particular link leans much more toward fringe pseudoscience than actual health information.
That’s a solid suggestion, truly, but I simply don't have the capital to make it happen right now.
My mother is fully aware that my daughter isn't being untoward; her issue is more fundamental, as she fails to grasp why her child would even need to see a gynecologist, viewing the whole ordeal as some sort of inherent trauma. So, naturally, things get complicated...
She will eventually visit that specific specialist—I've consulted him myself in the past, and he is an excellent physician. She intends to go in a month once she turns fifteen, following the advice given by the women at the social services office, so we shall see how it unfolds. If all else fails, I will step in and sign the paperwork myself.
I appreciate the input, ladies.
By the way, stormymaker24, I am quite certain that this used to be classified as primary healthcare; there is absolutely no way it only applies once someone reaches adulthood, especially since I know plenty of girls who saw a gynecologist long before turning eighteen without any issue whatsoever. The only problem is that I just can't seem to reach them lately...
I would much prefer if she simply registered there locally because, first of all, it is far easier to argue with my mother about seeing a gynecologist when the appointment is just down the street rather than having to debate an entire trip to NYC, and secondly, I want her to have her own dedicated physician she can rely on whenever the need arises.
However, the whole requirement regarding parental signatures for primary care physicians remains utterly baffling to me, and despite my inquiries, no one has seen fit to provide a straight answer...
I find myself dealing with a rather reckless younger sister who, quite recently at the age of fourteen, decided to take her first steps into intimacy with a boyfriend. I am currently insisting that she see a gynecologist—not just to establish a proactive approach to her health, but to ensure she undergoes a proper examination under professional supervision. While I am based in NYC, she is living in a small rural town, so she is navigating this bureaucratic mess on her own. She attempted to register with a local clinic, and while the nurse handed over the necessary paperwork without any fuss, she was subsequently turned away by Social Services because apparently, since she isn't fifteen yet, she requires a formal referral from her primary care physician. It is utterly absurd.
To be fair, this isn't an insurmountable hurdle since she turns fifteen in less than a month, at which point the process should be more straightforward. However, the real issue lies in the documentation, which explicitly states that parental consent is mandatory for minors. This strikes me as fundamentally flawed; the entire purpose of such medical access should be to allow young people to seek care without fear or coercion, rather than leaving it to the whims of a mother who decides whether or not she’ll go. My mother is incredibly conservative, and frankly, we have had our share of heated arguments over this, but a person's autonomy shouldn't be sidelined like this.
Has anyone here dealt with similar institutional roadblocks? Should she consider forging a signature or perhaps signing it herself to bypass the system? Since I entered adulthood without these hurdles, I am somewhat out of my depth here.
Laura Davis62, what you are doing here is nothing short of fearmongering, and frankly, it’s starting to veer dangerously close to hate speech. You ought to be more careful with your rhetoric. Not every individual living with schizophrenia suffers from paranoia, nor does everyone carry murderous intent. It seems you lack a fundamental understanding of how most people with this diagnosis actually function; if I am not mistaken, you are basing your entire worldview on a single segment from a program whose objectivity is already highly questionable. Perhaps you should try educating yourself. It is true that paranoid schizophrenics can occasionally become violent, and it is equally true that the government fails them miserably—there needs to be far more meaningful engagement and support. However, forcing people to take medication under medical supervision every single day... well, that is a different matter entirely. The law exists as it does for a reason; while I am certainly not suggesting it cannot be improved, there is a legitimate issue regarding forced hospitalization in extreme cases. But attempting to alarm the general public about the supposed "dangers of schizophrenia" lurking around every corner? That is simply hate speech and discrimination. Watch your step.
Cramps? Nausea? Then nothing about your situation is surprising. I recall starting out with rather significant doses myself—taking about 400mg of Ketorolac Forte daily over a span of four or five days—and I certainly wasn't increasing those amounts. Yes, the body builds up a tolerance, but only if you are consuming them with relentless frequency. As for Voltaren, for some inexplicable reason, I have never reacted to it at all. Not once. Currently, however, Motrin—just the standard version—is providing me with relief.
It is entirely plausible that the pain itself is simply intensifying, or perhaps you are reaching for pills far too often. You really ought to stop relying on headache medication; you would be much better served by sticking to herbal tea and actual rest.
I have come to realize that I am either developing a fever or already running one based solely on the sensation of my skin burning. There is no actual pain involved, just this persistent, searing heat. Since I don’t happen to keep a thermometer lying around the house, this has become my most reliable diagnostic tool lately.😁 It feels absolutely dreadful across my legs, my back, and my arms. Brrr. And it happens because... well, it is quite simple: the elevated temperature causes a certain hypersensitivity in the skin. To my mind, that remains the only logical explanation for such a phenomenon.🤷