Posts by rapidpanther41

Michael Ramos3 said:Alright, now I've really gone and done it!

Honestly, I think you picked the wrong handle—you should have gone with Unhealed, though, let's be real, that doesn't even have anything to do with psoriasis.

Robin Robinson8 said:In just one month, I managed to take my psoriasis from scaly mess to just redness by using nothing but Vaseline—so I highly recommend it. For me, the itching really kicks in once my skin dries out, so I’m constantly slathering on the Vaseline, and that's how I deal with the itch.
Good luck!

Checking in after a bit of a hiatus. I've been experimenting with some new ingredients and teas for the first time, and honestly, my psoriasis seems to be improving slightly. I’ve been drinking Tahebbo tea, and if you follow the instructions for prepping and using it properly, you shouldn't expect much—the first signs of progress didn't show up until about the 30-day mark. I also tried Vaseline, though it hasn't really done much more for me than other ointments have—not that I stuck with it long enough to be sure, mostly because I don't struggle with intense itching or major redness. So, I'm sticking with the Tahebbo tea and this salicylic acid ointment—I'm not entirely sure what the exact formula is, but my dermatologist at the Oakland hospital gave me a prescription for it, and the pharmacy prepares it specifically for me. It seems to be working quite well so far. I'll let you guys know if things keep looking up or if it hits a plateau.☕

Robert Clark2 said:Best regards to you all!👍

I actually had a friend look into this for me—now I’m just sitting here wondering if they’ll actually pull the trigger and buy it, since it's nowhere to be found in local pharmacies, at least not in any of the ones they checked.
To be totally honest, what gave me the most hope was seeing a photo of a woman who had a mastectomy—if she could find relief using this, then hey, maybe there's a chance for me too.

I told them right away: even if it doesn't work, whatever, it's not like I'm going to be the first person to throw money down the drain.😉

But I'm not throwing in the towel—and honestly, I try not to let the psoriasis get under my skin too much, because like someone once said, hope is the last thing to die.☕

Wishing everyone health and wellness,

I did a little digging on Google and managed to track down where you can actually get KALAWALLE, but man, the price tag is steep----- I'll let you guys be the judge of that.
http://www.americanlifestyle.com/the...cat=1989&cat=1

Robert Clark2 said:Hey everyone, I’m asking all you folks here—and specifically calling out phyto—to please take a look at this page. Seriously, check out those before and after photos they've posted; they're pretty eye-opening. KALAWALLE .
I honestly have no clue if ordering this stuff is actually worth it—but hey, I already pulled the trigger, so now we wait. I’m sitting here wondering if it’ll even show up or if I just flushed my hard-earned cash down the toilet... again. Seriously, take a look at the photos I attached so you can see what I'm talking about. Fingers crossed. Best to everyone.

If you’re looking for some insight into dealing with psoriasis, check out this page over at Organic Hope—it's worth a look if you're tired of the usual runaround. Dealing with psoriasis isn't just about a skin condition; it’s one of those things that really messes with your whole sense of well-being—your confidence, your comfort, all of it. It can feel like a constant battle against your own body, which, let's be honest, isn't exactly a fun fight to be in. You end up scrolling through endless forums and reading conflicting advice—one person swears by a specific cream, another says stay away from certain foods—and it just gets overwhelming. The thing is, there's no magic wand. I wish there were—I really do—but most of what we see in mainstream medicine feels like a temporary patch rather than a real solution. You get prescribed stuff like Anthralin or maybe some heavy-duty steroids, and while they might knock back the redness for a minute, the underlying issue stays right where it was. It’s a bit of a cycle—treat, flare up, repeat. What I find interesting about the approach here is the focus on a more holistic perspective. It's not just "slap some ointment on it and move on." It’s about understanding how everything connects—what you're eating, your stress levels, and how your internal systems are actually functioning. It's easy to forget that the skin is basically just a mirror for what's happening inside us. If things are a mess on the inside, the outside is going to reflect that—plain and simple. It’s definitely not a quick fix, though. Anyone telling you otherwise is probably trying to sell you something. But if you're willing to dig a little deeper and look at things beyond just the surface level, there might be some actual paths forward. Just take it slow, do your own research, and don't feel like you have to follow any single piece of advice blindly. We're all just trying to figure this stuff out as we go.

Hey Robert Clark2, I see you're out there hunting for a cure—honestly, it’s great to see you haven't lost hope yet. Looking at those photos, the progress looks massive, but you have to wonder if it actually translates to real life... I mean, you really ought to double-check that from a few different angles. Since the manufacturer is the one doing all the heavy lifting with the advertising, it makes you question if the results are truly that dramatic in practice. Anyway, since you went ahead and ordered it for yourself, I really hope it does the trick—but hey, if it doesn't work, we just keep moving forward.🙂

It’s actually pretty great seeing more people joining the conversation here—it feels like we're finally building a real community where we can swap stories and actual results. We aren't just talking about managing the physical symptoms of psoriasis, either; we're helping each other navigate the social side of this whole mess, too. Honestly, if you're looking for a hand, you'll find it here—and by participating, you're probably helping someone else out without even realizing it. We’re making progress every single day, fighting to hold onto our dignity while some scammers try to sell us overpriced snake oil... though, let's be real, those folks usually just wander into these threads while they're lost in their own dark clouds anyway.😉

Maria Chavez55 said:Thanks, rapidpanther41. By the way—when you say "partial effect," are you implying there actually *was* some kind of result specifically tied to using Megamin?

Chris Morgan67, are you still hitting up the Salad clinic for phototherapy?
Personally, I found the phototherapy worked pretty well for me—really decent results—but honestly, I just can't swing the logistics of getting over to the Salad facility during business hours anymore. Life happens, right?

Yeah, regarding Megamin—in this specific instance, the results were basically the same as they were with other ointments (like Psorcutan), except the price tag was ten times higher. So, naturally, she stopped using Megamin. As for other cases, I wouldn't know.👍

Maria Chavez55 said:Has anyone actually tried using Megamin before?

My friend’s mom used Megamin—kind of hit or miss, honestly.
From what I gathered through my buddy's stories, people claim Megamin helps support liver function, which supposedly regulates free radical production—and apparently, those radicals play a role in speeding up skin cell turnover, which is the whole headache behind psoriasis. At least, that's how it sounded when he was explaining it to me. Anyway, Megamin isn't exactly cheap, either. It's a bit of a splurge.

So, yeah, that's the deal with Megamin.

Yeah, I’ve had my own share of bad luck with Zorac ointment too. I haven't messed around with Psorcutan or gone the chemotherapy route, but a buddy of mine tried using a specific Salad—it actually helped for a minute, but then everything just went right back to square one. He usually makes regular trips to Petroleum, but honestly, that's just a temporary fix; he gets way more relief from the ocean and the sun. He’s been dealing with psoriasis way longer than I have, so we’re constantly swapping advice—though what works for him doesn't always work for me, and vice versa. So far, nothing has really stuck for longer than six months before it all falls apart again.👍

goldenstag213 said:Hey everyone!!!
It looks like things have gone totally silent here for days—honestly, it’s kind of a bummer because it feels like there hasn't been any news or any actual progress to report lately.

Just wanted to drop in, say hi to you all, and wish you a really happy upcoming holiday season.👍

We’ve all gotten a little rusty, I guess—maybe everyone is just waiting for someone else to come up with a fresh angle or a new topic regarding psoriasis, or maybe, just like me, people are finding they enjoy lurking and reading the posts more than actually typing them out.☕

Michael Ramos3 said:I really appreciate you all listening and actually giving a damn about what I'm going through.

The thing is, I just can't wrap my head around what your actual issue is here.

And honestly? I'm pretty sure you don't get it either.

Best,

Look, I have absolutely no clue what you're getting at—why are you stressing out so much if they just don't want your "magic potion" help? Just move on and live your life, maybe they'll change their minds down the road.☕

Michael Ramos3 said:I should probably emphasize that this is just my own subjective take—my personal perception of how things are going on this forum—which doesn't necessarily have to reflect the objective reality, much like anyone else's view or my own.

With faith in God

Well, obviously it’s just my subjective opinion—I mean, what else could it be? The actual facts are pretty much reflected in the state of everyone on this forum, and if we're talking cold, hard facts, the results are unfortunately pretty grim. That's exactly why we're still hanging around here, hoping those facts eventually start looking a little better.👍

It’s perfectly normal for interest levels to ebb and flow across all forums—this one included. It really just boils down to how many new faces show up to join the conversation. That’s how awareness about this disease spreads, and honestly, how treatment options evolve too, since there’s always someone popping up with a fresh perspective or a new discovery. Now, let’s be realistic here—we shouldn't sit around expecting that chatting on this forum is going to magically yield a cure for psoriasis in any reasonable timeframe, or if one will even be found at all. The whole point of this place is to lend each other a hand so we can navigate the daily grind of this condition a little easier; in that regard, our personal experiences and individual insights are absolutely irreplaceable. So, let’s not lose heart—let's keep helping each other out without holding anything back. Who knows? Maybe we'll actually pull it off!!!!!👍 👍 👍

George Fisher11 said:I was wondering—can someone living with psoriasis actually donate blood? Just curious if there are any specific rules or things to watch out for regarding that.

35. So, you're wondering what exactly they're looking for when they test a blood donor's blood? It’s a bit of a deep dive, honestly—kind of like when you realize a "quick checkup" at the doctor is actually an hour-long interrogation. When you go in to donate in the States, they aren't just checking your pulse and sending you on your way. They run a whole battery of tests to make sure everything is safe for whoever receives that donation. Usually, the big ones involve screening for infectious diseases—things like HIV, Hepatitis B, and Hepatitis C. They also look for things like Syphilis and sometimes West Nile Virus, depending on where you live or if there's been a recent outbreak. It’s all very clinical and thorough—they want to be absolutely certain that nothing nasty slips through the cracks. It’s a lot of science happening behind those lab doors while you're just sitting there trying to decide if you're going to eat all the free cookies afterward.
After every single blood donation, they run tests on every dose of blood or blood product to check for anything that could be transmitted through the bloodstream—specifically Hepatitis B, Hepatitis C, HIV, and syphilis.

So, who's actually off the hook when it comes to donating blood? It’s one of those things you don't really think about until you're sitting in that big recliner—you know, the one that makes you feel like you're at a very clinical spa—wondering if your recent choices have officially disqualified you from being a hero for the day. Basically, there's a whole list of reasons why the Red Cross might give you a polite "thanks, but no thanks." Usually, it boils down to safety—both yours and the recipient's. If you've got certain chronic illnesses, or if you've been traveling through areas where certain diseases are common, they'll probably pass. And let's not even get started on the medication side of things—certain antibiotics or even some skin treatments can throw a wrench in the works. Then there's the lifestyle stuff. If you've recently had a tattoo or a piercing (unless it was done in a super sterile, regulated clinic), they'll likely tell you to wait a few months. It's all about making sure everything is as clean and safe as possible. Oh, and obviously, if you're feeling under the weather—like, actually sick, not just a little "I stayed up too late watching Netflix" tired—you definitely shouldn't go for it. You want to be giving life, not passing around a nasty flu. It's a bit of a minefield, honestly, but it's better to be safe than sorry. If you're ever unsure, just ask the folks running the drive—they've heard it all before, trust me.
About 10% of donors end up getting turned away during the screening process—some just for the day, others are permanently blacklisted. It’s never personal, really; it always boils down to one of two things: either taking the blood poses a genuine risk to the donor's own health, or using that specific blood product could put the patient at risk. Safety first, I guess.
Look, there’s a basic rule here—you can't just go donating blood if doing so would wreck your own health, or if your blood might end up being a risk to the patient receiving it. It's common sense, really. Safety first, always.
Look, just a heads-up on the blood donation front—you can't exactly roll up to the clinic if you're dealing with anything acute or chronic, or if you're currently mid-antibiotic course (or any other meds, really). It’s also a hard pass if you're running on zero sleep, stuck on some long-term restrictive diet, or if your lifestyle leans a bit too much toward "risky behavior." They've got rules for a reason, I guess.
Look, I get it—you showed up ready to be a hero, rolled up your sleeve, and then got hit with the "sorry, not today" news. It feels a little personal, doesn't it? Like you failed some sort of secret test. But honestly, please don't take it to heart. It’s not about you being "unfit" in a general sense; it’s just a massive, complicated checklist that the medical staff has to run through to keep everything safe. I know you have a million questions burning in your mind, so let's just lay it all out on the table. First off, the whole thing about travel or where you've been—it’s not because we think certain places are "bad," it's strictly about local health trends. If you've recently spent time in an area where certain bugs or viruses are running rampant, the blood center has to play it safe. We aren't trying to judge your vacation choices; we're just making sure nothing hitchhikes in the bag. Then there's the stuff with medications. I know, it seems overkill to skip a donation just because you took something for a headache or a skin issue like psoriasis, but some drugs can interact with the blood or affect how the recipient's body processes it. It’s one of those "better safe than sorry" situations that sounds annoying until you realize the stakes. And yeah, the iron levels and the hemoglobin checks—that’s purely a "don't pass out in the chair" measure. We want you to walk out of here feeling fine, not dizzy and pale, and we definitely don't want to give someone else blood that isn't at its absolute peak quality. So, if you were turned away today, just hang in there. Check the guidelines, wait out the necessary window, and come back when the timing is right. You still want to help, and we still want you to help—we just have to do it by the book.

Permanently rejecting donors:
They’ll permanently turn you away from donating blood if you've ever dealt with—or are currently dealing with—serious chronic issues involving the respiratory or digestive systems. It’s the same deal for anyone struggling with heart disease, vascular issues, cancer, liver problems, HIV, diabetes, or even neurological and mental health conditions. Basically, if your body's been through the ringer with those kinds of stuff, they aren't interested.
2. People exhibiting high-risk behavior are being permanently rejected:
People who are hooked on alcohol or drugs—
Men who have had sexual encounters with other men—you know, homosexual relations—
So, we're talking about men and women who have been with sex workers—just putting it all out there.
People who tend to cycle through sexual partners pretty frequently—you know, the ones labeled as promiscuous—
People who have been using drugs intravenously—well, that’s a whole different ballgame.
People who have gone through treatment for STDs—you know, the whole syphilis or gonorrhea ordeal—
People who are HIV-positive—
- sexual partners of the people mentioned above.

Temporarily turning down a donor:
People who are temporarily barred from donating blood include:
With those milder, acute issues—you know, things like the common cold, digestive hiccups, or when your iron levels take a dip—
- following surgical procedures,
After getting some blood transfusions—and then having to deal with all those vaccines—
...with a slightly milder case of blood pressure issues, too—
Women dealing with everything from their monthly cycles to pregnancy and breastfeeding—you know, all those hormonal rollercoasters.

Look, if you're heading in for a blood donation, you absolutely have to be upfront with the doctor about any medications you're currently taking. It’s not just a suggestion—it’s a must. These drugs can actually travel through the bloodstream, and if they get passed along to the recipient, they could cause some pretty nasty side effects for them. Just be honest during your checkup; it's better to be safe than sorry.
This kind of information just comes out naturally during a conversation with the donor—you know, while they're going through their regular check-up.

Look, I’m just saying—please, for the love of everything, just be honest during every single medical checkup before you donate blood. Seriously. If you have any doubts or weird gut feelings about your health, just speak up and tell the doctor. It isn't about being difficult or making things complicated—it's about protecting your own health and, honestly, everyone else's too. It's common sense, really. Just be straight with them.

Becoming a blood donor is honestly such a privilege—but let’s be real, it comes with a massive side of responsibility toward the patients who are actually counting on you.

Not a single mention of psoriasis anywhere in the text—not even once.

Michael Ramos3 said:It’s a fantastic product—definitely something I'd recommend to all my friends for daily use.
You're better off using that hand cream mentioned above.

Look, I didn't actually recommend Zorac—if anything, I was warning people about Mayu-k and all its nasty side effects and what kind of treatment we're really dealing with here. As for any other products or their side effects? Well, at the end of the day, we can only find out by testing them on our own skin.

Charles Mitchell79 said:I saw someone mentioning Zorac gel on this forum, so I decided to ask you guys something. Can you tell me if I should buy this cream? I noticed it says you shouldn't apply it to the face, and I have acne iuvenilis (which isn't psoriasis) just on my face.

So, here’s the lowdown on ZORAC—it falls into the Tazarotene category.
Tazarotene
Basically, Tazarotene is an esterified retinoid that breaks down in your skin into its active form, tazarotene acid. That’s actually the only known metabolite of tazarotene that carries any real retinoid activity. This acid specifically works by regulating gene expression—basically modulating cell proliferation, skin tissue hyperplasia, and how skin cells differentiate. Now, don't get too technical on me, because the exact mechanism of how tazarotene acid treats psoriasis isn't fully understood yet. What we *do* see is that patients improve as their skin starts looking normal again, which happens alongside a reduction in inflammatory markers like ICAM-1 and HLA-DR, plus it helps with epidermal hyperplasia and those weird abnormalities in skin cell differentiation—you know, things like keratinocyte transglutaminases, involucrin, and keratin.
You’ll usually find Tazarotene in gels or creams used to treat mild to moderate psoriasis that doesn't cover more than 10% of your body. Most people start with a 0.05% concentration and then move up to 0.1% if they need more punch.
A quick heads-up: you definitely shouldn't use Tazarotene products if you're pregnant or breastfeeding because of the potential risk of birth defects (teratogenic effects on the fetus). Also, it’s a no-go for pustular or exfoliative psoriasis, and you shouldn't put it on hairy areas of the skin or in skin folds.
You also have to be careful using Tazarotene on skin that's already damaged or inflamed from psoriasis, since it can cause irritation. And please—keep it away from your eyes. Also, once you've applied a Tazarotene product, your skin becomes extra sensitive, so don't go out into direct sunlight or hit up a tanning bed.
The most common side effects? Itching, a burning sensation, redness, irritation, peeling, contact dermatitis, skin pain, and—believe it or not—sometimes even a temporary worsening of the psoriasis itself.
Registered in the US since 2006: Zorac (Belupo)

Since we aren't always living life on the edge of alternative medicine—let's take a quick second to actually look at what mainstream doctors are telling us!!!!
http://www.pharmacology.com

Just type "psoriasis" into the search bar.

Michael Ramos3 said:I honestly wonder what it takes for people to finally embrace something new—something "alternative"—that might actually help them.

no hidden ads here, just being real 😉
we get you, we're smart enough to know when we're being sold to
thanks, jadesailor14 🙂

Look, this cream definitely isn't going to cure psoriasis—let's be real about that—but it’s great for managing the symptoms. It works best if you apply it right after a shower, especially if you’re dealing with psoriasis on your knuckles and finger joints like I am. It doesn't have a scent, it's colorless, absorbs into the skin incredibly fast, and stays hydrated for quite a while. I'm not out here trying to hawk some product, I just want to share what I've personally tested and found helpful in my own fight against this thing.👍 👍

The absolute last thing I’ve been using—and honestly, it actually works—is this "cien bodicare" Hand & Nail cream Oliva I stumbled upon at Walmart. For a 125 ml tube, you're looking at $2.75. It’s got this mix of beeswax, Vitamin E, and olive oil, plus some Allantoin to soothe things out... oh, and it's PEG-free and dermatologically tested, too. I've basically been slathering it on every single spot where my psoriasis acts up.

Robert Clark2 said:Hey everyone,

- I’ve been dealing with psoriasis for over 37 years now—which, let's be honest, is a lot longer than some people on this forum have even been alive.
- I’ve tried everything mainstream medicine has to throw at me, but honestly? Not much of a significant breakthrough there.
- I’ve also messed around with all sorts of "old-school" home remedies—not going to list the specific makers or anything—but again, nothing really moved the needle.
- I actually have a contact list full of names and phone numbers for over 41 different herbalists whose products I’ve tested out.
- Living by the coast means I spend plenty of time swimming and soaking up the sun, so I probably understand how the elements affect skin a bit better than someone stuck in the Midwest.
- My diet is basically centered around using as much high-quality olive oil as possible (the local stuff).
- I have completely mastered my condition.
- Mentally, I'm doing just fine.
- My outlook is more than positive; if it wasn't, I wouldn't even be typing here—I'd be busy smelling flowers from the roots up.
When you've lived with psoriasis for 37 years, you learn how to read between the lines—and no, that doesn't mean I'm psychic.

Warm regards to you all,

It was clear to me a long time ago from the way you write that you genuinely want the best for everyone suffering from psoriasis. It's obvious you've explored almost every treatment option available to us today, but you also aren't about to let anyone lead you astray or sell you a bridge. You'll always have my support in sharing your perspective on this here, regardless of whether certain people want to hear it or not.👍 👍

Robert Clark2 said:It’s all very sweet of you to pretend you’re here to help us, but from where I'm sitting, that doesn't seem to be the plan at all. Honestly, I’d say your true motives lie elsewhere.
You posted this exact same thing over on the MyCitin psoriasis thread, so if you ask me, you're just out for a profit.☕

Best regards!

Glad to see you're keeping an eye on things and watching how this forum plays out. It seems like plenty of people are emerging from the fog—people who probably should have just stayed lost in it.