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Psoriasis [PLEASE READ FIRST POST!]

Started by mistybear4 · · 👁 44 views · 2.3K replies

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Chris Morgan67 Chris Morgan67 Member
49 messages
joined Jul 2007
#1921 ·
goldenstag213 said:Chris Morgan67...
Please, let me know the exact name and manufacturer of that cream you're using. I'm heading to Germany on business this weekend and was thinking of picking up a larger supply while I'm there...
Also, please let me know how to use it properly and if there are any side effects...
Thank you so much...

Just transcribing what's on the box...

Psorcutan ointment...

Intendis...
Intendis


They offer both 30 mg and 90 mg packaging...
The 90mg option is much better value; the larger size costs less than buying three of the 30mg tubes...

I've also heard they offer a Psorcutan scalp lotion, which might be worth picking up...😉

If there’s anything else you need to know, just let me know...

Generally, you just apply a very thin layer once a day. Don't expect to see any real progress right away; it usually takes a few weeks to notice a difference...

Side effects...
Clinical studies have demonstrated that Calcipotriol maintains an excellent safety profile... Instances of hypercalcemia remain quite rare...
Calcipotriol is a vitamin D analog used to manage psoriasis... It works by slowing down the overproduction of skin cells...

There are still several pages left, so feel free to look through them yourself...😉

There are fewer side effects compared to Belosalica, and since Psorcutan is generally considered safe, even small children can use it outdoors...
jadeheron12 jadeheron12 Newcomer
3 messages
joined Mar 2008
#1922 ·
Chris Morgan67 said:See? I really should have gone to pharmacy school.😍🤣

It's never too late to start a second degree.😛

Thanks for the helpful info.👍
Chris Morgan67 Chris Morgan67 Member
49 messages
joined Jul 2007
#1923 ·
jadeheron12 said:It’s never too late to start a second degree... 😛

Thanks for the helpful info...👍

Haha, that would end up being my third degree then...😍

Don't mention it, my fellow psoriasis warrior...😉😍
We're here to help one another...
Kate Williams41 Kate Williams41 Member
47 messages
joined Mar 2008
#1924 ·
Robin Robinson8 said:Welcome aboard!!! 🙂
Besides dealing with the panic attacks,😁 can you tell us how things are looking right now and what your current routine is?
The stares used to get to me too, but I'm over it now. First, because it isn't contagious—so there's nothing to be ashamed of or afraid of, and I'm nobody's threat. Second, I just figure there are plenty of much worse conditions out there that look way worse than this, so it doesn't bother me as much. Plus, when someone asks what's going on, I just tell them straight up without any drama. Most people around me already know what's up, so they usually just ask if I'm feeling better. 😁
I have zero issues wearing long or short sleeves. Long sleeves are easy since there are so many lightweight, breathable fabrics you barely feel. Short sleeves? Honestly, I just don't care who looks anymore. Thank Bog that they don't have to deal with this themselves.
If you're worried about swimming or being watched at the beach, you've still got options. There are so many beautiful little coves along the coast near the main beaches, so you can always find your own spot.
I'm really hoping—and I truly believe—that this will be my first summer without psoriasis since I've had it, if things keep going this way. I am genuinely excited. 🙂

I'm rooting for you to recover quickly, too. Cheers! 😍


Thanks for the warm welcome. 🙂
Lately... honestly, I haven't been using anything specific. Just the usual stuff: baby shampoo, Plivit D3 because my skin is fair so I have to stay out of the sun... salicylic acid cream and Diprosalic lotion... though I rarely use the latter since it's a corticosteroid!
BUT the only thing that actually worked was BETACORTONE cream!!!!!! My sister brought some over from Switzerland. I went to see a doctor there and he gave me five tubes, but I can't get them anymore because I don't have health insurance there... and you can't buy them without a prescription!!!! It made me want to give up on everything.
Right now, I'm hitting the tanning salon, and for the summer, I'm planning on garra Ruff !!!!!! Because I'm totally done with doctors and testing out endless medications... 👎
Kate Williams41 Kate Williams41 Member
47 messages
joined Mar 2008
#1925 ·
Robin Robinson8 said:Welcome to the group!!! 🙂
Aside from dealing with those panic attacks,😁 could you tell us how things are looking for you right now and what kind of treatment you're on?
I used to get self-conscious about people staring at my psoriasis too, but I don't let it get to me anymore. First off, it isn't contagious, so there's zero reason to feel ashamed or scared—I'm not a threat to anyone. Second, honestly, there are plenty of much worse conditions out there that look way tougher than this, which puts things in perspective. Plus, when someone asks what's going on, I just tell them straight up without any hesitation. Most of the people I hang out with already know what's up, so they usually just ask if I'm feeling better. 😁
As far as clothes go, I don't care if I wear long or short sleeves. Long sleeves are easy because there are so many lightweight, breathable fabrics that you barely notice them. And short sleeves? Honestly, I've reached a point where I just don't care who looks. Thank God most people don't have to deal with this, so they don't have to stare at it either.
If you're worried about swimming or being seen on the beach, remember you've got options. You can always find those gorgeous little secluded spots along the coast that aren't too far from the main beaches, so you still get everything you need.
I'm really hoping and believing that if things keep going this way, this will be my first summer without psoriasis since I've had it. I am genuinely looking forward to it. 🙂

I'm rooting for you to get better as soon as possible. Take care! 😍


See... Robin Robinson8... people didn't pay nearly enough attention to me... because I was just too good at hiding it... I'd get short bangs, wash my hair constantly... nothing stood out at all...!! For my arms,🙏 I'd use foundation because my doctor said it was fine... nobody noticed... and my legs... I wore mini skirts without a second thought back when I could... everything was great (even though I've been dealing with this for 5 years)!!!!!! 😁...until last year... my arms, my legs... it's just everywhere now... I don't even bother with Diprosalic, Elocom, Excipial, Zorac... I won't even list the rest... nothing works... 🤷
Mark Fox44 Mark Fox44 Member
17 messages
joined Jan 2008
#1926 ·
wearycrane11 said:Hey everyone, I have a quick question for you all. So, I’ve been dealing with some issues regarding my nails lately. It isn't that typical "tiny little pits" thing people talk about; instead, what I'm seeing is this dark spot appearing in the nail bed underneath. The thing is, it just keeps spreading and spreading until it hits a certain point and then finally stops. The skin in that specific area looks darker, and eventually, it starts to feel hard or calcified. Honestly, it's pretty unsightly! Does anyone know if there’s a specific vitamin or perhaps a cream that can help regulate this? Any advice would be much appreciated!🤷But really, does that even factor into the psoriasis struggle at all?

Hey everyone! I wanted to jump in and share something that’s helped me out. I’ve dealt with nail psoriasis on both my hands and feet a few times now, and honestly, it’s such a headache. It is incredibly difficult—if not totally impossible—to actually get any topical creams under the nail bed where the trouble is happening. Because of that, I found that treating it "from the inside out" was the only way to go. In my experience, every single time it flared up, I managed to clear it up by being really aggressive with my supplements for about a month. I was taking three capsules of Omega-3 daily along with one or two evening primrose oil capsules a day. Now, don't get me wrong—these are great supplements to have in your routine regardless, but for my specific situation, I found I needed those higher doses to see a real difference. Just something to consider if you're struggling with the same thing!
I was recently out in Bihać and picked up some Psorex ointment. Since I’ve bought this stuff a few times before—and honestly, it worked wonders on my scalp, keeping me completely clear for months after just two weeks of use—I had high hopes. This time around, I was actually pleasantly surprised by the new packaging and the updated ingredient list!👍!
So, Ms. Kajtezović really stepped up to the plate here. She took things quite seriously, conducting thorough research at the medical faculty institute in Sarajevo, securing the intellectual property, and getting the product officially registered. It reminds me of how Pero Antičević, that herbalist from Knin, handled things back in the day—he set up his own business and made sure his psoriasis ointment was fully protected and registered too.
I’m sharing this because, frankly, I’ve been burned before. I’ve fallen for those various "natural remedy" gurus more than a few times, shelling out quite a bit of money for products that didn't do a thing—or worse, actually made my condition flare up.😠I see that Michael Ramos3 is back at it.😕 He’s back at it again, popping up to point new forum members toward those specific pages where he used to run his ads. Honestly, it’s a bit much. I’ve watched this play out, and the result for every single person on this board hasn't been a "cure"—it’s just been pure disappointment.👎So, I’m going to ask that individual to please act like those other serious forum members and actually register the product properly. It would be much better than just using this space for self-promotion without any actual substance behind it. 🤷It’s honestly a bit frustrating to see people citing various institutes without providing a shred of actual evidence, or constantly preaching about these miraculous "cures" when there isn't a single piece of medical documentation to back them up. To make matters even more ridiculous, his username doesn't even reflect reality—the guy has never actually dealt with psoriasis in his life, let alone found some magical way to cure it.😂!
So, I was looking over the ingredient list for Psorex (based on what’s written on the label), and I wanted to get some thoughts from the group. Here is what we're looking at: yellow petrolatum, lanolin, salicylic acid, Peruvian balsam, beeswax, St. John's Wort oil, and olive oil. I'd love to hear your take on this formula! What do you all think about this specific combination?
Here’s the breakdown for the Antičevićev mast formula: it consists of 86% suet, 7% white beeswax, 3% English ivy, 2% common oat, and 2% black pine! As for those Latin terms you asked about, here is what they actually mean in plain English, along with a little thought on the mix: * **Adeps suillus (Suet):** This is essentially rendered animal fat. At 86%, it serves as the heavy-duty base of the ointment, providing that rich, occlusive barrier to lock in moisture. * **Cera alba (White Beeswax):** A classic stabilizer. It helps give the balm its structure and consistency so it doesn't just melt away immediately. * **Hedera helix (English Ivy):** Usually included for its soothing properties; it's often used to help calm irritated skin. * **Avena sativa (Common Oat):** A total superstar for skin relief. Oats are wonderful for soothing itchiness and calming down redness. * **Pinus nigra (Black Pine):** Often added for its antiseptic qualities and that distinct, refreshing scent. If you ask me, it looks like a very traditional, "old-school" approach—very much focused on creating a thick, protective layer to let the skin heal underneath. It’s quite a substantial formula!
I’d like to ask the moderator not to view this as an advertisement. These products are fully registered and available to anyone who needs them, and I personally have absolutely no financial incentive to promote them here. I only brought them up as prime examples of how herbalists can legalize their sales—you know, a legitimate way to operate, unlike those shady characters out there looking to make a quick buck under the table!
goldenstag213 goldenstag213 Member
32 messages
joined Jan 2007
#1927 ·
Mark Fox44 said:Greetings, everyone. I’ve been dealing with bouts of nail psoriasis on both my hands and feet quite a few times now. Since it is incredibly difficult—if not entirely impossible—to actually apply topical treatments directly under the nail bed, I have found that treating the issue from the inside out is the only practical way to go. In my experience, every single time this flared up, it cleared up after I committed to a month-long regimen of high-dose Omega-3 (three capsules a day) combined with evening primrose oil (one to two daily). While I certainly believe these supplements are worth incorporating into your regular routine, I wouldn't suggest taking them in such heavy doses unless you really need to get things back under control.
I recently found myself in Bihać and picked up some Psorex ointment. I’ve actually bought this stuff a few times before, mainly because it delivers results that are honestly well above average for my scalp—I can usually stay completely clear for several months just by using it for two weeks. This time around, however, I was pleasantly surprised to find they’ve updated the packaging and tweaked the ingredient specifications.👍!
Well, Ms. Kajtezović really stepped up to the plate here. She played it smart, conducting thorough research at the medical school institute in Sarajevo, securing her intellectual property, and officially registering the product. It reminds me quite a bit of what that herbalist Pero Antičević did back in Knin; he set up his own business and made sure his psoriasis ointment was properly protected and registered.
I’m only bringing this up because I’ve been burned before. I’ve fallen for plenty of those "natural remedy" gurus and herbalist types, wasting a small fortune on products that didn't do a damn thing—and in some cases, they actually made my condition significantly worse.😠I see that Michael Ramos3 is back at it.😕 He’s back at it again, once more trying to lecture the newcomers on this forum by pointing them toward those specific pages where he used to run his ads. It’s honestly exhausting to watch. If there's one thing I've noticed, it's that none of us actually found any kind of "cure" through his methods; instead, all we ever got was a massive dose of disappointment.👎So, I’m asking him to please act like these other serious forum members and actually register his product properly. It’s one thing to share what you're using, but it's quite another to just engage in blatant self-promotion without any actual credentials or official backing to support it. 🤷It’s honestly exhausting watching people cite studies from major institutes without providing a shred of actual evidence, or worse, preaching about miraculous "recoveries" while refusing to show any medical documentation to back them up. It feels incredibly disingenuous. To make matters even more ridiculous, his username doesn't even align with his reality—he’s never actually dealt with psoriasis in his life, let alone managed to "cure" it.😂!
Looking at the ingredients listed on the Psorex packaging—which includes yellow petrolatum, lanolin, salicylic acid, balsam of Peru, beeswax, St. John's Wort oil, and olive oil—I find myself wondering what everyone else thinks. I’d really appreciate some insight or commentary on this specific formulation.
Here is the breakdown of the ingredients in Antičevićev mast: it contains 86% suet (adeps suillus), 7% white beeswax (cera alba), 3% English ivy (hedera helix), 2% common oat (avena sativa), and 2% black pine (pinus nigra). Since you asked, here is the translation from Latin along with my own take on the formula: * **Adeps suillus (86%)**: Suet / Pork fat * **Cera alba (7%)**: White beeswax * **Hedera helix (3%)**: English ivy * **Avena sativa (2%)**: Common oat * **Pinus nigra (2%)**: Black pine As for my thoughts on this—it’s a pretty old-school, heavy-duty composition. With that massive 86% base of suet, this isn't some lightweight, watery lotion you'd pick up at a drugstore; it's an incredibly dense, occlusive ointment. It's clearly designed to sit on the skin and create a serious barrier, which makes sense if you're dealing with something particularly stubborn or dry. The inclusion of English ivy and black pine suggests a focus on soothing irritation or providing a bit of antiseptic support, while the oats are there to help calm things down. It’s a very traditional, "no-frills" approach to topical care, leaning heavily on lipid replenishment. It feels like something that would have been used for generations before we all became obsessed with high-tech synthetic polymers.
I’d like to ask the moderator not to view this as an advertisement. These products are fully registered and available to anyone who needs them, and frankly, I have absolutely zero financial incentive to be promoting them here. I only brought them up as prime examples of how herbalists can actually legalize their operations and sell their goods properly, rather than acting like those shady characters operating in the shadows!

Hey there, Mark Fox44,
I've been hearing some chatter about this herbalist, Antičević—apparently, he’s got this specific tea for psoriasis and some kind of green honey that people swear by.
So, tell me something—if my memory serves me right, you mentioned in some of your earlier posts that you had tried his products, but didn't see much of a significant breakthrough. I’d really appreciate it if you could go into a bit more detail about exactly what you were using and whether you noticed even the slightest hint of a change.
I should probably expand a bit on my experience using that Psorex stuff. From what I can gather by looking closely at the ingredient lists for both ointments, they seem to be entirely free of any nasty, harmful additives. So, even if they don't end up being the ultimate cure, at least I won't be making matters worse by applying something toxic to my skin.
Thanks in advance for getting back to me!!
Robin Robinson8 Robin Robinson8 Newcomer
7 messages
joined Jul 2008
#1928 ·
Kate Williams41 said:See, Robin Robinson8... people didn't pay much attention to me before... mostly because I was pretty good at hiding it... I’d just do short haircuts, wash my hair regularly... nothing really stood out...!! For my hands, 🙏I used powder since my doctor said it was fine... nobody noticed anything... legs... I wore mini skirts without any issues back when I could... everything was great (even though I've had this for 5 years)!!!!!! 😁...until last year... my hands, my legs... everything flared up big time... now I don't even bother with Diprosalic, Elocom, Excipial, Zorac... not to name them all... nothing works anymore... 🤷

If I were you, I'd honestly suggest stepping away from the corticosteroids—they haven't helped anyone in the long run; they just provide temporary relief. Plenty of people on this forum can vouch for that. Try switching to neutral products first, and if that doesn't work, definitely check in with your doctor. I know how frustrating it is—waiting around and feeling like the doctors are treating you like some sort of lab rat (I've been there myself)—but they prescribe what seems most effective for the majority, even if it helps or hurts everyone differently. Personally, I think they finally nailed my therapy after six years. And maybe it's just me, but through those six years, I've gained enough mental maturity regarding this condition that I don't let stress or certain people get to me as easily as I used to.
Hang in there, best 😍
Kate Williams41 Kate Williams41 Member
47 messages
joined Mar 2008
#1929 ·
Robin Robinson8 said:I would honestly just advise you to move away from corticosteroids. They don't really help anyone in the long run; they just offer temporary relief. Plenty of people on this forum can testify to that. Start using more neutral options, and if that doesn't work, talk to your doctor. I know how hard it is to wait and deal with doctors treating you like a lab rat—I've been there myself. But they prescribe what works for most people, even if it's an individual process of trial and error. It took six years before they finally found the right therapy for me. By then, I’d also gained some mental maturity regarding this illness, so I don't let stress or certain people get to me as easily as I used to.
Hang in there, best 😍

Thanks for the support... especially since I'm new to this forum!
Can you tell me what kind of therapy you're on now? Like, if it actually worked for you... P.S. I'm not sure if you've already posted about it, so sorry if this is a question for half if you have...

Best, 😍
Kate Williams41 Kate Williams41 Member
47 messages
joined Mar 2008
#1930 ·
Robin Robinson8 said:If I were you, I’d just suggest moving away from corticosteroids. They haven't helped anyone in the long run; they only offer temporary relief. So many people on this forum can back that up. Try switching to more neutral options first, and if that doesn't work, definitely talk to your doctor. I know how frustrating it is to wait around while doctors treat you like a lab rat—I've been exactly where you are. But they prescribe what works for most people, even if everyone responds to treatment differently. It took me six years to finally find the right therapy. By then, I’d gained enough mental maturity regarding this illness that I don't let stress or certain people get under my skin like they used to.
Hang in there. Best wishes! 😍

Thanks for all the support... especially since I'm still the new kid on the block here!😁
So, can you tell me what kind of therapy you're on right now? Only if it actually worked for you, of course.
P.S. Sorry in advance if you've already covered this topic!😕

Hey there!😍
Robin Robinson8 Robin Robinson8 Newcomer
7 messages
joined Jul 2008
#1931 ·
Kate Williams41 said:Thanks so much for the support... especially since I'm still pretty new here! 😁
Could you let me know what kind of treatment you're on right now? If it's actually worked for you, that is...
P.S. Sorry if I'm repeating something you've already shared... 😕

Best, 😍

I have mentioned it quite a bit, but honestly, there's no harm in repeating myself. Right now, I'm just using Vaseline and taking Sandimmun Neoral—you can find more info on that Medicine in the previous pages. My psoriasis has cleared up almost entirely 👏, going from covering 90% of my body down to about 15%. There is still some left, but it’s very minimal and doesn't really flake anymore—it's just red. It's been such a struggle, but I'm really hoping they hit the mark with this one. If it turns out they haven't, my last resort would be biologics. I'm praying to God that this stays effective 🙂
Best regards!! 😍
Michael Ramos3 Michael Ramos3 Active Member
196 messages
joined Apr 2007
#1932 ·
Hey there, "sunce cacino".
Thanks for worrying so much about me and my situation. That’s real nice of you. I’ll take your advice into consideration.
I think you missed the mark on one specific point regarding success and disappointment, though.
I don't know what your angle is here (since mine is already pretty obvious), but you're ignoring the facts.

You’ve got plenty of "regards" coming from Dragon1000, lide 74, and a bunch of other people on this forum who aren't even bothering to chime in anymore—probably because they have no reason to (thank God).

The only disappointed members here are silentheron25 and you, since you both used the stuff wrong despite the instructions and now you're complaining. Correct me if I'm wrong.

I get it.

Regards again, and thanks.
silentheron25 silentheron25 Newcomer
5 messages
joined May 2007
#1933 ·
Regarding Psorex, I’ve used both the cream and the ointment from Antičević, so I have a few thoughts. To get the best results with Psorex, you really should pair it with honey to help detoxify—basically eating it while applying the cream. When I first tried this combo, it worked wonders; almost everything cleared up. Since I tan easily, once my skin darkened a bit from some sun exposure, the patches blended right in with my normal skin tone. Years ago, Antičević recommended tea and cream to me, but nothing actually worked until I started using Psorex; it acted incredibly fast. Just a heads-up: apply it lightly because it’s potent. That was the advice I got from the lady at the shop. Its main advantage is that it’s herbal and natural, unlike the industrial chemicals I’m currently using. Honestly, I’m not sure if I’d switch back to Psorex or just quit this current stuff entirely and see how my skin reacts. I think it's vital to drink a cleansing tea or use honey to clear out whatever is happening inside your system, because that's where the root of the skin issues usually lies.
silentheron25 silentheron25 Newcomer
5 messages
joined May 2007
#1934 ·
Look, stop hating. You posted some garbage that didn't actually work. Maybe it works for someone else, but it didn't work for me, and that’s just a fact. I wasn't even talking about that. It didn't help, period; we move on. You're constantly jumping into arguments with everyone and becoming a real nuisance. I'll tell jadesailor14 to ban you. I followed the instructions myself and ended up in more pain than before because of your advice—and honestly, who cares about what happened to that old neighborhood anymore? It's all gone anyway. If you're so adamant that your method provides permanent results, then show me some photos. Show me people who had this issue before and how they look now. Give me names. The reality is you don't have any solid arguments. It always comes back to "it helped..."—helped who? I don't care. I'm reporting you to jadesailor14 now. 😂
Michael Ramos3 Michael Ramos3 Active Member
196 messages
joined Apr 2007
#1935 ·
The only thing about your level of culture that needs banning on this forum is you.

I don't bother jumping into a discussion until someone actually calls me out.
Chris Morgan67 Chris Morgan67 Member
49 messages
joined Jul 2007
#1936 ·
Michael Ramos3 said:The only thing on this forum that needs banning is your level of sophistication...

I typically only join a conversation when someone addresses me directly...

Oh, so we’re just supposed to take your word for it that Dragon1000 and Lida are better?🤣

Please, what about Octo? That guy probably ended up in the ER because he used your medicine...

No, let everyone see exactly who you are and what you're planning. Thank God everything on this forum is recorded...

With faith in God, my regards to you...😂😂
jadesailor14 jadesailor14 Regular
314 messages
joined May 2006
#1937 ·
Michael Ramos3,

1. So far, nobody on this thread has actually come forward to say your ointment helped them.
2. Lately, you've been mentioning that you have all the official paperwork for the remedy and that it’s available in pharmacies. I've suggested a few times that you should just upload those documents online and list where people can officially buy it, but you haven't done it yet.

You've been overhyping yourself on the forum way too much—please, let's dial it back!
Until you follow through on point number 2, everything you say about this ointment is just talk; until then, it's just some cream you whipped up in your kitchen.
Plus, hearing a real testimonial from someone would be a huge help!
goldenstag213 goldenstag213 Member
32 messages
joined Jan 2007
#1938 ·
silentheron25 said:Look, let's not get ahead of ourselves here; you suggested some nonsense that didn't help anyone. Maybe it works for someone else, but it certainly didn't work for me, and that is simply an objective fact. I wasn't even planning on bringing this up, but we move on regardless. You seem to constantly engage in these endless arguments with everyone, and frankly, you're becoming quite exhausting. I might just suggest to jadesailor14 that she bans you. Personally, I followed the instructions to the letter, and honestly, all that talk about how certain things aren't what they used to be is useless; it’s all gone to waste anyway. If you are so adamant that your method provides permanent results, then show me some proof—show me photos of people who had it before and after, or give me actual names, because the truth is, you lack any solid arguments. It always comes back to "it helped..."—helped whom? To be perfectly honest, I couldn't care less. I'm going to report you to jadesailor14 now. 😂

Listen!
Up to this point, I have never once attacked Michael Ramos3, nor do I intend to, though I find it quite peculiar that those claiming to be "CURED" have all quietly vanished from the forum.
To finally settle the mystery surrounding Michael Ramos3 and his ointment once and for all, I am prepared to make the following proposal:
Currently, my psoriasis has flared up significantly, covering large areas of my legs and arms.
Therefore, Mr. Michael Ramos3, I am asking you to send me your preparations (I will provide my address via private message), free of charge. In exchange, I will follow your instructions strictly and, if necessary, take daily photos of the progress to post here on the forum.
If this actually works and clears my psoriasis as you claim it will, I won't just send you fifty bucks to cover the cost of the therapy; I will send you a full $1,000, not to mention the massive influx of new customers you would gain if my photos prove your claims are true.
I believe I have put forward a very fair offer, and I suspect most of my fellow sufferers would agree with my terms.
Best regards to everyone, and hang in there; spring is coming, and we all know how much that can trigger a flare-up.👍
Michael Ramos3 Michael Ramos3 Active Member
196 messages
joined Apr 2007
#1939 ·
jadesailor14 said:Michael Ramos3,

1. Nobody here has actually come forward saying your ointment worked for them.
2. Lately, you've been claiming you have the paperwork to sell this stuff in pharmacies. I've told you a few times to just upload those documents online and list where it’s officially sold, but you haven't.

You've overhyped yourself on this forum too much. Please stop.
Until you address point number 2, all this talk about the medicine is just words. Until then, it's just some cream you squeezed out of your savings account.
And honestly, some actual testimonials wouldn't hurt either.


Can someone explain how and where I should put my paperwork online? Like, do I scan it, where do I upload it, and what's the process?

THANKS !!!!!!!!!
Kate Williams41 Kate Williams41 Member
47 messages
joined Mar 2008
#1940 ·
Robin Robinson8 said:I’ve written quite a bit about this already, but I don't mind repeating myself. Right now, my routine is pretty simple: just Vaseline and Sandimmun Neoral (you can find more info on that medicine on the earlier pages). It’s actually working. My psoriasis has cleared up almost entirely—it went from covering 90% of my body down to just 15%. There's still some left, but it's minimal. It isn't even flaking anymore; it's just red. Honestly, I've dealt with so many issues, so I'm really hoping they finally hit the mark with this one. If it turns out this isn't the answer, my last shot will be biologics. I'm praying to God it stays exactly like this. 🙂
Hey there!! 😍

THANKS !!!!!!!!!🙂
Fingers crossed... hope it stays that way.👍God willing, things only get even better from here!🙂
Hey there!🙂

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