Posts by placidorca14

I neglected to mention that people dealing with arthritis are supposedly supposed to cut red meat and dairy out of their diets entirely, as they're claimed to be primary triggers for the condition.

I’m constantly hunting for things that might actually be beneficial to include or, more importantly, things we should probably cut out entirely. I read somewhere that sipping sage tea three times a day for twenty-one days does wonders, provided you don't steep it in boiling water for longer than three minutes. My husband has been on this regimen for two weeks now, so we’ll see how it plays out. He’s already ditched coffee, and while he used to indulge in a couple of beers every now and then, he’s completely stopped; he never really drank much alcohol to begin with, but apparently, even that needs to go. He's also cut out tomatoes and citrus fruits.

Yesterday, I came across a story about a woman in a clinical trial studying the impact of food additives on autoimmune issues. Once she eliminated all processed foods containing artificial additives from her diet, her symptoms cleared up within four weeks. I’m not sure if that specific case is a universal rule, but I find it hard to argue against a diet that avoids chemical fillers; honestly, those synthetic additives seem designed to do nothing but destroy us, whereas real food has such a profound effect on the body. For instance, I dealt with a 1.7-inch gallstone, and by switching to a specific dietary plan and drinking peppermint tea, I managed to shrink it down to about 0.6 inches, which helped me avoid surgery.
We’ve made a pact at home to stop buying or eating anything containing those artificial additives. My daughter and I are going to stay disciplined to support my husband, though there's really no downside for us—if anything, it's purely beneficial. I'll keep you posted on our progress.

My husband went through a nearly identical experience. He didn't show any outward skin symptoms at first; instead, he just dealt with constant, widespread pain. He used to travel to Saratoga Springs for the springs, which offered some relief, though nobody could actually pinpoint what was wrong with him. About two years ago, his wrist joints started swelling to the point where getting out of bed in the morning became a struggle. They kept prescribing him Ibuprofen, yet they never bothered with actual testing or a formal diagnosis. It wasn't until a patch of scaling finally appeared on his scalp that things changed—and even then, the doctors were dismissive. It was only when a physician happened to notice that specific scaling that she immediately identified it as psoriasis. Following her lead, we finally pushed for the right tests, which confirmed he’s dealing with psoriasis, arthritis, and spondylitis. That was our first real answer. Nowadays, he only gets occasional scaling on his scalp, but since his skin otherwise looks clear, the psoriasis is primarily confirmed through blood work. Much like your husband, the disease manifested internally rather than externally. I did some digging, and apparently, that's a known way this presents itself. We'll just have to see how things progress from here.

silentheron25 said:I was back at the clinic again this morning. It’s a relief to finally have some clarity, though I still can't quite wrap my head around the fact that I’ve been dealing with psoriatic arthritis since my twenties.

Yeah, that's a tough diagnosis to swallow. I was actually reading through an arthritis support group thread about disability benefits and early retirement provisions. My husband deals with the exact same thing, so I looked into whether he qualified for any special labor protections, and apparently, he did. He was able to secure those benefits based on his diagnosis from late 2015. I’m not sure if you’re currently working, but if you are, it would be a mistake not to look into your options while you're eligible. You should also check if you qualify for those annual wellness retreats or medical spa stays—some plans allow for about three weeks of coverage every year.

Ethan Perez4 said:Thanks for the reply, but that whole situation sounds incredibly complicated—and waiting nine months is just insane!
I honestly can't afford to sit around waiting that long; I'm losing my mind dealing with this psoriasis. I’ve been struggling with guttate psoriasis for ten months now, and it's driving me crazy. I think I'll just head over there and pay out of pocket for the full treatment and therapy, because waiting nine months is simply not an option for me.

Thanks,

I think that would be an incredible move for you, provided you follow the doctor's orders to a T. My husband had to undergo about eight different treatments every single day. He always says the doctors and the entire staff were absolutely amazing and truly went above and beyond for their patients. He was extremely satisfied with the care. The guy who stayed in the room with him had psoriasis covering his entire body, and my husband swears the skin started clearing up right before his eyes. He received a copy of the bill—which was covered by his insurance—so we saw exactly what the cost was. For three weeks, it came out to roughly $2333. But don't hesitate; the results make every cent worth it.

Ethan Perez4 said:Could anyone tell me if they've been to the ExxonMobil facility in Indianapolis and if it actually worked? Also, what’s the protocol for getting admitted there for treatment?

Thanks in advance for the help

My husband went to the Petroleum facility. It was excellent for him. He deals with psoriasis, though it isn't severe, but his arthritis is the much larger issue. He saw people there with psoriasis covering their entire bodies who claimed their skin cleared up right before their eyes. There were some guys who refused to follow the prescribed therapies, and obviously, nothing helped them. They insisted from the start that it wouldn't work, skipped the treatments, and predictably, saw no results. Those who stuck strictly to the medical instructions were satisfied. You have to stay for at least three weeks to see anything.
His coverage came through insurance. First, a rheumatologist made the recommendation, followed by a physical therapist and a dermatologist. Based on all that, his primary care doctor submitted a referral to the board. Initially, the board denied him, but after a heated argument and threatening legal action, they finally approved it. He sent everything to Petroleum and waited nine months on the list. However, if you pay $33 per day, you can get in within one or two months. If your board referral expires after six months, you have to go back through the whole process—which is exactly what happened to us because we didn't know the rules. You end up back at the board, and it's the same cycle: they deny you, you fight them, and then those jerks finally give in. That's easily the worst part of the whole ordeal. Apparently, if you only have psoriasis, you aren't eligible, but you should double-check that, since he only got approved based on his arthritis.
My husband thinks that if they actually realized how much Petroleum helps people, they would approve everyone without hesitation. They also have this incredible cream they manufacture there.
That's basically it. Ask if you need more details.

Nicole Lee78 said:Alright everyone...
I've been dealing with psoriasis for about 15 years (I'm 22 now). It started off incredibly slow and wasn't much of an issue, but over the last three years, things have escalated, and now it's flared up on my arms and legs. My scalp used to be the worst part, but Dr. Temt Black Shampoo actually helped quite a bit there. It isn't a permanent fix since the issues tend to crawl back once I stop using it, and it does make my hair pretty greasy, but considering my scalp was completely covered and looking terrible before, I’d say it’s actually decent.

Now I REALLY NEED YOUR HELP. I'm heading to the coast in three weeks, and this time it is incredibly important to me that I can finally walk down a beach in a sundress without feeling self-conscious. I'm not looking for a lifelong cure; I just need something to calm it down for three weeks—even if it only stays quiet for fourteen days. Right now, I have Zorac gel and Psorcutan cream at home, but I know I shouldn't use them simultaneously, and I don't have the luxury of testing one then the other. Could you please share your experiences with these creams? Which one works faster or more effectively, even if it's just short-term?

THANK YOU SO MUCH IN ADVANCE!!!!!!!!

I might be able to help. My husband deals with psoriasis, specifically on his scalp. He has tried Zorac, Besalix, and basically everything available here, but unfortunately, nothing really worked. We recently picked up a cream from Italy, and I have to say, it is incredible. I applied just one drop to him the first night; by the second day, the scales had lifted so much that I could comb them right out with a fine-tooth comb and reapply. By the third day, I could barely see any scaling left on his scalp, so I reapplied to those spots. I stopped after that, and a week later, the scaling was completely gone. His skin looks totally clear.

The product is called "Flubason 0.25% emulsione cutanea." It comes in small 2g sachets. You get a pack of 15 for about five dollars. It's manufactured by Pfizer in Milan. The only catch is that you can really only find it in Italy. See if you can track some down and give it a shot. It worked for him, and I honestly couldn't believe my eyes.