121 posts shown.
ambertiger10 said:Please, just tell me what kind of medicine this is? Does it actually work? And what about the side effects?
Sophia Martinez3 said:Hey there! How has Neotigason been working for you? Personally, I’ve had some amazing results with it...
Grace Hughes42 said:That’s exactly what scares me—how everything seems to be connected lately, unfortunately.
Tell me, do you know if liver enzyme levels have anything to do with psoriasis? My son's GGT levels came back lower than normal.
Grace Hughes42 said:the spot looks white in the middle now with a red ring around it,
is there a link between high triglycerides and psoriasis?
Sandra Gomez56 said:Has anyone ever heard of those KALAWALLA capsules for psoriasis and vitiligo? What’s the deal with them? Where can I actually get my hands on some?
Sandra Gomez56 said:Thanks a million, best wishes!
Michael Ramos3 said:🙂🙂👋
Robin Robinson8 said:I'm not sure if anyone here has dealt with erythrodermia or even knows what it feels like, :
rapidpanther41 said:I did a little digging on Google and finally tracked down where you can grab some Kalawall, but man, that price tag is brutal—take a look for yourself!
http://www.americanlifestyle.com/the...cat=1989&cat=1
rapidpanther41 said:if not, we just keep moving forward.🙂
Michael Ramos3 said:Hey there.
Look, I've checked with some top-tier experts and scoured the web—none of those addresses or phone numbers actually exist in the US.
Just remember: online shopping is basically a playground for scammers.
Olivia Ramos66 said:From what I can tell, Kalawallai is basically just a plant extract. Polypodium leucotomos. Clinical studies have actually shown this stuff works for treating vitiligo, senile dementia, psoriasis, and atopic dermatitis. It acts like a shield against UV damage, stops angiogenesis in its tracks, and provides immunomodulatory effects—basically helping to dial down the immune system a bit.
It's taken orally. It seems pretty safe, but since this plant is still relatively new to the world of herbal medicine, we don't fully know the long-term effects of taking it constantly or what the exact "safe" dose really looks like. Your best bet? Stick to the specific dosages used in clinical studies.
Check this out: http://www.ncbi.nlm.nih.gov/pubmed/6...RVAbstractPlus
There are more studies out there, but unfortunately, I can't even get my hands on the abstracts.
Carol Johnson3 said:A friend of mine deals with psoriasis, and a few years back, her dermatologist suggested she try tanning beds. Honestly? It worked wonders. She’s feeling so much better now. Good luck to everyone out there!😉
EkatarinaVelika;11508945 said:Hey everyone 🙂
For quite a while now—maybe 5 to 8 years—I've had these tiny little dots on my nails. It looks like someone poked them with needles. I’m wondering if this could be linked to psoriasis.
Aside from that, I don't see any other changes on my nails, the skin around them, or my cuticles.
The nail situation is really starting to worry me. Even though things haven't changed much over the years, those little spots seem to be spreading and covering more area.
🥳
It definitely can be related to psoriasis. There's actually a specific type calledPsoriasis unguium that shows up pretty often. With that, the nail ends up looking kind of like a thimble.
You might also see stuff like brittleness, roughness, ridges, or even yellowish spots under the nail.
That's basically what I know, though maybe some other folks here can give you a more detailed breakdown.
Either way, it's probably best to go see a dermatologist. They can give you a real diagnosis and figure out the right treatment plan for you.
Take care!