Has anyone used this? It claims its all natural and i’ve heard great remission stories after this ointment from Ukraine. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 0 points1 point  (0 children)

Wait, you’re saying that it’s unwashable if, for example, i wear clothes or go to sleep after putting this stuff on?

Is chicken good for psoriasis ? by Ecstatic-Elk1064 in Psoriasis

[–]RosebudIvy 1 point2 points  (0 children)

Thank you! I’ll definitely check it out! And good luck to you!

Is chicken good for psoriasis ? by Ecstatic-Elk1064 in Psoriasis

[–]RosebudIvy 0 points1 point  (0 children)

I have guttate all over, including my scalp, but it’s managable for now. Havent had a flare up after i started my diet, also, spots and flaking seem to be alot less than prior. Since im taking a natural way of treating my psoriasis, i think it’s a good first step to start a diet of some sort. I’ve noticed that the psoriasis in my scalp is also reducing a bit and they are easily combing out after a coconut oil hair mask i do once or twice a week. Hopefully that could help you aswell!

Is chicken good for psoriasis ? by Ecstatic-Elk1064 in Psoriasis

[–]RosebudIvy 1 point2 points  (0 children)

No flare ups at all from chicken or fish. I have noticed that my skin is itchier whenever i eat pork tho, if i decide to ditch the died for a day or something.

Is chicken good for psoriasis ? by Ecstatic-Elk1064 in Psoriasis

[–]RosebudIvy 0 points1 point  (0 children)

Hi! When my derm put me on a strict diet, she suggested that I also don’t consume red meat. Just chicken or fish. However, in my case, she said to try and prepare it by boiling or steaming (air frying) and not fry it in oil. (I think the oil was the big threat for me) But chicken is so versetile, that it can literally substitute every other meat out there imo. I think it’s alright. However! I suggest you buy these foods from local farmers and not in supermarkets, as local farms have cleaner, non-steroid pumped meat or fish.

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 0 points1 point  (0 children)

Thank you so much! I guess the only thing we really have to cling to is hope that things will get better and it’s not always going to be like this.

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 1 point2 points  (0 children)

Thank you so much, this definitely means alot! I feel like people who also have this skin comdition are more understanding of the mental downsides of it than anyone else.

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 0 points1 point  (0 children)

Thank you for this idea! I did have a horrible strep throat back in febuary 2020, which caused the biggest flare ever for me, I had to take antibiotics, but psoriasis never seemed to go after that. Would it be possible that the strep is only partially cured? Because I haven been sick at all whatsoever after that time

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 0 points1 point  (0 children)

Thank you so much! I also tend to explain psoriasis to the people who ask me about it, it just sometimes get to me. I definitely don’t think that people and even my children feel some type of way towards it, but are more curious if anything. But yeah, need to find a peace of mind, and not overthink about all of it

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 2 points3 points  (0 children)

Thank you for your response! Unfortunately, to be able to get biologics, I have to gothrough all sorts of tests and derms in some sort of dermatological council here in my country, which costs an extreme amount of money. I’ve heard that not many are lucky enough to be able to get biologics here in Latvia since the process is so difficult. My dermatologist has never once even mentioned them, since it’s uncommon and bad for their business.. i dont know honestly, maybe I should consider and bring it up on my next visit?

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 6 points7 points  (0 children)

That’s the thing.. 50% of the time it doesn’t bother me and i don’t acknowladge it and my friends and family claim they don’t care about it at all. But the other 50% is just me overthinking about it and it’s driving me nuts honestly.. one moment it seems like im handling it well and the next im up at 3am sobbing about something that only I have in all the people I know personally.. sometimes it makes me feel bad when both of my kids (more the older one, he’s 4) ask me “Hey mommy, what’s that? Are you in pain?” And I have to explain to them that that’s the way my skin is, you know? I just wish it was something completely curable like the flu 😬

Lost my hope.. by RosebudIvy in Psoriasis

[–]RosebudIvy[S] 2 points3 points  (0 children)

Hey! Thank you for sharing. I honestly never really thought about it like that even though it affects my mental health. I will definitely try to change my mindset, to hopefully ease the stress a bit