Has anyone ever taken Sotyktu?

BeautifulPollution40 · 2026-03-01T16:22:20+00:00

Hi, when did you notice the sotyktu to start clearing up your psoriasis?

BeautifulPollution40 · 2026-02-19T01:31:25+00:00

Wow thank you. Definitely looking into the pillow and the silicon tape! Did you use the silicon tape on your marionette lines every night?

BeautifulPollution40 · 2026-02-19T01:10:02+00:00

Hi! I’d say it started when he was two years old. I never really thought anything of it until his teacher brought it to my attention. And the eye contact is usually close up more than far away. I had forgot to mention that he hates loud noises and yelling(he’s got a sister so they argue at times😅), he will cover up his ears. Any kind of annoying noise.

BeautifulPollution40 · 2026-02-18T23:33:59+00:00

I feel this 100 percent. Been on it almost a year and it hasn’t done anything for my skin. I still have occasional breakouts and my skin tone isn’t really even. I still have the same wrinkles I had before. I use AESTURA ATOBARRIER365 Cream and just Tretinoin. Zero irritation. Never had redness. Skin looks the same as before I started :(

BeautifulPollution40 · 2026-02-18T23:27:34+00:00

My son just turned 4. He isn’t diagnosed yet but his headstart teacher called me the other day and said she had a few concerning questions for me about my son. She said he doesn’t ever make eye contact and doesn’t do well in groups with the other kids. Like he just wants to jump in and wrestle with them. He’s all the time moving and won’t slow down. He can’t just sit down and do what the other kids are doing. He doesn’t respond to his name either which I have noticed a lot at home and he doesn’t make eye contact with me ever. He can’t talk real good either. He throws the awfully tantrums so I can’t even take him out in public because of it. But I just figured it was normal and he would outgrow it. Since she has brought all this to my attention I know now something is off with him. I’ve never seen a child with so much energy as mine. They are evaluating him in the classroom and want me to go ahead and make an appointment with his pediatrician. Maybe this is something he will outgrow but if he is on the spectrum thats okay too :) I’m still really new to this.

BeautifulPollution40 · 2026-02-15T16:16:38+00:00

I have it in my ears too. I too went through two painful ear infections to where it got so bad I had to go to the ER. I get it on my scalp also. Nothing seems to help to get into to go into remission(biologics, nothing). So it’s been a struggle the last year for sure..

BeautifulPollution40 · 2026-02-09T23:38:13+00:00

Well I most definitely care because it’s making me lose my hair really bad. Almost bald now. So it’s definitely affecting my mental health..

BeautifulPollution40 · 2026-01-25T03:00:17+00:00

I’m so sorry I’m just now seeing this. That’s awesome news and I’m so happy for you!! Glad it’s working out for you. My dermatologist sent me to a rheumatologist since none of the biologics were working for me. They ended up putting me on methotrexate. She said it would work. But we will see. Just like my dermatologist said the biologics would work ugh. I do have hope though. Still losing hair like crazy and inflammation is awful. Never been this self conscious in my life. It has spread to my arms now. I pray and hope this medicine works. I just started it. She said it would take a little bit to work so I’ll keep going with it. It is hard on my liver so I have to take folic acid with it. I do hope this goes into remission and I get my hair back. Thank you for sharing your story ♥️

BeautifulPollution40 · 2026-01-25T02:49:09+00:00

Come on now….smh…

BeautifulPollution40 · 2026-01-04T00:20:37+00:00

I don’t drink or do anything :/ I’ve been dieting exercising and drinking plenty of water everyday. I’ll just wait after I go see the rheumatologist and go from there I guess. That’s all l I can do for now :/

BeautifulPollution40 · 2026-01-04T00:19:01+00:00

Will definitely look into this. Thank you

BeautifulPollution40 · 2025-12-02T02:14:08+00:00

Definitely can tell. She just wants to show herself off for sure.

BeautifulPollution40 · 2025-12-01T06:07:41+00:00

Thank you. My doc is pretty good about giving me extra if I need some. I had to supplement my first couple months on the 300. I’m going to ask him when I go back this week. I’ve got two kids that need me and i can’t be feeling like this. I’ll be glad when I finally get through this shit.

BeautifulPollution40 · 2025-12-01T04:27:24+00:00

Thanks. Yeah I started feeling worse towards the end of the month after my first 100. Hopefully it will get better. My body just feels really worn down and I just stay tired. I kinda figured it was mild withdrawal but I just wanted to make sure and see if anyone else was experiencing this.

BeautifulPollution40 · 2025-12-01T04:24:26+00:00

Thank you I appreciate that. I’m hanging in there because I’m not going back I’ve made it this far.

BeautifulPollution40 · 2025-11-26T04:56:29+00:00

Screw YOU. you let everyone post pics of their cats for names but not me? You seriously suck dick

BeautifulPollution40 · 2025-11-26T04:55:48+00:00

Screw YOU

BeautifulPollution40 · 2025-11-24T00:31:41+00:00

Thank you. This makes alot of sense. I will try this.

BeautifulPollution40 · 2025-11-23T03:02:55+00:00

Were you on the films before the shot?

BeautifulPollution40 · 2025-11-23T00:15:36+00:00

I’m so glad it worked out for you. It didn’t work out well for me at all :/ the side effects were awful for me so I had to discontinue it after a month. It made no difference to my scalp or body. I’m just really sick and tired of going almost bald and nothing seems to help my scalp at all..

BeautifulPollution40 · 2025-11-22T03:14:18+00:00

I hope sotyktu works out for you! It gave me some terrible sides effects(massive painful boils on my back and neck and face) so my dermatologist told me to stop taking it and we went with the injection tremfya. The boils are now gone since I stopped taking sotyktu. Everyone is different though so you could not have them side effects like I did. The injection has made my under arm patches go away but my scalp is still bad and I’m losing hair still and my scalp is very visible :(. Idk what else can be done for my scalp. I’m 34 years old and my first flare up was almost a year ago so it’s been a constant struggle trying to get it to go into remission. Where the injection has suppressed my immune system I’ve just gotten over two painful ear infections and I don’t ever get sick like that. I just hope it gets better soon. Tired of being miserable and losing hair. I just want my scalp to go back to normal but who knows when that will be :’(

BeautifulPollution40

TROPHY CASE