I had my first vaccine yesterday all is well arm just sore

Hey P Vets, So I'm considering Ozone treatments for the the P Monster, any one ever tried ozone before and how was your experience with it ?

Hi guys, I hope everyone are well! Anyone on bio T had the covid vaccs? I was told to wait a bit more before taking the vaccine..

Lately I've been getting tiny dots that turn into welts. They feel like mosquito bites, they itch really bad but after a few hours of not touching them, they disappear. Does anyone else haves this issue? I can't figure out if its part of psoriasis.

Covid was downgraded to the flu in March 2020. You may all think I am crazy but you can get the truth at drcharlieward. Do your own research before taking the vaccine, don't take my word for it.

Anyone went for the vac and if you have, how do you feel? Been reading up on it and a bit weary to go for it. It's safe for us to go for it? I heard that should I decide to take the vac, I should take the Oxcord jab as its not as strong?

Hi my lovely Flaymers. Haven't been on here in months. Moved to the UK to be with hubby and I'm surprised to say my skin still looks good. I hope you are all well?

Hey There! I am uninsured & have both Psoriasis and Psoriatic Arthritis. I'm wondering if anyone else is trying to navigate Psoriatic Arthritis, which is currently flaring out of control, with no insurance.

Got the covid19 vaccine at work today nhs nurses came in to do it have any of u had it yet any side effects?

Hi everyone, I'm new here! I'm a 16 year old female in the UK and I'm taking methotrexate for my scalp and body psoriasis. Does anyone know how strong this medication is, I've been taking it for 10 months and want to know any other stronger options?

At work we have been given letters to call up to book appointments for the covid19 vaccine has anyone heard how psoriasis sufferers react to this or have any information on it ?

Its the cold weather season and it always flares up at this time anyone any ways to sooth it can be awful ive had it since i was 8 and its only gotten worse not better

I hope life is treating everyone well as we stay safe from Covid. I was on Stelara but due to a lay-off, I am without insurance. I am seeking alternatives. Does anyone have any recommendations that have worked for them for behind the ear psoriasis?

Hello everyone! Hope you are doing well.

Just joined the Flaym Community. Glad to meet you, people :)

Hi my lovely Flaymers. I haven't been on here for a long time but I do hope you all are well? Our lockdown has moved from level 3 to level 2 so I'm happy. How are you all keeping?

I’ve been on methotrexate for over 25 years and it works for me I have 3 monthly blood checks

I'm writing from the middle of California where Covid-19 is blooming. My family has immune issues so we've been home for 84 days. I officially have psoriatic arthritis. I've started on methotrexate. How have any of you found that to work?

Has anyone been home during Covid-19 and find themselves worried to go back out into the world?

Hey my lovely Flaymers. All has been quiet. Tell me about your struggle with Psoriasis. I hope you are all keeping well? We are here for you .

Rheumatoid arthritis.: Who is the best doctor to see in the UK?