Flares and Psoriasis

Posted on March 12, 2018

"I don't have any psoriasis flare, but the arthritis pain is what gets to me. I have no energy, joints hurt and just want to lay and do nothing but that hurts also. I make myself get up and do some things but I'm in continuous pain." -A member on MyPsoriasisTeam

On MyPsoriasisTeam, the social network and online support group for those living with psoriasis and psoriatic arthritis, members talk about a range of personal experiences and struggles. Flares are one of the top 10 topics most discussed.

Here are a few question-and-answer threads about flares:

How do you cope with a flare up on your scalp and ears?

Has anyone else had the problem of a biologic that has stopped working? I've been having flare-ups.

After years of being mostly free of the dreaded rash, my scalp has suddenly decided to flare up. Any advice till I can get to see my GP?

Here are some conversations about flares:

I dislike cold weather... I get more flares when it's cold!

My job is becoming too stressful and making my psoriasis and psoriatic arthritis flare.

Currently in the midst of the worse flare up ever!

Have another topic you'd like to discuss or explore? Go to MyPsoriasisTeam today and start the conversation. You'll be surprised just how many others may share similar stories.

Feel free to ask a question here.

3 mini

A MyPsoriasisTeam Member said:

I’ve had great result with XTRAC on scalp and insurance paid for all of it.

posted 3 days ago

hug

MyPsoriasisTeam My psoriasis Team

Get the latest articles about psoriasis sent to your inbox.

Not now, thanks

Privacy policy
MyPsoriasisTeam My psoriasis Team

Thank you for signing up.

close