Psoriatic Arthritis Warriors

Psoriatic Arthritis Warriors Psoriatic Arthritis Warriors was founded by Emily Kate! Join our Facebook group! Follow on Instagram! 💚

Some days I swear I am the Tin Woman. 🤖🩶🛢️My joints feel stiff. They creak. They protest every movement. Mornings can fe...
07/24/2026

Some days I swear I am the Tin Woman. 🤖🩶🛢️

My joints feel stiff. They creak. They protest every movement. Mornings can feel like someone forgot to oil my hinges. 😅💔

Living with psoriatic arthritis isn’t just about sore joints….it’s about navigating chronic pain, fatigue, stiffness, and inflammation while still showing up for life. Some days I move a little slower, but I never stop moving forward. 💪✨

I may need a little extra “oil” (or coffee ☕😂), a little extra rest 😴, and a whole lot of grace… but this warrior heart keeps beating. ❤️

If you live with arthritis, know this: You are not lazy. You are not weak. You are fighting a battle most people can’t see. 🫶

We’re stronger than our diagnosis. Together, we keep going.

✨ I’m incredibly honored to share that I’ve been selected as a Health Union Social Health Awards Finalist in the Communi...
07/21/2026

✨ I’m incredibly honored to share that I’ve been selected as a Health Union Social Health Awards Finalist in the Community Cultivator category! 💙🏆

Building a community where people feel seen, heard, and supported has always been my mission. As the founder of and the admin of the Psoriatic Arthritis Warriors Facebook group, I’ve had the privilege of connecting with over 18,500 members from around the world. 🌎💚

What started as a way to share my own journey has grown into an international community where people living with psoriatic arthritis and psoriatic disease can ask questions, share victories, navigate challenges, and remind one another that no one has to face this disease alone.

This recognition belongs to every single one of you who has shared your story, offered encouragement, answered a question, or simply shown up for someone else. Thank you for trusting me, believing in this community, and helping make what it is today. ❤️

Here’s to continuing to raise awareness, educate, advocate, and empower patients around the world. The best is yet to come! 💙

💙 The hardest parts of chronic illness are often the ones no one can see. 💙It’s not just the pain, fatigue, or flares. I...
07/10/2026

💙 The hardest parts of chronic illness are often the ones no one can see. 💙

It’s not just the pain, fatigue, or flares. It’s the constant explaining. The second-guessing yourself. Grieving the life you thought you’d have. Saying “no” when your heart desperately wants to say “yes.” Watching life continue while you’re simply trying to make it through the day.

If this resonates with you, know this: You are not alone. Your strength isn’t measured by how much you push through—it’s measured by the courage it takes to keep showing up, even on the hardest days. 💪🦋

To every warrior reading this: I see you. I believe you. And I’m proud of you. 💙

👇 Which one of these hits home the most for you? Let’s remind each other that none of us are fighting this battle alone.

07/06/2026

When your biologic kicks in and you start feeling gooood!

💜 Chronic illness doesn’t just affect our bodies, it can affect our minds too.There are days when we feel down, isolated...
06/24/2026

💜 Chronic illness doesn’t just affect our bodies, it can affect our minds too.

There are days when we feel down, isolated, angry, or overwhelmed. Living with a chronic illness can be exhausting in ways others may never fully see. But even in the hardest moments, we can discover strength, grace, resilience, and sometimes even a little humor along the way. 🌷✨

Healing isn’t always about being symptom-free. Sometimes it’s about learning to give ourselves compassion, finding joy in small victories, and continuing to move forward one day at a time. 💚

If you’re struggling today, please know this: you are not alone, and you are so much more than your diagnosis. Warrior, keep going. ❤️

💜 Chronic illness can feel incredibly isolating. The cancellations. The pain. The invisible battles. The feeling that no...
06/21/2026

💜 Chronic illness can feel incredibly isolating. The cancellations. The pain. The invisible battles. The feeling that no one truly understands.

But here’s the truth, warrior… you are never alone. ❤️

There is an amazing community of people who get it. People who understand the flares, the fatigue, the grief, the victories, and everything in between. Together, we lift each other up, celebrate the small wins, and remind one another that we are stronger than our diagnoses.

✨ Join the Psoriatic Arthritis Warriors Facebook Group
✨ Follow for daily support, education, encouragement, and connection.

No matter what diagnosis you carry, there is a place for you here. 🤗

You don’t have to fight this battle alone.

💜 Different journeys. One community.
💜 Different diagnoses. One warrior family.
💜 Strong alone. Unstoppable together.

Gentle Reminders For Difficult Days! ❤️🫶🏼
06/16/2026

Gentle Reminders For Difficult Days! ❤️🫶🏼

Psoriatic arthritis doesn’t just affect the joints, it can impact the skin, nails, eyes, spine, heart, lungs, mental hea...
06/11/2026

Psoriatic arthritis doesn’t just affect the joints, it can impact the skin, nails, eyes, spine, heart, lungs, mental health, and overall quality of life.

That’s why many of us believe it’s time to start calling it what it truly is: Psoriatic Disease.

A name that reflects the full-body, systemic nature of this condition helps raise awareness, improve understanding, and validate the experiences of millions living with it every day.

Because it’s more than joint pain.
Because it’s more than skin deep.
Because every part of the disease deserves to be seen.

Our condition can be invisible but we are not!
06/09/2026

Our condition can be invisible but we are not!

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