BECAUSE WE MATTER
We can all live a higher quality of life! Let's Empower, Encourage and Educate Each Other Together! Make An AppointmentAbout MeHelp Our Cause
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Live Chat
Come on by for a quick chat @bezzypsa.com. #BezzyPsA partnership. @bezzycommunity @bezzypsa. Come on in. It’s “LIVE CHAT” time at Bezzy PsA. We are here to inspire and support each other. You might think you are alone, but you’re not. If you have psoriatic arthritis, we encourage you to sign up for the Bezzy PsA platform. You can download the Bezzy PsA app. I will be there, Diane Talbert as advocate and Patients Rising’s moderator. There’ is Jenny Parker, the community’s guide, and PsA advocate. We are here to support the psoriatic disease community.
Learnings from the 20th Century: Innovative Mediums Used to Identify and Elevate Health Disparities
Amgen‘s Panel and Discussion
Connect with other members of the community and empower each other to move beyond this disease.
Los Angeles Times Studios
A producer with the Los Angeles Times Studios (not the newsroom) would like to speak with women in the Southern California area who have experienced being dismissed or not heard by healthcare professionals. Her deadline is Wednesday, so she’d appreciate hearing from folks early this week. She can be reached at: karen.foshay@latimes.com
VISION STATEMENT
Power Beyond Psoriasis is a nonprofit organization designed to raise awareness and embolden the communities of people suffering with chronic diseases everywhere.
Power Beyond Psoriasis raises awareness and emboldens communities by:
- providing a blog, podcast of personal experiences,
- and helping other people find support through advocacy.
We are passionate about bringing awareness, boldness, and strength to our community to help people that have suffered and are still suffering.
Put your needs first. The goal is to inspire hope and contribute to health and well-being by helping people locate the best care. Patient advocacy is here to help every patient through integrated clinical practice, education, and research.
WE ARE STRONG TOGETHER
- @ghlf is committed to producing resources and support initiatives personalized to patients’ needs.e stick together.
- Gain reassurance that we can make a difference
- Learn about our COVID19 Patient Leadership Council.
- Meet the patient leaders who are working with GHLF to serve chronic illness patients during this critical time.
- No one knows what it’s like to live with a chronic condition more than patients themselves. GHLF
PATIENT ADVOCATE EXPERIENCE
With over 50 years of experience, I’m here to tell my story so that others may learn how to cope with psoriasis.
I’ve come a long way, and I’m here to share my insight with others.
SNAPSHOTS FROM THE LIFE OF A PATIENT ADVOCATE
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Washington, District of Columbia, United States