General
Photos Member photos and videos Blog This is an archieve of Blogs from the old site Young Fighters While being young is great, being young with PsA is definitely not. We have found, and likely, so have you, that teens and young adults with rare illnesses are often have a hard time finding what they need: information, support, like minds, and others to share ideas or simply commiserate with. We are looking to change that. This is a place for the teen and young twenties crowd to talk about the things that matter the most to us as we carry on in our PsA battle. Share your stories, challenges, triumphs and worries with people that understand you the best. Medications Want specific information or others experiences with a specific medication? This is the place for it. Support Feeling down? Need to rant? This is the place. Let it rip, we are here to listen PsA Articles, News and Research This is the place to post links to scientific readings which enhance our understanding of PsA and treatments for it. The articles listed here have their roots in evidence-based research, and they have been directly or indirectly peer-reviewed. Other types of articles have their place in one of the other discussion categories. Although they may be peer-reviewed and evidence-based, articles and even studies don't always represent "fact". Articles and studies are largely the way scientists communicate ideas and opinions. They are are a great basis for discussion and learning but rarely should they be the basis for medical decisions. If you post a link, please state the topic of the article in the subject line. If you are posting more than one article, make separate posts for each.
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Join Us in Strengthening Our Rare Disease Community
I hope this message finds you well. As a valued member of our Ben’s Friends community, I’m reaching out to share an important initiative that directly impacts the support we provide to individuals like you who are affect… |
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1 | 7 | November 15, 2024 |
| About the General category |
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7 | 4031 | December 29, 2020 |
| Tips starting Humeria? |
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1 | 11 | November 21, 2024 |
| Become a Champion for Our Rare Disease Community |
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0 | 5 | November 19, 2024 |
| Medial knee pain |
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43 | 656 | November 15, 2024 |
| Biologics running out of steam |
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11 | 57 | November 15, 2024 |
| Checking In 11/24 |
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2 | 18 | November 14, 2024 |
| Seenie’s back |
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16 | 389 | November 13, 2024 |
| Enthesitis again |
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4 | 55 | November 13, 2024 |
| Stem cell treatment |
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7 | 712 | November 13, 2024 |
| Strange Throat / Neck Issue |
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4 | 66 | November 8, 2024 |
| Rant - Chicken? Egg? Rheumatologist(S)? |
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7 | 44 | October 30, 2024 |
| Now on Simponi - Have questions |
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10 | 93 | October 24, 2024 |
| Biologics Infection |
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5 | 56 | October 16, 2024 |
| COVID decreased my pain?! |
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7 | 60 | September 28, 2024 |
| Peripheral Neuropathy- PsA just keeps on giving |
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6 | 86 | September 4, 2024 |
| Hip replacements |
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5 | 515 | August 19, 2024 |
| Bruising on fingers |
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7 | 68 | July 27, 2024 |
| How to lose weight with PSA/Help Needed |
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9 | 75 | July 22, 2024 |
| We Need Your Financial Support |
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3 | 26 | July 17, 2024 |
| CVS and Abbvie - Gotta Love them (or hate them) |
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9 | 52 | July 15, 2024 |
| Ch ch ch changes! |
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16 | 220 | July 8, 2024 |
| Heart cath |
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2 | 62 | July 4, 2024 |
| Totally lost with it all |
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5 | 150 | June 20, 2024 |
| Seenie Inspired |
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16 | 228 | May 28, 2024 |
| Anything but dogs |
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5 | 132 | May 28, 2024 |
| Red Dots and The Frustration of the Unknowns! |
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0 | 114 | May 23, 2024 |
| New Rheumatologist.., am I crazy? |
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37 | 618 | May 22, 2024 |
| Has Mtx Helped anyone? |
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46 | 2407 | May 19, 2024 |
| CCP level |
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14 | 240 | May 7, 2024 |