Profile picture of Sullypsa2019

Sullypsa2019 posted an update 1 hour, 33 minutes ago

Diagnosed 2 weeks ago. Trying to be optimistic. But mornings are getting worse and worse. 1 knuckle, then 2. One foot then the other. I am refusing the Big Pharma route. Working on food triggers and allergies 1st. Today is a tough one. I just joined the forum because I have no idea what to expect and when. Wondering if life will ever be back to…

Profile picture of Sullypsa2019

Sullypsa2019 posted an update 1 hour, 33 minutes ago

Diagnosed 2 weeks ago. Trying to be optimistic. But mornings are getting worse and worse. 1 knuckle, then 2. One foot then the other. I am refusing the Big Pharma route. Working on food triggers and allergies 1st. Today is a tough one. I just joined the forum because I have no idea what to expect and when. Wondering if life will ever be back to…

Profile picture of bumster Hi I'm new 12/2018

bumster Hi I'm new 12/2018 replied to the topic Cosentyx/Extreme Fatigue in the forum Treatment Issues 3 hours, 25 minutes ago

Hello hope everyone is well as for cosentyx when I started I couldn’t walk very good but on my 4 mth dose in a couple wks and walking pretty good after my recent flare yes still get flares but overall doing better I hated the fatigue and headaches but stuck with it so yes give it time and hopefully you can get the relief you deserve. take care…

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Rebecca posted a new activity comment 3 hours, 58 minutes ago

I’m so sorry you’re going through this, Smbarco….it seems like so many have issues with doctors and not getting the treatment you deserve. Many here have normal bloodwork. Trust your body and know you aren’t alone in this.

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Smbarco posted an update 7 hours, 58 minutes ago

I am very nervous because I just went to a rheumatologist for the first time Tuesday. He gave me a diagnosis of PSA from description alone, and a prescription for methotrexate. Since my symptoms started, I went from one doctor to the other, all my labs are perfect or at least not alarming. The doctors then lose interest and I’m left with my pain…

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Michigan Nana commented on the post, Accepting My New Normal: A Few Tips From Someone Still Struggling 23 hours, 43 minutes ago

I’m still hoping for a diagnosis. I’ve had psoriasis for over 50 years. And my elbows wrists and hands are hurting. They don’t have OA. Next rheumatologist appointment I plan on asking for something to take for my psoriasis. I’m stuck in depression again waiting for something, someONE to help me. Thanks for writing this Leanne. It means a lot.