I don't have much time to stop and write today, so a picture will do (A picture speaks a thousand words, right?). I feel this picture explains my life.
Psoriatic arthritis (PsA) affects every part of your life, even in subtle ways – including your friendships. After living with PsA since childhood, I assumed I knew everything there was to know about navigating friendships with arthritis. But after graduating from college and entering “the real world,” I was in for a huge shock. As it turns out, maintaining adult friendships is much more work than I anticipated. View the full article at HealthGrades.com .
In this post, I talk about a very hard time after I was diagnosed with arthritis. I share this because I think it's important for others to know that this is a hard disease. For the longest time I felt weak and that I was the only one weak enough to feel this way. But I know now that that is far from the truth: Many people feel this way and it's because they are strong. I know I'm not the first when I say 'I don't want to be alone in this disease.' I don't think anyone has ever said, 'I want to fight this alone,' and actually meant it. It's an ongoing thing that never seems to end, with surprises at every corner. I couldn't go on if it weren't for the wonderful people behind me. I know that for a fact because there was a point when I had almost no one. I did it almost alone for a long time. I had my mum, and she had me. Even then, sometimes there was a wall of fatigue between us. I was newly diagnosed and was taking methotrexate. It ...
Photo credit: Psoriatic-Arthritis.com If I could use one word to describe my time taking methotrexate (MTX), it would be: sluggish. Frankly, I felt like a zombie sometimes. I had no energy and was very tired all the time. And I had lots of other not-so-fun side effects, like nausea, cankers, and hair loss. Read the rest of the post at Psoriatic-Arthritis.com
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