"You Should Live at the Doctor's."

-
That's the biggest joke between my friends and I. They find it amazing how often I'm at the hospital: Once a month to see My rheumy, once a month to get blood drawn, and sometimes because I'm ill. Since I take the day off to see my rheumatologist as I have to travel by train to see him, I naturally have many funny or amusing stories for my friends to help pass the time in school. One of my very good friends understands the severity of Arthur and he has said the most memoriable things about it:

"One day I'm going to make a charity for whatever you have so it can get cured (Me: 'Awww') so I don't have to hear it anymore."

"Why don't you just live at the hospital?"

Granted, these sound very mean but they were said comically and I was dieing laughing. Honestly: He's one of my best friends and we are always teasing each other.

Speaking of which, I'm seeing my rheumy soon: Hopefully he'll say I'm getting closer to remission just like last time.

Comments

Post a Comment

Popular posts from this blog

Balancing Friendships and Psoriatic Arthritis

-
Image
   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 .
Read more

My Arthritis Depression

-
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
Read more

Leflunomide, Calcium Oxalate Crystals, and Kidney Stones

-
Updated: October 2022 My name is Elizabeth and I will never have an easy disease to diagnose. It took several years ro get my diagnosis. I've taken a few different drugs, but none of them truly worked out for me. Methotrexate didn't work well. But Leflunomide changed my life. Not so much arthritis-wise, as I responded well. However, I began experiencing possible thyroid and kidney problems while taking leflunomide. I have calcium crystals in my kidneys, which could later become stones. As my mum says, "I'm sparkling on the inside."  We found this as blood was found in my urine many times. I also had to do a twenty-four hour urine sample, which is when you collect all the urine you produce in twenty-four hours. It really is quite embarrassing walking into the hospital with a container of your own urine, but it's worth it. I'm currently seeing a specialist for this problem and we are taking care of it right now by discontinuing leflunomide and lett
Read more