Life has been a little... chaotic since starting hospice care for my mom. And by “a little chaotic,” I mean I now live in a sleep-deprivation experiment sponsored by Alexa, arthritis, and appliance failure. Mom has developed a habit of waking me up throughout the night because she can’t work the remote, needs help getting... Continue Reading →
Hospice chaos, caregiver exhaustion, biologic crash, emotional overload, and survival mode—with just enough rest to breathe for a minute.
I’ve had one hell of a month. Like… if there were an Olympic event for emotional whiplash, I’d be standing on the podium with a gold medal and an ice pack. It started with my almost 10-year-old cat, Jaxson. He had a cough. Just a cough. I did what any responsible pet parent does—I took... Continue Reading →
Living with chronic illness for almost 30 years gives one a thick skin. I've met so many people who love to give me free advice. For the most part, it's all good intended suggestions, but I often feel stumped on how to respond. Today someone said, "My friend says those infusions you take are bad,... Continue Reading →
Someone recently asked me if I wrote an "advice blog". The answer is NOPE. As My Joints turn is more of a journal of living with chronic illness and debilitating pain. I share my experience with doctors, medication, treatments, and daily life. I am not a medical professional, so any "advice" I give would be... Continue Reading →
I haven't blogged in a while. Recovering from pneumonia was difficult, then I caught COVID..... After 2 years and 8 months of avoiding the dreaded virus, I tested positive. I had a mild case. Bad cold without a fever. Due to my immunocompromised status, my doctor prescribed Paxlovid, the antiviral medication. Although my COVID symptoms... Continue Reading →
I've completed the last loading dose of my newest bio similar infusion drug, Inflectra. I know most of my family and friends are waiting to know....do I feel better. That is a tricky question to answer. I met with my rheumatologist and had to have an answer to that very question. My answer: Maybe Not... Continue Reading →
Life is scary for all of us right now. None of us have experience with this, so I've been following the recommendations of WHO (World Health Organization), the CDC (Centers of Disease Control), and the ACR (American College of Rheumatology). I did reach out to my personal rheumatologist and her advice was to get blood... Continue Reading →
IFAA just put out the 2nd part of our first episode of Rheumy Rounds™, a breakout series from our ArthritisVoices360 podcast. In this episode we talk about the doctor/patient relationship. We also touched on what a patient expects to accomplish during visit as opposed to what a rheumatologist expect to accomplish during a visit. It's... Continue Reading →
I recently started a foray into podcasting with my IFAA cofounder Tiffany. She is the brains behind the project, in which patients co-host a podcast to discuss issues impacting patients in the autoimmune/autoinflammatory arthritis community. Our latest series is called "Rheumy Rounds". Personally, I think it is ground breaking. How many of us (patients) have... Continue Reading →
asmyjointsturn.com 