The disability community is up in arms about statements made by a woman who is described as "American conservative author, talk show host, political commentator, and producer." I will NOT be identifying this woman by name because it's obvious she lives for these moments where she feels she is being unfairly vilified so she can... Continue Reading →
March is both Autoimmune Disease Awareness and Women's History month. To honor both, I'm highlighting female advocates who have inspired me, motivated me, and befriended me. In this third issues, I've decided to feature three women that make me want to be a better advocate. First up is Kerry Wong from Float like a Butterfly.... Continue Reading →
I was scrolling through facebook today and saw a post for "walk 50 miles with your dog this month" for XYZ charity. I looked at my dog and said, "When this new medication makes me feel better, we can do this." A friend asked me to go to a large mall in the area, and... Continue Reading →
The holidays can be both enjoyable and stressful when you are dealing with a chronic illness. I've learned that boundaries are important. I'm not always the best at enforcing my boundaries, but after being sick for the past four months, I need to be extra cautious with my health. 🎄You may want to do everything... Continue Reading →
I've lived with Chronic illness for over 20 years. During that time, I admit, I haven't always been good at communicating what I needed from friends and family. Over the years, I've learned how to set boundaries and ask for what I need. The issue is, I've become more discerning of whom I choose to... 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 →
It's been a hot minute since I've posted a blog. There are 15 blogs in my drafts that I just couldn't finish. I feel like I lost my voice for a bit. I've lived in pain for over 20 years. This past year; however, I feel like my disease is out of control. Medication barely... Continue Reading →
My health has been a roller coaster lately. This past week my disease is basically out of control. I had to break out my cane because walking and balance were an issue. I woke up Friday morning feeling exhausted, but I got out of bed and forced myself to drive to work. I lasted 1.5... Continue Reading →
Today was a tough day. It was a typical work day with all the typical hassles that occur, but I felt like I counted down each and every moment until 2:25 pm. You see at 2:25 pm, I was scheduled for my first COVID-19 vaccine. My journey to this moment has been painful for many... Continue Reading →
Last time I posted about my dad losing his fight with COVID. Since then, I lost another family member. My uncle called the day after my dad died to tell us that he fell. My uncle had a myriad of medical issues, with one being severed COPD. My family (parents, cousins, etc.) followed guidelines and... Continue Reading →
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