It’s Saturday August 28th. My “sick-anniversary” is September 20th and this is always a really weird time of the year for me. I avoid most the memories on my phone because the thought of my old life still makes me sick. I can still put myself right back into my life in 2018. And to… Continue reading Lupus, Diabetes, Spine..
I haven’t written in awhile. I got the diagnosis of Lupus March 4th and since then have been fighting with insurance to approve the immunosuppressant my rheumatologist wanted me on (Abatacept/Orencia). My doctor went through all the appeals he could and then it was turned back over to us to file a grievance through the… Continue reading Lil update- The good, the bad, and the in between!
We spent 5 weeks at the Mayo Clinic. We were blessed to be able to stay with family because we went over the course of the entire summer (2020). We started with rheumatology where they ran another whole blood panel for autoimmune diseases and other disorders. In the meantime of those results, she sent me… Continue reading Diagnosed Pt. 2
I tell people all the time that my life was probably the least affected by COVID compared to others in my world. I know people who have lost jobs, been forced to move, lost family members or friends, are frontline workers. But me? I’ve been homebound with my parents for the last 2.5 years due… Continue reading This Is Our Everyday: How Covid Has Changed Life For The Chronically Ill
I loved baths as a kid but as I got older, I grew out of them and then eventually grew to hate them. I tend to run on the warmer side and I didn‘t find sitting in hot water, dripping in sweat any fun. When I was first getting diagnosed with Interstitial Cystitis last year,… Continue reading Bath Time!!