When I was first diagnosed with SLE, there were also blood trace and protein in my urine indicating that my kidney are also under attack. The rheumatologist advised that I get a renal biopsy to determine the extent of damage the SLE has caused to my kidney.
I was hospitalised to undergo treatment and renal biopsy. I had to collect 24 hours of my urine to obtain a more accurate reading of the level of protein leakage.
“Every time you go away, you (I) take a piece of me (you, kidney) with you (me).” Paul Young’s song could be the theme song of a biopsy room. Continue reading “Lupus Nephritis Stage IV – When it started to sink in”
Ever since I started to feel the existence of my nagging inconvenience, I have been hoping that it will go away eventually. 16 days and tonnes of painkillers later, it seemed that my unknown partner is here to stay. It greeted me every morning with pain, left me alone for 7 hours, and reported to me again until I close my eyes. I could no longer go climbing, lift weights, even moving around is difficult. I decided that I needed to put a name to this nagging inconvenience of mine, and have a heart-to-heart conversation with it. Continue reading “Lupus – When you fight you”
Solo tripping in Germany and England with my nagging inconvenience.
Despite experiencing pain every day, I still managed to make the most out of the hours when I am less in pain, and I never regretted proceeding with the trip.
I spent one week in Germany, and another one in England.
I would say that I was an extreme optimist and hopeless romantic. Continue reading “Days in Europe (Pt 1)”
29 November 2015, 5.30am.
It was a Sunday, and I was looking forward to a short hike with fellow hikers in Bukit Saga. The alarm went off at 5am, and like any usual days, I stretched my hand to reach out to my mobile phone on the table ahead of my bed. However, today something did not feel the same.
I had problems lifting my hand. Continue reading “The nagging inconvenience”