Black Tuesday
I know my posts are getting to be far in between lately although there were a lot of significant events (like our new puppy, Jordan) to write about. Due to some recent setbacks, I decided to take another respite from blogging just so I can sort things out in my head. It might not be of utmost interest to everyone but I came to a conclusion that it's best to write about it. If by some measure, people learn a little bit more about something, then it's worth the effort. I've often said that each of us are just a tiny speck in the grand scheme of things but now that I have come to appreciate my bit role in the Internet global community, I aspire to make a positive dent in someone's life if possible and whenever given the opportunity.
When I first wrote about my problem with Carpal Tunnel Syndrome , joint pains and my subsequent attempt to detoxify, I left out a lot more issues that were somewhat of clandestine nature. As candid as I try to be, some things are still better kept private. But after today's events, I felt like I owe it to my friends and faithful readers to disclose and get it over with.
After working the night shift, I dashed out of the hospital to meet up with Kenny for my doctor's appointment (Rheumatology) at another building. It was a freezing, wintry and windy day and I struggled to keep warm. My fingers and toes were icy cold, deathly pale and unbearably numb despite my gloves and Ugg boots. These days, it doesn't take much to make them look and feel that way. Even just washing my hands with a cooler temperature water will do the same trick. If you ever have the occasion to see a dead person's hands and feet, that's the closest I can describe my predicament (Raynaud's Phenomenon).
On the surface, I managed to keep a facade of composure. Inwardly, I was bombarded with a jumble of emotions threatening to overwhelm what little vestige of restraint I have left. It has been a drawn-out process but I finally have the chance to obtain answers, whatever they might be. After all these months of numerous hospital visits and tests, the speculations and uncertainties will hopefully come to a resolution.

It was probably one of the longest and most thorough consultation I've ever had with a physician and in the end, the verdict was handed out. I have Systemic Lupus Erythematosus (SLE or lupus).
Brief background: Lupus is an autoimmune disease that can affect various parts of the body, including the skin, joints, heart, lungs, blood, kidneys and brain. Normally the body's immune system makes proteins called antibodies, to protect the body against viruses, bacteria, and other foreign materials. These foreign materials are called antigens. In an autoimmune disorder like lupus, the immune system cannot tell the difference between foreign substances and its own cells and tissues. The immune system then makes antibodies directed against itself. These antibodies -- called "auto-antibodies" (auto means 'self') -- cause inflammation, pain and damage in various parts of the body.
My worst fear was confirmed and I have to finally deal with the fact that things are going to be different from now on. I know this was coming but I was in a state of denial for the past few weeks, hoping for a better outcome. I am not going to lie and put up a brave front. I am scared as hell. I am mad, despondent, panic-stricken and feeling like I had been hit by a runaway train. I desperately wanted to move away from its path but my whole body was bolted down, succumbing to the inevitable ruin.
Why me? I'm sure a lot of you got some words of wisdom, reassurance and sympathy. In time, I'll come to appreciate them and thank those who really care. At the moment, all I want to do is just to run off and lick my wound. What better place to do it but warm and sunny Maui? Yes, I'm headed off to Hawaii on Friday with some friends and I'll try to enjoy every bit of this short escape although I might spend more time hiding away from the sun (photosensitivity). Before long, the real world will loom bigger and I'll have to continue living in it for as long I can.

Right now, I have some packing to do and that is something I have control of. I will try to keep blogging during the trip. I just got a brand new camera and I'm not afraid to use it. So, catch ya later, folks! Take care of you and each other.
For more info on SLE or Lupus, here are some links:
http://www.lupus.org/newsite/index.html
http://www.medicinenet.com/systemic_lupus/article.htm
http://www.emedicinehealth.com/lupus_systemic_lupus_erythematosus/article_em.htm
http://www.visualdxhealth.com/adult/systemicLupusErythematosus.htm






