For those who are still not in the know, I’m a patient of LUPUS/SLE (Systemic Lupus Erythamathosus). It’s a chronic disease that is fatal if the patient has no strong will to fight the disease. That usually happens when somehow the disease attacks the brains. I have heard about 4 deaths so far that had died due to the attack of the disease to the brains.
Lupus is not something contagious. In fact, it’s allegedly hereditary. However, as to note, there is no one in the immediate family history with Lupus in my family. But, I concour to the fate that Allah has decided for me.
I accepted the disease since I was first diagnosed - 1st June 2002. I’ve concede to the fact that I had a major illness the moment my hair started to drop off in March 2001 and my joints swell and hurt in Dec 2001.
Remedy? There’s no cure at present. But the disease can be controlled via prescribed steroids and medications. It is NOT a cure… just to stabilize the condition.
Time and time again, people ask me what IS LUPUS? The simplest short answer would be it’s an autoimmune disease; in other words - antibodies that help prevent any illness from getting worst in your body; decides to attack and kill a fellow antibody. The antibodies in the body fails to recgonize the other and turn bad by killing fellow antibodies.
What’s effected…? The system of the organs and skin in the body.
Many patient starts off with "butterfly rashes" on their face. It’s a symptom that a person HAS the disease. The disease is NOT a skin disease, as many would perceive (thankx to the publicity from the National Service gal not too long ago).
It’s a disease thats real but not heard off. People perceive it as rare, but in actual fact, many has this disease. If you don’t believe me, pay a visit to HUKM, Cheras or Sunway medical Center or even General Hospital. You will see a range of women and some men patients with the disease.
If you’ve heard of this disease, it’s because you have a relative and/or friends who have it. For that I wish them well and hopefully the disease is controlled.
Why is it that people could not recognize if that person has SLE? Simple, we walk, talk and breathe the same as any of you. We have an extra smile on our face due to our positiveness. We believe we can change the world through our hardships.
Patients of SLE are vulnerable to any form of illness. We have low antibodies due to the fact that the steroids medication supress the antibody level.
Love and support is what a patient needs. Stress free environment & no direct sunlight as the layers of the skin is thin and that it’s a trigger for SLE to react again.
Me? I’m under controlled. The disease is sleeping for now. It has signs sometimes that something is not right… but, nevertheless the blood tests and other tests shows that I’m doing just fine. *winks*
This blog tonight is to create awareness for the disease that had caught me offguard four years ago. Through love and support of families and friends, I am where I am now. They had believed that I could get through the days well, and I am still fighting one day at a time. Lupus does not have a point of stages. It could be the most silent or it could be at its peak and fatal.
For my friends and people who came across this blog… I’m inviting you to join me this Saturday, 10th March 2007 to Starbucks, Sunway Pyramid. In this event, FlyFm Malaysia is giving out the cash prize of RM1,000.00 to the person who brings the biggest crowd to Starbucks and stays the longest.
Time : 1pm to 4pm.
The more the merrier! If I win the money, it is pledged to go to SLE Association. You can check them out at http://www.lupusmalaysia.org
A special shout out to Razlin. Thank you for your effort girl. I hope your blog will be noticed and people will come.