Thursday, September 14, 2017

What is lupus and why does it occur 10 times more in women than men?



An autoimmune disease, it can turn fatal if not treated early 

If you are a young woman and having a butterfly-shaped rash on cheeks, coupled with fever, joint pains and fatigue, better watch out! It probably is Lupus, an auto-immune disease, which could turn fatal if not treated early.

Lupus is a chronic disease. It causes inflammation (pain and swelling), affects the skin, joints, kidneys, lungs, nervous system and other organs of the body. It mostly affects women in their 20s and 30s and occurs 10 times more in women than men. The other symptoms include weight loss, blood clots, poor circulation to fingers and toes. Pregnant women could have miscarriages.

In Lupus, the immune system, which normally protects the body by making antibodies that attack foreign germs and cancers, starts producing auto-antibodies targeting the patient's own tissues. “We are seeing more patients with the disease now,” said Dr. Raj Kiran, Consultant Rheumatologist, CARE hospitals. However, due to lack of awareness, patients were turning up late when the disease has progressed and affected vital organs like kidneys. Describing it as a “peculiar disease”, he said it needed more attention because young women in childbearing age were affected.

Side effects

If untreated, the disease would progress and the patient would die. At the same time, medications for the treatment cause side effects. Unlike in many other cases, Lupus patients require constant monitoring as the disease could flare up suddenly. A judicious balance needed to be maintained to prevent its progress and reduce side effects of drugs. While no definitive data is available in India, the prevalence could be one in every thousand, he added. The mortality rate could be one in 100 patients if vital organs like kidneys or brain were affected. It mostly gets triggered by some infection, environmental changes and at times by drugs. However, drug-induced Lupus would be mild most of the times, he added.

With women from weaker sections increasingly getting affected, Dr. Raj Kiran said that he planned to establish a foundation with the help of NGOs to extend support to such patients as the treatment was quite expensive. The foundation would also take up research and build data on Lupus patients.



Monday, July 3, 2017

Christina Harvey

Christina Harvey



Please give this a watch. As most of you know I was diagnosed with Lupus in Jan 2017 after almost losing a few of my toes. I had absolutely no idea what Lupus was. These people inspire me and give me hope. I can relate to just about everything they are saying. I teared up watching just knowing Im not alone. I hate disappointing people and lately I have had to cancel many event due to the pain, lack of energy or drs appointments. Its hard making people understand a disease you dont even understand yourself. I am really thinking about organizing a walk and/or some fundraisers for Lupus awareness and research. Would any of my family and friends be interested??? Tommy Wright Stephanie Wright Jennifer Wright Jessica Wright Frankie David Harvey Alexandra Wright-Phipps Maxine Poteet Joseph Hunt Nikki Wilkins Angela Brown Sarah Stine Mickie Knuckles Selena Johnson Larry Ferguson


https://m.youtube.com/watch?feature=share&v=uip4ChFbeVo

Monday, June 26, 2017

TAME THE WOLF AND TAKE CONTROL


 “TAME THE WOLF AND TAKE CONTROL’
The word ‘lupus’ originated from the Latin word ‘wolf’. It’s attributed to a 19th century physician who used it to describe rashes or scarred irritations on the skin of his patients that looked like the bite of a wolf.

The wolf is considered as a ferocious animal which ravages just like lupus does. 

Lupus is life – threatening, unpredictable and can damage organs in the body.

Living with lupus is like living with a wolf in the inside. Do we allow the wolf (lupus) to ravage our bodies or find ways of taming it?

Taming the wolf involves taking measures to ensure we keep lupus under control.

Together we can make a difference by joining forces to educate lupus warriors and the public about Lupus.