I just heard about this great thing called bloggy carnival. I wanted to get in on the act. Of course I"ll have to start small but small is better than nothing I guess. I'm giving away one coupon good for a free 8.45 oz Cascade Crystal Clear Rinse Agent.
To enter the drawing:
* Leave a comment telling me what you know, if anything, about Lupus
* Deadline August 1
* The winner will be posted in the blog
* Valid email address required
* U.S. only
For more contests, visit my other blog at: Weird News and Other Stuff!
And the winner is.... Ginny! Thanks to all who entered
Bloggy Giveaways
Fever Subsides, Nasua comes on
I did run fever one more night, but that wasn't so bad. I'm always thankful when I make a quick recovery or if it doesn't keep me out of commission for longer than a day or two. I feel okay except for an occasional bout of nausea and dizziness. The last time I was in the hospital it was for low blood pressure. It was way to low and couldn't even stand up for a few minutes without almost blacking out. I have no idea why or how it was so low. The doctors never did/could give me an answer. I don't want to repeat that. I will do my on research and find out what are some possible reasons for your blood pressure being low.
Fever Chills
Last night I went to bed feeling fine. I read a book while waiting to drift off to sleep. I keep a small heater by my bed because I get chilly at night and can't sleep if I'm cold. While reading the heater made this funky, weird noise and stopped blowing. Of course it had conked out. I bundled up and hoped I could go to sleep for the night.
A few hours later I woke up in a sweat. Sweating all over really. I was running fever again. I keep a thermometer near by, since I run fever so often. I checked and it was 99.7 which is a fever for me. My temperature is always lower than 98 degrees normally. I tossed,turned, and sweat all night long. When I awoke, I felt just fine. When this happens it usually is a pattern for a couple days. Oh happy days.:(
Contacts to be colored
I got a call from my eye doctor. They just wanted to check in and see how the contact they gave me were doing. Without the contact I'm mostly blind in my left eye. Everything looks like colorful blobs and blurs. To top it off I've lost the color also. I now have one brown eye and one light blue eye. It is very noticeable and makes me self-conscious. This is all thanks to Lupus. Saying it's been tough losing my eyesight is the understatement of the year. Anyway they called to say it was time to have the contact colored to match the eye since I was doing well with it. And now I will no longer be this baby's twin. Adios.
Restrictions
Job hunting can be a bit of a chalenge with Lupus and the various thing associated with it. Anything that requires prolonged standing is pretty much out. A lot of repetitive motion or heavy lifting is also out. Any kind of extreme temperatures, especially the cold, is out. This narrows the field down considerably. And that doesn't even take into account all my restrictions.
Working a full-time job is hard for me. I can do it, but not much anything else that constitutes a life. Working part-time does not provide enough income to make ends meet. And not working is not an option. What's a girl to do? Right now, I am exploring work at home possibilities to supplement my income. I'll keep you posted on the development.
Chronic Fatigue Syndrome
Yesterday I went out job hunting. I just moved to Texas and wanted to find a summer job to earn some extra cash. The searching lasted maybe 4-5 hours tops. When I got back home out of the heat, I was exhausted. A person in their twenties should be able to go a full day without needing rest, but that's not the case with me. So, I took a nap, only intending on it being and hour or so. It ended up being almost four. This is the main reason my sleep patterns are so out of whack. Some days I have the energy of a normal (non-lupus person) and other days it's almost non-existent. Chronic fatigue is no fun.
Lupus is an autoimmune disease that can affect various parts of the body, including the skin, joints, heart, lungs, blood, kidneys and brain. In an autoimmune disorder like lupus, the immune system cannot tell the difference between foreign substances and its own cells.
There are four types of lupus: discoid, systemic, drug-induced and neonatal lupus. I have been diagnosed with Systemic Lupus. This type lupus is usually more severe and can affect almost any organ of the body. So far the main issues that I have to deal with are Arthritis, Raynaud's Phenomenon and fatigue. Lupus also attacked my left eye and left me mostly blind in it. I struggle with the symptoms from day to day. Some days are better than others. But I keep on keeping on.
I guess a good start to this blog is to define what Lupus is exactly. The MedlinePlus Medical Encyclopedia defines it as this:
Systemic lupus erythematosus (SLE) is a chronic, inflammatory autoimmune disorder. It may affect the skin, joints, kidneys, and other organs.
SLE (lupus) is an autoimmune disease. This means there is a problem with the body's normal immune system response. Normally, the immune system helps protect the body from harmful substances. But in patients with an autoimmune disease, the immune system can't tell the difference between harmful substances and healthy ones. The result is an overactive immune response that attacks otherwise healthy cells and tissue. This leads to chronic (long-term) inflammation.
The underlying cause of autoimmune diseases is not fully known. Some researchers think autoimmune diseases occur after infection with an organism that looks like certain proteins in the body. The proteins are later mistaken for the organism and wrongly targeted for attack by the body's immune system.
SLE may be mild or severe enough to cause death.
SLE affects nine times as many women as men. It may occur at any age, but appears most often in people between the ages of 10 and 50 years. African Americans and Asians are affected more often than people from other races.
Introduction
Hi, I'm Nia. I'm a 27 year old woman in Texas living with Lupus. This blog is not only to be a journal of my day to day struggles and successes, but also an insight into life with Lupus. Join me as I learn more about my own disease, what helps, what doesn't and how to cope with it. I hope to see you back often and I welcome your thoughts and comments.
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