Lupus Disease - Symptoms with Pictures
77Lupus Disease
Lupus means "wolf". Erythematosus means "redness". In 1851, doctors thought the facial rash that frequently accompanies lupus looked like the bite of a wolf, thus the name. I've had the "butterfly rash" as I prefer to think of it, which is one of the more classic signs of lupus. The wolf name just doesn't sit well with me! I like to be well informed and have found "The Lupus Book: A Guide for Patients and Their Families" by Dr. Daniel J. Wallace to be very helpful. There are many other helpful books available.
Systemic Lupus Erythematosus is one of the autoimmune diseases that involve your immune system turning against your body. It is a multi-system disease. Lupus varies greatly in severity in individuals from mild cases with minimal intervention to those with significant symptoms and potentially fatal damage occurs to vital organs, such as the lungs, heart, kidney and brain. The disease is also characterized by flares of activity interspersed with periods of improvement or remission. It is a difficult disease to diagnose as many of the symptoms are also found in other diseases
Common Symptoms Include:
- Malar "butterfly rash over the cheeks of the face (only affects about 15%)
- anemia ( may be low red or white blood cells or low platelets)
- low grade fever -over 100 degrees
- chronic fatigue
- arthritis - two or more tender, swollen joints of the extremities
- kidney damage - spilling protein, red blood cells or white blood cell casts into your urine
- pleurisy - an inflammation in the lining of your lungs which causes pain
- pericarditis - an inflammation in the lining of your heart, also very uncomfortable
- photosensitivity
- alopecia -hair loss
- Raynaud's phenomenon - an autoimmune disease affecting the circulation of blood in your fingers causing numb, purple fingers
- Brain irritation -causing seizures
- Mucous membrane disorders -ulcerations of the mouth or nose
- Antinuclear antibody -positive ANA blood test
Lupus Symptoms
The more symptoms a person has from the above list, the greater likelihood they have lupus, usually 4-7 confirm a diagnosis. There is no one specific test for lupus. The ANA blood test is usually positive about 97% of the time if you have lupus. A Very Good Rheumatologist is a must. They are specifically trained in autoimmune diseases. They will do a complete physical, a battery of blood and a urine test to help confirm the disease. You need a good working relationship with your rheumatologist, so that you are comfortable talking with them about any problems you are experiencing. Then, you will get on the right medical regimen for you.
Depression is often a problem found in lupus patients, especially when their symptoms develop slowly for years and they have no explanation or if their disease is advanced. If you are in an active disease time, more sleep us required, but it seems poor sleep quality is also a problem when you have lupus and adds to the fatigue problem. It is a "bone weary" tired that nightly sleep does not remedy. I find an afternoon nap helps me tremendously. Obviously this is not an option is you are working and you may need to find a way to have extra down time on the weekends, times outs when possible, take your lunch to work and put your feet up are just a few suggestions.
The America with Disabilities Act does insure you can request proper lighting at work, as florescent lighting is not healthy, a wrist support if you do a lot of computer work is helpful or perhaps a chair that is more comfortable to you. I would certainly suggest you check into what your company might be willing to do to accommodate your disability. Another helpful consideration is carefully prescribed exercise which will help maintain your joints and muscle tone, plus range of motion in your joints.
Lupus Affected Areas of the Body
Lupus- understanding signs, symptoms and treatment
Lupus Organization
Another problem the Lupus Organization explains is the term "lupus fog". It is almost universally known to people with lupus. The phrase reflects the difficulty that you may have in completing once-familiar tasks, such as remembering names and dates, keeping appointments, balancing your checkbook, or processing your thoughts. Properly termed "cognitive dysfunction" or "cognitive impairment," this inability to recall information can be extremely frustrating. These symptoms may come and go, but may also be continuous, making school or work difficult or even impossible in extreme cases. People with both lupus and Fibromyalgia are even more likely to experience cognitive problems".
In Conclusion
In conclusion, lupus is a complicated disease, which is why a good rheumatologist is so important. It is also important to develop a strong support group within your family and friends. Learn to live within your ability for activity, which means sometimes skipping that shopping trip, or cleaning the house perfectly. The most important thing is to find some stress relief and if you don’t take care of yourself, you sure can’t help anyone else.
The copyright to this article is owned by Pamela Oglesby. Permission to republish this article in print or online must be granted by the author in writing.
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My daughter has lupus and has had many of the problems listed. This is a good informative article.
My oldest sister (I have 4) has had Lupus for as long as I can remember. It was only in the past few months that I started getting information about it and truly educating myself. I think a lot of people, myself included, don't realize the toll Lupus puts on people. Thank you for this hub!
When I asked you what exactly lupus was I guess i should have looked at more of your hubs! here it is! :O)
Thank you Pam! Tomorrow is actually just a consult with the breast surgeon to schedule the biopsy. Everything seems to take forever. As far as my Mother she lived In AZ and I live in the Seattle area so i didnt see her as much as I would have liked to. I din't know all of her symptoms but I do know it seems as though every organ you could have removed she had removed as well as open heart surgery but I actually witnessed her talk the dr's into that one, they said she didnt need it and would be fine with a stint (spelling?) she had been there, done that and wanted a better fix she said. One day she went in for routine hernia surgery and was said to come home the next day. My brother called me from AZ and told me the nurses found my mother in her hospital room ...she had died. I still have no idea why as my brother took it upon himself to cremate her etc. It was a terrible situation, alot more to that story...
Play by play description on what we go through here with my wife's illness with Lupus. Thanks for the clear explanation
I see that most of the comments are more than a year old. Diagnosed w/ SLE about 10 years ago, it was then an minor inconvenience. Now it runs my life with potentially life-threatening problems. Donate clothes, the extra $5 bill that you might save by not going to Starbux one day; donate to the Lupus Foundation, so that there might be a cure for this horrible disease.
I need help....I am a 48 yr old who was diagnosed 15+ years ago. I had no idea at that time, how much my life would change. I was an RN who loved my job.Spent most of my life "helping others". Little did I know my dreams would be shattered...lupus would cause me to lose so much! . It wasn't long before I was unable to work because of being so sick. The stress took it's toll on my marriage and it wasn't long before I had to face the reality that I was unable to care for my own children. As the medical bills increased, so did the financial stress I eventually ended up in a homeless shelter. Now I am the one needing to reach out for help!
Hi Pam im diagnosed with mixed connective diseases,ive been confused alot fatiged ,loss of sleep ,pain all day every day for years in 2010 i learned about this.also inflammed disc. how does one cope.depressed and hospitalized in2011 of july.because i had anervous break down, the flare ups are so bad ,i stay home in bed alot need support group help me.
















breakfastpop Level 8 Commenter 2 years ago
Great advice, horrible disease. I give all my old clothes to the Lupus Foundation to help them raise money for research.