Lupus: Support and Survival
Common Secondary Conditions in LupusThis is an over-view of some of the common conditions, which often accompany Systemic Lupus, but is by no means intended to be a complete listing of all such conditions. As SLE produces the greatest number and widest variety of symptoms found in any disease that type of listing would be near impossible to accomplish. Fibromyalgia Syndrome
Central Nervous System (CNS) Vasculitis
Menstrual Problems and Menopause
Conditions of the Eye
Cognitive Dysfunction (Brain Fog)
Fibromyalgia SyndromeFibromyalgia Syndrome, also called simply Fibromyalgia, FM, or FMS is a condition, but not a disease. FM afflicts some 6 million Americans, 90% of whom are women. About 20% of all lupus patients also have FM, and the two are sometimes confused. It has been estimated that at least 10% of patients diagnosed with Systemic Lupus actually have only Fibromyalgia. While FM can be extremely painful with debilitating fatigue, it is not life-threatening nor crippling, and does not damage organs.
There are 18 designated tender points in all four quadrants of the body (right side, left side, above the waist, below the waist), and a person must show pronounced tenderness in at least eleven of these eighteen points to be diagnosed with FM. If a patient has tender points in less than the four quadrants, they have a regional myofascial syndrome.
The cause of FM is unknown, but it is triggered by trauma, viral infection, an inflammatory disorder, or can happen as a reaction to physical or emotional stress. The most common symptoms of Fibromyalgia are joint and muscle pain throughout the body, especially in the jaw, neck, and shoulders; painful muscle cramps or spasms; muscle weakness; sleep disturbances or non-restorative sleep (waking up after 8 hours of sleep and not feeling refreshed); functional bowel symptoms such as abdominal cramping, bloating, and swelling; numbness, tingling, and burning sensations in the limbs and extremities; profound fatigue; headaches; and cognitive dysfunctions, such as memory loss, difficulty concentrating, and anxiety.
About 10% of FM patients have a positive ANA. Since these symptoms are also common to Systemic Lupus, many physicians make the mistake of taking the symptoms at face value, especially if a positive ANA is present, and diagnosing the patient with SLE without further laboratory findings to validate the diagnosis. While these symptoms in lupus patients are responsive to steroids and narcotic pain relievers, the same drugs cause these symptoms in Fibromyalgia to worsen. This is particularly a problem to patients who do actually have both, SLE and FM.
Fibromyalgia is best treated with NSAIDs (Non-Steroid Anti- Inflammatory Drugs) and muscle relaxants for pain; various types of medications that promote restful sleep; mild, non-strenuous exercises, and deep-muscle massage therapy. FM is a chronic process that worsens and lessens, but most patients respond to treatments.
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Sjogren's SyndromeSjogren's Syndrome, named after the man who discovered it, Henrik Sjogren, (pronounced show-gren) is usually thought of as the "dry-eye" syndrome. Those individuals, whose mouth and eyes are exclusively affected, are said to have "Sicca Syndrome," a milder presentation of Sjogren's.
However, Sjogren's can be much more inclusive than this. Mucous membranes throughout the body, such as eyes, ears, nose, mouth, salvitory glands, larynx, lungs, stomach, and vagina can all become extremely dry, along with the skin, hair, and nails.
Sjogren's Syndrome can cause blurred vision, ringing in the ears, crops of mouth sores, constant thirst, and bouts of laryngitis. Sjogren's can be a secondary condition to other autoimmune diseases such as SLE, or it can exist by itself.
Possibly as many as one-third of lupus patients have secondary Sjogren's Syndrome. It should be noted that most people do not experience all the above listed symptoms, but any combination of these.
Primary Sjogren's is, in itself, an autoimmune disease that can affect joints and damage organs. In severe cases, loss of vision can occur due to cornea damage, dry lungs can lead to pneumonia and lung disease, severe gastritis can result from dry stomach, pericarditis can result from inflammation in the sac surrounding the heart, and nerves may be damaged, particularly in the face. The liver, pancreas, spleen, kidneys, and lymph nodes may all be affected.
Sjogren's Syndrome is the only autoimmune disease that has a potential for malignant transformation. Up to 5% of Sjogren's patients develop a blood disorder, particularly lymphoma. It is easily confused with SLE, as the signs and symptoms are shared by both conditions. Sjogren's patients often have a positive ANA and rheumatoid factor.
Sjogren's is usually a benign process and is treated symptomatically. The problems associated with Sjogren's are highly responsive to medications and can usually be managed quite successfully.
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Raynaud's PhenomenonPrimary Raynaud's, which occurs independently from an autoimmune disorder, is called Raynaud's Disease. When it occurs as a secondary condition to an underlying disease, it is known as Raynaud's Phenomenon. However, the symptoms are identical in primary and secondary. Between 60 and 90% of those with Raynaud's are young women.
The condition is the result of small arteries, usually in the fingers and toes, going into spasms, causing the skin to become pale or a patchy red to blue. These spasms come on quickly and may last minutes to hours. Anything that stimulates the sympathetic nervous system, such as exposure to cold or intense emotion, can cause arterial spasms. Vascular migraine headaches are also associated with Raynaud's.
Symptoms include the affected area turning a patchy red and white, usually in a spotted fashion. During an episode, the individual usually experiences numbness, tingling, pins and needles, and a burning sensation.
When the episode ends, the affected skin may be pinker than usual or bluish. If exposure to cold triggered the symptoms, warming the hands or feet restores normal color and sensation. Sores sometimes develop on the affected areas and in severe cases, can cause peeling of the skin.
There are specific drugs used to treat Raynaud's disease, as well as using preventative measures, such as protecting their trunk, arms, and legs from cold and by taking mild sedatives. In the case of Raynaud's Phenomenon, the symptoms improve with the treatment of the underlying disorder.
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As you can see, the term CREST is an acronym. It is a syndrome made up of five different disorders presenting together. CREST Syndrome is a less severe form of an autoimmune disease called, Scleroderma.
CREST is named for its symptoms:
· C - Calcium deposits throughout the body;
· R - Raynaud's Phenomenon;
· E - Esophageal dysfunction;
· S - Sclerodactyly (skin damage on the fingers);
· T - Telangiectasia (spider veins).
Although this syndrome is usually less severe than Scleroderma, CREST can cause calcium bumps to form on bony areas or at the joints; severe acid reflux, heartburn, and difficulty swallowing; intestinal infections; and severe muscle and joint pain and weakness. It can also lead to high blood pressure, causing heart and respiratory failure. CREST is treated symptomatically.
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Systemic VasculitisSystemic (meaning throughout various body systems) Vasculitis (meaning inflammation of blood vessels), is not a disease, but rather a disease process that occurs in a number of autoimmune, connective tissue diseases. Vasculitis can also occur without connective tissue involvement.
Lupus is the result of the body's immune system producing too many antibodies, and these turn against the body, attacking healthy cells and resulting in inflammation. This same process occurs in vasculitis. The auto-antibodies attack blood vessels, causing inflammation that damages the vessels and the tissues they supply.
The blood vessels can become either leaky or clogged, and both conditions disrupt blood flow to nerves, organs, and other parts of the body. These affected areas can be damaged permanently.
Symptoms may result directly from the damaged blood vessels or from the damaged tissues or nerves whose blood supply is restricted. Any vessels can be affected, and symptoms depend on whether small or medium veins or large arteries are affected. It has been suggested that a large number of Lupus symptoms result from vasculitis.
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Central Nervous System (CNS) Vasculitis
Vasculitis of the CNS is an inflammation of the brain's blood vessels due to lupus activity. The most serious of the CNS syndromes associated with lupus, it was the first to be described and is one of only two CNS syndromes (the other being psychosis) that fulfill the ACR criteria for defining lupus. Vasculitis of the CNS usually occurs early in the disease course; over 80% of episodes take place within 5 years of diagnosis.
The typical patient experiences high fevers, seizures, meningitis-like stiffness of the neck, and may manifest psychotic or bizarre behavior. 10% of lupus patients develop CNS vasculitis. Untreated, their course rapidly deteriorates into stupor and ultimately coma.
CNS vasculitis is diagnosed either by a conventional angiogram, a magnetic resonance angiogram, lumbar puncture, or tests to detect high levels of antineuronal antibodies in the serum. It is treated with high doses of corticosteroids, or cytotoxic drugs, & can be treated successfully.
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Menstrual Problems and MenopauseScientists are not certain what role hormones play in Systemic Lupus, but there does seem to be an obvious correlation. Thus, the menstrual cycle can be affected in some women with SLE.
Those taking birth control pills (made up of the female hormone, estrogen), sometimes experience a decrease in disease activity, as do some women who have passed menopause. Lupus is much less common in men, yet males with lupus tend to experience more serious complications of the disease.
About 15% of women with SLE develop menorrhagia (excessive blood flow during menstrual periods) which may be due to clotting problems. Some lupus patients may also experience amenorrhea (lack of menstrual periods). Early menopause has also been noted in women with lupus.
It has been estimated that the symptoms of menopause (mood swings, hot flashes, night sweats, irregular and/or unusual periods) actually begin some 3 to 5 years before the woman is pronounced as being in the process of menopause. Each of these conditions can be a direct result of Systemic Lupus, or a side effect of steroid therapy.
All lupus pregnancies should be considered high-risk and closely monitored, yet there is no reason for a lupus patient to avoid conception, unless she has moderate to severe organ involvement.
However, for those whose organ involvement had been controlled prior to conception, an increase in organ disease occurs in only 10% who become pregnant. All women with lupus are at a higher risk of miscarriage, but especially those with the Lupus Anticoagulant Syndrome.
In 40% of lupus patients, no change in disease activity occurs during pregnancy, disease exacerbation in seen in another 40%, and improvement of symptoms occurs in only 20%.
Since the fetus produces additional cortisone, the withdrawal of this increased hormone after childbirth can cause a flare in the mother's disease. Such exacerbation is usually mild in patients who have been treated prior to and during pregnancy, but can be quite severe in those who hadn't yet been diagnosed and treated.
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Conditions of the Eye
Whether due to Lupus itself, certain lupus medications, or secondary conditions such as Sjogren's, Raynaud's, or Vasculitis, the eyes are often affected in a variety of ways.
Cataracts and Glaucoma are often seen in lupus patients, but the disease is not associated with either of these eye conditions. However, extended use of steroids, such as Prednisone, can cause Glaucoma and almost always produces cataracts.
Since lupus patients are more susceptible to infections, Conjunctivitis (more commonly known as "pink eye") commonly occurs, but is easily treated with antibiotic eye drops.
Should you ever be given antibiotic eye drops, which cause the affected eye to burn, itch, or worsen, discontinue use and contact your doctor immediately. These are indications of an allergic reaction to the particular solution, and there is more than one type of antibiotic drop available to treat eye infections.
Inflammation of the iris, known as Iritis, is a recurrent problem in about 2% of lupus patients. It has been observed in almost every autoimmune disease and can also exist by itself. It is usually managed successfully with steroid eye drops. The symptoms of iritis include hazy vision or floating black spots. Severe pain, redness in the white of the eye, and sensitivity to light are especially common.
Blood vessel disorders of the eye, called Retinal Vasculitis cause bleeding behind the eye, inadequate blood supply, and blood clots causing blockage to the vessels. These disorders lead to decreased vision and sometimes blindness. They also indicate that the person is at a high risk of other problems, such as stroke. This condition is usually a complication of the Lupus Anticoagulant Syndrome.
The decreased ability of the eyes to produce tears in persons with Sjogren's Syndrome prevents the cornea (outer covering of the eyeball) from being adequately lubricated. Left untreated, this excessive dryness results in the development of pits, leaving scarred areas on the cornea surface. This can be effectively treated with artificial tears.
Optic Neuritis, inflammation of the optic nerve, can also occur in SLE. The optic nerve is the primary nerve leading from the brain to the back of the eye, through which all sight responses are transmitted and received. This condition is not as common in lupus as it is in Multiple Sclerosis (MS). However, lupus mimics the symptoms of many other diseases, including MS.
Optic Neuritis can be painful or painless, depending on which section of the optic nerve is affected. It can cause blurred or cloudy vision or blindness, depending upon if the inflammation has actually damaged the nerve. Optic Neuritis is usually limited to one eye, but not always. The blindness can be temporary or permanent, and is treated with steroids.
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Cognitive DysfunctionKnown by lupus patients as "brain fog"'! Symptoms include confusion, profound fatigue, and difficulty in articulating thoughts, memory impairment and difficulty concentrating. Cognitive dysfunction may come and go on its own, but antimalarial drugs, tricyclic antidepressants or serotonin blockers, or DHEA may help.
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Lupus headacheCompared with the general population, lupus patients are perhaps twice as likely to suffer from migraine-like headaches. Many patients also have antiphospholipid antibodies, while others display Raynaud's phenomenon.
Lupus headache is managed much like conventional migraine, using painkillers, anti-inflammatories, vasoconstrictors, and sometimes beta-blockers, or tricyclic antidepressants. Lupus headache is different to most migraines, since patients may respond to a one week trial of 20-60 milligrams of prednisone daily, which is rarely useful to migraine sufferers.
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SeizuresSeizures can result from acute brain inflammation, scarring from prior vasculitis, acute strokes, or reactions to medications used to treat the disease, such as corticosteroids or high-dose antimalarials.
There are different forms of seizures - 'grand-mal' seizures are characterized by total body shaking, loss of consciousness, incontinence, and after seizure lethargy. Temporal lobe/partial-complex seizures are characterized by perceptual distortions, odd smells, altered emotional states, staring, and no loss of consciousness.
Electroencephalography (EEG) can be used to diagnose, CT and MRI scans are used to rule out other causes. Anticonvulsant medications are normally used to treat seizures.
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PsychosisSome lupus patients may demonstrate symptoms of psychosis. Psychosis is defined as an inability to judge reality, marked by disordered thinking and bizarre ideas, often including delusions and hallucinations. It usually results in an inability to carry out the ordinary demands of living.
About 10 to 15% of lupus patients will display acute psychosis during the course of their disease. Most psychotic episodes occur with CNS vasculitis, but others occur as a result of steroid therapy, water intoxication with low blood levels of sodium, seizures, central hyperventilation, or antimalarial therapy. It is managed with corticosteroids, and antipsychotic preparations.
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Unlike the joints, the muscles can be seriously damaged by SLE. This damage may result in muscle weakness and loss of strength unless early, appropriate treatment is given. Inflamed muscles may not only be painful, but may also be tender to the touch. Muscle weakness is the most common symptom of lupus myositis
Characteristically, the muscles of the trunk of the body are affected (i.e., neck, pelvic girdle and thighs, shoulder girdle and upper arms). Pain in the small muscles of the hand or weakness of the grip are not symptoms of SLE myositis. However, nerves as well as muscle fibers can be caught up in the inflammatory process and, occasionally, some weakness of the wrists and hands or the ankles and feet may occur as a result of nerve damage.
The diagnosis of SLE myositis is relatively straightforward. There are chemical enzymes (e.g., CPK, SGOT, SGPT, aldolase) which are normally concentrated within muscle fibers and which escape into the blood circulation when muscle fibers are being damaged by inflammation.
Thus, tests for these chemicals in the blood are abnormal in SLE myositis. These tests can also be used to determine the severity of muscle involvement: more severe myositis results in a higher level of these enzymes in the blood. Such tests are therefore useful in the diagnosis of SLE myositis, and in following the course of the disease and its response to therapy.
Just as the electrocardiogram (EKG) reflects damage to heart muscle, the electromyogram (EMG) can be used to determine the character of muscle damage in lupus myositis.
When inflammation is present, the EMG shows a characteristic pattern of electrical response. A microscopic examination of a sample of muscle tissue a biopsy) may also be taken from a painful muscle to confirm the presence of inflammation and to help identify the severity of the inflammation.
Corticosteroids (Prednisone) are necessarily prescribed for the treatment of SLE myositis. High doses (50 mg. per day or more of Prednisone or equivalent) are initially given for prompt suppression and control of the inflammation. The steroid dose is gradually reduced as the inflammation subsides, as determined by the patient's symptoms and enzyme levels in the blood.
The vast majority of people with lupus respond promptly and well to corticosteroids. It is seldom necessary to augment treatment with cytotoxic or immunosuppressive medications.
Once the acute, inflammatory phase is past, a well directed exercise program should be started to help the patient regain normal muscle strength and function.
Do Your Part to STOP THE SICKNESS!
Lupus is a disease that destroys the muscles, joints,
major organs, and the lives of millions of Americans.
So why is so little being done about it?
Maybe because most of its victims are women.
Contact the Lupus Foundation of America or the local Chapter that serves your area for more information about lupus, or the programs and services the LFA offers including support group information and physician referral.
Lupus Foundation of America., Inc.
1300 Piccard Drive, Suite 200
Rockville, MD 20850-4303
Information gathered from :
Searching for ways to deal with the depression, the frustrations, the questions about lupus, I joined a support group online. LUPIES has been a wonderful gift. I have learned more from the information I found on the support web site from other sufferers of Lupus than I did from my doctor. Thank you fellow Lupies! With a very special thank you to Deanna!
May your days be pain free!
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