Friday, September 2, 2016
10 Early Signs of Lupus
What Is Lupus?
Lupus is an autoimmune disease that causes swelling (inflammation) and a wide variety of symptoms. Lupus affects each individual uniquely. Some people have only a few mild symptoms and others have many, more severe symptoms.
Symptoms usually start in early adulthood, anywhere from the teen years to the 30s. As with some other autoimmune diseases, people with lupus generally experience flare-ups of symptoms followed by periods of remission. That’s why early signs are easy to dismiss.
Because early symptoms are similar to those of so many other conditions, having them doesn’t necessarily mean you have lupus.
Fatigue
whopping 90 percent of people with lupus experience some level of fatigue, according to the Johns Hopkins Lupus Center. An afternoon nap does the trick for some people, but sleeping too much during the day can lead to insomnia at night. It may be hard to do, but if you can remain active and stick to a daily routine, you may be able to keep your energy levels up.
you are living with debilitating fatigue, speak to your doctor. Some causes of fatigue can be successfully treated.
Unexplained Fever
One of the early signs of lupus is a low-grade fever for no apparent reason. Because it may hover somewhere between 98.5 and 101 degrees Fahrenheit, you won’t necessarily think to see a doctor. People with lupus may experience this type of fever in an on-again, off-again fashion. Low-grade fever could be a sign of inflammation, infection, or imminent flare-up. If you have recurrent, low-grade fevers, make an appointment to see your doctor.
Hair Loss
Thinning hair is often one of the first signs of lupus. Hair loss is the result of inflammation of the skin and scalp. Some people with lupus lose hair by the clump, but more often, hair thins out slowly. Some people also have thinning of the beard, eyebrows, eyelashes, and other body hair. Lupus can cause hair to feel brittle, break easily, and look a bit ragged, earning it the name “lupus hair.”
Lupus treatment usually results in renewed hair growth. However, if you develop lesions on your scalp, hair loss in those areas may be permanent.
Skin Rash or Lesions
One of the most visible signs of lupus is the butterfly-shaped rash that appears over the bridge of the nose and both cheeks. About 50 percent of people with lupus have this rash, according to the Johns Hopkins Lupus Center. The rash can occur suddenly or appear after exposure to sunlight. Sometimes the rash appears just before a flare-up. Lupus can also cause non-itchy lesions in other areas of the body. Rarely, lupus can cause hives. Many lupus patients are sensitive to the sun, or even to artificial lighting. Some experience discoloration in the fingers and toes.
Pulmonary Issues
Inflammation of the pulmonary system is another possible marker of lupus. Not only can the lungs themselves become inflamed, but the swelling can also extend to lung blood vessels. Even the diaphragm may be affected. These can all lead to chest pain when you try to breathe in, a condition often referred to as pleuritic chest pain.
Over time, breathing issues from lupus can literally shrink lung size. Also called vanishing (or shrinking) lung syndrome, this condition is characterized by ongoing chest pain and shortness of breath. The diaphragmatic muscles are so weak that they appear to move up in CAT scan imagery, according to the Lupus Foundation of America.
Kidney Inflammation
People with lupus can develop a kidney inflammation called nephritis. Inflammation makes it harder for the kidneys to filter toxins and waste from the blood. According to the Lupus Foundation of America, nephritis usually begins within five years of the start of lupus.
Symptoms include swelling in the lower legs and feet, and high blood pressure. You may notice blood in your urine, or have to go more frequently at night. Also, you may have a pain in your side and your urine may be a bit darker than usual. Early signs may go unnoticed. Once diagnosed, monitoring of kidney function is recommended. Untreated lupus nephritis can lead to end-stage renal disease (ESRD).
Painful, Swollen Joints
Inflammation can cause pain, stiffness, and visible swelling in your joints, particularly in the morning. It may be mild at first, gradually becoming more obvious. Like other symptoms of lupus, joint problems can come and go.
over-the-counter pain medications don’t help, see your healthcare professional. There may be better treatment options, but your doctor must determine if your joint problems are caused by lupus or another condition, such as arthritis.
Gastrointestinal Problems
Some people with lupus experience occasional heartburn, acid indigestion, or other gastrointestinal problems. Mild symptoms can be successfully treated with over-the-counter antacids. If you have frequent bouts of acid indigestion or heartburn, try cutting down on the size of your meals. Avoid beverages containing caffeine. Don’t lie down right after a meal. If symptoms continue, see your doctor so other conditions can be ruled out.
Thyroid Problems
t’s not uncommon for people with lupus to develop autoimmune thyroid disease. The thyroid helps control your body’s metabolism. A poorly functioning thyroid can affect vital organs like your brain, heart, kidneys, and liver. It can result in weight gain or weight loss. Other symptoms include dry skin and hair, as well as moodiness.
An underactive thyroid is known as hypothyroidism and an overactive one is called hyperthyroidism. Various treatments to get your metabolism back on track are available.
Dry Mouth, Dry Eyes
If you have lupus, you may have dry mouth. Your eyes may feel gritty and dry, too. That’s because some lupus patients develop Sjogren’s syndrome, another autoimmune disorder. Sjogren’s syndrome causes malfunctioning of the glands responsible for tears and saliva. In some cases, women with lupus may also experience dryne
Your doctor can prescribe medications that help increase tear and saliva production.
Other Symptoms
The list of potential symptoms of lupus is lengthy. Other symptoms include muscle pain, chest pain, osteoporosis, and depression. Rare symptoms include anemia, dizziness, and seizures.
Fortunately, not everyone gets every symptom. While new symptoms can appear on the scene, old ones often disappear.
Saturday, July 9, 2016
Living With Lupus: Part 1 By Michaela
A LIVELY GURL
Living & Loving Life
Living With Lupus: Part 1
Hello, its been a couple of days since I have posted. Not to make excuses or anything but I haven’t been feeling all that great. I have said before that I want this to be a real experience with you guys and that this is my life blog. With that being said, Tuesday I went for another Benlysta infusion(that was my fourth infusion) for my Lupus and everything went pretty good for the most part but I did experience some of the side effects the rest of the say and most of the night. I was very sleepy because of all the before meds that they gave me to prevent allergic reactions and I had some nausea and a headache the rest of the day. That night, my headache got worse and turned into a migraine and 1:30 in the morning. Along with that my nausea returned. So I had a pretty hard night and to make things worse I had to get up early the next day and go to work after not getting much sleep.
Overall I do think this drug is helping control the Lupus and I have been feeling better the last couple of weeks. In august I will go see my doctor and will get to evaluate how much progress I have made in the last couple of months.
On an even more positive note I received my debit card from the Benlysta company to help pay for the treatment because believe me they are not CHEAP! I was so happy to hear that we qualified for the financial assistance program that the company offers. If any of you are currently on Benlysta or have been of the drug previously, feel free to leave your comments below on how it affected you. Also if any of you would like some more info on the drug I will add a link to their website you can check it out. This is not a sponosered post in any way. I am just writing about what i am currently going through because this is part of my life and i want this blog to be open to you guys and make you feel like you really know me. Anyways thats my update on my Lupus. Let me know what you guys think about these kind of posts or leave comments below about hard times you are going through.
Talk to you guys soon
Her blog is
https://mcbeautymatters.com/about-me/
Monday, June 13, 2016
Arachnoiditis Often Misdiagnosed as Chronic Back Pain
/ DR. MUHAMMAD MIRZA
An arachnoid is a membrane that covers and helps protect the nerves of the spinal cord. When these membranes becomes inflamed it can lead to pain, burning, tingling, and even neurological problems. Long-term sufferers experience bowel dysfunction, autoimmune disorders, and even lower-extremity paralysis. Until now, there have been no common symptoms used to diagnose this condition. Clinicians did know that it usually affects the nerves of the legs and back. But now a new report finds that many of those suffering from arachnoiditis are often misdiagnosed with mere chronic back pain.
Those who have leg tremors or experience intense pain after standing for too long are now thought to have this condition. Forest Tennant, MD was the lead author in this study. He is a pain specialist from the Veract Intractable Pain Clinic in West Covina, Calif. Dr. Tennant said that those patients who come in complaining of severe back pain, and have an inability to stand for long periods without having to sit or lie on the floor, could have arachnoiditis.
Tennant conducted this study to help better understand and identify the symptoms of this worrisome condition. He recruited 26 patients who were diagnosed with the spinal cord disease via an MRI. Next, he examined what specific symptoms they reported. Patients all talked about tremors in the legs, and having to sit or lie down after standing for too long. Most patients also had difficulty defecating and urinating, felt increased episodes of intense heat and sweating, and occasionally experienced blurred vision. Never before has consistent symptoms for arachnoiditis been isolated like this.
There are many causes to the condition including compressed nerves in the spine, back injury, infection, exposure to certain chemicals, and more. Researchers say though uncommon, the condition very often goes undiagnosed. Spinal manipulations, epidurals, and spinal taps have increased over the last decade, and Dr. Tennant wonders if these are contributing to the increase in arachnoiditis cases. If you suffer from chronic back pain be sure to visit a doctor or specialist. You never know what may be causing it, how serious it is, and to what extent you are in need of medical intervention.
Sunday, May 15, 2016
Suffering the Silence
Hey lupies,
Be sure to check out this awesome video of two young girls, best friends, who both suffer from chronic illnesses. Ally who battles Lyme disease and Erika who battles Lupus.
See how they’ve started a movement and have inspired millions of others suffering in silence to speak up and speak out!
Thursday, May 5, 2016
Butterflies of Hope Spreading Lupus Awareness One Butterfly at a time Let this butterfly flutter all over cyberspace! May 5 Lupus Fact
Lupus can cause inflammation of your heart muscle, your arteries or heart membrane (pericarditis). The risk of cardiovascular disease and heart attacks increases greatly as well. Heart disease is now a leading cause of death among people with lupus. Blood tests, chest X-rays, an electrocardiogram (EKG), or an echocardiogram may be used to find out if you have a heart condition caused by lupus.
This is your fifth butterfly of hope.
We need awareness and a cure!
Encourage everyone you know to let it FLY!
Labels:
butterfly,
heart,
LUPUS,
red heart,
rid butterfly
Thursday, April 21, 2016
My Story: “I Won’t Let Lupus Beat Me” By BlackDoctor

Nakita is a Lupus Butterfly. She wears her purple colors loud and proud with a mission to inspire other women. And when she met fellow lupus sufferer Jakita, she knew she was someone special. Jokiva is the founder of the popular Facebook group; “The Real Housewives of Lupus,” a group for women with Lupus and a platform to network, vent and motivate each other to fight.
Here, Nakita speaks with Jokiva one on one about what living with and fighting lupus is all about:
Nakita: When were you diagnosed with Lupus?
Jokiva: I was diagnosed with lupus at the age of 18. I had a rash that looked like eczema and they started me on skin cream but the rash became worse and then I started to experience joint pain and they sent me to a rheumatologist where I was then told I have lupus.
What’s the biggest challenge you’ve faced since being diagnosed?
The biggest change I’ve had in my life since finding out I have lupus is how I live my life. I barely go out. I currently do not work or go to school because my condition is not so good right now and it makes me depressed at times because I want a normal life.
I used to hate to go in public because people would often look at me as if I was contagious and that was not the case at all. They did not understand that they were more of a harm to me then I were to them. It’s kind of hard to go out in society and want to be accepted for who you are and what you’re going through. People don’t understand unless you educate them about your condition because everyone’s lupus symptoms are not the same. I’ve met wonderful people whose condition is way worse than mine, and it hurts my soul that they have no real support team.
MUST READ: Singer SEAL Tells About The Lupus Marks On His Face
Describe your daily routine.
Every day I get up around 8 in the morning and eat something real light on my stomach. But I don’t have a day-to-day regiment because I never know how my body will react that day. Sometimes I wake up to vomiting or in pain to where my day will not go as planned. It’s very stressful to plan things with friends and family and all because I may become sick.
I always tell people who are not aware of what I go through, that lupus is not something I could just hang in my closet and go to it when I want. I have no choice but to accept my condition which I have. I take my meds…
Saturday, April 9, 2016
Subscribe to:
Posts (Atom)




