Lupus Research Institute Is The Only Nonprofit Organization

     In conclusion Lupus is definitely a very serious disease that we must learn more about. My great aunt had Lupus for over ten years and during that time suffered in ways no person should have to. She would fall down constantly and break bones. Near the end of her life, she would break bones doing stuff as simple as getting out of bed.

As a group, we have close personal connections to people that suffer from this disease. Our efforts are to raise awareness with students of the symptoms because people who suffer with lupus are among us every day and we cannot comprehend the struggle that they are going through. When creating the pamphlets that we will use to educate the masses, we will include stories of people who suffer from this disease. By including the personal testimonies it will allow students to understand how lupus affects the victim’s everyday life. Once students understand how painful it to live with this disease, they will be aware of the symptoms and be able to educate others. Grasping what people with this disease go through and what they suffer from, has motivated our group to inform others of how important knowing the symptoms of lupus and how important the quest for a cure is. The reasoning is that this is a genetic disease that is affecting 1.5 million Americans and a total of 5 million throughout the world, and there has yet to be a cure for this disease, just treatments to help the sufferers through their

Lupus is a chronic inflammatory disease of unknown cause that can affect virtually any part of the body. The medical term for Lupus is Systemic Lupus Erythematosus or better known as SLE. With Lupus there is a malfunction in some of the cells of the immune system. "In Lupus, the body overreacts to an unknown stimulus and makes to many antibodies, or proteins directed against body tissue. Thus, Lupus is called an autoimmune disease. ”#

If a person has lupus there are places to get help. The Lupus Foundation of America provides a lot of help for lupus’ patients. For help you can write to them at: Lupus Foundation of America, 1300 Piccard Drive, Suite 200, Rockville, MD 20850.

The foundation give hope to people that is dealing with Lupus. The website gives a person an idea of what is Lupus and the types of Lupus. It also gives different pages to look at and learn and better understand the disease. The website is very helpful for a person that feels like they have these symptoms. The information that is giving in this website is very credibility and very useful.

Juvenile lupus is a “disease in which the immune system is overactive and does not function properly” (College of Rheumatology). As with many autoimmune conditions, the immune system attacks healthy tissues. In the case of juvenile lupus the immune system attacks different organs in the body, which results in painful inflammation in the child (College of Rheumatology). There are multiple possible factors included in the cause of juvenile lupus, like hormones and the environment, but because the cause of lupus is still unknown, no one really knows how to prevent it from happening in children (College of Rheumatology). There is no cure for lupus, but there are many successful treatments to help children and teens with juvenile lupus (College of Rheumatology).

Our staffs consist of Grace, a marketing specialist, Levi a writer/editor, Lakysha, a staff assistant and her husband who is a photographer. And we have Alexis as director of external affairs, and also the stakeholders.

Approximately 1.5 million americans (5 million worldwide) live with lupus, but lupus is more common in women of African American and Native American than Caucasian women. More than 16,000 people are diagnosed with lupus each year. Everyone can get lupus but it’s mostly common in women and the specific type of women is African American women. Lupus is a systemic autoimmune disease driven by the inflammation in the immune system. Women of color are 2 to 3 times more likely to develop lupus than a Caucasian women. 90 percent of the people diagnosed with lupus are young women. Black women are diagnosed at much higher rates and are more likely to experience complications from the disease. There should me more research done, they should spend more

We are completely aware about certain diseases such as Cancer and Diabetes but yet we rarely see any type of public service announcement providing information about lupus. I am interested in finding out more information about lupus dealing with testing, treatment and pain management so then I can educate people about it.

Lupus can lay in remission making all symptoms improve and thus, making the patient feel better but can also have fares-ups that can be chronic which create symptoms that can last several weeks and often for many years causing the individual it affects to feel

A butterfly to many individuals may speak of love, trust, or opportunity yet to some a butterfly could speak of trouble, pain, and vacancy. The butterfly, now attached to a sickening infection, has turned into the image of a rising disease known as Lupus. For many the fight to cure Lupus has taken a major role in their lives.

Systemic Lupus Erythematosus is an autoimmune disease within the appearance of autoantibodies that fights against nuclear antigens within the body of a person who is living with SLE and the involvement of their organ systems, including the kidneys. The rigorous events that cause an onset of medical signs of SLE are not yet well understood. However, the researcher are usingnumerous mouse strains spontaneous and inducible lupus to find a cure because as of now there still is no cure for lupus.

Lupus is known as “the cruel mystery” in the world of disease/medicine. 1.5 million Americans are currently diagnosed with Lupus, with the number possibly being a lot higher since it is one of the most difficult diseases to diagnose in the WORLD (5 Million some form of Lupus)

Most lupus patients are followed very closely by many different types of physicians and specialist due to the multisystem organ involvement. These doctors may include but are not limited to Rheumatologist who specializes in diseases of the joints; there are also Nephrologists the kidney doctor, the Optometrist doctor for the eyes, the Neurologist for the brain and central nervous system, the Cardiologist for the heart and the Primary Care Physician. All of these doctors work together to manage S.L.E. It literally takes a team to help the patient manage and cope with the changes someone with lupus will undergo throughout the entire disease process.

Seems Lupus is getting disobedient ... It’s time to teach it some discipline. But, before that you have to bring it in your life.