Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
4602 E. Grant Rd Tucson, Arizona 85712 520-622-9006 www.lupus-az.org Lupus Foundation of Southern Arizona, Inc. 2014 Annual Report Lupus Systemic Lupus Erythematosus is an autoimmune disease in which the immune system produces antibodies to cells within the body leading to widespread inflammation and tissue damage. The causes of SLE are unknown but are believed to be linked to genetic, environmental, and hormonal factors. SLE may be characterized by periods of illness and remissions. SLE has a variety of clinical manifestations and can affect joints, skin, brain, lungs, kidneys, and blood vessels. People with SLE may experience fatigue, pain or swelling in joints, skin rashes and fevers. A team approach in treating lupus is often warranted due to the number of organ systems involved. Lupus is a autoimmune disease with a wide array of clinical manifestations such as rash, photosensitivity, oral ulcers, arthritis, pleuritis, pericarditis, kidney problems, seizures and psychosis and blood cell abnormalities. Patients can have symptoms and signs of lupus along with other immune system diseases (mixed connective tissue disease.) Statistics show that systemic lupus is primarily a disease of young women during their childbearing years. However, lupus can occur from infancy to old age with peak occurrence between ages of 15 and 40; neonatal lupus occurs as a result of passively acquired auto-antibodies from a mother with lupus. According to the Center for Disease Control, lupus is three times more common in black women than in white women. It is also more common in women of Hispanic/Latina, Asian and American Indian descent. Hispanic/Latina and Black women tend to develop symptoms at an earlier age than other women. Patients with lupus have an increased frequency of related autoimmune problems such as Sjogren’s syndrome (i.e., dry eyes, dry mouth) and antiphospholipid syndrome (i.e., clotting problems, strokes, fetal loss), that require additional treatments. Accelerated atherosclerosis is a newly recognized phenomenon responsible for premature mortality. Diagnosis can be very difficult. The American College of Rheumatology (ACR) uses a standard classification requiring 4 of 11 criteria for diagnosis, although this is recognized to miss early and mild cases. Even so, there is underdiagnosis because the presenting symptoms and signs are often not specific; and over-diagnosis because doctors mistakenly use a positive blood test (present in 5% of the healthy population) by itself, to make a diagnosis. Treatment consists primarily of immunosuppressive drugs such as hydroxychloroquine (Plaquenil) and corticosteroids (prednisone). In 2011 the FDA approved the first new drug for lupus in more than 50 years—belimumab (BENLYSTA®). Since lupus is highly individualized, and no two cases are exactly alike, the treatment also varies depending on the symptoms and needs of the patient. Lupus is usually treated by a rheumatologist who specializes in treating diseases that affect the joints and muscles. Prevalence of lupus ranges as high as 1,500,000 in the United States. A recent study estimated a 2005 prevalence of 161,000 with definite SLE and 322,000 with definite or probable SLE. Among rheumatic conditions, lupus has a high mortality rate—14.5% of all rheumatic disease mortality in 1997. At the same time survival has been improving, suggesting that more or milder cases are being recognized. To address the multi-dimensional needs of people with lupus physicians and primary health professionals need to be able to recognize the disease early; the public needs to be better educated about symptoms and treatment; and funding needs to be directed for medical research on lupus. Lupus Foundation of Southern Arizona, Inc. Mission Statement The purpose of the Foundation is to: · Provide support, resources, referral and encouragement to lupus patients and families information · Promote the development and enhancement of health and social welfare services at the local level to assist individuals suffering from lupus · Promote public education to increase knowledge and understanding of the disease and its ramifications · Encourage and support research programs related to the diagnosis, treatment, cure and prevention of lupus · Promote the exchange of information among health professionals and collaborate with the professional community to improve the standards of diagnosis, care and treatment of those affected by lupus HUMAN HEALTH AND WELFARE SERVICES PROVIDED BY THE LUPUS FOUNDATION OF SOUTHERN ARIZONA, INC. COUNTIES SERVED: Cochise Graham Pima Pinal Santa Cruz PUBLIC AWARENESS & INFORMATION During 2014 the Lupus Foundation presented onsite Health Fair and Education Tables throughout the city including the University of Arizona Arthritis Living Healthy Fair, Tucson Estates Health & Education Fair, Arthritis Foundation Expo, Saddlebrook Community Health Fair and the Armory Park Health Fair. Additionally, to educate and encourage support for the work of the Foundation, Health Fairs were held for City, State and Federal Employees. Our Green Valley members benefitted by visiting our table at the Green Valley Community Center and learning about our resources. Lupus Newsletters were sent to 79 hospitals, clinics and rheumatologists. Additionally lupus information was sent to 60 public schools and public libraries in Tucson and surrounding communities. The Lupus website, www.lupus-az.org provided details about lupus and our services. Apple Annie’s Orchard in Wilcox promoted the Lupus Foundation and its mission at the Orchard as well as adopting the Foundation as one of its annual charities. The Tucson Plush Club passed out lupus information packets to its guest during a fundraiser, A Phoenix Arizona concert distributed lupus literature and donated proceeds to the Foundation as well. KGUN 9 television interviewed lupus staff on The Morning Blend promoting the Foundation’s mission and services; COMCAST, KVOA and the Journal Broadcasting Company highlighted lupus, the difficulty in diagnosis as well as the resources provided at the Foundation, for several months on television by way of videos and radio broadcasts. At the site of The 2014 Annual Lupus Walkathon held at Reid Park walkers and guests were able to ask questions about lupus and pick up information about the Foundation, lupus research and our services. In addition to television and radio, this event was promoted by the Arizona Daily Star, U of A Wildcats Newsletter, online and Facebook. PATIENT EDUCATION & SUPPORT Lupus Quarterly Newsletters Newsletter Distribution The Foundation produced and distributed Lupus News to 343 lupus patients each quarter of 2014, providing information on current research, new medications and clinical drug trials. The Lupus Annual Meeting Luncheon has continued to host guest speakers who provide information on lupus research, alternative lupus treatments, and Arizona assistance programs for lupus patients and their families. This is an opportunity for our members to ask questions about lupus and current research as well as become involved in fundraising events, and join lupus support groups During 2014, The Foundation provided Emergency Medical Funds to cover the cost of monthly medication for 1 southern Arizona lupus patient and to cover the physician visit expense for a lupus patient unable to afford the procedure. During this fiscal year, 11 patient Support Groups were held in Tucson and 8 patient Support Groups were held in the Douglas, Arizona area. Support Facilitator Helen Butler, RN arranged educational speakers including home health care, pharmacy, nutrition wellness, and Medicare representatives. The Lupus Self-Help Course material was provided for three lupus patients without cost. This year bi-lingual Support Groups were made available and our after-hours bi-lingual staff assisted 12 lupus patients. 165 lupus inquiries were made during the year and 287 lupus information packets were mailed, including packets to public schools for specific student families, and local hospitals for specific lupus patients. There were 33 lupus patients referred to physicians, and 116 lupus patients provided resource information for housing, medication, and social security disability counseling. This fiscal year, two Native American reservations were provided with lupus information for newly diagnosed patients. The Lupus website www.lupus-az.org provided basic lupus information, a current list of the Foundation’s resources and an ongoing lupus calendar of events for the community. The Foundation is grateful for the 4,012 hours of time donated by over 90 volunteers along with our volunteer Board, this fiscal year to help us meet our Mission Statement. Lupus Foundation of Southern Arizona, Inc. Fiscal Year 2014 Board Roster Board of Directors Board Officers: President Joni Broussard, Personal Trust Administration, Northern Trust Bank Vice-President Patty Powell, Occupational Therapist, Amphi School District Treasurer Jeanie Moga, Vice President & Sr. Banking Officer, Northern Trust Bank Secretary Julie Gates, Public School Teacher, Amphi School District Co-Secretary Jill Schneden, Registered Nurse, U of A Board Members: Dr. Miranda Adelman, Research Assistant Professor, Arizona Arthritis Center Lani Baker, MBA, CPA Finance Manager for Holualoa Companies Carolina Hinds, Student, Pima College Ricardo Hinds, Project Manager, Molex Inc. Carlotta Flores, Owner El Charro Restaurant Rebecca Shields, MBA, CS, Director Corporate Philanthropy, Finley Distributing Co., LLC Why A Butterfly? The butterfly has long been the symbol of lupus because in many individuals early onset lupus manifests in a facial rash that extends across the face in the shape of a butterfly. The appearance is somewhat similar to a butterfly in that the wings are covering the cheeks, and the body extends down the bridge of the nose. The butterfly rash is not a condition but rather a symptom of other underlying disease that may or may not be serious or life-threatening. www.lupus-az.org 4602 E. Grant Road Tucson, Arizona 85712 Ph. 520-622-9006 Toll-Free E-mail [email protected] 1-877-822-9006