5 juin, 2005 14:33
Lupus Education Program in Dallas June 25
Lupus Now: State of the Art Approaches from the Experts
A free education program for individuals with lupus, their families and health professionals
The Lupus Foundation of America and its North Texas Chapter are pleased to announce free public and professional education programs on the "State of the Art Approaches from Lupus Experts." The programs will be held in Dallas on Saturday, June 25 at the Adolphus Hotel, 1321 Commerce Street, Dallas.
The free programs aim to educate physicians, individuals with lupus, and their families on the latest advances in the management and treatment of lupus. Come and listen to experts discuss genetics, skin disease, renal disease, and clinical challenges of lupus, including osteoporosis, atherosclerosis and pregnancy.
http://www.123enroll.com/eventinfo.asp?EventId=24128
The afternoon program from 1:00 p.m. until 4:00 p.m. is for individuals with lupus and their families. Leading lupus experts will answer your questions. Click here for the public education program faculty and agenda. Click here to register on-line for the pubic education program. (If these links do not work, copy and paste the URL addresses at the end of this message into your web browser.) To register for this program by telephone, dial 1-800-238-9620, enter PIN 7451.
A program for health professionals only will be held from 8:00 a.m. until 12:30 p.m. The target audience is specialists in nephrology, dermatology, rheumatology, immunology, and internal medicine. Click here for the health professional education program faculty and agenda. Click here to register on-line for the health professional education program. To register for this program by telephone, dial 1-800-238-9620, enter PIN 5240. Continuing Medical Education credits will be awarded for this accredited program.
The program is produced by the Lupus Foundation of America, the nations leading nonprofit voluntary health organization dedicated to finding the causes and cure for lupus. The mission of the LFA is improve the diagnosis and treatment of lupus, support individuals and families affected by the disease, increase awareness of lupus among health professionals and the public, and find the causes and cure. The LFA operates programs of research, education, and advocacy through a nationwide network of 264 chapters, branches and support groups.
Weblinks:
Patient Education Program Information and Registration:
www.123enroll.com/lupusnowpatients
Health Professional Program Information and Registration:
www.123enroll.com/lupusnowphysicians
Hotel Information:
Lupus Foundation of America website:
gigi*/Karen Please pass on to our sisters so those who live in, Texas can
make plans to attend.
