Melissa Conrad Stöppler, MD
Melissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology.
William C. Shiel Jr., MD, FACP, FACR
Dr. Shiel received a Bachelor of Science degree with honors from the University of Notre Dame. There he was involved in research in radiation biology and received the Huisking Scholarship. After graduating from St. Louis University School of Medicine, he completed his Internal Medicine residency and Rheumatology fellowship at the University of California, Irvine. He is board-certified in Internal Medicine and Rheumatology.
In this Article
- Lymphedema facts
- What is lymphedema?
- What does lymphedema look like (pictures)?
- What causes lymphedema?
- What are the symptoms of lymphedema?
- How is lymphedema diagnosed?
- What are possible treatments for lymphedema?
- What are complications of lymphedema?
- Can lymphedema be prevented?
- What is the prognosis for lymphedema?
- Where can one get help and support for lymphedema?
- Find a local Internist in your town
What is the prognosis for lymphedema?
Lymphedema cannot be cured, but compression treatments and preventive measures for those at risk for secondary lymphedema can help minimize swelling and associated symptoms. As mentioned above, chronic, long-term edema that persists for many years is associated with an increased risk of developing a rare cancer, lymphangiosarcoma.
Where can one get help and support for lymphedema?
Many hospitals and treatment centers have support groups for people dealing with specific chronic conditions. Health care professionals may be able to recommend a local support group for those with lymphedema.
The National Lymphedema Network (NLN) (http://www.lymphnet.org/) is a non-profit organization founded in 1988 to provide education and guidance to lymphedema patients, health care professionals, and the general public by disseminating information on the prevention and management of primary and secondary lymphedema.
Find support and advances in treatment.