James W. Dooner, M.D. was on hand to discuss the latest in research and treatment options for macular degeneration. The audience was fully engaged, asking informed and thoughtful questions. Doing his best David Letterman impression, Mark Levitan, M.D. presented "Answers to the Top 10 Questions about Macular Degeneration." Levitan went through the list, covering some of the basics and the questions that most often arise about the disease.
Kelly Teese, COT took the stage to present "Answers to the Top Questions about What Low Vision Services Can Do for People with Macular Degeneration." Levitan returned to the stage and joined Teese for an informative and lively audience Q&A session.
Also on hand was Mary Betty Roeder to talk about how to live well with macular degeneration. She opened up with the audience, sharing her own experiences with macular degeneration, how it has affected her life and how she has learned to cope and thrive with it.
Back to topThe program was introduced by Lea S. Bramnick, Executive Director of MVRF, which is based in West Conshohocken, outside of Philadelphia, Pennsylvania. Ms. Bramnick explained that the mission of MVRF is to fund research into the cause, prevention, treatment, and ultimately the cure for macular degeneration is aided by the fact that one hundred percent of all dollars raised go toward this goal, as the organization is entirely underwritten for all administrative expenses.
After Ms. Bramnick, Dr. C. Armitage Harper talked about the newest research and treatments for macular degeneration. Then Dr. Jack W. Pierce addressed the possibility of a hereditary link to this disease, which was of particular interest to the audience.
People with advanced macular degeneration often have to be accompanied by a helper when they travel, because they are unable to drive when their vision is severely impaired. Often, these companions are their adult children, and both the patient and the caregiver are keenly interested in the genetic links and the possibilities for prevention.
Dr. Pierce addressed this concern for family members, and talked about the need to share tips for prevention with children and grandchildren. He said that people have to know how to protect their eyes from all types of harm, and that everyone should always wear sunglasses and hats with wide brims. He also said that healthy eating habits and not smoking can contribute to the prevention of macular degeneration.
Back to topThe first speaker, Lea S. Bramnick, Executive Director of MVRF, talked about the mission of the organization, which is to raise funds for research and to provide support services to people who suffer from macular degeneration. Ms. Bramnick explained that 100 percent of all administrative costs of the foundation are underwritten, enabling them to donate every single cent raised to research and support.
Dr. Jack W. Pierce provided an overview of the latest treatment and research on macular degeneration. Dr. C. Armitage Harper gave a very interesting talk on how diet and nutrition may affect macular degeneration.
Mary Betty Roeder, a speaker for MVRF, discussed how her own life has been altered by macular degeneration, and how important support groups have been for her. Ms. Roeder is funny and fearless, and her positive outlook on life, and macular degeneration, is infectious. As the program concluded after her talk, the audience was laughing, smiling and clearly feeling life can be good, even if one has macular degeneration.
Back to topDr. Coleman Driver Jr., started the session by updating the eager crowd on the history of macular degeneration treatments and the newest innovations in research and treatment.
Next the group was treated to a lively presentation by Mary Betty Roeder, a patient who has long suffered from macular degeneration. Ms. Roeder’s positive outlook and amazing resiliency was evident in the way she discussed her methods for coping with her disease, sharing many tips that will make a big difference in the lives of the people who came to hear her speak.
Lea S. Bramnick, executive director of the Macula Vision Research Foundation spoke about the work the foundation is doing to raise money to fund research into further prevention, treatment, and ultimately, a cure.
Finally, Kelly Teese, a caregiver for a patient with macular degeneration, offered a compassionate talk about how to provide assistance in order to help someone maintain and maximize their independence and dignity, explaining that offering too much help in a way that is not welcomed can be actually be damaging, and may unwittingly strip away any remaining independence. Ms. Teese gave the audience a list of positive and pro-active ways to live with macular degeneration.
The Macula Vision Research Foundation’s mission is to find the cause, prevention, treatment and cure for macula vision diseases with the goal of saving sight and providing public education about the condition. One hundred percent of every dollar raised goes directly to the funding of research, as all of the administrative costs of the organization are underwritten. The organization can be reached, toll-free, at 1-866-4-macula. (866-462-2852.)
The Macula Vision Research Foundation Support Group’s mission is to enhance the quality of life of the ever-growing population who are affected by or concerned with macular degeneration through public education. The 866-4-macula hotline will respond to the needs of patients, their families and loved ones, through question and answer sessions following all public education programs and providing printed and taped literature.
Back to topMacular degeneration causes deterioration of the macula, resulting in a loss of sharp, central vision. An impaired macula prevents a person from clearly seeing objects straight ahead, such as words on a page; television or the faces of loved ones. At its worst, sufferers of macular degeneration have only very limited peripheral vision.
Receiving the Diagnosis
C. Armitage Harper, III, M.D. of Austin Retina Associates discussed:
Mary Betty Roeder, an 81 year-old legally blind macular degeneration patient from West Chester, Pennsylvania discussed:
Lea S. Bramnick, Executive Director, Macula Vision Research Foundation discussed the Foundation and its history and commitment to research and support for those with macular degeneration.
A lively and informative question and answer session followed each speaker’s presentation.
Age-related Macular degeneration“There is a critical need for education and information among patients with macular degeneration and their families,” said Armitage Harper, III, M.D.
Macular degenerationAn 89-year-old patient of Austin Retina Associates was diagnosed ten years ago. He cannot read or drive, and his computer is outfitted with a voice reader so he can check his email. He relies heavily on his wife, and she, too was recently diagnosed with the disease in one eye. “I think the disease should be publicized,” he said. “I think the support group will be helpful as there is great benefit in sharing little pointers for coping with other people facing the same fate.”
Macula Vision Research Foundation“I was shocked at how little people knew about this issue, which is becoming an epidemic with the growth of the aging population,” said Herbert Lotman, Founder, Macula Vision Research Foundation. “This organization was founded to find the cure for this disease and to save the sight of the millions affected. This can and will be done, but only through fundraising support for critical research, some of which is discussed at these seminars. We are also aware of the great need for support for patients with macular degeneration and their families.”
Back to topWould you like to volunteer?
Do you need more information?
Macula Vision Research Foundation SupportSight
Five Tower Bridge
300 Barr Harbor Drive, Suite 600
West Conshohocken, PA 19428-2984
Please call Lea Bramnick
Toll free 1-866-462-2852
1-866-4-macula
Email: lea@mvrf.org
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