Neurologists, ophthalmologists, nurses, and other allied health professionals that want to support the work of the MGA. The Committee provides knowledge, skills, credibility, and recommendations. They act as ambassadors and assist with fundraising .
Founder of the MGA
The first few years were filled with growth and excitement and little did these early MGA pioneers realize that they were laying the foundation for an association that would become an innovative health services non-profit in the greater Kansas City area that would help thousands of people living in Kansas and Missouri for over 55 years.
We serve those living with MG, their family and friends in Missouri, Kansas and Northwest Arkansas by providing services, events, and information. We are devoted to our mission to increase public awareness and provide MG-specific educational opportunities.
Please call or e-mail us at any time if you have any questions or need a a list of neurologists seeing MG patients in your area. We are here to help you at any stage of your diagnosis.
Our Board of Directors and Officers are elected each year at our Annual Meeting. Members serve a 3-year term and are expected to attend all meetings and functions of the association.
In 1962, Dr. William Wu, MGA’s first Medical Advisory Board Chair, and Joan were instrumental in establishing the first MG outpatient clinic at Menorah Medical Center to be under the direction of Dr. Dewey Ziegler. In 1964, Dr. Ronald Youmans assumed directorship and established a MGA office space at the hospital. Soon after, a MG Drug Bank through the Menorah Pharmacy was developed and made it possible for those living with MG to afford costly medications. In the 1960’s being diagnosed with Myasthenia Gravis meant that there were limited treatment options, lack of understanding, and fear. An organizational emphasis was placed on increasing public awareness and providing professional education as well as educating patients, providing support, and linking patients with MG-knowledgeable neurologists and community resources.
Staff at the MGA of the Heartland have a combined 40 years of expertise in Myasthenia Gravis and are equipped to answer questions from first diagnosis to resources of providers in the area. Staff work diligently to raise awareness, provide educational opportunities and bring to light the needs of this rare auto immune neuromuscular disease.
Medical Advisory Committee
Board of Directors
In 1954, while Joan and Rev. William Stackhouse were in West Africa, Joan was diagnosed with Myasthenia Gravis. Joan and Bill were missionaries with the United Presbyterian Church, but after Joan’s diagnosis, they returned to New York so that she could receive treatment. Just as Joan became aware of the MG Foundation of America in NYC, Bill was transferred to Kansas City where there wasn’t an MG group and the nearest MG clinic was at the Mayo Clinic in Minnesota. In 1960, Joan set her sights on forming a local association and received support from their pastor, his wife, and other parishioners of the Southridge Presbyterian Church in Mission, Kansas. Joan met Cecile Wu, who was also living with MG and motivated by their shared diagnosis, and with the cooperation of other MG patients and doctors in the community, the MGA was established. The charter meeting of the Kansas City MGA was held at Menorah Medical Center on April 9, 1961. Later that year, the United Campaign (United Way) provided the association’s first grant of $2,500 enabling them to hire the MGA’s first Executive Director.
Cecile (Franki) & Dr. William Wu