Come and join us for the 2017 Inland Empire MG Walk as we continue taking “steps” toward the ultimate finish line…a world without myasthenia gravis! Register now to join an existing team, or to start and Captain your own!
All that’s left after that is to create and customize your FREE personal fundraising page, share your connection to myasthenia gravis and start fundraising!
David Bolger was diagnosed much later in life with MG, starting his journey back in 2014 at the age of 74. It started with only the symptom of droopy eyelids which led David to get checked out by his eye doctor and, from there, was referred to an eye surgeon. Because of his age, the surgeon wanted to have the approval of his primary care doctor. It was a good thing he was checked out by his primary care physician because she became concerned, not just with his eye, but the slurred speech he had now developed as well. Her mother had MG for over 20 years, so she was very aware of the symptoms. After running some tests, she confirmed her diagnosis of myasthenia gravis and called of the eye surgery. She then proceeded to explain what MG was and what the next steps to take would be.
The diagnosis was all very new to David and his wife Esther, who immediately did all the research she could do to learn more about this disease. As they learned more about the disease and dealt with it on a daily basis, they wanted to seek out even more support, which led them to the MG Support Group in Culver City. While the group was fantastic, it was a 2 hour ride to get there and the travel just completely wiped David out. However, with the help of their support group leader, Jerry Friedman, and the staff at the MGFA, Esther was able to start a support group in her area.
Leading a support group has been only one important way the Bolgers have gotten involved in the cause. Esther has been very diligent in sending materials to the doctors in her area to make sure they are all aware of MG and what it is, and also works to make sure anyone who wants to learn more about MG has access to those resources.
The Bolgers have also been very excited to become involved in the MG Walk, getting involved with the new Inland Empire MG Walk started last year. Their oldest daughter rallied their entire family including 7 kids and 12 grandkids, and worked hard in getting the word out on social media. This year, they’re getting their efforts started even earlier and have been spreading the word to get as many people involved and to grow this Walk. The MG Walk has been a very positive experience for them both, allowing them the opportunity to meet others going through MG at various stages and the chance to support each other. It has shown them that they are on the right path in this journey and has inspired them to keep staying involved and keep growing their efforts to provide support to the MG Community.
Esther and David are very excited to see the growth of the MG Walk and the increase in awareness of MG in their community. They look forward to seeing even more people coming out to support the cause and fundraise to help provide even more resources and hope for the MG Community.
Not sure where to begin? Check out our fundraising tools to help you raise MG awareness and increase your fundraising!
On MG Walk Day, we gather to celebrate those we love who live with MG, commemorate the research we’ve helped to develop with funds raised!
Share your fundraising page and links to donate via email and on your social media accounts. If you have checks or cash funds to turn in, please let us know and we can help you add them to your fundraising page. Checks may be mailed to the address below. Please be sure you’ve written your team name in the memo field!
MG Walk Office
1707 N. Randall Rd, Suite 200
Elgin, IL 60123
If you have questions or want to know more, contact us today:
Checks should be mailed to: