09/22/2026
MG News Forum member Ken Miller’s summer with myasthenia gravis has been full in more ways than one.
Ken lives with generalized myasthenia gravis, which has changed how summer activities are approached from day to day.
When we asked Ken for one word to describe summer with MG, the answer was simple: “‘Stable’ fortunately.”
That stability still comes with planning. Ken shared, “Every day is set with calculations on limitations for that day so I am constantly aware of my body.” Sometimes activities have to be cut short for rest, and experience has taught Ken to approach plans with more caution.
When asked what advice they would give others navigating summer with MG, Ken said: “Learning, respecting and staying within your limitations.”
Heat has also been a major factor. Ken shared, “The heat/sun definitely impacts me more than it ever had so anything outside is done early and allowing myself to take it easy is very important. The pool is a big help but the sun still ways heavy.”
But adapting to MG has not meant putting life on hold. Ken and their wife have continued traveling, spending time with family, enjoying the pool with their grandchildren, working with veterans, and fitting in cruises and a trip to the Lake of the Ozarks.
As Ken put it, “We’ve had a pretty full summer and our next trip is not until September so we’ll be enjoying our pool with our Grandchildren working with our Veterans and taking on whatever life throws our way! We had a wonderful time at the Lake of the Ozarks last month!”
One of the biggest constants through all of it has been Ken’s wife and best friend of nearly 47 years. When we asked what has helped keep that bond so strong, Ken answered: “Friendship, we are still best friends as well as husband and wife.”
Ken’s summer has been a mix of travel, family, service, rest, cooling strategies, and the daily awareness that can come with MG. Thank you, Ken, for sharing your summer with our MG News Forums community.
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