Delayed memory response
Hi, firstly I am very grateful to be a part of the MG support group. Having others share their experiences has made me feel a whole lot better about my diagnosis. I'm understanding a lot more about MG and how it affects individuals. I have had delayed memory response for some years now, and since my diagnosis 12 months ago and starting on medication I'm noticing improvement. When in conversation I used to stop mid sentence, not really knowing where I was going with it. Totally forgetting what I was thinking. My friends now know me with this condition and I'm getting better, if I'm given a minute or two , to regain my train of thought. It's very frustrating and embarrassing but I feel better at least knowing why I'm a bit of a foggy brain at times. I'm worse when tired or stressed 🤔. Jules
Thank you for sharing your experience with the group. It’s inspiring to hear how you’ve found some comfort and understanding through your diagnosis and the support of others. It’s great to know that you’ve noticed improvements since starting your treatment. I truly believe that acknowledging and accepting change and obstacles is a significant step toward feeling more in control.
Jodi, Team Member
