January 30, 2019 | Kerry Jones
My main symptom was primarily memory loss of time and place. I still remembered people and faces, just not events and experiences.
Initially I was started on Prednisone infusions by IV. They were given daily for five days and then weekly for several weeks, then it was going to taper to every other week. However, I was finding that I felt good the day of, and a couple of days after, the infusion but was feeling really bad by the end of the week. I switched to daily pills and have been on those since. They’ve evened out the ups and downs, though I do still have some of both.
Earlier on, I would find that I’d just start crying for no apparent reason. I had frequent dizzy spells, and many emotional swings, along with several minor seizures each day. I haven’t had a seizure now for about a month and the other symptoms also come less frequently. There are still big gaps in my memory but if I work really hard, I can call up some memories that seemed to have been lost. But it’s odd. I was talking to my wife the other day about trying to remember where we lived in California. I could remember the last place we’d lived there, but none before that. But after concentrating I was able to remember the place I thought we’d lived in before that. I remembered the place alright, but we’d lived somewhere else in between the two but I have no recollection of that place!
Spending time with my Grandson at the beach is my last memory before becoming ill with Limbic Encephalitis
As I progress in my recovery, I seem to be able to remember recent stuff and some older stuff, but mostly I’m just trying to observe what is happening with my memory. Early on, I would get quite distressed when we’d go somewhere, I’d been to many times and fine I could not remember it all. Now, I’m just looking at it as a new experience. I still have dizzy spells on getting up, and I get very winded with very little effort, but do feel that I’m getting better.
My recent appointment at Mayo, in late December, was when we planned to start tapering me off the Prednisone.
It’s been a long ride, but, at least for me, I think I can see some light at the end of the tunnel, and hopefully you all will too with proper care.
International Autoimmune Encephalitis Society (IAES) is a Family/Patient centered organization that assists members from getting a diagnosis through to recovery and the many challenges experienced in their journey.
Driven by the knowledge that “Education is Power”, International Autoimmune Encephalitis Society manages an educational support group for patients diagnosed with Autoimmune Encephalitis and their loved ones, empowering them to be strong self-advocates and advocates that will lead them to best outcomes and recovery. We are the premiere organization leading in these vital roles.