I just wanted somebody to share this with cause I'm so excited. Six months post hospitalization I played my first field hockey game since August last year (2020) today! I'm so happy cause I've played it most of my life and love it I was worried and getting prepared for the fact I wouldn't play again (I'm also 30 years old too lol) but I played for 40 mins, substituting in between, but I felt like I was on a high! Although I'm still worried that I might drop in the middle of the game with a seizure :/
Leading up to the game, 2 months prior, I began walking and then breaking into short runs and also small HIIT sessions at home, but even still I didn't think I'd be able to play. I still struggle with fatigue and I'm sure I will feel it in the next couple of days.
I just wanted to share that milestone and hope it gives people hope too 💕
I would love to hear if you have similar stories of being able to return to sport or other activities post discharge/recovery?
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Elle2090
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That's great, we're all in that situation where just getting back to our 'normal' is almost an impossible dream. Well done and keep pushing. Best Wishes G2
Wow! You should feel so proud of yourself for getting back into exercise and hockey. It's all steps in the right direction. About a year after my e, I was also so chuffed with myself when I started going to a keep fit/yoga group. It's like a breath of fresh air.
I played a full game last Sunday, scored 2 goals and made players player for the match which I'm super stoked about. However the week after I was severely fatigued which didn't happen the last time I played 😶
Aww that's awesome, thank you for sharing - I can imagine that being an emotional game for you! I hope you have many more hockey games ahead of you 😀
I am recovering from a relapse last year which was finally treated with aggressive therapy just a couple months ago. My recent milestone is getting some psychometric testing done, which was compared against testing I had gotten last year. Last year's was from when I "claimed" to be relapsing, but certain doctors wouldn't believe me and disputed my original encephalitis diagnosis because the overall test conclusion was that I was still performing cognitively in the normal range. But I felt debilitated and had to quit work!
The recent testing showed MASSIVE improvement, and I feel more and more like myself again - it was very validating to receive, especially after the gaslighting that I underwent through much of my health journey.
My primary symptom of AE has been immense cognitive dysfunction, and over the span of a couple weeks I felt the onset of what I imagine a rapid onset dementia feels like. I used to write a lot for work, and composing sentences became a massive undertaking. Thanks for the support!
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