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Today is the most important day of my year, #WorldEncephalitisDay 2021. #Red4WED
Encephalitis is the rare brain disease I had age 20, which was misdiagnosed as being a mental breakdown, left to worsen for 3 months in a psychiatric ward and ultimately led to me becoming (1/9)
Encephalitis is the rare brain disease I had age 20, which was misdiagnosed as being a mental breakdown, left to worsen for 3 months in a psychiatric ward and ultimately led to me becoming (1/9)
permanently disabled, both visibly and invisibly.
It may be hard to imagine if you are a newer follower that there was a time just a few years ago that I couldn’t walk, talk, read or write – and by just looking at my pictures on Instagram, you’d probably have no idea that(2/9)
It may be hard to imagine if you are a newer follower that there was a time just a few years ago that I couldn’t walk, talk, read or write – and by just looking at my pictures on Instagram, you’d probably have no idea that(2/9)
I am living with an acquired brain injury which has completely altered the direction and path of my life. I choose to speak about Encephalitis wherever I can, because I know that despite the fact that there are hundreds of thousands of cases of the disease worldwide per year(3/9)
