I came across this article on the brain and spine foundation Facebook page and thought I’d share it. I’m over 5 years past my BI and one of the biggest things I still deal with on a daily basis is other people’s lack of knowledge and understanding. I look fine, therefore to them, I am....
If anyone is finding it difficult to communicate their difficulties, showing this article might help. And also for those who know someone with a BI.
Thanks for the link. I have downloaded the info to use when I finally get my esa assessment. Hopefully it will help them understand a little better......You never know it may enlighten them.
Thankyou for posting this article. So helpful and accurate. It states so many issues my son struggles with that others, including me at times, don't understand because he looks 'fine.'
It could even be my son talking as we've had these discussions often.
I'm going to print it out as a reminder to me, and to raise awareness with others. It may be helpful for his children too.
I’m so glad it has helped, when I read it, it was like me talking and trying to explain myself to others, especially in the early years after my brain haemorrhage. I wish I’d had this to show my friends, family and my boyfriend, as it’s so difficult and exhausting to explain and put into words why and how I feel.
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