Syringomyelia Saturdays

Syringomyelia Saturdays is a new series of posts that I’m planning to put together that will, obviously, be all about syringomyelia. This short series of posts will probably be fortnightly & will included facts about syringomyelia, its charity The Ann Conroy Trust, as well as some stories written by people with syringomyelia. My story has been active on my blog for some time but if you haven’t read it yet you can find it here:

My Neurological Fight

2 thoughts on “

  1. I had not heard of Syringomyelia before this post and having read your discovery, I am just so sorry that no one took you seriously for so long. I’m glad you know have a diagnosis and I think it is great that you’re using your blog to make the condition more known. This is incredible. I hope that you are doing well 🙂

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    • Thank you so much for taking the time to read about it, especially as you’d never heard of it before. Unfortunately the NHS is so stretched now that they’re not able to take everyone seriously & because of my gender & age I ended up being on of the people who wasn’t believed! I’m unfortunately one of many people that get treated that way; I’m hearing of it more & more now. Thanks again for taking the time to read my post, it means a lot to me!

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