Posts Tagged SUDEP
Thank You
Posted by tialys in Life in General on November 14, 2022
I just wanted to say thank you to everybody who reacted to my last post about the loss of our daughter Bryony last Christmas.
Whether you commented or didn’t have the words but let me know you’d visited with the ‘like’ button, some for the very first time, I really appreciated your kind thoughts and the fact that some of you shared some personal stories of your own with me. Most especially, I am glad to have passed on some information about SUDEP (sudden unexpected death in epilepsy) – especially to a few of you who have more cause to be aware of it – in the hope that lives will be saved in the future.
Christmas is fast approaching and, obviously, will be a very difficult time for our family. We are not going to hide from it though – we do have another daughter to think about after all. Bryony absolutely loved everything to do with Christmas and we will continue to celebrate it as I’m sure she would have wanted us to. There will of course be more tears but also some smiles and, hopefully, even a bit of laughter as we share memories of our funny, brave, loving daughter and sister.
I will hopefully return more fully to blogging in the new year but, in the meantime, I hope you will all enjoy a healthy and peaceful festive season.
If you would like more information about this little known risk associated with epilepsy you can find it here.
Slowly Resurfacing
Posted by tialys in Life in General, Uncategorized on October 19, 2022
Today is SUDEP Action Day – an annual awareness day to shine a light on SUDEP (sudden unexpected death in epilepsy) and other causes of epilepsy-related deaths.
So, hard as I’ve found it to write, it seemed like a good day to explain the reason for my prolonged absence from blogging to those of my readers who don’t know the circumstances and also show my support for the work of SUDEP in the hope it will help somebody else by acknowledging the risks of epilepsy and thus taking informed decisions in managing the condition.
Our youngest daughter – known to some of you as Miss Tialys the Younger – was due to come over last Christmas Eve with her sister to spend Christmas and New Year with us.
Her habit was to phone us every evening around 7 and, when she didn’t phone on the evening of December 23rd I thought it strange as she was excited about Christmas and I expected her to be asking what time we’d arrive to collect her the next day so, when I couldn’t get her to answer the phone, I became so worried I decided to drive over to her flat which is an hour and a half away.
When I arrived and could get no answer by knocking on the door, I let myself in with our spare key and found her collapsed on the floor where she must have been since the morning. I called the paramedics but it was too late. The police came, I gave a statement, they drove me home. She was 26.
The post mortem was inconclusive but, as there were no suspicious circumstances, an interim death certificate was issued so we could go ahead with her cremation. However, they needed to do further investigations on her brain and, after six months, we had an official cause of death which is ‘sudden unexplained death in epilepsy’ also known as SUDEP.
She was on medication after she had a seizure in 2020, while her father and I were still in France (on lockdown) and her sister had taken her to hospital in the UK where they kept her in for almost a week and prescribed the anti seizure meds on her release. So, in a way, the post mortem result was a relief because it was sort of what we anticipated and not something more sinister but also because we take comfort from thinking she wouldn’t have known much about it. However, it’s also a bit surprising because although she was on anti-seizure medication, she wasn’t what I think of as being ‘properly’ epileptic – whatever that is.
She was on the autistic spectrum and I worry that, on certain occasions where she told us she’d felt ‘weird’ or had episodes where she couldn’t speak, these might well have been petit mal seizures rather than the autistic ‘meltdowns’ we put them down to.
None of this speculation changes the fact that she has gone from our lives at the age of 26 and that we are still coming to terms with it and nothing will ever be the same again.
I registered her death with SUDEP Action and filled in their questionnaire to help with their research into this fairly uncommon cause of death and, hopefully, it will help people in the future.
I would like to start blogging again but forgive me if, although I do try to read your blogs, I don’t always feel like commenting and sometimes might just press the ‘like’ button.
The urge to sew/crochet/knit etc. has only fairly recently come back again – strangely those things were of no help at all to me during the darkest days. My only salvation was reading – I read so many books that I’ve lost count – but it was the only way I could escape and, still now, when I wake up in the night or early morning and my thoughts won’t let me rest, I reach for a book.
She hated having her photo taken as she got older but I can’t resist putting one of her on here from when she was little and didn’t care.
Bryony Kate 24th February 1995 – 23rd December 2021
Please don’t feel as if you have to comment – I know it’s difficult to know what to say. A ‘like’ will do and will let me know you’ve read it.