Tag Archives: upset

If i die young.

Ok im not going to be depressing or dramatic here. Yes ive had some really down days… Life has been difficult but im ok. Things wont change but i have them all in my head into their little neat spaces instead of making my head muddled and a mess. 


I was asked to do another video by so many people. I didnt know where to start. I began with a song a jessie J number.
I then went away on holiday to see my best friend for a week,  I had such an amazing time. During that time though my world changed  that little bit more and epilepsy took a little bit more from me. I ended up in hospital as you know from my previous blogs and then when I came home i was again in hospital some more.
During this time I was told by drs that with the amount of seizures Im having and the amount of times im suffering from status epilepticus where I have repeated seizures without regaining consciousness and where my breathing changes and stops on occasions my future is not looking good. my future may hold brain damage and death if this continues. Luckily so far Ive escaped with only slight  blurry  left eye. I was also told my epilepsy is no longer limited to starting in my temporal and occipital lobe on the left but has now spread and is on both sides of my brain. Surgery is not a viable option as this would also cause brain damage.
Depressed, upset and at a turning part in my life I looked through some songs and found this one. (if i die young) It seemed to fit what i had just been told.
Im not being depressive about all of this but it is the harsh truth. So many people think epilepsy is just a condition where you take a pill and no more seizures …. If only it were that easy for us all.
Mothers and fathers have lost sons and daughters to epilepsy, Ive lost good friends. The truth is that epilepsy kills over 1000 people in the UK alone every year.

More awareness needs to be raised and this is my wish and goal to do so. I love life and love my friends and family who help me when im struggling. Im still the happy bubbly person I normally am… I do have my down days but most of the time im still happy and enjoying life.
This video is just to make you think a bit more about how precious life is… it is not to be taken for granted. 


I hope you like the video and it raises a few questions of your own.
Love you all guys. Please leave comments if you like. its nice to know who is reading this… I just get a counter thing telling me people are here otherwise which is a bit boring. Would be lovely to hear some of your stories too. 


Love you all and remember Just keep swimming. 




Ruling my life

I am sick and tired of people trying to rule my life. If i dont have enough issues without not being able to make any decisions without them being contested at every point.

So yes I went to the ball last night…. I felt a bit like cinderella when the beast came out at midnight ha ha (it wasn’t midnight) but you know what i mean.
I now find out that apparently mum was so cross last night cos when pauline came to the door she said “she’s fitting, she’s fitting!” mum was rushing about getting her coat and bag thinking she was coming to get me and then i was there… i wasn’t fitting i had had one fit , one seizure. i was ok and i was home. Slightly dramatic in the way pauline started her introduction had mum on even higher alert!

I was so told off last night I felt like a little child. This morning no different. I was getting more than the third degree. I have a gig to play at this afternoon (sunday) and I am going, Yes ok my tolerance without oxygen at the mo is incredibly bad, bout half our to an hour at the most but today its been basically non. Had to have oxygen in all day. Well obviously mums not happy bout me playing at a concert blowing into a flute but you know what I want to give it a go. I dont even know if i can play with oxygen but if i can without effects I will. If not its a lovely sunny day and I can sit and watch the rest of the band. Its not the end of the world. I will deal. I do not want to be cooped up in doors on this lovely day with mum moaning on about me and life and how I should be more careful.

CAREFUL ! ! well how careful can you be with epilepsy ? it is unpredictable… you never know when the next seizure will strike. The only way i can be 100% careful is if what? i stay in bed and dont bother moving? that way i wont hurt myself (oh but then again i may suffocate myself on the pillows!) there is no 100% way to be careful with epilepsy. Its unpredictable seizures that strike you down at any time.
Without putting everything in life on hold which is ridiculous and like i told her i may as well be dead anyway then …. I just need to live.

Well I tried to talk to her. after all she is my friend as well as my mum. We normally have a ok relationship and are pretty close. I started to talk to her and try and get her to see it from my point but all I got was shouting about all I am doing is thinking of myself and Im being reckless and stupid and pushing it. Im not pushing it im just trying to live while I can i said. from this i got “well you wont be living vey long at this rate… your going to kill yourself” !

Well what can you say to statements like these!.
I was really upset that she couldnt see it from my point of view.

I put across that just let me finnish what i want to say..
When you were my age you were travelling all over the UK. You were married, had a job and a life.
now look at me. My partner who I was going to spend the rest of my life with left me because epilepsy became to much trouble to understand and he was a nurse! my next partner couldnt understand I couldn’t travel all round the world cos i couldn’t afford insurance and taking all my meds means alot more preparation than oh lets go here tomorrow.
Im a fully qualified nurse who has given up her pin number because she can not pass the occupational health assessments (not to mention I had just been accepted to my dream job in nursing! )
I have been stuck at home since being taken into intensive care where I nearly died.
Ive basically lost the sight out of one eye and live in a constant un-knowing of when the next seizure will strike.
You lived your young life with nothing hanging over you. You never had to worry that your body would let you down. You never went into hospital… Ive been in and out of hospitals since I was 4 years old. You see it from a mothers view, you wont even try to see it from mine.
I do not want my life to be “Just” full of hospitals, pills, injections, oxygen and all the other medical stuff. I want to have the good bits too. I can see it from your point but you need to see it from my point.

If I die tomorrow I want to die with no regrets that I wish i’d done that or this. I want to do what I like and love while I can, when I can. I have no way of knowing what the future will bring but while I can do things I will.

Anyway I went to the concert and I managed to play with oxygen. It went really well and i enjoyed it.
When i got home though I had another argument as mum and dad started moaning a me.
I was being told how much i was hurting them – they could not even see how much they were hurting me more than they could know. I couldn’t bare no more. Im not allowed to go anywhere on my own.. haven’t since being in ITU the first time as Drs say its not safe. Despite this  I got dressed grabed my portable oxygen and ipad and went out …. Im not saying where I went cos its my place to get away. Im not normally like this I have only once done this before in the last 4 years I need to be with someone 24/7. However this really was a get out or go mad situation. I was so so upset that they would not even try to see it from my point of view. I just sat and cried for a long time. I then reached out to a really good friend. Amongst this mum text me and did in her words did say sorry. I waited for a while before I went home though… I was actually enjoying the being on my own thing. it was nice to be alone. The sun was setting and it was beautiful, still and quiet.

I came home exhausted though. I went to bed.