Skip to main content

Just a update on me myself and I

14.

I just want to start off by saying I feel Sam Smith is a beautiful singer and song writer, his songs resonate with so many people just like Adele's 21 album. I love listening to his songs and singing a long to them, but I will never inflect that ear pain to you my loves.

I just want to update you on things with me, what I've been up too etc. 

First of all, I have completed my first booklet to my dementia course and posted it off to my assessor, I'm just waiting to see if there are many changes I have to make to my answers. I took my time getting started on it, I think I answered 12 questions out of 29 in the first two weeks, I have four weeks to complete the first book. So on Sunday 31st of August I put my head phones on blasted music from Paramore, A Day To Remember and Alexisonfire (very different music to what you all may know me to like, but I've love that style of music since I was 15) and got the book finished :) Fingers crossed for me please lovely's. 

Last week I ordered a colouring book, I know I'm 24 and wanting to colour in but trust me on this one, the book is amazing!! It's called Secret Garden, I saw it in one of Zoella's YouTube videos and thought 'oo that looks interesting' I got all prepared for it, I bought myself some Sharpies and well, that's all I did while waiting for it to arrive BUT I love it. I would recommend NOT using Sharpies because they print onto the other side of the page so I can't colour that page in boohoo. 



That is the first one I've coloured so far, half way through, the smell of the pens is quite strong so I can't focus on it for too long. What do you think? All the pages are super detailed and really lovely pictures to be honest. 

Yesterday 3rd of September was my brother Jacks birthday, he is now 27 woo. Myself and Rob went to Flamingo Land with him and his girlfriend Emma, my niece and Emma's little boy. It was such a nice day, I'm not a ride person because I'm a pansy, I went on the carousel (which I loved) and the ferris wheel (which I had a mild panic on) I adopted the role of bag looker after, which was fine by me because I only really wanted to see the Giraffes. When we eventually went to see them I did feel slightly emotional because I just love them so much, I wanted to buy everything giraffe related in the gift shops but managed to restrain myself from doing so. There's a picture to show my excitement :)


Today I am going to the hospital to see my Neurologist again, for those who don't know, since December I have been struggling with dizziness/imbalance. When it started I was back and forth to the doctors because I felt I couldn't walk in a straight line or stand with nothing around me for me to hold onto. I'm not a person who goes to the doctors a lot, so for me to go and keep going showed those around me that something wasn't right. In around April/May time I was referred to a Neurologist who decided I needed to have an MRI on my brain and spine to see if there is any visible blockages so I had that done in June and finally today I am getting those results. I'm guessing nothing showed up because they would have called me back in sooner but my dizziness/imbalance is still there. I had a few months of it being okay, still there but not as strong unfortunately last Saturday it was full force again. I feel like it's lights that causes it because I get it the worst at work which has strong artificial lighting but I have no idea because it can happen anywhere randomly. I hope to find out something today about what it could possibly be, we shall see. 

They are the most exciting things that have happened with me in the last two weeks, how sad! (I say sarcastically but totally meaning it.)

I hope you enjoy the rest of your week and weekend :)

Much love
Beth xx

p.s if you would like to leave a comment just select the name/url option in the drop down 








Comments

Post a Comment

Popular posts from this blog

This may upset you...

50. Hello my loves. WOW we've made it to the fiftieth blog post, if you're reading this one and you've read all of the ones before, thank you for sticking with me and my public diary entries. If you are new to my posts then Hello and welcome to my life, my little world of, well, I'm not to sure...this. I'm listening and watching Sia - Elastic Heart, I absolutely love this song and I love the video! It's so incredibly powerful , I watch it without knowing what it is that is keeping me so drawn to it (maybe Shia's body...) but seriously please go and watch it, don't read the comments of the video if it's the first time you're watching it and let me know what you believe it is portraying. I won't tell you what I believe because I don't want my view to alter what you may initially feel.      I feel like it might be a good time to update you guys on my Dad. By the way, everything I write is solely my feelings and from my point of vie

In difficulty there is strength and laughter

53. Hello my loves... This may seem like a very strange time, some may think I shouldn't write at all right now but as I'm just sat here, waiting, I feel I should (plus I've been given permission from my sister Kellie and Rob) On Wednesday 4th February, which seems like a lifetime ago, I got a phone call to say things with Dad had took a turn and we all needed to get to the home as time was looking short. I can't explain the fear that was going through me. The panic was so strong I was physically shaking until i got to the home to see him.  I had no idea what to expect, what had happened or what was going to happen, I just had to go with it. I guess we all do when faced with these extremes.  I have to admit I was pretty shocked to see that once the sedation had worn off he was back to his smiley self, even dancing along to the music.  But we knew it was serious when they said he was now completely nill by mouth, no food, no liquid.  An influx of fa

Our story with MND so far..

6.  These are my feelings and my thoughts, no one else's, just mine. In June 2013 my Dad was dealt the card of Motor Neurone Disease, a horrible disease. MND attacks the central nervous system and causes muscles to weaken and waste away. People with MND have to struggle everyday with activities that wouldn't have affected them before. It can be different with each person but sadly the outcome is always the same, there are no survivors, only true fighters! There is no cure... In some cases of MND the person can also have Frontotemporal Dementia. A less common form of dementia but nevertheless devastating. My Dad also has this... I first realised that something wasn't quite right around January 2013, my dad and I were sat in a cafe and he couldn't open a folded lottery ticket my exact words to him were "can't you use for hands or something" his reply was "no, my hand has got really weak" I asked him to make a fist with his right han