Thursday 21st March 2019

I got a surprise today, not one of those awesome surprises sadly but I could really use one of them right now. Okay I got sidetracked sorry about that but what happened was the receptionist from my doctor's surgery called me saying that the hospital wanted me to go and have blood tests done today. Now if you are someone who uses the health care system a lot you know that things like that very rarely happen so I made an appointment for later that afternoon. At the moment I still need to get my mum to drive me places because I haven't yet overcome my anxiety enough to start driving again yet but I am determined to overcome my anxiety and be able to drive myself places whenever I want.

I went in and got my bloods done by the phlebotomist today which was good because normally getting blood out of me with the first poke is hard to do because my veins are so bad but she managed with no bother at all. I expected them to do all the normal bloods that I get done but they didn't which I found strange. When I mean normal bloods for me I get my kidneys checked because my potassium can be low at some times, I get a liver function test to keep an eye on my struggling liver, I get a CRP to check my inflammation levels as I have an chronic illness that causes inflammation in my body and the final thing that gets checked is a full blood count which checks a number of things in my body but all the surgeon wanted is a kidney function and full blood count for some reason.

There was something that I forgot to include in my last entry and that was I can't go down to Essex and visit my friend for her birthday which has really upset me because I promised her that I would go down and stay for a week. I feel so terrible letting my best friend down who is like a sister to me but because she is so awesome she understood why I couldn't come. Deep down I know myself that travelling down is not a good idea, it took me 4 hours to get ready for my hospital appointment. I had a massive 5 day bleed from the Thursday to the Monday and it took a major toll on my body. the blood lost caused me to feel dizzy, I was feeling cold, my normal heart rate is around the 60's but when I was getting ready for the hospital yesterday it was up at a 120, I was having a hard time breathing and was feeling more fatigued then normal. As much as I really want to go it's just not safe for me to do so, I just wish my heart and head would agree but my heart says I should go and my head doesn't. I know I will get to visit her one day I just have to be patient.

Well that's it for today's post, I hope you enjoyed reading the post. I am already working on a draft for my next post so everything being well you should be able to read it by the end of this week but until next time................

Keep strong

and 

Keep fighting

💓💙💚💛💜 

previous post - Wednesday 20th March

next post - Tuesday 26th March 

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Groups I have set up for my chronically ill family
The IBD family facebook group
Spoonie bookworms goodreads group
Spoonie warrior gamers steam group
Chronically ill and disabled equestrian's facebook group

Wednesday 20th March 2019

So today was the important surgical appointment. I don't know what happened but the anxiety that I have been having about this appointment completely disappeared, I don't know how it happened but it did which was amazing. It was a good thing my anxiety was gone because the doctor was running over an hour late and I think if my anxiety had been as bad as it normally had been I would have walked out of that clinic.

So after an hour of waiting I finally got seen by the consultant. I have met most of the surgical consultants at my hospital but not this one, she seems really nice though and reminds me of the surgeon that did my previous operations so that's good. The one thing that sucked about this appointment is I had to wait over an hour for 5 minutes with her. To be honest there really isn't much she can do apart from look at it as there is so much over granulation tissue now that it's covered the actually wound opening, even if she could see the opening she can't see what's going on in the inside and the number 1 suspect in what caused this  wound thing is an abscess so she really needs to see whats going on in the inside.

Due to not being not being able to see what's going on the surgeon who I am going to name Miss S has decided the 1st thing that needs to be done is a pelvic MRI and once they get the results they will decide if a small bowel study MRI is required. I really hope that I don't need one of those because the Klean prep that they give you makes me really, really, really unwell and by that I mean violently sick and poop for Scotland because the prep is actually a laxative. After the MRI is done Miss S will be doing surgery to clean up the wound so the healing process will begin again. I honestly don't know how they can take away anymore skin and tissue because they took so much away the first time round, I actually did wonder if it reopened due to the skin being too tight but no one has ever mentioned that could have been the cause.

Another thing I got told today was if I start bleeding again I have to go to A and E and get seen because the last thing Miss S wants is for me to pass out but the problem is I really don't want to have to go. The issue with going to A and E is it will be a waste of their time and mine because there really isn't much they can do and surgeons won't do surgery because what I have really isn't an urgent thing. I suppose right now all I can do is wait and I hate waiting.

Well that's it for today's post, I hope you enjoyed reading the post. I am already working on a draft for my next post so everything being well you should be able to read it by the end of this week but until next time................

Keep strong

and 

Keep fighting

💓💙💚💛💜 

You can also follow me on 

twitter | facebook | instagram | google+
youtube | twitch


Groups I have set up for my chronically ill family
The IBD family facebook group
Spoonie bookworms goodreads group
Spoonie warrior gamers steam group
Chronically ill and disabled equestrian's facebook group

A prefect time to restart this blog

Hello there all you wonderful people, it's been a very long time since I posted something on here and I am sorry about that.

Sooooooooooooo you may be wondering why it has been so long since you last saw a post from me and the reason for that was my depression and anxiety, it was really bad and I let it take control of my life. Thankfully though my mental health is better then it was and the desire to write blog posts has returned plus with upcoming events I thought now would be the perfect time to start blogging again.

Well that's it for today's post, I know it's a short one but I have to start working on my next post which will be live on my blog in the next few days so keep your eyes peeled for that. Until next time................

Keep strong

and 

Keep fighting

💓💙💚💛💜 

You can also follow me on 

twitter | facebook | instagram | google+
youtube | twitch


Groups I have set up for my chronically ill family
The IBD family facebook group
Spoonie bookworms goodreads group
Spoonie warrior gamers steam group
Chronically ill and disabled equestrian's facebook group

I am broken

Hello there everyone, it's been a very long time since I last wrote a blog post and there has been a reason for that and I am sure that some of you can guess by the title what has been happening.

I have been suffering from depression for a number of years but last year it started to get  a lot worse and instead of asking for help again I just let it get worse and worse and a couple of weeks ago I reached my breaking point and had to get an emergency appointment with a G.P. as I was having thoughts of it would be better not to live plus many more symptoms.

• lack of energy which I originally put down to anaemia but apparently lack of energy is one of the symptoms
• feeling tired which again I put down to anaemia and medication I was taking
• getting agitated when around people
• not wanting to spend time with others
• shutting myself in my bedroom
• using dihydrocodiene to help numb the emotional pain
• finding it hard to cope with with everyday things including simple things
• not enjoying what I normally enjoy doing
• not looking after myself properly e.g food
• having thoughts it would be easier not to live
• trouble sleeping because I can't relax or switch my brain off
• not being able to stay asleep
• not being able to concentrate
• feeling that i have failed in life
• fear of something going wrong when out of the house that makes me land in hospital
• Scared that I become ill after say a trip away (this one and the one above are more related to anxiety)

I think the worst thing is I have all these symptoms despite being on 3 medications to help with my mental health and I am on 4 when I am really bad. The 3 medications that I take everyday are maximum dose citalopram which is an SSRI anti-depressant, a low dose 25mg of quetiapine which is used as anti-depressant also and maximum dose propranolol which is used for anxiety. You really would think with the amount of medication that I wouldn't be suffering with depression and anxiety so bad.

So the plan for the moment is to see the urgent care mental health team so they can review the medication I take and put some support in place to help me make improvements. I have been told that the improvements will be slow but any improvement is better then the way the life is right now.

I do have this massive bucket type list which I prefer to call my to do list ,which has all these big plans but I will tell you the smaller things I use to and want to get back to doing first.

• pc gaming 
• streaming on twitch 
• being with and riding horses 
• blogging
• cooking
• baking
• crafting
• reading books and comics
• going to the cinema
• going to concerts
• spending more time with animals

I think that is everything for this blog post. I am sure once I post it I will remember I forgot to write something else. I will try my very best to document my journey to getting better but with the way my depression is I sadly can't promise anything.

I hope you all are doing well and until next time................

Keep strong

and 

Keep fighting

💓💙💚💛💜 

You can also follow me on 

twitter | facebook | instagram | google+
youtube | twitch


Groups I have set up for my chronically ill family
The IBD family facebook group
Spoonie bookworms goodreads group
Spoonie warrior gamers steam group
Chronically ill and disabled equestrian's facebook group

I'm back

Well hello there it's been a very long time since I last posted on here and I am sorry about that but for some reason I just couldn't write a blog post. I have no idea why it happened it wasn't like I didn't have any ideas I just couldn't write things down and when I did force myself to write a blog post it just didn't make any sense.

I am pleased to announce that I have got my blogging mojo back and my brain is brimming with ideas so that means there will be new blog posts coming your way on all my of blogs.

Well that's it for today's post I know it's a short one but I just wanted to let you all know that you will be seeing new blog posts in the future so until next time keep strong and keep fighting. 💗💙💚💛💜

Wednesday 27th December 2017

Well today has been one those days where I needed to take care of the essentials, these are not my favourite type of days but they need to be done to so I can have better health. Better health = being able to do everything I want.

So today was an early start as I had appointment at the health centre to get bloods done at 8.40am. Before Christmas I phoned the IBD nurse because my anemia has got so bad that I can no longer wait for the portacath to be placed. I have tried to take the Ferrous Fumarate tablets that they have always prescribed in the past but my stomach and bowels does not like them tablets at all.

With it being the week between Christmas and New Year people didn't want to see the doctor so I managed to score myself a doctors appointment for that afternoon. I didn't just manage to get one appointment, I manage to a get two and having a double appointment meant I could get all my issues seen too. 

For the longest time now I have had this problem with my right shoulder, it's not the easiest thing to describe, I don't really get pain as such it's just really uncomfortable and it doesn't stay in the one place it goes down to the bicep. The best way to describe it is my shoulder is being pulled out of it's socket, I take paracetamol and dihydrocodiene but it doesn't seem to work and now I am at the point where I can't cope with it anymore plus it's taking it's toll on my mental health too. The GP did numerous things but he couldn't really say what it was, I had full range of mobility and more because I am hyper mobile. He decided to give me a prescription for diclofenac gel which I am concerned about using because it is a NSAID (anti-infammatory medication) and if you have Crohn's you are not suppose to use NSAID's. I did mention to him that people with IBD are not suppose to take NSAID's but he says as it's going on to the skin so it won't be absorbed into the body but I am still not a 100% sure if it is a good idea to use it. 



Well that is it for this post, take care everyone and til next time keep strong and keep fighting. 💗💙💚💛💜

previous post: Thursday 16th March 2017

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Thursday 16th March 2017

Well what can I say it was a disastrous day.

Today I was suppose to have a dentist appointment because my top set of false teeth (dentures) doesn't fit properly but there was a family emergency which meant I couldn't get a lift. My grandma has had this cellulitis infection for a little bit now but she had to go to the doctor this morning and they wanted her to go into hospital urgently because the they thought she might have a deep vein thrombosis. As some of may know a deep vein thrombosis can be a life threatening problem so it was more important that my mum took my Grandma to the hospital instead of me to the dentist. I am glad to report though that the tests game back and she got all the clear which means a massive weight has been lifted.

I wish I could have said that was the worst part of my day but it wasn't. As many of you know I have dyspahgia (swallowing disorder) due to a Crohn's stricture in my oesophagus so for that reason I eat a pureed diet. Well for a while now I have been pureeing pot noodles in a small blender and they have always gone down with no problems until this evening. I was eating sweet and sour one and there was a piece of pepper that hadn't blended properly which is now lodged either at the top of my stricture or further down. I have had things get stuck before because that's what can happen when you have a stricture but I have never had an issue getting it to pass or come back up until tonight. I have tried so hard to make it come back up and I have tried drinking fizzy juice but the juice won't pass so I have to bring it back up too, at this point I am now out of ideas and all I can hope for is it moves by it's self. 

Well that is it for this post, take care everyone and til next time keep strong and keep fighting. 💗💙💚💛💜

previous post: Losing my best friend

You can also follow me on 

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