Tag Archive for Portsmouth Hospitals

Thankful yet Frustrated

So, it had been a bit of an eventful weekend.

Not in anyway the weekend I had planned on having.

Sorry for the riddles. I won’t keep you in suspense anymore.

On the weekend beginning Friday 7th June I ended up in hospital, suspected of having suffered a TIA or ‘mini-stroke’…. The pre-curser to an actual stroke.

Something that having never smoked and only ever drunk alcohol occasionally I didn’t think I was at risk of.

After all I kept saying “but I’m healthy, I’m active” but actually as one lovely nurse explained to me stroke can affect ANYONE! From babies, children, teenagers, young adults, fit adults, unfit adults right through to older people.

Before I continue let me just confirm, thankfully the initial suspicions were incorrect. I had not had a stroke or a TIA or actually any form of brain bleed.

I feel very fortunate for this, yet I felt the urge to write this blog to help others understand what happened, why this was suspected and how I am now.

Friday evening I was sitting having just eat a regular sized dairy milk bar (other chocolate bar brands are available) when I suddenly got a tingle in the left side of my mouth and chin.

Initially thinking maybe I was having an allergic reaction on the advice of a friend I reached for my phone and took a selfie. Ten minutes later the tingling was persisting, yet now it was moving. It was also beginning to spread down my shoulder, left arm and left leg.

Another photo, yet no swelling.

A call to 111 (out of hours Dr) a quick ‘check-list’ of symptoms and the call handler said something that left me shocked

“we have sent an ambulance to your house, please do not eat or drink anything, please lock away any pets.”

This is when I explained I had a guide dog, I would put her on her lead, but wouldn’t lock her away and before I could ask why there was an ambulance coming the call handler told me to keep my phone to hand, not to call anyone except for 999 should my symptoms start to get worse ….. then goodbye.

I messaged friends but tried to tell them not to worry (even though I was actually beginning to feel quite concerned)

Thankfully I didn’t have to wait long. The ambulance arrived and the paramedics quickly explained why they had been called.

Although after initial checks and having me smile at them, the paramedics were not sure what had happened; but felt that it wasn’t a stroke.  But with the nature of my eye condition they were unable to test my eye movements for reaction.  So after a call to another Doctor it was decided the best thing to do was to take me to hospital.

At this point two of my small group sisters arrived.  Even I could see the panic in their faces…. The paramedics explained to them, I reassured them and with the promise that I would most definitely call when I needed to be collected from the hospital (hopefully in the next few hours) I left in the ambulance.

Off to Queen Alexandra Hospital we went, but no blue lights, no panicked rush; which I actually found quite reassuring.

It even appeared that Fizz’s comfort was more a priority for the paramedics and then the staff in Accident and Emergency than what had actually bought me here in the first place.

Because I was certain I would be discharged after some bloods, I had kept her with me.

But when I was moved onto a ward to undergo a CT scan and an MRI I knew I wouldn’t be found home soon.

But it was important that Fizz did…. She moved to the ward with me, walking beside the bed as I was transported.  The nurses took it in turn to take Fizz out for walks and wee’s … They even made her a makeshift bed of towels so she could be as comfortable as possible.

I think the nurses were most upset when Fizz was collected on Saturday morning to go off for a break with friends, where she could relax and not be worrying about me with all the noises and smells of the hospital.

I had been moved to the stroke ward, where I spent the weekend as I needed an MRI scan that wasn’t available until Monday morning.

I discovered that it was standard procedure to serve me soft almost puréed food.  Thankfully a friend had dropped off my Herbalife Nutrition shakes so that I could take care of my own food and actually enjoy it.

Monday morning saw my MRI scan followed by a visit from the consultant who explained that my results and scans showed no signs of stroke or TIA.

But with the continued weakness and numbness in my left side he could offer me no explanation of what it could be, as he explained his expertise was strokes.

Thankfully a friend was able to collect me and drop me home where it was great to be able to lounge on my own sofa.

For now I am to rest when I feel I need to, not push myself to do anything strenuous and hope my symptoms ease and improve.

As the title suggests, I am so very grateful I have not had a stroke.  But not knowing what this is means it’s hard to know how long recovery will take?  If I will recover?  And more importantly, not knowing what THIS actually is?

Reflections

Photograph of Tee, Weston a grey t-shirt saying “climb on” stood in front of a black and white canvas of a misty hence in Greenwich Park

Photograph of Tee, Weston a grey t-shirt saying “climb on” stood in front of a black and white canvas of a misty hence in Greenwich ParkThis November it will be 10 years since I was registered SSI (Severly Sight aimpaired aka BLIND) it was the appointment with my consultant that EVERY seemed to change, yet at the very same time NOTHING changed.

What I mean by that is that my eye sight didn’t actually change at THAT appointment.  I  simply became aware of just how bad it was.

Having had my Nystagmus (involuntary eye movements) and having worn pretty strong glasses for as long as I can remember my sight had never been great.  But in terms of the distance I could see (I have always been short sighted) had changed very little.

Rightly or wrongly so; when I was in my early teens I had been discharged from the consultant at the hospital, where I was given into the care of my opticians.  With the strength of my prescription And it was through this team that in July 2008 they used their new camera equipment to try getting a photo of my retina.

My optician wasn’t happy with what she saw, but she couldn’t explain it to me as she explained it could simply be that with my eye movement the photograph wasn’t actually true.  So she referred me to the hospital for a thorough check up.

Having been rushed in as an emergency after the hospital were concerned I had detached my retina (a common issue that if caught early enough can be reversed) I discovered that this was not the case, the registrar discovered I had cataract in both eyes, I will always remember what she said;

With laser treatment we can remove them and that would actually improve your vision.

But as she was simply confirming I hadn’t detracted my retina, she didn’t actually comment on the fact that my retina wasn’t ‘complete’.

So, you can probably understand my total shock when I returned a few weeks later to see the consultant to be given the news of just how bad my sight was.

I did have cataracts (my left eye had been diagnosed when I was 12) But the laser surgery suggested wouldn’t be easy and would have very little affect at this time.  And actually with my retina dying away my sight would actually only get worse.

Many people ask me

How did you not realise you were going blind?

Its simple, the changes in my peripheral were suggested to be something that had been happening steadily for many many years, and as I only likely lost a small amount at a time I didn’t actually realise.

I did notice ‘little’ things after my daughter was born in 2006, like how I was bumping into things, like low level tables or benches.  But I put this down to ‘baby brain’

I had also noticed that it was taking me longer for my eyes to adjust to light changes; like walking indoors after being out in the bright sunshine, but because I had reaction lenses this went in-noticed as an actual change in my sight (as I assumed it was just the glasses)

So…… Reflections.

I have decided I want to celebrate this anniversary.  I want to acknowledge that as me I have changed from the person I was before.  It hasn’t always been happiness and celebrations, but I have tried to embrace my blindness (and now deafness)

It may sound like a cliche

But in these last ten years I have had so many amazing opportunities, so many doors open to me.  I want to move forward with me and celebrating the good seems the best way to do this.  I am human, I can’t be postmitive ALL THE TIME.  But in this instance I want to look for the good, rather than dwell on the bad.

But the question is (and this I hand over to you my readers) ….

How should I celebrate???

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