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Showing posts with label buzzing sensation in legs. Show all posts
Showing posts with label buzzing sensation in legs. Show all posts

Wednesday, 9 October 2013

The Story So Far - Part Two: No Man's Land

No Man's Land

After being discharged from Hospital on the Sunday I came back home with Bear for complete relaxation and recuperation.  The Consultant advised that I should take sick leave from work for at least the beginning of the week, which, for a change, I listened to!  Bear was great; fetching me cups of tea and making dinner, even though he had to go to work himself!  During this period the only symptoms I was having were problems with vision (everything was easily blurred and I had to really concentrate to focus, however putting my glasses on helped quite a bit), my balance was poor and my walking was very slow and deliberate.  I had to really concentrate on putting one foot in front of the other and I felt like my legs didn't belong to me - like I couldn't tell how much weight or pressure I was putting on them so I had to be careful.  The tingling that I had experienced earlier when in the hospital had started to ebb away and my concentration and mood were significantly improved.

By Thursday I was gagging to go back to work and have some semblance of normality in my life.  At work my colleagues were understanding and concerned, and I was open and honest about what was happening.  Although to be fair, I didn't really know what was happening myself - just that something wasn't right and there would be further investigations.  I have a great rapport with my senior colleagues and peers at work, I do my job well, and although I think some of them were guilty of thinking bad of me for taking such a large amount of time off, I think they understood when they saw me at work that Thursday and Friday that this wasn't a minor illness or over-exaggeration.  My boss, unbeknown to him that I had even been in hospital over the weekend, exclaimed loudly whilst I walked to the printer, "Is this the World's slowest walking competition?"  I saw the funny side, how could I not?  But I just couldn't walk any faster.  I shook when I got the milk out of the fridge to make a cup of coffee, I was holding on to desks as I walked by for balance, I had to squint at the computer screen (even with my glasses on) to see what I was typing, I couldn't hold my pen properly to write, my speech was slurred to the point where someone asked in a meeting if I had been drinking at lunchtime.  I found typing whilst listening to someone explain how a specific portion of code flowed through the system impossible.  This was the most worrying thing for me.  I'm constantly doing three things, never mind TWO, at once - I can't just watch TV, I have to be playing a card game on my iPod whilst also texting friends and flicking through a magazine.  I PRIDE myself on my ability to do two things at once - I did it at work ALL of the time.  So why did it sound like the person sitting next to me was speaking Vulcan whilst I was knocking out the simplest of requests by email?

I found that relaxing would temporarily take my symptoms away, and one minute I felt almost back to normal again and so would do something like clean the bathroom with a surge of energy, only to get half way through and collapse in a heap on the sofa unable to move.  Despite this my spirits were positive and I was sure that it was all still a big fuss about nothing still.  I wouldn't have been surprised if my GP or a consultant had suggested that I was just stressed and needed some time out - besides I hadn't had any proper time off from work since December 2012!

On the 17th September I had a brain scan, which I found out about purely by coincidence!  That day I had woken up feeling like someone had repeatedly been hitting me all over my body.  My skin felt bruised, my legs were so weak that even walking to the toilet was difficult, I had an awful headache and I couldn't see properly.  This was the first time that I experienced real vertigo.  Everything seemed unreal, like I was existing in a bubble and it just wouldn't stop moving!  All sounds were muffled and my brain wasn't registering what I was seeing straight away - there seemed to be a slight delay.  I had taken Valium before whilst admitted to hospital in 2011 for a severe panic attack and I felt similar.  Needless to say, I called work to explain and they were thankfully understanding.  Half an hour later I received a call from the Imaging Department at Charring Cross hospital to say that my appointment for a brain scan that day would have to be cancelled as the MRI hadn't switched on properly.  This was the first that I had heard about any brain scan!! I had received no letters, phone calls or emails!  The radiologist, although sympathetic and most probably not very surprised at the lack contact, said that if they had to re-arrange they would try and make it ASAP and before I went on holiday.  Deflated and angry at the obvious failings in NHS administration I expected not to receive a further appointment for months BUT the Radiologist called back and said that the MRI machine was now working and if I could still make it today that would be great! :)  I wasn't really in any state to go anywhere and the thought of getting on the tube from Ealing to Hammersmith made me want to cry, but I did it and I got there (with a very large Costa Coffee caramel latte in hand!).

Some people find MRIs scary.  I don't often get the opportunity to lie down and think of nothing (certainly not without feeling guilty about it!) so for me, being enclosed in a coffin like environment and having loud noises radiated through my ears didn't bother me in the slightest!  The concerned face of the Radiologist when she asked me if I had an appointment to see the Neurologist urgently did, though.  She knew something and when asked if she spotted anything told me that it would have to be confirmed by a Neurologist.  I was still hanging on so desperately to the hope that I would be shooed away and told to shake myself off and get on with it because it was just a little dose of stress.  But at that moment, I knew it wasn't.  I knew that the organ upon which I relied so heavily to make me ME had let me down in some way or another.  It hit me that I wasn't making it all up (irrationally I think we all worry that we are doing this, whether it's narcissism or self-preservation, I don't know) and then I started to get scared.  Surely she would have told me that 'everything looked OK and not to worry' if it had all been fine?  I decided that I needed to take action and be in control of something, so I went to the Outpatients Appointment department to check if I had any other tests or appointments booked in without my knowledge!  I did! Neurology Outpatients appointment on the 19th NOVEMBER!!!  But that was two months away!  Surely that wasn't right?  Didn't they know that there was something wrong with my brain?!?!  It takes a while to become rational in these situations and realise that:

a)  There might not actually be anything wrong - a worried Radiologist's face does not a tumour make;

b)  That there are probably thousands of people in the same boat - I'm no more special.

I struggled through the Friday at work and relished a weekend of relaxation and no plans.  The weekend came and went and although I managed to go to Ikea with Bear and pick up a few home furnishings I didn't get overly tired, mostly probably because I insisted that we sit down and drink coffee every hour or so!  On Monday, however, around 11am at work, the fatigue hit me like a punch in face, torso and legs all at the same time.  My brain swam and my eyes dilated.  I couldn't concentrate on what people were saying in meetings, I just stared in to space willing myself to concentrate and understand.  I felt humiliated and just glad that we didn't have clients with us that day.  I couldn't go on like this so I called my managers in to a meeting and explained how I felt and admitted that I was struggling.  they admitted that they could see that i was too.  We decided that it was time for me to take some time out and to use the time to try and find some answers from the Consultants.

That afternoon I called my GP who suggested that I see her the next morning where she could take some more bloods and she would try and chase up my brain scan results.  For the first time that all of this had been going on, I sobbed down the phone to her and I think she recognised my utter desperation and confusion.  I just wanted my life to go back to normal - why was this happening?!

At the time the waiting for results seemed worse than actually having the results - but I think this is only when you are still clutching to the naive insistent hope that you are going to be told that it's 'just stress'.

The Story So Far - Part One: The Beginning

The Beginning

Firstly - welcome to my blog! :) If you are reading this then probably:

a) You stumbled across it when searching for MS Blogs.  You have MS or you are a relative of someone with MS and want to more about how the disease affects all involved.

b) You are my boyfriend who wants to know more about what is going on in my head because I won't talk to him about it!

c) You are my parents who want to know more about what is going on in my head because I won't talk to them about it!

d)  You are my friends who want to know.......  you get the drift...!

e)  This one is a long shot:  I have been nominated as best 'Blog of the Year' and you want to send me on an All Inclusive holiday to Mauritius as a well done.  Yeah, I will keep dreaming about that one....

On  26th August 2013, Bank Holiday Monday, it was a glorious day (for a change in the UK!).  Bear and I woke early and decided to go for a walk in the sunshine to a local village for some breakfast, which was delightful until we started to walk back.  Fatigue, weakness, imbalance, a blinding crashing headache and sensitivity to the sunlight hit me like a brick wall within 2 minutes of leaving the cafe.  I had absolutely no idea what was wrong but I suspected that it was hayfever or I was coming down with the flu.  The 1.5 mile walk home was difficult and I spent the rest of the day and night in bed, moving only to use the toilet and to try to eat something (unsuccessful!).  The next day I woke up feeling only slightly refreshed after the day in bed but able to shower and go to work, but within 3 hours of being at work the debilitating weakness and tiredness had hit me again.  I felt like my legs were made of lead weights and I could barely hold my head up.  My speech was slurred and I couldn't think or see properly.  I was sent home from work for more rest and I made a doctors appointment for the next day.  I slept all day but again it did little to relieve the utter exhaustion.

I had originally booked to see my GP on the Friday of that week to discuss my lower back pain, which had been nagging for 2 years on and off but had been a constant deep aching for a number of weeks.  She prescribed me some Naproxen 250mg twice daily (every 12 hours).  I then told her about the "funny turn" that I had on Monday and how it had left me in bed for two days, she took some blood and then asked about my obvious difficulty walking.  I told her that my legs felt like weights and that it was like walking through water.  She examined my reflexes and did some basic neurological tests before confirming that I had marked weakness in my left hand side, and that if I began to have any numbness in my legs that I should call her immediately.  I left with the Naproxen feeling a bit baffled by it all and thinking that it was all just a fuss about nothing; the last month or so had left me feeling exhausted - that was all. After all I had competed in the Virgin Active London Triathlon, gone to V Festival with Bear where we had spent pretty much three sold days getting pissed, and work had been crazy busy. I spent the rest of the afternoon and evening on the couch, hardly moving a muscle and insisted that I just needed a good holiday and some time out.

The next morning I woke up and felt remarkably better - the fatigue had lifted and headache had disappeared.  I was elated!  However my left leg just didn't feel like it belonged to me.  I had a constant buzzing feeling in it, it felt numb and my toes were so cold!  It was weak and caused me to walk like it was dragging behind me.  My balance was also very bad and I had to walk slowly to stop myself from falling over or walking in to people!  But I felt better so I didn't worry.  I managed to get in to work, and sat at my computer I felt fine and worked away happily.  My GP called me that afternoon to tell me that my bloods had been rushed through and there was no evidence of iron deficiency to explain the fatigue, but my white blood cell count, although still within the normal levels, was slightly elevated.  Upon asking about how my legs felt, I told her about the weakness, tingling and numbness, and she promptly told me to go to Charring Cross A&E to get an urgent lumbar spine MRI as she suspected Corda Equina.  I had no idea what that was and told her that I was fine, was at work so couldn't really get away, but I would wait and see if it got better on its own before making such a drastic decision to go to A&E.  It felt silly to walk in to A&E feeling relatively well apart from walking a bit funny and demanding an urgent MRI!  I could imagine the scathing stares of 'who the hell is she' already!

The next day she called again and asked if I had been to A&E yet, to which I replied no.  She reiterated her advice and explained what Corda Equina is and if it's found quickly then it can be treated within minimal complications.  If it is left then it could lead to paralysis.  Needless to say, this was enough to make me get my coat and explain to work that I needed to go and get an urgent scan of my spine.  Off I limped to Charring Cross A&E, where after a 36 hour wait I had a lumbar MRI and the Neurologist confirmed that there was nothing compressing my spinal cord.  Phew!  However I did have a dehydrated spine, something which the consultant sandwiched in to the conversation, somewhere between telling me that it wasn't Corda Equina and that it could be another neurological condition.  I don't even remember them saying anything about a 'dehydrated spine', it was Bear who picked it up and told me when we discussed it later that evening, I think we were both so stupefied by the idea that it could be Neurological that we didn't think to ask.  At the time I remember thinking, HOW can my brain have anything to do with me not being able to move my leg?!  Oh how naive I was!

I stayed in hospital from Friday until Sunday evening and had a number of neurological tests, including reflexes, pin-prick, coordination, balance and strength.  The consultant didn't give me any feedback on my performance in these tests but just muttered a 'good' after each one.  Steadily, after two whole days of lying in a hospital bed, my symptoms improved and I started to regain feeling and strength in my left leg.  On Sunday evening a Medical Consultant (not Neurologist) informed me that I could go home and that they would request a brain MRI and a NCS/EMG as an outpatient and then I would be seen in Neurology Outpatients.  They also sent some blood samples off to Serology to test for Weil's and Lyme Disease.  When I asked what they thought was wrong with me, they 'ummed' and 'ahhed' and just wouldn't give me a proper answer - it was so frustrating.  So we left the hospital none the wiser but just glad that I was starting to feel a bit better.