Sometimes I wonder what is Multiple Sclerosis? Is it just a figment of someones imagination or a trick by a sick and invisible entity. I mean really how can you be sat quietly at home just chilling out and suddenly for no explicable reason you have a tarantula walking across your forehead! No really that’s what it feels like.
I wont put up an image as I know some people have phobias over spiders. I can remember clearly trying not to panic as I assumed a spider had crawled onto my face, so carefully without panic got up and slowly scared out of mind and hanging onto my hand rails for dear life, walked to the mirror located in my hallway. Expecting to see this long haired creature on my forehead instead of which there was NOTHING! I could still feel it walking across my forehead. Jeez I must have been going insane or something. It was a horrible sensation. Quickly I washed my face, and the sensation did go away. It was warm I remember that.
This was a madness and period of my life when I suddenly was invaded by ants, and nits in my hair, and fleas running across my face. I got more exercise going to the mirror to see all these crawly things but never found one.
Invisible nits which made you scratch your scalp raw. Boy that Joker card was aving a larf with me. What else was he going to chuck at me.
I did have a giggle though when I found out what this sensation is called. Formication, my brain being my brain immediately went to the naughty step lol, but basically it’s a type of paresthesia. Paresthesia happen when you feel sensations on your skin that don’t have a physical cause. Paresthesia can take many forms. These can include burning, tingling, or numbness. With formication, you might also describe the “crawling” sensation as feeling like “pins and needles.” Formication is also called a tactile hallucination. This means that you’re feeling a sensation that has no physical cause.
Oh yes also Withdrawal from alcohol or drug use can also trigger formication
So knowing what it was and it had a name kind of mind it easier to cope with but at one point I was totally paranoid thinking my house was infested with little crawlie things. Eek.
Another wonderful sensation was the biting bee. I was actually in the garden with my chickens when I suddenly felt a bee or wasp sting me really hard, jeez it made me jump out of my skin and my husband came into view just as I was screaming in pain, crying “omg omg omg” I have been stung by something, as I hastily started to drag my trousers off myself trying not to fall over to find the offending perpetrator of my body. Mike came rushing up to me to help, and between us we managed to get my trousers off but nothing fell out onto the floor and there wasn’t a mark on my leg where I felt the bite.
No way how could that be? (bee get it lol).
This was getting ridiculous now. I was really being dealt the Joker card, what was going to come next I wonder.
Have you ever stood say in the kitchen and feel someone is looking at you from behind? You just have that feeling that there is someone there and kind of hold your breath because your scared to death to turn around, then suddenly you actually feel someone push you? Now it was either a spirit and I can assure you it wasn’t an alcoholic one or it was another weird symptom perhaps some sort of spasm, but I swear to god I had been pushed although I never actually moved.
Ah the joys of MS.
A new one for me was trickling cold water down the back of my legs. Yep this is true. I again would be minding my own business and going about my day probably just musing about life or something similar when suddenly the back of my legs would actually feel wet and I could without doubt feel what was like water or wet going down my leg. Well for someone with a disability I could sure move when the needs must and lucky for me I was stood very close to our downstairs toilet. Making a Beeline for that as I assumed without realising it and with some horror at myself had peed. Expecting to see urine soaked underwear and the back of my trousers wet there was NOTHING. Nope all dry and nicely groomed where I left it all in the morning after I had my shower.
Now this only really happened a few times and it was earlier on in my journey. I did read about a disease that is mistaken for MS or vice versus called Arachnoiditis, but for me I feel as that is caused through nerve problems in the spine perhaps this had caused it for me. I belong to MS groups and have read others who have also experienced this with MS. If it had happened more often then perhaps I would have been worried, but I did mention it to my neurologist and he just looked at me and smiled and with a reassuring pat on my hand told me it was all down to my illness.
Weirdly enough one of the first symptoms that presented itself to me at the beginning was the strange sensation of wearing wellie boots running through a frozen field with a hole in your wellie, and freezing water making your toes feel like they had frostbite. Now that was a great one and I was convinced if I looked at my toes they would be encased in ice lol.
I did mention these things to my neurologist who said they were all forms of parenthesis.
To be honest writing this down I am feeling like some sort of nut job lol. I mean how can all these weird things happen to me or do they happen to others too. I don’t remember playing a game of cards or actually being handed the Joker card, but somehow somewhere I must have really ticked someone off, as even though these symptoms were not in themselves serious they were driving me mad.
I know I am not the only one who suffers with all these things and thankfully that is kind of comforting to know.
One of the worse ones I had though was the pain in the front of my shin. Usually my weirdo symptoms exhaust themselves very quickly and disappear as mysteriously as they came, but the shin pain was horrific. I remember at the time pushing myself to walk more with my dog. This was early onset. When I got home and was just resting on my recliner the pain started. I swear to god that someone an invisible entity had stabbed me in the front of my shin with a large knife. The pain was so intense I grabbed hold of my shin and shouted out and nearly scared mike to death. Now this pain lasted days so bad was it I really had to see my GP. As usual I got THAT LOOK, and yes you guessed it well it was down to whatever was going on with me at the time. I was told to take paracetamol and rest.
Thanks doc, so I did, and roughly 2 weeks later it finally had gone, just like it came.
Oh dear the bee is back. Yep I must have wished it on myself. At the moment living in my little sheltered flat I am trying to make an area outside which makes it more homely or like the home I left. On one side is a border which was so neglected. I had asked if I could maintain it, and was granted permission, so all the old overgrown plants which were so neglected were removed by my gardener, and the ground was given a good feeding. I decided to turn it into a little bee garden by having planted only plants that would encourage bees. Within 2 weeks I saw my first bee and was quite excited I know right I live such an exciting life. But there was the little bee, flitting away busy from Borage to flowering Thyme, gathering pollen to make the honey.
Since then I have had more and more arrive and I believe its like one is the scout who goes back to a hive and communicates that there is a bounty to be had follow me boys …………
Bees off to feast
Ah where was I oh yes, the bees starting to come to my area and I love watching them always so busy. Then just a few days ago the biting came back. Sting, sting sting……….. on my knee of all places really bad. I did lift my trouser leg up but in my heart I knew it was just an hallucination another Joker card, like he was saying “you want bees………….well your going to get bees”! There they were like magic back on my leg biting me.
Fleetingly in my brain I wandered is it true you get what you wish for? I am not scared of it now though, and just ride it through until it decides to try something new the last attack was yesterday after being at the neurologist and the heat was exhausting, so I wonder what will be on the cards today…………………..!
If you’re reading this with MS and suffer similar please share as we are not alone.
I have thought long and hard about writing this but it is no good it is really bugging me. I hope that whoever reads this does not find it offensive its not meant to be, but its my way of trying to find a perspective into something that is constantly being dragged up on forums and groups.
What is it? Hum well have you ever gone out say to the shops and noticed anyone looking at you in an odd way? Maybe you think why is that person looking at me like that?
Nearly every week I go on forums or groups and there will be someone on there literally “spitting feathers and full of indignity”
Angry and indignant (not thirsty). Drawing by Hannah Scully .
Now you would think World War III had started. I would have an image in my head of some person with arms under their breast standing there and taking real offence………. I am drawn in to the conversation as it seems so intense something awful must have happened to induce such a vitriolic and angry post.
It would sometimes start with…….. “How dare they look at me like that? (Hum reading on thinking this might be juicy), who do they think they are for gods sake”! I could literally feel the fire of anger coming off the screen…what had this person done to illicit such a response……..so holding my breath I would carry on reading.
“The nerve of the them. I was just walking into the supermarket with my walking stick, and this moron standing in front of me, looks at me like I am diseased or something and steps out of my way and the look they gave me was disgusting like I was dirt under their shoe, just because I am disabled and use a stick how dare they look at me like that………….”
I know my brain is very slow and it would take a few seconds to comprehend what on earth this person was moaning about.
It would seem the person had some how purposefully or inadvertently given the impression that they found the look of their disability as distasteful or not real, perhaps the person with the stick was some how playing games and just doing it to get attention or money off the state, who knows, but the writer of the piece would be so mad one would think they had been physically assaulted.
I have had a think back about times when my disease first got so bad i needed a stick and an arm to lean on. I would go to the supermarket and by the time I got to the check out would be exhausted and out of balance.
I had often stumbled and needed to hold onto my carers arm to stop me falling. Yes I would admit that someone in the queue by the side of me would look at me with a look of sadness which would prompt me to say “oops I need to put more water in my gin in the mornings” and this would break the ice and the person would smile and giggle with me which broke the tension of the moment. I would always turn these awkward times into a scenario where one could laugh and smile alongside of me. My illness never made me sad, frustrated yes but never sad.
I was proud actually that even though I had a life changing disability that I could still go out and that I could still quip about it and interact with people to show them well there is nothing to be scared of not really, hell no I may have MS but I am not dead yet there is still life in the old dog yet lol. Below just a few photos of me over the years of having MS, I just got on with it, and never bothered about what others may have thought. I never stress over what I cant change.
I kind of felt sorry really for the posters as my feeling is they were not angry at this person but more angry with themselves and what was going on around them, and it was their way of dealing with it, by focusing on a tiny thing that may have happened and turning it into a major incident. Maybe a need to be noticed perhaps, for people to feel sorry for them, or even feed their insecurities about their disease.
After thinking about it I realised that people with MS or any other chronic illness can be very insecure, and some of them needed to be supported but didn’t know how. So they use the media to feed it to feel loved and supported.
You could almost imagine them sat in their room lonely and sad, lapping up all the answers of support, lapping it up like a cat would lap up a bowl of tasty cream. The person who had unwittingly looked that way, would never know that they had caused such a drama which would be unfolding and getting more and more intense and down right nasty towards them.
I am sure they would have been horrified. Its almost like someone being stoned like in the days gone by, but verbally a trial by media. It would almost become mob rule as other posters would get wired up and angry for the first poster.
In days gone by people would be stirred up by verbal communication and things could get pretty nasty. Now its all down to lonely people living in their own seclusion feeding off each other the object of their hatred was not known or seen, but it didn’t matter not really as they could feel for the poster as they too were in the same situation and perhaps similar had happened to them too, so a simple moan could turn into hours and hours of posts from all over the world.
With the Internet you can start a post at night in the USA and it would be picked up some time in the morning for example in the UK, then posters would pass on their thoughts, and come the afternoon in the UK it would be the morning in the USA etc, and so that one small post could be doing the rounds for many many hours all over the world and getting bigger and bigger. At least in times gone by you reacted and it was done and dusted there and then. I feel now its so much more unhealthy. We tend to hold onto our anger and never let it go which cant be good for us surely.
Then just when you thought it had calmed down someone else would find the post and kick it off again, and indignity would reign once more around the satellites…….
Stone throwing the old fashioned way.
An innocent glance taken totally out of context had been used to feed someone else insecurities. Perhaps the indignant person needed to GET over themselves and find a life………yes they were disabled they had been given a rotten calling card but they needed to learn to deal with it for themselves not stir up a emotional feeding frenzy by others in the same place. All these people responding for me feeding the insecurity were the same sadly.
Life with a disability doesn’t have to be the end of their life but the start of a new one with lots of challenges yes, but we have to choose our paths in life. It is so much easier to take the easy path of just not dealing with it, and passing it all onto someone else and live the rest of our lives indignant because someone LOOKED at us in a weird way and make a huge thing about it which would feed us for a week and prop up our fragile egos.
As Humans I believe we are an innately self-absorbed species. Partly down to the fact that we have an instinct for survival. Could this person who is sharing this awful experience on say Facebook be using it as a way to survive another day. Using this exaggerated incident to enable them to cope through their own day, isn’t this a bit selfish really?
This could be dangerous unintentionally. There are a lot of people now living with a Mental illness who also have alongside a chronic illness they have to deal with. By sharing this story it could unintentionally stir up someone else who may not be as equipped to deal with it. It could even stir up hatred to all things NORMAL.
We have no idea how fragile minds are and the Internet is now a breeding ground for many things some of them not so good. By Normal I mean a focus can then turn onto someone who unwittingly one day looked at someone and without realising it set off a chain of events, because they appeared to be a “normal” person with no visible disabilities…………….
This doesn’t mean they have no disabilities just that the poster couldn’t see any, but perhaps their innocent look was of sorrow, or they may not have been looking at the person but through them as they were reminding themselves of something that happened to them that day. DON’T assume they were looking at you in a bad way.
Perhaps if you are reading this just be aware that if there is an issue with someone LOOKING at you in an odd way, look at yourself, and how you deal with things in your life at that point in time, and keep it to yourself, as innocently you could be putting other peoples lives in jeopardy.
You see that look, the best thing is to Stop – Take a deep breathe – Think of something funny – move on.
We all need to learn to GET over ourselves, yes we are disabled, but we are not a unique species with special privileges in life, we have to learn to deal with what we have been given, and not expect others to prop us up, as these same people may be more disabled then we are, more fragile then we are, and more scared then we are.
Let us all try to be a bit more tolerant of each other. We are humans and we are all just trying to survive the best we can, we don’t need to be stirred up and stressed to support someone as it just makes their day worse too.
Your needs shouldn’t always come first. Just remember whatever you post on media can have a ripple effect that leads to a tsunami, be mindful that others may be way more fragile. Just try to look at the funny side of things. Make yourself laugh, and the incident will just fade away.
I have another saying too when someone says to me “well you look really well” and I quip back well why shouldn’t I? I am not ill I am just NEUROLOGICALLY CHALLENGED, and it makes them smile and they know I am ok.
If you really want to be happy, you need to take a step back. You need to engage with the people around you, and with the rest of the world. Because this individual focus really isn’t working for anyone. Certainly not for you as it just leaves you having a bad day and a constant reminder inadvertently that yes you are disabled………. Turn the computer off, get out of the house, sit in the sunshine, do something, don’t focus on the bad things in your life, look around you, there is beauty you just need to look for it.
Beauty is everywhere you just have to open your eyes.
Good company in a journey makes the way seem shorter. — Izaak Walton
Brazil 2000 – July
To say I was excited would be an understatement. I never in a million years thought we would have the money to afford a holiday in Brazil as the rates were really expensive. It was one place i have always wanted to visit, and believe me I have been all around the world at sometime in my life.
To be honest the thought of seeing a few hunky maybe footballer types running around on the beaches wouldn’t go amiss either….but i would never tell my hubby that.
I had gone to my local travel agents and there in the window was NEW THIS SEASON holiday in Recife Brazil on a “package” holiday. I couldn’t believe my eyes. There was the perfect holiday for Mike and I it was in a small Hotel in Recife the name of it now escapes my memory. It was so cheap and we could afford it. The Hotel was located close to the town and the beach was yards away. I booked it without hesitation for July 2000.
Mike my hubby was excited as I was even though he was well travelled himself. Finally the day came to leave and we got there after a long flight and journey but the Hotel was fine, had a swimming pool and beach was amazing like the beach on the old Bounty chocolate adverts. We soon found our bearings and hired a beach buggy fabulous so much fun. The beaches were virtually deserted as the PACKAGE holiday had only just started and we only saw a few other holiday makers, it was all just a trial anyway to see how it went down with the British customers. Well we were hooked and even talking about returning again the next year.
We had a great time really was fun, the weather was a bit unsettled though but still we enjoyed beach-combing, watching beach football, swimming, and just chilling and oh yes eating the local food which was brilliant just what we liked. We ate in the Brazilian restaurants and met lots of new people and just whiled away our days chatting and sightseeing as well.
Towards the end of the holiday we took a visit again to the town and decided to mooch the shops for presents to take home. I was in one when suddenly I had no vision in my left eye it was scary and bizarre. I remember clutching hold of Mikes arm and almost in tears was telling him “I cant see, I cant see, out of my left eye, get me out of here quickly”. He was shocked but didn’t argue and took me outside. I just held onto him as hard as i could so frightened i was going to die there and then in a strange place without my family. He calmed me down and i managed to open my eye again and the vision was weird i couldn’t see to the side at all, and it was so blurry and fuzzy. We took the quickest route back to the buggy and mike got me back to Hotel. By then my vision was slowly returning. He spoke to the receptionist and she got the local doctor out to see me.
He was a very nice kind man and made me feel comfortable and safe again. He checked me thoroughly and said in good English i hadn’t had a stroke but i must see my doctor as soon as i went back to the UK. He said i should be ok to stay for the next few days of my holiday but should rest for a day or two.
When he went i just wanted to go home, i was so scared and frightened, Mike got hold of the representative of the holiday company. He explained by the time it took to organise me a flight i would be going home anyway, and it would be just as easy if I just stayed there and finished the rest of my holiday.
In the morning things were almost back to normal my eyes felt better and my left wasn’t as painful or blurry.
So we spent the next few days just enjoying the rest of our holiday and time together.
Thankfully I managed to survive the homeward bound journey.
When I arrived home; the next day i popped round to see my daughter with her presents, and to tell her all about my holiday and the scary happenings to me I had. Whilst she was in the kitchen making a cup of coffee for me, well it happened again. My left eye went blind, like a black spot in the middle of the eye, all blurry and out of focus and the pain when i moved it.
My daughter insisted i went to the doctor so an appointment was made for the next day.
I went there and explained what happened. The doctor almost looked bored as I described the symptoms and finally just looked at me and said I expect it was the travelling, the heat and anxiety, I wouldn’t worry too much as it resolved itself the first time, and as you have just said to me, it feels better that day. He didn’t even bother to check my eyes.
I left that office feeling totally deflated how can someone potentially go blind TWICE, and yet not even have tests?
I was back at work the next day, and slowly the memories of my scary episodes started to fade until the next episode a few years later…………
“Was I losing my Sanity”?
Life after Brazil settled back down to the usual routine of rushing around in my job. I had a wonderful job i was an Educational Developer for a small college in our city. I was responsible to create and support accredited I.T. programs and also recreational classes throughout the 11 learning satellite centres which were attached to the college.
I was responsible for 54 tutors as well. On top of all that i taught I.T. and also basic cooking in the community.
I never stopped probably worked 60 hours. I was so proud the day i went for the interview as i was working for another college closer by in their flexible learning centre supporting members of the public in I.T. based learning. I loved the job but it wasnt challenging enough for me. I LOVED to be challenged. Maybe it was the Leo in me, or i took after my father who was just the same.
The interview consisted of a 2 hour interview the first was an hour on power point on how i would develop the necessary accredited programmes and deal with the quality, training, and variety of courses to present to the local community. By the time i had finished i was totally drained and whacked out. I was told I would hear back in a few day, and started to drive home.
I had to suddenly stop the car as i felt so ill i thought i was going to pass out. My eyes were so blurry i couldn’t see. I took long sips of cold water and just tried to chill back down. I just thought it was the stress i had just been through. Finally i was able to carry on with my journey home. I must admit i didn’t take much notice of the journey home i was just thinking about what i had just been through. It was like torture, jeez they wanted to know everything. I was up against a panel of people all firing shots at me about my “VISION” for their new programs in the community.
A few days later I received a thick envelope and it was a job offer, i was so excited i squealed like a stuck pig when i read it and Mike my hubby came running out thinking i had hurt myself. The money was good too and it would really help us.
I put my notice in that day I was working in a local colleges Flexible Learning suite (supporting learners in I.T.) and started to research on the Internet about all the I.T. programmes which i worked with now anyway but i had never had to actually deal with the qualification side of the courses. It was going to be a long hard road for me but i was so excited to have such a challenge.
Eventually I started my job, i had a PA, Dylis who had been working with me several years came with me, sadly she died a few years ago and is sadly missed.
Dilys the best PA anyone could have had sadly missed RIP.
Things started to go wrong in 2001 well i had been getting subtle little life disturbances before that but i had just ignored them. When I started my new job things i had noticed a little bit prior started to really show up.
I mean how come every single day when i went into the city office I would enter the office and immediately drift to the right and bang my arm or leg on the row of filing cabinets? It was madness i was getting black and blue, and the girls in my office started to tease me about being a secret drinker. Hardly yes i liked a glass of the old vino at night to relax but i would never drink for my breakfast lol I wasn’t that desperate.
Then Dily’s would find me ASLEEP on my desk about 3pm i just couldn’t stay awake, omg meetings were such a chore for me, as they got warmer i got more exhausted.
Oh dear then the invisible “Genie” only i could feel turned up. He would sit on my chest and viciously stab my body with a knife i had no idea where the pain would be at any given time, it would just suddenly hit me and i would shout out at times in shock. Dily’s would look at me old fashioned “you alright zen”, no I had that stupid pain again its bizarre. Was i losing my mind?
The days turned into weeks, then months and a few years on with me still experiencing all kinds of weird stuff had settled down into a routine and things were going good. I had all the I.T. qualifications in place, managed to sail through an ECDL audit with full marks, had written a full workable procedure for my tutors, had put together copious amounts of exercise books all on Microsoft suite, taken qualifications myself, taught cooking to recovering addicts and even had time to become an NVQ assessor just so we could offer Teacher Assistant and Administration NVQ to the local community.
To say my life was on full sail would be an understatement.
2004 the eyes hit me again, massive urinary infection and a period in my life when i could barely function, but i did. My GP once again put it all down to stress, and high blood pressure.
Then the next stage of my madness turned up. The proverbial dropping things. There i would be with car keys in hand then they would be on the floor. UGH every day i would drop something. What the hell was going on. I was an avid car boot Queen. I loved collecting and my second passion apart from my job was collecting and learning about antiques. I had a bedroom full of stuff. I would research and then if i thought they would sell they would go on Ebay. I sold a lot of stuff and prided myself of my collection of stuff and my quirky likeness for all things odd.
I had a little studio with a sheet over a table where i would lovingly arrange my latest piece i had found. Suddenly without warning that lovely piece i had treasured would be just on the floor in well more pieces then it started with. After i had massacred a few nice items I said to Mike that’s it someone else will have to photograph for me. I was so upset what was happening to me I didn’t even know i had let go of the item until i heard it smash.
It was madness.
The tiredness crept back in, and then the balance issues came back and I was constantly banging myself i was literally black and blue at one point and Dily’s commented one day jeez you look like your being beaten or something. I assured her i was not, well she knew that anyway mike being a friend.
Then the pins and needles arrived so bad in my legs i found myself struggling to drive thank god i had an automatic i thought to myself. I think Mike was beginning to think i was going nuts too…….pins and needles in my legs yet i could feel them, how weird was that, maybe i needed a new mattress.
It got so bad i had to ring Dily’s up and ask her to take me to work.
Every meeting was a challenge as i got so hot and felt sick and couldnt even focus on the contents.
Life just got weirder and weirder and more odd things would pop up and I really thought i was loosing my mind. I mean you should be able to have a bath right without getting stuck in it, and i mean that in a way that no i wasn’t so fat i couldn’t get out, the heat of the bath just sucked the life out of me.
Poor Mike my hubby tried to get me out on one occasion when my legs refused to work, and he went flying backwards as he wasn’t very strong himself suffering with his COPD. It was hopeless i was sat there scared and more scared. I suddenly thought well maybe its the heat of the water, so i pulled the plug and let the water drain out……………………. it took about 10 minutes laying in that bath for me to feel able to attempt getting out of the bath again, so this time with Mikes help i was successful and just flopped on my bed and lay there for ages, just like a balloon and been burst or a tyre let down and deflated, i had no energy whatsoever.
I realised that my days in the bath were over. Not only for my safety but Mikes too i didn’t want him hurting himself trying to extricate me from the bath. So we had a shower installed. Oh dear well errr that was a fairly good idea, but then when i was having a shower i had areas on my body which I literally couldn’t feel the water hitting the skin, I mean what was all that about?
I started to convince myself i was loosing my mind.
(Since then my illness progressed so much that even a shower was a real chore and i hate them even more so now they wipe me out all day, sometimes two.)
Until 2006 my life was ok sort of, but the mystery of my illness continued and there was always a new challenge for me to face.
We had booked a holiday for Malta in 2006 with my sister and her husband and we were really looking forward to it. I thought as did Mike perhaps getting away would do me good as i had been working non stop sometimes 60 to 70 hours a week, what with the teaching and qualification developing, keeping teachers in work, and making sure all the paperwork was done correctly and still writing exercise sheets and books, and lesson plans and checking my tutors too; really took it out off me.
Just before we were to travel the worse urinary tract infection hit me. Two weeks of antibiotics would not shift it, and I felt awful too, really tired and in pain for the first time especially in my back. I couldn’t get rid of this infection and it got closer to the holiday my doctor advised me not to travel, as my medical insurance would be invalid if anything to do with that happened. Sadly, we decided not to go ahead it was a hard decision to make, but because my doctor had supported me with this i was able to get my money back thank goodness, but it was sad as i was looking forward to the holiday with my sister they still went and enjoyed it.
I still know the exact day and date that my life changed for ever. It was the 11th September 2006 a Monday.
On the Friday our college had a big award ceremony for all the students who had done well. I wasn’t feeling special i had been suffering more with really bad backache and the heat was wiping me out, we were having a late summer. I went to the ceremony but have to say I was glad when it was over and I could go home to rest.
Every weekend I would usually go to a local car boot sale, they were my joy and relaxation. I would buy lots of things usually as i was a collector and I sold stuff on Ebay. It really helped me to wind down. There was the usual one not far about 10 minutes away by car.
Mike took me and parked up. I was still aching in my back but was determined to have a walk around. It didn’t take very long for me to realise something wasn’t quite right. My legs were so stiff i could barely move them one foot in front of the other. It was almost like walking with concrete boots on. I tried to enjoy myself, but stiff legs, and cramp in the back of the shins was starting to take a toll. I found Mike and told him i needed to go home. He knew there must be something wrong for me to do that, i had never done it before even in the freezing winter.
I got home and just had to go to bed and lay down. I cold barely move and my left foot i remember was almost dead. I stayed there and eventually after Mike ensuring i had some food for the evening i fell asleep.
When i woke up in the morning my legs were so stiff and in pain I could barely move. I nudged mike awake and told him he would have to help me get out of bed. I just couldn’t even swing my legs out of the bed, they were dead weights.
I remember trying to stand up and nearly falling over. Eventually Mike managed to get me to the bathroom but it was a real struggle.
There was no way i was going to be able to get to work in this state. Mike rang Dily’s and explained, then he rang the doctor, who eventually came to see me around lunchtime. This was a new practice as i had left the old one. She did some quick tests and told me she thought there was something neurological going on, and would make a referral to a neurologist and i was best to just rest for now, and come and see her when I felt a bit better as a referral in those days would take several weeks.
Mid week I felt a little better and went to see her. She did more neurological tests and confirmed she was on the right track. As I wanted to go back to work as soon as I could I agreed to see the neurologist privately.
That was the second part of my journey was I going insane or was I really sick…….it took 10 long years to find out the answer to that question…………………………………………….
Testing testing 1,2,3…
Getting a diagnosis of whatever it was that was ailing me was not going to be an easy thing. I realised that after my first visit to the neurologist. Because I wanted an urgent answer i even went private for the first MRI. I just wanted to go back to work.
My first meeting with him was positive. He let me ramble on about things that had gone on. Then I was asked to lay on the bed and he started a barrage of tests jeez it was like being in a torture chamber, I mean what did i do to deserve having long sharp pins sticking into my legs……………………..
You would think OUCH would be the first thing out of my mouth nope. He started on my left leg knee down to foot and under foot. I just lay there wondering what on earth he was doing come on for gods sake get on with it. He kind of looked at me from under his arm and said can’t you feel this? “Feel what I said”? I should have been ouching and snatching back my leg but it just lay prone. However, when he went to stick it on the other leg and asked me SHARP or DULL i shamefully have to say i nearly kicked him hard boy I felt that. Flipping heck ouch and double ouch.
The next thing to be revealed to me was a TUNING FORK…. I looked at it thinking out wow what is he going to do with that give me a TUNE UP ba boom lol.
Basically he tapped the fork onto the edge of the bed and said prior to that please let me know if you feel the vibrations… Well left leg from knee down and foot, toes and ankle NOTHING much on my foot and ankle zero. Right foot i could feel the vibrations.
So then we did other tests i believe to test my gait, and one where i had to stand with my eyes closed and I nearly fell over. I still cant do that. The tests seemed to last an eternity. (See illustration below I had them all and a few added)
He told me i needed further testing as i had left sided weakness and other issues going on. So we agreed an MRI of the brain, which i paid for at The Cobalt Centre in Cheltenham surprisingly not massively expensive and got seen very quickly no waiting when you pay private you get seen in a few days not weeks or months.
The results of that were some degeneration top of spine some SWEDISH NODES, but also large patch of high signal foci in the deep white matter of my brain………..WOW sounds good right…………. WRONG.
The radiologist had simply seen the date of my birth 1951 and put it down to more LIKELY my age and not a demyelinating disease.
Now folks this is the truth i had no idea what was wrong with me even from the bizarre weirdness and i had deliberately kept away from Dr Google, but i did ask my Neurologist what was he looking for when i saw him for the results. He said then MS. He also told me quite honestly it could take a long time to finally get a diagnosis as certain criteria had to be met.
One thing I can say in the defence of my neurologist it was one of the times he was actually honest with me when he said those immortal words……….it could take a long time to get a diagnosis…..jeez literally did I know how right he was.
Ok fair enough I would see him again after the New Year I cant remember the dates, but there is a reason for that.
I got through Christmas I think ok. Mike then in the New Year had to make a trip to China and would be gone about 2 weeks. I know I shouldn’t say this but I found his trips away BLISS, because they gave me time to recharge my batteries and chill down a bit. Yes of course I missed him but sometimes a break is good especially as i was a miserable old bag with all this stuff going on, i think even Mike needed a break from me to be honest.
Well i was bored, not allowed to work as i was signed off. There is only so much you can do in a day and i found the simplest things would wipe me out soon it became obvious i wasn’t going to be bored not for a long time anyway……..
Ground Hog day……..it really exists……..
I am sure it was the 17/18th January this date seems fixed in my mind so we will go with either one for the sake of argument. I remember my daughter Miranda rang me to tell me not to PANIC….she had a car accident coming out of the road from the riding school she worked at…..whenever anyone says don’t PANIC well hell you do. She was ok, just bashed about phew but shook up and resting, her husband Greg was looking after my grandson.
I woke up the next morning so we will go for the 18th early. I got up stiff as usual and crampy legs. Looked in the mirror and thought hell girl you look old. I used to dye my hair which had gone prematurely grey regularly but since my illness had not bothered. My hair was a mess so I decided Mirror Mirror on the wall, Zenda sure as hell was not the fairest of them all, so went off downstairs carefully to get my scissors, i was going to trim my fringe. I remember coming back up getting my dye ready as i was going to cover that grey, and giving the hair a snip I can even remember chucking the hair into the loo. I kind of remember a little bit of rinsing but i am not sure about that one.
Next thing I remember is sitting on my settee fully dressed and my hair done talking to my daughter and it was my time to FREAKher out…………………………………………..
Groundhog day came to me that morning in the form of an episode of what the doctor called Transient Global Amnesia. Sounds posh doesn’t it like my memory had suddenly gone off globetrotting lol.
My daughter tells me (as i cant remember most of the times I rang her up), I kept ringing her up and asking where my husband was I couldn’t find him anywhere. She would tell me he was in China then i would repeat myself over and over again just like a scene in Groundhog day, until i would suddenly put the phone down. She said I rang 4 times saying the same thing, in between my daughter freaking out she managed to get hold of her sister and begged her to come to my house to see what was going on, as the accident she had the day before had rendered her immobile.
Well oh dear all i remember is suddenly sitting on the settee talking to her i suppose on the fifth call and my global wondering memory was coming back to me. I felt weird i can tell you the feeling was horrible like you were so drunk you just couldn’t remember what you had said. She told me to sit tight her sister was on her way to me. Now weirdly enough I must have remembered my daughters phone number to ring her i never really worked out why.
Slowly it was like coming out of a fog and I started to remember where I was and who I was like awakening from a long sleep maybe i was in a production of Sleeping Beauty but some how the Beauty doesn’t quite fit my profile.
The door bell rang and i got up to answer it, and there was my older daughter looking at me very anxiously. “Mum are you ok what is going on?” I think i just repeated what I knew. She quickly took charge and before i knew it, I was sitting in the doctors office in front of my doctor explaining what I think had happened. He checked me over, I had a slight temperature and a normal blood pressure, he said he didn’t think it was a stroke but classic of what they call an episode of TGA and my memory would slowly come back but i would never remember what i had actually done in the approximately 2 hours I was blacked out. Golly it was scary. He explained it was quite rare and even more rare to have another episode of it……………….errrrrrr well he got that one wrong.
See below with caption.
This is me in 2015 after another big episode of the rare TGA. Trust me to prove my doctor wrong. I don’t remember any of that day and ended up in hospital.
Well I spent about two weeks trying to get over my rather scary and bizarre episode of TGA. My husband had been contacted and was brought home early as the doctor didnt want me left on my own. I slowly recovered but never got my memory back. I do know when my daughter bought me home she went upstairs to check the bathroom, and the place was spotless. I had dyed my hair and put all the empty boxes and rubbish in the bin, the towels were in the washing machine, my bed had been made and my bedroom tidied up.
Of course I had to research this phenomenon and it could have been triggered either by my daughters accident or actually hanging curtains as the day before I had hung one set up.
As the days turned into weeks and then months i felt better about it, but still could not remember much of that day.
But lots of weird things were afoot I was convinced at one point my father who had died in 1997 was haunting me as so many odd things were happening but that’s all another story for another day…………all I know is the doctor I saw that day who said it was rare to have another episode got it wrong completely trust me to be different…………….
Rare ……. that’s a laugh
If you have been following me the last blog explained my attack of TGA, and the doctor assuring me it was rare and he doubted I would ever have another attack.
Can’t remember what year or what day, but I was still driving even though I struggled to walk and my mobility was compromised I had gone into my town which is about a three minute drive away. I came out of the supermarket and stood there like a blank lemon where was my car? I always parked it in the same place or close to the shop.
I did panic I found my illness made me panic more now so I rang my daughter I was crying I mean really. “I cant find my car someone has stolen it”, I was convinced. She calmed me down and came straight to me and parked up. “Come on mum” are you sure you didn’t go anywhere else. I assured her I hadn’t. Quick thinking she got my handbag and had a look inside. There was my building society book and clearly inside was a deposit I had made that exact day. Well the Building Society is a few minutes walk from the supermarket.
I had a blank look on my face so she made me stay in her car and went off to have a look around the car parks. She came back about 10 minutes later. “Mum I found your car it was parked outside the post office with your disabled badge displayed. Well I had no memory whatsoever of going there I still don’t.
I started to have odd things happening to me where i would have no memory of doing something but it would only last a few minutes. It was kind of scary, and I found myself writing down such things as I HAVE FED THE CATS or DOGS, I had to constantly remind myself as the animals were getting fatter and fatter. I was also over feeding the fish as i had no memory of feeding them at times.
I started having weird hallucinations with regards smell, it would be onions, or burning, I spent many a day walking around the house scared that I was going to have a fire.
My husband was concerned as he was away a lot but i had a care worker by then who kept me safe.
I have since found about MS and BRAIN FOG…..was I actually suffering from this or was it something else?
I always thought that brain fog in MS was more cognitive issues bit like getting old, cant remember a word or going into a room and not remembering why you went there in the first place. I mean I get all of that anyway. Also like the image I can read a sentence and just not be able to comprehend it at all. I cant concentrate on things for long so tend to flit from one thing to the next. Also my typing deteriorated I would write things and read them back and find words in there which had no meaning to the actually subject whatsoever. I spent ages checking over my work, my spelling well its really not good now and thank goodness for spell check. To me that is brain fog well my version.
What I seemed to be suffering with was more total memory loss. I would for example give someone one of my chickens, and they would comment on it one day, and I would blankly look at them as i had no memory of even talking to them, never mind giving them one of my beloved birds.
I found myself repeating things all the time, I would totally forget what I had said to someone and even that I had said it. This was ongoing and got tiresome but well you just put up with these things don’t you. Until the day you end up kind of waking up in hospital with a blank expression on your face.
It was 2015 I believe October. I had gotten up as normal early Mike and I had hatched chicks and they were about 4 weeks old, so I had to attend them, clean them out and make sure they had fresh water and food. They were so darn cute. I remember doing some of that, then vaguely remember saying to Mike “I feel sick and my stomach felt weird I need to go and sit down”. That was it.
BLANK memory.
Just imagine for one minute not being able to make any new memory whilst you were having an “episode”of whatever it was…..no memory you just sit there like normal hell you even look normal (well as normal as possible), but you are just repeating yourself over and over again, as you don’t remember saying anything…..yep we are back to the old ground hog again………….reliving the same thing over and over again.
I just suddenly and slowly remember looking to the right of me in a hospital bed, as yes I woke up in hospital its like waking up I suppose and realising your surroundings. My daughter was sitting there my eldest you could see how worried she was. She explained what happened, then Mike came in. He had to call an ambulance as i was just sat on the settee complaining of feeling weird and sick and repeating myself over and over again. I have no memory of the ambulance ride, or the ambulance men, or the doctor who saw me when i got there.
I was moved upstairs to the neurological ward, and slowly my memory BEFOREthe attack started to come back. I still have no memory of the hospital. I do remember the next day talking to a very dishy neurologist who after taking my medical history decided i was suffering with Transient Epileptic Amnesia which is quite rare, yeh trust me; way too greedy by halves, not only did I finally get told in 2016 I had progressive MS but in 2015 I was given a cup of TEA…..get it……and I HATE TEA bleurgh never drink it so that’s another joke the Joker has played on me, give me the one thing i really cant stomach…….
T.E.A. = TRANSIENT EPILEPTIC AMNESIA
I take a special tablet every night to ward off other attacks, but I have to say I do suffer with some weird things but then I wonder if they are down to MS brain fog, so much stuff we get is kind of similar and you never know where one thing starts and another finishes.
Sadly this disease has robbed me of some of my autobiography and I lost quite a bit of stuff from my child hood and later, although there is no rhyme or reason to what has disappeared from my brain, and actually lately I have suddenly had flash backs of things I thought I had forgotten.
I don’t think anyone can really understand how scary the episodes have been its left me anxious I know that, and I wont go out on my own unless it is just to pop my dog over the road to our local park just in case I have another attack. 2015 October was a bad month, but November 2015 until the 21st February 2016 was even worse then I could have ever imagined……………………………………
Just when you thought your life was stabilising……….fate kicks you in the stomach….and the EYES have it.
Well where was I? Oh yes 2015 was a very weird year for me and even now I find it difficult to recall stuff after my visit to hospital in a blank wiped out memory state.
I saw a different neurologist in the hospital who diagnosed me with TEA but he told me I needed to see my own neurologist urgently so whilst I was in there they made me an appointment I told them to do it privately as I would see him very quickly.
I had an appointment within a few days.
I saw my neurologist who had my notes and he agreed with the findings as we had been together for 10 years and obviously I had been telling him over that time of all the weird stuff I was experiencing. Also I told him my eyes were playing me up again so whilst I was there he proceeded to test them with cards they use to test for colourblindness. If you have Optical neuritis it can dull your colour perception, I didn’t know that until it was all explained to me. Ishihara Color Test I believe it is called. You get presented with these cards and have to say what number you can see.
Well I failed somewhat I have no idea why, but my neurologist booked me for another Visual evoked response test, VEP for short. If you have never had one of these don’t be frightenedby it as really its nothing to worry about honestly. You just sit down and have wires attached to your head with small patches. The wires record your brain’s responses as you watch a screen that displays an alternating checkerboard pattern.
The test measures the speed at which your optic nerve sends signals to your brain. If it’s damaged, they’ll move more slowly. A piece of cake the worse thing about having them done is the stuff they use to attach the patches to your head its sticky and hard to get off.
Nothing to worry about if your a Motorsport enthusiast its like watching the chequer flag go down for another win for Lewis Hamilton on the Grand Prix.
It doesn’t take long and there are no after affects just matted hair. Now I have to go back again in time sorry folks…..but I had already had one of these in 2008 I think it was. You see from 2007 until 2015 I like you my readers will have been through a barrage of tortuous testing. Some of you will have been lucky in some respects as your tests would have given a clear cut diagnosis of this insidious disease.
However a lot of us poor mortals would end up back and forth being forced into tiny spaces for our MRI, sitting in front of the chequer flat, having a large needle in our back, and more MRI with dye as well (don’t forget the dye) but i don’t want to dwell too much on them as I will write about the tests I went through and the results I had, but yes I had this VEP test before.
The results were wait for it………………..Slowing of the brain bilaterally. The test measured the speed at which my optic nerve was sending signals to my brain and as it was damaged they were moving more slowly. Which indicated I had a bout of Optical Neuritis. When was that, I cant see it would have been in 2000 as Optical Neuritis usually mends itself, so it could have been anytime between then and 2007. Who knows.
So no more answers for me, just more tests. I was put on the tablets for my TEA and my neurologist assured me taking them I would never have another attack, and he sent for an urgent VEP to be performed.
Woopee lucky me. I had that done very quickly which was surprise as I actually didn’t pay for it I was done on the NHS, I believe it was end of November something like that. I just had to wait for the familiar white envelope with the NHS mark on the back to get the results which never came until about end of January 2016.
As you guys reading this know we spend most of our time either waiting for an appointment, OR being put in queue for our tests, then yes waiting and waiting for the results. no wonder a lot of us have high blood pressure.
Life continued after the test in November and I went to my sisters birthday party on the 17th December. It was held in a small cafe about a 30 minute drive away from me, and my care worker took me there. All my family were there including my mum, and all my other brothers and sisters. We are a large family as mum was Italian and there were six of us. The only person missing was my eldest brother who was living in Australia, sadly I would meet him way too soon.
The cafe was like a hot house yes you know what I am going to say, heat and MS do not mix do they. I was struggling to eat my egg and spinach on gluten free bread, when suddenly the vision issues really appeared with a vengeance, they were so bad i could barely see out of my left eye I knew the signs, and sadly had to get out of there. Heat exacerbation is a bitch isn’t it? Sadly I had to split as I felt ill and needed to go home and rest.
Oh the joys of Utoffs syndrome. Hands up all of you who suffer from it? I think for me it is one of the worse symptoms as it can come in many guises.
I will leave my story here for now as what happens after my test is still painful for me but I promise you I will continue my story in a few days.
I will leave you with a laugh for now as it was December I thought this would give you a chuckle. I will be back in a few days.
Following on from my sisters birthday party…………………..
After I had the issue with the heat induced attack of Optical Neuritis at my sisters birthday party, it was only a few more days for Christmas. Just slightly over a week. I cant for the life of me think what we did that Christmas I am sure Mike and I just wanted a quiet one but knowing my family I expect we had a few more for lunch.
What has happened over the last few years has taken away some of my memory sadly, and it is hard to recall events, BUT I remember what happened on Christmas day 2015 not because it was a happy holiday, because the events that enfolded would change Christmas for ever for myself and I believe my family. The main player of this event was sadly my beloved mother.
Mum was going to my older sisters house for Christmas.
Mum had rung my brother up to tell him she couldnt get down the stairs and was in pain in her hip, as he only lived five minutes away he and his wife went straight away to help her. In the meantime they had already told my sister what was happening.
I am not going to dwell on the events that slowly unfolded as I still find it all incredibly difficult, and sadly after weeks of pain we lost mum on the 21st February. To say I was in emotional pain is an understatement. I have still not gotten over her loss, maybe I will write about it one day on another blog but this is my blog about my MS Journey. Yes these events had an impact on my health as any form of stress will trigger off pseudo flares and exacerbation’s.
The kicker for me was just after my mothers death, I finally had an appointment with my neurologist. A letter had plopped onto the door mat and it was from him inviting me to make an appointment as the results of my last VEP test back in November were positive once again for slowing of the brain………………………..Oh the irony of it, the results came to me by snail mail obviously and if only the results had come before I lost mum, I could have finally told her what was ailing me all those years. I could have finally told her, that the times I wanted to come and see her but had to cancel last minute was because I had Progressive Multiple Sclerosis which was slowly bit by bit eroding my life and abilities, much like one of those cliff edges that slowly crumble over time and you end up splat in the sea.
Like the house about to fall over the cliff edge; having PPMS eventually I too will eventually tip over the edge. Mine is slowly tipping over in the form of my disability. Since my mothers death and another horrendous event which I will talk about soon, my health has eroded so it is now precariously hanging……I am trying hard to stop it because I have the strength and genes of two wonderful people who made me strong my mum and dad.
I could have told her “mum I wanted to see you but my MS is playing up”. Not going to see her when I had arranged it, always made me feel bad about myself and frustrated to hell as I just didn’t understand why. I do now sadly.
Life after mums death was hard; my MS had gone into a tail spin, I had lost interest in life I just couldn’t get out of the depression that was surrounding me like a black cloak. I hated feeling this way. I don’t know how I got through my mums funeral but I did, and I managed to respect and repay all the love she had shown me over the years by talking at her funeral even though I was supported by my daughters trying to keep me upright, I managed from deep inside of me to quote a wonderful poem…...you can read it here.
If you want to know more about my mum you can read the tribute I wrote for her here.
(The tribute is in a form of a tri-fold sorry it was the way I handed it out at the funeral.)
Because of the nature of her death, I had a job to do which helped me grieve and get through these dark days, my job was to make sure that no other over 90 year would be treated as badly as my mother was that fateful Christmas day 2015. I put together a case of complaint with the help of my sister, and eventually the surgery where my mother attended was taken to task over her unnecessary and untimely and painful death. She would have been 93 on the 6th January. A wonderful women born in Italy, I will write about her one day and link it here but not now, this is about my journey I dont want too many distractions.
Life slowly came back into balance. My label of Progressive MS made no difference to me not really, it just made it easier for other people to understand why I was who I was now.
Anyone reading this with MS knows how hard stress can affect our lives. Probably stress could be one of the main factors which triggers off this disease. Mine started not long after I lost my father in October 1997 so perhaps it is right. For those with MS this is an interesting article about how to deal with it, and for those reading this because they are my friends and what to join in my journey and understand more about me and my partner MS, the link will give you a little insight into what things I have to avoid and why.
Now I finally had my label I was scheduled on a round of appointments. My first one was to see the doctor at the Pain Clinic. Yes MS sadly does give you pain. Did you not know that? Some doctors say it doesn’t, but it does and it really depends on what type of MS you actually have. Did you know there was more then one type of MS?
Relapsing-Remitting MS (RRMS). This is the most common form of multiple sclerosis. …
Secondary-Progressive MS (SPMS). In SPMS, symptoms worsen more steadily over time, with or without the occurrence of relapses and remissions. …
Primary-Progressive MS (PPMS). …
Progressive-Relapsing MS (PRMS).
I am blessed with PPMS. This one is probably rarer then the first one RRMS. It can show up later in life …. although I am not convinced as I can remember having wierd episodes way back in 1981 but one neurologist told me if it was MS then I would be more disabled….err more disabled then whom? Every single person with MS the effects are different that is why MS is called a SNOWFLAKE disease. There you go you see if you stick with me you will all be MS experts.
Millions of snowflakes that’s us
Every person with MS will have different symptoms. Their diagnosis will come about different to another. Everyone of us our treatment will be different.
So THINK on all of you reading this who don’t have MS do not make the fundamental and errr annoying mistake of saying to someone with MS well I KNOW Joe Bloggs who have MS and he can still go on holidays. Good for Joe Bloggs but remember whoever you say this too may not take it well.
I have had it said to me and believe you me it really is annoying, because don’t these people actually think I would like to go on a holiday? Don’t these people think that if I had the energy even to travel 30 minutes without it wiping me out I would be the first in the queue to do it? Just remember there are approximately 2.5 million people in the world with MS and we are ALLdifferent. …………………….
Where was I, sorry I do have a tendency to wonder off ……. ah yes the good old Pain Clinic……PPMS has pain oh yes. Now again we will try and tell someone I have pain I am in pain and you will usually be encountered with “oh yes me too” I have the same. Meaningful people, wonderful people who have to encounter with something. IF you don’t have MS and your talking about your hip or poor knee joints, or arthritis etc etc et el….yes you will have pain BUTit wont be anything like the MS pain………….. yours will be crumbling joints, dry joints, slipped joints (joints i.e. bone not the smoking kind), its a different kettle of fish. (I love that expression……….now Zenda don’t get distracted).
Mine is down to a wonky nervous system. The signals from my brain to my body are all screwed up, so my pain in essence is actually well not real but equally its horrendously painful and lasts 247 unless I am asleep.I hate nerve pain.
Sometimes I actually feel like that photo as though I am on fire. Its horrendous. Nothing makes it better. Going back to the pain clinic my doctor told me all he can offer me is drugs they use for depression/Psych drugs which I have tried most of. He actually was quite honest with me and said all they do really is turn you into a zombie. I decided as they don’t suit me I would go naked. I only allow myself one 2mg diazepam at night which I take when I have been woken up with a spasm. So the pain clinic for me was a bust no point really it was just a case of get on with it, like I had been doing anyway.
I find my self management as good as anything the NHS (in the UK the NHS runs our medical care) can chuck at me.
Whilst at the pain clinic I was encouraged to attend an evaluation by a special type of psychologist cant remember her exact label or name. I went with my care worker. It lasted ages and exhausted me. The up shot of two exhausting hours was for me to attend a Mindfulness Class. Really? I was to say the least shocked after all that talking about my MS AND how it affected me a course on Mindfulness was going to be my saviour. I was given a sheet of paper with links on it and told to go away and have a look at the classes and what they were about.
Eventually after waiting weeks i was given an appointment to attend one. The class was in the City at 2pm for 2 hours. Now I explained quite clearly to this therapist the afternoons were a NO for me as by then I was exhausted and also to attend a class which meant I needed transport was impossible as I didn’t drive. It seems the therapist as per usual just didn’t bother to listen to me.
I often wonder if they get some sort of pay back to fill these classes as really the point of them well you can now get an APP and download it and get cured without even leaving your chair. https://www.healthline.com/health/mental-health/top-meditation-iphone-android-apps#headspace
After that appointment I gave up with doctors, and specialists, and spent the rest of my time filling in forms and writing letters of complaint about the way my mother had been treated by her Primary Care Surgery.
I just muddled on to be honest coping the best way I could and was at least pleased that our family were given an apology for the poor way my mother had been treated. It went some way for me to cope with her senseless death.
I don’t remember much of 2016 and I know Christmas was quiet as i couldn’t bear to think about it without my beloved mum being able to be part of it.
Life moved forward and I just learnt to get used to having my MS and did it my way as good old Frankie would say in his immortal song. It worked for me.
Yes life was just well………. trying to cope with my illness and my husbands COPD and life in general until that awful and fateful day of 3rd October 2017 at 05.00 hours when my world came crashing down the cliff edge.
I will talk about this on my next blog……………….
When Grief came knocking on my door……….
It suddenly went deathly quiet when my husband took his last breaths on earth it was surreal, I looked at him laying in the hospital bed he looked asleep but I knew he wasn’t as he was finally quiet and peaceful. I felt a sudden sense of disbelief he was gone, just gone like he never existed. I started to cry and rant “he cant be he cant be”, I tried to shake him awake he wouldn’t wake up. I just cried by burying my face into his thin dead arm and just cried until I thought my heart would break.
It was the 3rd October 2018 at 5.00am.
Grief swaddled me tight and wouldn’t let me go, I just wanted to be with him there right now. How could this be happening my mind was in a turmoil thoughts racing, Mike Mike don’t leave me please I need you I love you……how could it happen, how.
Just a week prior we were so happy. It was the weekend of the 23rd of September I remember it. Mike had woken up and as usual he was sitting in our conservatory in his chair and we started to talk about our future. We had been mulling over for a long time after he retired if we should move for our health.
He suffered with COPD, and I of course had my MS. Both of us yearned to be near the sea. It was almost like it was calling us both. “Mike said to me that morning, what do you think about me going over to the Isle of Wight and do a reccy for places that might suit us. Can we afford it?” “Yes of course we can” I replied. “Will you be strong enough though hun to do the journey”, and he looked at me with those blue eyes of his and said of course he would be, he hadn’t felt so good for ages.
Well I know that is true, as well I was constantly nagging him about his hoarding and if he was really serious about us moving he would have to start chucking out some of his treasures he had saved for years otherwise we would never be able to move. I found him one day not long after actually tidying up his bedroom cupboard I nearly collapsed with shock. He was obviously serious then about moving.
Going back to the conversation, I agreed if he wanted too then I would book him a ferry passage and find him a nice hotel. Whilst he was there he hoped to meet up with his son who lived there. It would be like a little holiday for him, he deserved it as recently he had a scare with his health on top of his COPD in a form of a lump in his breast. After tests it showed it was benign, phew one less thing to worry about, but worried I knew he was.
We agreed the date he would set off which was the 26th of September. He was full of it for the next few days, chatting about the IOW, the areas he should look at and I went off on Google and found some properties for him to have a look at outside.
It was time for him to leave, he was packed and ready to go to catch his ferry. Its not too long a drive to Southampton from where we live and he made good time. When he got to the ferry he rang me and we chatted a bit until he boarded.
Whilst he was away he rang me regularly with updates on areas, which I would mark down as good, bad or plain right ugly. He met a young couple in his hotel and he told me they chatted on the Wednesday night and he was so happy animated like the Mike I used to know a funny caring Mike who could sure spin a yarn and make people smile.
I asked him if he wasn’t too tired, and he assured me he was fine, he was a bit sad as he hadn’t managed to catch up with his son, but he was busy at work, and well it was short notice so couldn’t take any time off. Still Mike wasn’t too upset as we were going to go back anyway and would make sure the next visit was more organised. I had already found a few self catering cottages to stay and they would allow us to take our dog Lucy.
He finally arrived home on the 28th September, tired but happy. After a bit of rest he was off to town to buy his usual beer and fags, and asked me if I wanted anything. You see he was sort of my carer too as I was limited.
I couldn’t drive or go out on my own, so having him leave me on my own was quite daunting for me to be honest. I hadn’t been on my own for a long time now since he retired when he was 70. Mike was just always there and I knew if I needed him he would be there for me, so it was with a sense of relief when he came home I felt safe again. I asked him for some Maltesers my very naughty and sinful treat I allowed myself now and then.
Off he went on his big black mobility scooter. He loved that thing. You know I never would have thought in a million years I would see my husband driving one of them instead of a Hillman Imp or Mini, as Mike was an amazing driver and won many awards for Hill climbing and grass track driving.
He had no fear whatsoever. Seeing him drive off on his scooter was a far cry from the days he was trailing his cars, although to be fair only a few months prior to this he had come FIRST IN CLASS in a competition not bad for an old man of 71.
The first image below is his very last trophy he won a tropy Piston. This was for the last competition he did in his Corsa with my grandson Conner. (Mike with his mini and favorite Imp).
Going back to Mike driving off on his mobility scooter I really must stop this habit of mine of going off on a tangent.
He was out for a good hour I wasn’t in the least bit worried, as Mike was a talker, and I expect he was chatting to all and sundry on his journey to the shops he was a very sociable guy, he just loved talking and the locals new him and respected him, as well. Mike was a good guy one of the best and would help anyone who needed it.
Finally he came home….and yes you got it did you, he forgot my Maltesers he was so engrossed in talking to everyone about his journey to the IOW. Oh well I forgave him they only give me a stomach ache anyway as they have gluten in them. (A bit of useless information a lot of people suffering with MS have a gluten intolerance).
Where was I, oh yes. He was back home safe from his travels.
The next day was Friday and I had an appointment at the doctors the 29th. I heard Mike coughing in the night, but well that is normal for him. He had the worse cough most days, but still insisted on smoking, it used to drive me mad, but well what can you do, it was his body not mine.
Jade my care-worker was with me to collect me, and Mike started to come into the sitting room, we could actually hear him before we saw him, as his chest was whistling and wheezing so loud it was like an old steam train. He didn’t look special. Instinctively I took his temperature, it was up not high but up. When you have COPD you have to be careful as you can get chest infections very quickly. As I was going to the doctors anyway when I got there I asked the receptionist if she could arrange for a doctors visit as I didn’t want Mike going out with a temperature.
When I got back from the doctors, he was still feeling a bit rough. The doctor arrived soon after I did, and checked him over, and said he couldn’t hear any congestion, but put him on steroids and a course of antibiotics just in case. Jade went off and got them from the pharmacy and Mike started them straight away.
On Saturday he was better his temperature was normal again. I just assumed he was tired from his trip. He felt so well he went off again on his scooter to talk to his friend who owned a shop in the town and tell him all about his trip. He came home about an hour later. He did look tired, so I told him to rest.
On Sunday, he wasn’t well. Now I know that with my MS I just deal with it, nothing much else I can do, but someone suffering with COPD is a different thing. Its quite limiting, and Mike was at the point he got breathless very easy and tired. I would always regulate his condition, so I took his oxygen levels, his blood pressure and temperature, and bizarrely they were all low, which puzzled me. I had never known him to have low oxygen as even though he had COPD his oxygen was always good.
I told him I felt he should see a doctor but he wouldn’t hear of it and got anxious and unusual for him, irritated with me for suggesting it. I said fair enough go and have a sleep and I will see how you are when you wake up. Three hours later he woke up so i did the tests again and they had improved so I decided not to stress him more by talking about doctors visiting.
During the night I could hear him coughing again.
It was early about 6am I heard him go to the bathroom. He would always pop his head around the corner when he got up to see if I needed help getting downstairs or if I needed anything. I waited for what seemed an eternity but he didn’t come in, and I strangely enough I never heard him leave the toilet which set alarm bells off.
I felt anxious and worried so I managed to get up and go and see what was happening.
Never did I expect to see him like that.
I have a fold down support bar between our shower and the toilet, and he was hanging on to it, and well he looked terrible. “Mike whats wrong hun I asked”. He struggled to even look up at me, his blue eyes were gone they looked lifeless and his mouth was opening but nothing sensible was coming out of it. I could clearly see he was in distress and pain, and was clutching the side of his chest where he had the breast lump, I sort of heard him say PAIN, PAIN, help me..but it was like his tongue was swollen and the words were almost unintelligible.
They say when you are in a position of stress and fear your Adrenalin kicks in. I have no idea what I did but somehow I put a blanket over his shoulders and told him to stay where he was, i was getting our neighbour.
I managed to get my neighbour who was shocked when he saw Mike, we decided to leave him on the toilet with a blanket as he was simply unable to move. I finally got the ambulance and two paramedics make to attend to him.
They said it was urgent they got him to hospital. It was easier if they just got him and go, rather then wait for me to get things sorted out.
I went out with them, and when they put him the ambulance and he turned around and looked at me I knew he was in for a rough ride, his oxygen mask was filling with moisture from his breath as he struggled to get air, and his eyes were beseeching me to follow him to be with him.
I must have been so shocked as I fell right in front of the ambulance men I had forgotten for a minute I had MS and was just not thinking about my own safety it was blank gone. They helped me up and made sure I got back to the house safe. I was fine, just scraped a bit when i fell against our wall. They told me they would get the doctor to ring me with an update then I would be able to go and see him I had one last look of Mike before the doors were shut and the blue light started to flash and they were off taking my Mike with them.
The phone call finally came, it was bad news. She said he had pneumonia with sepsis and the next 24 hours would be crucial. He was in resuscitation ward and i could go and see him. My daughter picked me up and we raced off to the hospital.
Now really what would you think if your husband was rushed to hospital, gasping for breath given 24 hours to either live or die……really what would you think?
My daughter pushed me in my wheelchair to the resuscitation unit I was dreading going through the doors to see him, probably laying down with bits of machinery coming out of his body.
I felt sick with fear. When we got into the ward the first person we saw was Mike. Sat up in bed eating DRIED BISCUITS and having a drink. I was so shocked if I had been standing I would have fallen down.
He even managed a cheeky smile. I just cuddled him and hugged him with relief. He was telling us both he thought he was being pumped through with steroids and felt not too bad.
We talked and he said something odd, he told me close to my ear that he had lived the best 25 years of his life with me and he was really happy and then he said those immortal words I will never forget as long as I live……..
“Zen, I don’t want to go to the IOW to be truthful its a real DUMP lol…………………… can you start to look at Minehead?
Well I wasn’t sure whether to laugh or cry, that was the Mike I knew. He was back. My immortal Mike who had been through some terrible diseases and always bounced back.
He wanted his phone and a few other bits so I told him I would go home and his son could collect them from me, and give them to him, as he was desperate to see his sons.
All went as planned and phones and bits taken to the hospital for him. Mike rang me at lunchtime, said something about it not being the right phone, not quite sure what that was about, he was ok, and his other son was coming about 7pm to see him. He told me not to go back as I would be too tired, and would prefer me to visit him in the morning. I had no thoughts in my head I wouldn’t see him again so agreed.
I had a phone call about 7.15 I think off his son. He almost sounded relieved as when he saw his father he was fine, tired yes, but making his usual jokes. He did tell me later that when he was there he told him, he didn’t want to die, not really he wasn’t scared, but he didn’t want to die as he would miss ME too much, those words have been a comfort to me in my dark times to be honest. I felt relief he seemed to have rallied and was looking forward to seeing him in the morning.
I had taken my MS medication and was almost asleep it was about 9.15. It was the ward Sister. I knew straight away by her voice it wasn’t good. “You need to come now she said”. Your husband is declining fast. I thought I had misheard her, she repeated herself, I just said ok put the phone down and on auto pilot rang my daughter who collected me and we were in the hospital and by his bedside very quickly. I managed to get hold of his sister and sons who came to be with him.
He wasn’t there. He just wasn’t. The person in the bed looked nothing like my Mike, he was in a coma and breathing was so loud and laboured every breath must have been painful.
I stayed with him all night which brings us back to 5am 3rd October 2018, when he took his last breaths and left me and the uninvited guest grief came to visit me.
The fall out from his death was like an atomic bomb going off.
THE FALLOUT FROM MY HUSBANDS DEATH TRIGGERED A PROGRESSION OF MY MS
I always thought that brain fog in MS was more cognitive issues bit like getting old, cant remember a word or going into a room and not remembering why you went there in the first place. I mean I get all of that anyway. Also like the image I can read a sentence and just not be able to comprehend it at all. I cant concentrate on things for long so tend to flit from one thing to the next. Also my typing deteriorated I would write things and read them back and find words in there which had no meaning to the actually subject whatsoever. I spent ages checking over my work, my spelling well its really not good now and thank goodness for spell check. To me that is brain fog well my version.
Like the house about to fall over the cliff edge; having PPMS eventually I too will eventually tip over the edge. Mine is slowly tipping over in the form of my disability. Since my mothers death and another horrendous event which I will talk about soon, my health has eroded so it is now precariously hanging……I am trying hard to stop it because I have the strength and genes of two wonderful people who made me strong my mum and dad.
My Journey with MS 