Gadgets and gizmos

 So, today the riser recliner was taken away. As you know, it was no longer performing its function and Roch rarely chose to sit there. But a huge thank you to the MND Association – that chair helped out for eighteen months (see blog post Tuesday 8 November 2011) and became part of the furniture in our house (ha ha). It’s kind of sad to see it go, but it makes way for a new model, one which will hopefully be not only comfortable, but practical too.  The new model hasn’t arrived yet but I will keep you posted.

 As with all people living with MND, Roch is passing through the different stages of reduced function, more slowly than most, it must be said.  There are so many innovations, so many gadgets and gizmos to help out. Mostly, as functions fade and strength diminishes, one of the professionals will have a suggestion to help.  Inevitably, the time comes when each gadget fails to perform its original function and then we move on to another stage.*

There is a cupboard in our bedroom in which I store many useful things but lately I’ve noticed that items end up there which have outgrown their usefulness, at least for us. A bag of ‘foot ups’ and ankle straps – those were life savers and allowed Roch to continue walking by keeping his feet up and preventing his big toe from dragging on the ground or catching on the pavement as he lifted his foot. It was the foot ups that got Roch noticed when we were in Venice in July 2010. A friendly American, travelling on a vaporetto with us asked Roch why he wore them and that led to a conversation about MND and about the research the American was doing in Venice (involving saints and their dogs, which naturally included Saint Roch – coincidence or what?) and so we met Lerick and made a new friend. When we were in Venice, Roch was using two sticks – his sticks have been put away now, too, although one of them comes in very handy when the toaster sets the ultra-sensitive smoke alarm off in the kitchen. Sometime soon, I will blog about other trips after diagnosis in the days before the blog (New York October 2009 and Tenerife February 2010).

Roch went on from using sticks to using the rollator. Ah, the day the rollator arrived, I remember it well (see blog post Friday 26^th March 2010 where I recorded Tom’s reaction when he saw it). Roch hated it at first, but it became his best friend. Now we all call it ‘rollie’. This morning, for the first time in ages, Roch was able to get out of bed by himself and, using old rollie, went to the bathroom and then the kitchen to make himself an espresso. A good start to the day.

In other good news, the OT reminded us that we had a handling belt somewhere and I went in search of it. Yes, it was in the famous cupboard! Yesterday Roch had lunch out with friends and the belt proved really useful when helping him to stand.  Another great innovation.

The ‘sock putter-on-er’ is also in the cupboard now. Roch continued to dress himself for as long as he could. I remember remarking to someone only last year how I would use the time he spent putting on his socks and shoes to put on my make-up (it took longer and longer for him to put the socks on but my face never looked any better).  Eventually it took him so long and he was so tired that he surrendered this task to others. But the ‘sock putter-on-er’ was another Godsend.

Sometimes I hardly notice when one stage is over and another begins. When I saw the bag of ‘foot ups’ in the cupboard I sat back on my heels to think. I couldn’t remember the last time he used them.

A new phase is beginning for us with the new car. We have our first test drive tomorrow in a WAV (wheelchair accessible vehicle) which is exciting. We are test driving the Fiat Doblo SpacePlus. I can’t wait to be able to drive off to new places together. The fly in the ointment is the new wheelchair. The other day (hot and sunny – remember what summer felt like?) Roch spent most of the day in the garden in the new chair, which was fully charged. He may have come in and out of the house a few times over the course of the day, but by tea time, the indicator on the chair was suddenly down to one light (from full) and the chair would not respond to commands. He called me outside and we were just working out how to get him in to the house when the lights flashed on and the controls responded again.  Back inside, I plugged the chair into the battery charger and the charger showed empty although the arm control pad showed full. How can we trust this chair on the streets if we can’t even trust it to take him back into the house from the garden? I say we need a brand new chair as clearly this one is a mess. But we will use it for our test drive tomorrow, because we are sick of waiting and our lease is nearly up on the old car. Frankly, I need to be able to get him out and about, further afield than the High Street.

So, if anyone wants a sock putter-on-er or some foot ups, you know who to ask.  Actually, you can probably get them from your OT, but if anyone wants ours, that’s fine too.

*Liam Dwyer has a really helpful website called www.disabled4disabled.co.uk  which is worth a visit. Liam has spent a lot of time and money researching suitable equipment/facilities to suit his needs as a person living with MND. On his site you will find a useful A-Z listing positive experiences not just from Liam but from his readers too. You can add to the information on his site with useful tips and ideas. 

The curious incident of the man in the bathroom

I have thought about whether it’s entirely fair to Fred (see below) to blog about this, and I have my doubts, but really, I find that I cannot let it go unrecorded. I mean, what is a blog for,anyway? There is a funny side to it and I can see that now. But when I heard about it first, it left me feeling stressed, angry and anxious. Bear with me in my attempt to maintain a fiction of pretence. “Names have been changed."

 

It all began as a certain person living with MND (let’s call him Rodney) and one of his personal assistants (let’s call him Fred) prepared for the daily shower. Fred felt the unmistakable signs of an imminent bowel movement and he alerted Rodney to the possibility that the shower might have to be postponed as he answered nature’s call. However, the urgency of the sensations appeared to fade and so he told Rodney it was safe to proceed with the shower. This was a mistake. Having settled Rodney on the shower seat in the wet room and begun the process of washing Rodney’s hair, Fred’s bowels once more called for attention. This time they could not be ignored. Rodney suggested that Fred use the upstairs toilet, for obvious reasons, and Fred concurred. Now, I have often observed that when necessity demands, many people prefer the privacy of their own bathrooms, and clearly Fred belongs to this group of the population. Earlier, he had mentioned his intention to use the toilet at home, as Fred lives only a few doors away from Rodney’s house, but Rodney had objected to this, insisting that he use the toilet upstairs and not leave the house.  Now, in the wet room, as Fred informed Rodney of his urgent request, Rodney once more told Fred expressly to go upstairs and not to go home. Fred agreed. “Ten minutes,” he promised and left the room. Moments later, Rodney, sitting naked on the shower seat in the wet room, heard the front door slam and his heart sank. Fred had locked himself out of the house. Rodney was trapped on the shower seat, wet and dripping. Now, we know that Fred has a short term memory problem, but this is ridiculous. It is a few short steps from the door of the wet room to the bottom of the stairs in Rodney’s house but in the length of time it took for Fred to traverse this space, he forgot that he was to go upstairs. After a time, Fred returned to the house and soon realised what a stupid thing he had done. They conversed through the window of the wet room. Happily, Rodney made no attempts to stand up alone. It was 8.30am on a Wednesday and he figured he only had an hour to wait until the cleaner arrived. And so it proved. As usual, on the dot of 9.30am, the cleaner arrived and let Fred back into the house. Rodney had carefully arranged a selection of shampoos and shower gels on the shower seat to preserve his modesty, just in case she was standing with Fred when he opened the door. But there was no necessity for this precaution. In Rodney's own words, "Disaster had been averted".

 Reader, if you saw it on TV, you wouldn’t believe it could happen. Short term memory loss is tragic and Fred was very contrite.  Rodney was fine, the room was warm and he came to no harm. No further incidents have been reported to date. Precautions have been taken and the matter discussed but what will happen next? Tune in next time...

 

Me time

It’s a beautiful sunny Bank Holiday Monday.  The good news is that Roch has gone to watch the football at Brentford – and I am so pleased for him! He hasn’t brought the new wheelchair, although it has been returned to us and they say they have fixed it. We are not entirely convinced, and felt that it was too risky to rely on it for Brentford today. He has gone in ‘old reliable’, which they have left with us for the present. The bad news is I feel pretty shit today so although I now have some precious time to myself – I have no interest in doing anything or going anywhere.   I do have to do some grocery shopping, however, so first, I drive to Tesco.

Before I leave, I make a list. I am good at lists. Half way there, I realise that I have left my list behind, but I figure I can remember most of the stuff, so I drive on, somewhat distracted by the maniac who appears to be rally driving behind me.  However, as I take my turn for Tesco, he races off somewhere else, much to my relief.  It is then, as I park the car in the Tesco car park that I realise I have left my wallet and purse behind. No worries, I think, although my heart sinks at the thought of having to drive home and back again, but back home I go. Having retrieved my list, wallet and purse, I set off once more. This more or less sets the scene for the rest of the afternoon. In Tesco I drift around the aisles in a mental fog but aided by my list (I would never have been able to make a decision without it) I finally arrive at the checkout and manage to behave like a normal person, even remembering my pin number and smiling in a friendly way at the young man who serves me. Somehow it all seems so boring and pointless.  But I’m pleased with the bunch of white roses, which I buy for the bedroom, to replace the wilting stems presently adorning the sideboard.

Home again, I tear a bottle of mineral water from its plastic packaging and drink thirstily. I need to put the perishables in the ‘fridge but as I cast an eye over the shelves I remember guiltily that a number of items are past their best and need to be chucked. Trying not to think about the wastefulness, I duly remove the bad food and replace with the fresh stuff. By now I am hot and bothered and anxious to use my free time for ‘myself’, so I hurry upstairs and select a sun top (a bit revealing but no-one will see me, at the same time I notice a stain on my trouser leg – dammit! – so I change into different trousers – why I think I have to do this, is beyond me). Flip flops replace my ‘good’ sandals. I should use this time to paint my toes, really, I think. Pink nail varnish beckons. On my way out of the bedroom I hesitate – should I put on a wash? I glance at the pile of clothes on top of my laundry basket. I suppose I should. Grabbing the clothes plus my mineral water (I am already clutching my nail varnish plus base coat) I hurry downstairs and fill the machine. Now, ME time. It’s a sun trap out there, so I spray some sun protection on (brand new from Tesco) and I’m just about to go outside to the garden when…I spot my roses. Oh no, I can’t leave them there, have to organise them. But now I’m in a hurry so I randomly start choosing stems, cutting them and sticking them in my lovely vase. I stand back and realise that although the blooms are gorgeous I have pretty much made an arse of the arrangement. This figures but I can’t be bothered to give them more attention. The roses go into the bedroom. Great, now all I have to do is sit down in the sun and do my nails. I settle myself on one of our rickety garden chairs and prepare to enjoy my ‘me’ time. Base coat on, I close my eyes and try to relax. But there’s too much going on in my head.  

We’ve had a bit of a setback of late. Over the past few months, Roch’s shoulder muscles have wasted considerably and this has led to new problems. It’s uncomfortable for him to lie on his side, especially his right side, and some mornings his right shoulder has been painful. We were advised by the physio to try some gentle exercises – lubricate the joint, so to speak. I must say I haven’t been great at remembering to do this. It’s only been when Roch has complained of the pain/discomfort that I’ve remembered, and each time, after exercise, the shoulder has improved. Last Thursday his shoulder was giving him problems and so we did some exercising.  The physio was due to visit that day and so I suggested that he mention it to her, just to make sure we were exercising it properly. It was one of my work days and when I got home, Roch told me that his shoulder was so painful, he couldn’t use it at all. She had done some work on it, although he said it hadn’t hurt at the time. Perhaps it was a coincidence and would have happened anyway, but I couldn’t help feeling cross. I was cross with myself, too. I can’t help wondering if I had been more consistent with exercising that shoulder, would it have reacted so badly when she worked on it?

 It hurt so much that he couldn’t put any weight on it, which meant he couldn’t use his rollator at all or help himself up using his right arm, so having a piss by himself, which he can sometimes manage, was out of the question  – even eating was a problem.  We adapted quickly and once more, the hoist has come into its own. Thank goodness we had had the bed moved, as I can position the hoist perfectly in the bedroom now, and lower him onto the bed/raise him up, as required. The Lenor bottle must be used at present all the time. Not having the use of his shoulder and arm has made him more dependent.  I look at him and see how physically diminished he has become. Today I find it hard to be optimistic.

Tom has helped out on a number of occasions, using the hoist and helping his father to piss into a bottle.  I wasn’t sure about asking him to do this but they have managed it between them with a mixture of humour and mutual respect. It can’t have been easy for either of them.

I guess last night didn’t help either – I am so hopeless when my sleep is disturbed, and last night Roch needed the toilet at 3.00am. It must be hard to have to wake your partner from a deep sleep to ask them for help. How rotten not to be able to just get up and go off to the bathroom yourself? With the bad shoulder, he could never attempt it, so I duly stumbled round with the hoist to bring him out but whenever I have to get up at night (and it’s not often) I find it harder to face what lies ahead.

Roch went to the doctor on Friday and she prescribed strong anti-inflammatory medication, together with tablets to protect the stomach. His shoulder is improving and today he used the rollator again. But as I sit in the sunshine, painting my toes a frivolous pink, I cannot fully relax. I just can’t do it. I feel anxious, depressed and tired. The sunshine is lovely, our garden is, as always a haven of greenery and birdsong but I know that what I really need to do is sit down at my laptop and blog. And so, sitting at our kitchen table with a cup of rooibos tea and that same bottle of mineral water, I start to type.

 

 

 

Being normal

You may have noticed that I slyly mentioned a weekend away in my last post (Wheelchair woes). That weekend was made possible by Roch’s brothers. Paudie stayed with us for a few days before I went, which meant I could prepare everything and catch up at home before heading off, and Mairt came the day before I went away, and stayed for an extra day after my return.  My personal  thanks to Paudie for fixing my bike and getting the car washed!  And to Mairt – thanks for the little kindnesses like a cup of rooibos tea in bed (luxury!) and fixing a hot water bottle for me, as well as Roch.

 I spent the weekend in Bath with a good friend and had a lovely, lovely time. I knew that Roch would be well looked after in my absence and I think the brothers had a good time together.  I now know they are willing to help more often  – I said to Mairt that we had been trying to continue as normally as possible – i.e. not asking for help and going it alone, so to speak (maybe that was just me). He said, “Part of being normal is going away sometimes.” I realise that he is right – so thanks boys for the ‘dig out’ as Roch would say. Plans are going ahead for another break in July!! See you then...

My time away was paid for by the annual one off Carer’s break payment – which I applied for before the deadline (end of March) and happily was granted. Last year it was £350, this year it was £250 but very welcome, all the same.   

The sun goes down over The Royal Crescent, Bath 12/04/13

Wheelchair woes

It’s been a while now since Roch and I have been out together in the Berlingo (I can’t get him in or out on my own) and it’s been a while since he has been able to get out of his riser/recliner on his own. Most evenings he will sit in his wheelchair to watch TV as he feels trapped in the recliner and very much dislikes my having to use the hoist for him. But the wheelchair isn’t so comfortable for him to sit in all day long. That’s why we were so delighted when the new power chair was delivered two weeks ago. The new chair should have been the solution to several problems at once.

I had the last two weeks off work and we had planned that last week would be spent test driving new WAVs (wheelchair accessible vehicles). Something we couldn’t do until we had the new chair. Just the thought of being able to get out and about together, without having to rely on taxis, really cheered us up. Lately it’s felt like a long hard winter and Roch has just recovered from a heavy cold, which left him feeling pretty low.

The new chair also has several new features including a head rest, also the back can recline, the footrests can be elevated (this will help with circulation, as his poor feet get icy cold) and it will be so much more comfortable for him to relax in in the evenings, until the new riser/recliner chair arrives. Most of all, it is the key to a new freedom of movement – new wheelchair = new WAV,  and in my mind was connected to thoughts of Spring and a feeling of renewed optimism – which is why it came as such a crashing disappointment when, fully charged, it came to a halt in the middle of the High Street the first time he rolled out in it. Thankfully he was with one of his brothers at the time. I certainly couldn’t have pushed it two inches, never mind to the nearest pub! But Paudie managed with some difficulty to do just that and Tom got the distress call and headed off from home with the charger. Back they came, having charged the chair in the pub (no great hardship there) and we just assumed that it hadn’t charged properly in the first place. No harm done. So we left it charging overnight and next day Roch, this time accompanied by two brothers (Mairt had arrived in the meantime) – headed off down the road to enjoy lunch out together. Five minutes later Paudie was back. This time the chair had stopped at the end of the road! So Paudie brought the manual chair back, they transferred Roch to this and came back, one pushing Roch and the other with the power chair (no easy task to push this). Again, how lucky that his brothers were with him?

This all happened 12 days ago. The day after the second breakdown, Serco sent someone round.  At the time I felt like I was deserting the sinking ship, as I was on my way out the door to catch a train for a weekend away. But I knew that Roch and his brother would be able to manage and secretly I was pleased that I wouldn’t have to deal with this particular Serco guy as in the past I had found him at best uncommunicative and at worst downright rude. So as I sped away in my taxi (!) I took a deep breath, and let go…

Meanwhile, back at the ranch, Roch was trying to explain the problem to Serco man. The experience was frustrating to say the least – Roch told me that he felt that he wasn’t being listened to and that this guy had no appreciation of what it meant to Roch to be without a reliable motorised chair – not to mention having been stranded twice. It is an essential piece of equipment and he has to be able to rely on it.  Serco man was unable to say what was wrong with it, he was unable to get it out to his van – so in the end he left it with Roch and told him it would be collected on Monday and a substitute chair provided until it was fixed. This left Roch with the unreliable chair for the weekend. It worked intermittently and brought him round the house, had to be constantly charged – but he could not trust it to the great outdoors.  Serco did bring the old chair back the following Tuesday and they took the new chair away again for repair – but here we are with all the same problems – our purchase of a WAV has been put on hold, we are back to taxis and we still don’t have the riser/recliner either, so he is trapped in the old recliner for the evening or has to sit in the old wheelchair all day and all evening too. It would have been nice to go out somewhere over the last weekend before I go back to work, as the weather was lovely.  I guess at least we have the garden, which is delightful to sit in when it’s sunny and warm, so it could be worse.

Roch has made a complaint to Serco and they have responded by apologising profusely for their operative’s attitude and behaviour, which is good.

But we still don’t have the new wheelchair and frankly I am fed up with it.

A warning for Carers - don't try to do too much!

 

 

Doing 'nothing' is the new busy

 

There are so many things to do. My life is made up of scores of lists. Some days we get up late and by the time we are up and organised it's midday and I feel I have achieved so little (those lists in my head, reproaching me!). Today I said this to Roch. He said to me, "Doing 'nothing' is the new busy." I've been thinking about it.  I realise that my lists don't include all the essential tasks carried out as a Carer. Once I have helped Roch up, to the toilet, with his shower, dressed him, given him his meds, coffee, breakfast (if he feels like it) and he has everything he needs to hand - then the other tasks begin. By midday today all this was achieved (plus one wash on the line, another in the machine) and he was enjoying the sunshine. Not bad.

 

Sometimes we Carers need to forget about the lists and relax and give ourselves some credit for all the things we just do without thinking. Maybe we should all start to write lists entitled 'All the things I have done today.' But then, that would just be something else to do, wouldn't it? Maybe just put your feet up and feel smug instead.

 

For those of you who dislike sentiment, look away now...

I find that I dream a lot about the past these days. Last night I dreamt about Roch. In my dream he was well, and whole again. He was the young Roch, the Roch I knew in University - kind of jittery, always on the move, thin, blond and sexy. Somehow, the dream me knew there had been problems between us but in the dream those first feelings of overpowering attraction and love were flooding through me again and I needed to tell him how I felt. That nothing had changed. I needed to make him understand that, to tell him that we could work out our problems, and that nothing was as important as being together.

Those first feelings of a brand new love are long gone now. They were replaced by another, calmer love and a shared history together. But last night’s dream allowed me to experience something like those feelings again and I am grateful. In the morning, it went the way of all our dreams and left me only with the memory of what we had shared in the beginning. I felt a little sad when I woke, not least because of how he is diminished now but - what a sweet dream it was. I felt as though I had received a truly astonishing gift. The dream me had felt what it was to love him like that all over again. What we feel may be different now, but nothing is as important as being together. The real me, the MND wife me, can hug that dream close in the days and weeks and months - and years to come.

Young Roch