My Open Letter to Personal Care Assistants | Muscular Dystrophy Trailblazers

All my life I’ve required care, whether it be from family members, friends or paid employees. For over a decade now I have been hiring assistants to help me with an array of tasks, including personal care. I have always chosen to recruit my own staff rather than use agency workers. This has given me much more flexibility in terms of when, how and for the duration of time I use my PAs. It also means that I know exactly who will be providing my care, which is not always the case when going down the agency route. However, with this comes the added responsibility of being an employer, which in itself can be rather daunting and stressful.

I’m in the fortunate position of having been gifted the best family I could ever hope for. I do appreciate though, that not everyone has the invaluable support of relatives to rely on. For these individuals their only option is to pay others, often strangers, to assist with their needs. Like me, they might advertise, interview and hire independently, paying for their care with council funded Direct Payments (available in England, Scotland and Wales). Alternatively they may decide to use an agency.

For others though, in times of desperation, they have no choice but to leave their residence and spend time in respite care. I know of cases where young people in their 20s have been placed in nursing homes for the elderly, where staff have no knowledge or experience of their condition and specialist needs. Personally I can’t imagine such an experience and count myself lucky that I’ve never had to resort to this.

Over the years I’ve had several carers (or personal assistants) – whichever label you prefer. For the most part, I have found them through friends, associates or word of mouth.

Several months back my longest serving employee had to leave for personal reasons. It came as quite a shock but couldn’t be helped. She worked for me for eight years and had seen me at my worst and most vulnerable. She is a good friend close to my age, whom I trusted and relied on, and so the news of her resignation was somewhat distressing. Thankfully she was good enough to stay until her position had been filled, which she was under no obligation to do. Nevertheless, I was abruptly faced with the immediate and unavoidable task of advertising for her replacement.

I was under no illusion that finding someone who could and would meet my needs was going to be a simple endeavour. It certainly was not. I’ve been casually told social workers, who carry out my annual Needs Assessment, to simply advertise and hire, as and when needed. As if I’ll be flooded by pools of applicants to choose from. Then again, I guess these social workers have never had to find people willing to drag them from their pit every morning and get them ready for the day ahead. Trust me it’s no easy undertaking when job seekers are sadly too often put off to discover that personal care does in fact mean personal care!

I placed ad’s everywhere I could think of; online and locally. After several weeks of limited interest, I arranged interviews with each candidate in the hope that at least one would be suitable. Most were let downs, failing to turn up without notice or changing their mind after showing initial enthusiasm. My expectations were raised only to be shattered.

I was surprised by the casual disregard and lack of consideration from some of the applicants. I spent whole days at home waiting for interviewees to arrive, as if I have nothing better to do. Is it really that difficult to send a text message or make a quick call to say you cannot attend for whatever reason?

Time was ongoing and I was increasingly aware that I would have to find someone – anyone – as soon as possible. I live rurally in a town populated by less than 10,000 and so inevitably I wasn’t getting as much interest as I might if I lived in a city. This was an incredibly tense and stressful time for me.

Although my carer had said she would remain with me until a replacement could be found, I knew it was too much to expect her to stay as long as it was taking. I couldn’t be without the care I needed to live my life – to simply exist. Yet at the same time I couldn’t find anyone to provide this care. I was facing an almost impossible challenge.

In the end it was once again through friends of friends and frankly sheer luck that I found someone to take on the essential role. I won’t lie, it’s been a difficult transition and my daily routine has had to adapt. But, several months on, things seem to be coming together and all the initial doubts and struggles have been ironed out. I do still worry about the future prospect of having to go through the whole hiring process once again. It’s an unenviable task but one that is an essential and unavoidable part of life for those of us with a disability.

I realise it’s difficult for those applying for positions as PAs to empathise with our unusual and complex situation. If you’ve never needed care yourself it’s understandably difficult to grasp the necessity and importance of the role of caregiver.

For this reason, I have written an open letter to carers and prospective PCAs (personal care assistants). It has been published on the Muscular Dystrophy Trailblazers website. If you’re interested to read the edited version of my letter, click here.


Open letter to carers

On behalf of all of us who require personal or social care, I invite anyone considering taking on the role of personal assistant to think carefully about what it really means before you do apply.

Firstly, this is not a choice for us. We’re not, for example, hiring a cleaner because we’re too busy or too lazy to clean our own homes. When we advertise for carers, it’s because we NEED them and not necessarily because we want them.

As physically disabled individuals, many of us cannot independently carry out essential everyday tasks such as washing, dressing and toileting. To have no option but to entrust such intimate activities to another person – a stranger – is unnatural and unnerving. We are in effect placing our lives in your hands when you take on the vital role of personal carer.

Recruiting carers can be a lengthy and extremely stressful process for us. There’s the initial worry over whether there will be any applicants at all, followed by the dreaded interview process.

We often find ourselves waiting around for interviewees to attend, only for them to carelessly fail to show without any notification. Please do bear in mind that just because we are disabled, like you we have lives too, so don’t waste our time. We appreciate there are valid reasons for failing to attend job interviews, but it’s no hardship making a quick phone call or sending a text message to let us know in advance. As you would with any potential employer, be professional and courteous.

If and when we are able to successfully recruit, it can be incredibly frustrating and disheartening when that person flippantly decides to resign days later. You may wonder how and why this can happen but the sad fact is that for many disabled people it is a reality. We are not afforded the luxury of being able to manage until a replacement is found. No, we can’t simply wait for the right person to show up.

Some of us even have to resort to respite and residential homes in the meantime, thereby taking us away from our own homes and everything we hold dear. Try to imagine if you will, how demoralising and distressing such a situation would be if it happened to you. I therefore reiterate how important it is to think before applying for a role as a personal carer.

Are you trustworthy, reliable, willing and able? Ask yourself: are you entering this area of work for the right reasons? Your role will involve a range of tasks and you will be responsible for the safety and wellbeing of your potentially vulnerable employer. So, if your attitude to care work is casual and indifferent, then this is most definitely not the job for you!

Flu Jab: Get Yours Today!

Well, it’s upon us again; Flu season is here. Every year my family and I get the Influenza vaccination, which is free of charge here in the UK, courtesy of the NHS.

For as long as I can remember, I’ve had the Flu jab to protect myself through the harsh winter months. It’s important that not only I am vaccinated, but that those closest to me are too. My immune system is much weaker than average, and my condition makes it considerably more difficult to overcome respiratory infections. For me, a common cold can quickly develop into something much more serious. It’s therefore very important that I am not unnecessarily exposed to the Flu virus.

As I have aged, my declining respiratory function has become the most concerning symptom of my disability. Ullrich congenital muscular dystrophy causes muscle degeneration and scoliosis. Not only are my lungs squashed and unable to expand as they should, the muscles that make them force air in and out are slowly wasting away.

Over the years, I have fought recurrent chest infections, several bouts of pneumonia, pleurisy and an acute pneumothorax (collapsed lung), requiring a chest drain. Many long, drawn-out days have been spent in hospital trying to overcome serious complications resulting from respiratory viruses.

For this reason, I implore and encourage you all to go and get the Flu shot. It takes no time at all and I promise you, it’s completely painless. There are fables floating around that will attempt to make you believe the Flu jab can give you the Flu. This is not the case at all. Yes, the vaccine does contain a small dose of the inactive virus. This triggers antibodies, which within two weeks will protect you, if and when you’re exposed to seasonal Flu.

Like all viruses, there are various strains of Influenza which change annually. For this reason, it is essential to ensure you are vaccinated every year.

I visited my local pharmacy, without appointment, a few weeks ago to get my free vaccination. If you haven’t already, please don’t delay. Go and get yours NOW!

For more information on the Influenza vaccine visit the NHS web page here.


Related Blog Posts:

Flu | The Facts

Winter | Top Tips to Keep Warm

Winter | Top Tips to Stay Well

Cough & Cold Season | Chest Infection

Why ‘Life on the slow lane’?

I have so many ideas buzzing around my head for future blog posts, but as yet no specific aim or objective. This blog, at present, lacks a specific purpose and serves no function other than to allow me the space to vent. However, in time I hope that I may also be able to advise others in a similar position. By this I mean I endeavour to help, support and share information with others living with muscular dystrophy. I’m not in any way professionally qualified to counsel on this topic. All I have to offer is my own personal experience, that being almost thirty years with me, myself and Ullrich congenital muscular dystrophy. I will get to the ins and outs of how this condition affects me at a later date, but first I feel I should explain my reasoning behind the naming of my blog.

So, why ‘Life on the slow lane’? Well first of all, I don’t walk. At all. I roll. Let me clarify, I’m not a skateboarder, a rollerblader, a cyclist or a car enthusiast. I’m a wheelchair user. My chair of choice is the Quantum 600 powerchair by Pride Mobility. It allows me to go wherever a 16+ stone wheelchair can go. But it can only move at a maximum velocity of 5mph. This limited, ambling pace can be considered a metaphor for my life.

I regard myself to be living life on the slow lane as everything I do takes at least twice as long as it would an able bodied person. Being non ambulant does not lend itself to speed or spontaneity. Every task, however insubstantial, requires careful consideration, support and time. From washing and dressing, to eating and travelling, every activity depletes both time and my meagre energy reserves.

I would love to be one of those carefree, go with the flow types. You know the kind; those people who are seemingly fazed by nothing, never forward plan and simply take life as it comes. But I can’t. I see them cruising along, living life in the fast lane, taking risks and seeking adventures unknown. I see them fly by me as I trundle along in my slow lane.

My body is weak and fragile, and consequently I can’t afford to be daring or gamble with my health. For instance, catching a cold for your average Joe is an annoyance yes, but it passes after a few days and it isn’t a cause for concern. If I catch a cold the consequences are severe and potentially life-threatening. Sounds dramatic doesn’t it! But because my condition affects my respiratory function, a simple viral infection can and has on multiple occasions led to complications including pneumonia, pleurisy and pneumothorax (collapsed lung). Many days and nights have been spent on hospital wards and in ICU; time seeming to slow with every tick of the clock. You know how they say time flies when you’re having fun? Well it drags like Hell when your sole focus in life is to just keep breathing.

My disability has effectively prevented me from flooring the accelerator pedal and pursuing my wildest childhood dreams. I’ll never be able to book a flight on the spur of the moment, jump on a plane and jet off to some mysterious destination with only myself for company. I’ll never experience the thrill of running to the edge of an exotic waterfall, to then dive into its frothy waters without a care in the world. I’ll never have children and since UCMD is progressive, I won’t reach old age. On the contrary, my life is slow, monotonous, routine and unexciting.

Don’t get me wrong, by no means am I saying that being confined to a wheelchair is not synonymous with leading a happy, fulfilling lifestyle. I can only speak from personal experience and how my condition has impacted on me. There are so many things I desire to do but cannot. Sometimes I get frustrated and wish I could get up & go for a country walk to let off steam. It would be such a relief to grab a quick shower whenever I want and not at a regimented time. I will lie awake until 3 o’clock in the morning, wishing I could drag myself out of bed to make a midnight snack. But I can’t because I’m stuck on that slow lane.

This is the card I’ve been dealt and that’s ok; I’ve adapted and learned to live within my means. I do what I can and I enjoy what I do. I have the wackiest and most wonderful family anyone could hope for, and an eclectic band of friends! I appreciate that this is more fortune than a great deal of others ever experience, and for this I’m thankful. My loved ones more than make up for missing out on living life in the fast lane.