January 25, 2019

Grief before death

Disclaimer: this is quite long and will take a good ten minutes of your life to read! I hope it doesn’t upset or offend anyone it’s only my views and experiences.

When you hear someone is grieving, you may automatically assume that they are bereaved. But many people will be grieving through the entire process of a loved one being unwell, long before they pass away, sometimes years.

 

I always struggle to describe how grief feels for me. I’ve described it as feeling like my heart is a balloon and when I’m sad, it’s filled with water, sinking heavier into my chest. Other times it feels like it’s being squeezed, and my throat feels tight, nausea sets in, my stomach twists and then ‘click’… it’s time to deal with it because my Mum needs something, I need to sort Rosa, or go to work ready to deal with whatever call comes in.

That’s the reality of life, time never stands still. We live in a time where we are all busy, rushed, struggling to make ends meet and won’t say to someone we’re struggling because hey, that makes us weak right? and like we can’t cope when we “should be” because we have to? We all know that bit is rubbish, but why do so many of us still struggle to talk? I’ve got rather good at dealing with grief through being a paramedic for nearly 8 years now, I see grief in so many circumstances and the different ways people deal with it.


For me, I don’t know what it is, but it is probably a mixture of factors. Sometimes I worry that if I let my feelings out who knows when they’ll stop flowing. My Dad was asked a few years back during a time where he found himself very low through sheer Carer exhaustion and stress, “how do you not cry?”. His answer was “because if I do I’ll never stop”. Nothing has ever rang so true as that statement.


When someone you love becomes unwell, the grieving process starts right there. You might not realise it, perhaps you go through an element of denial or trying to think positive, but it’s sitting there alright. Lurking in the background and pulling at your chest and stomach every so often, perhaps a memory pops into your head, or a song, or you see your loved one sad or in pain.

So how is grieving for the living any different to grieving for the lost?

I think we put enormous pressure on ourselves to seem perfectly ok for our loved ones and surrounding family. I know as a Mum myself I feel a responsibility not to break, sometimes it even feels like a lack of choice. I can’t break, who will go to work for me? How will Rosa feel seeing me this way? How can I keep supporting my Mum and Dad? All of these questions float around, and you get up, put your big boy/girl pants on and carry on with your day.

Thrown into the mix is often a nice splash of guilt too: how can I feel like this when it’s not me suffering? How is my child suffering this way when I am meant to protect them as a parent? How can I even consider having a break when my loved one is struggling so much with their illness? How can I forgive myself for having paid carers or looking at a nursing home? Guilt… guilt… guilt... Unnecessary guilt of course when you look at it objectively, but I’ve never met someone in this situation that hasn’t experienced the feeling of guilt.


The pressure to cope and carry on regardless of your feelings is real. The system makes it very difficult to access formal help at times. Sometimes paying for private carers until you must sell your home just doesn’t feel like a fair option, especially when your wage just about meets the carer fees, but that’s quite often the only option available these days with the lack of money that social services have available. Many carers are working hard to keep their home going, food on the table, care costs, and they don’t catch a true break. Whilst they’re doing all of this, they’re also meeting complex needs of their loved one, it’s no wonder that many carers don’t find the time to look after themselves.


I am quite happy to be open and tell you that I grieve a lot, on the inside. I did a post recently discussing this exact topic and it was rather cathartic because I knew so many people would relate. This grief for the living applies to so many situations.

Perhaps you have a disabled child and you’d do anything to make sure life is not more difficult for them than another child who doesn’t have that disability.

Perhaps your loved one has terminal cancer, with no date when that person will be taken from you but you watch them daily wondering how in the world you’ll enjoy life when they’re gone.

Perhaps your loved one has dementia, and when they give you that glazed look straight through you, unaware of their surroundings, you crave for them to just smile at you and recognise who you are.

I grieved in the first few days I had my daughter - I feel horrific writing that but it’s something that took me a long time to accept after realising I was probably suffering from post-natal depression and anxiety. I wanted my Mum there and she couldn’t be, and I’d spent my pregnancy caring for her as she was deteriorating rapidly, I didn’t prepare for how it would hit me with those wonderful post-partum hormones.

My wedding was planned meticulously around Mum’s care needs, and all I wanted was to be able to get pissed on Prosecco with her the night before. Don’t get me wrong, I am so grateful she could be there and we boogied on the dancefloor in the evening, but it isn’t what you think life will be like when you think of your wedding as a young girl.


For me it was difficult growing up as a teenager and coping with the prospect of Huntington’s Disease. I felt guilty saying this in the past but now I reflect back on the emotional issues I had in my teens and early twenties, it is all because I never talked to anyone. I was grieving the whole time. We weren’t allowed to tell people about Mum’s diagnosis, she was so ashamed of it ad the stigma attached, and didn’t want to be treated differently. In retrospect this made it hard to digest because me and my sister were both too proud to talk to each other, and my sister shortly after went to Lancaster University for 3 years.


I’ve always been protective of my Mum, she always seemed delicate to me even before we knew, perhaps intuitively I knew she had a vulnerability? As a teenager I would have my strops, shout at my parents, drink the alcohol they told me to stay away from. The difference for me was every time we did row or have teenage tantrums, I felt tremendous pain after, and I didn’t understand what that was at the time. I would cry but be too stubborn to go and talk to my Mum. I wanted to hug her but couldn’t bring myself to do it. So, I would isolate myself, not talk to my parents and just deal with it. I remember my Mum putting a card in my room (I still have this card), and it said, “I’m always here if you want to talk to me, love you darling Ems”. I’ve lost the opportunity now, what an idiot I was not taking up the offer, but when you’re young you don’t think about the future.


One day, my Mum got an unexpected letter to say that the DVLA had suddenly revoked her driving license. I remember wanting to take away her anguish so badly. I felt like I was just watching this surreal drama happen to my parents and I felt totally helpless, as I expect my parents did too.

When my Mum started to display psychiatric symptoms, I didn’t quite understand the disease fully, nor did my sister as we hadn’t known for long. I was about 15 years old and Kelly was 19 visiting from Uni. Mum had come home from her line dancing and Dad had not washed up the dinner pan. Trivial right? I could hear the argument building, and my Dad trying to calm it, distract her and keep it quiet so we wouldn’t hear. He had obviously recognised a change and knew what was coming. He would always try to sort it without involving us but inevitably we would be at home to hear it anyway. This moment erupted into a barrage of screaming and crying, and me and Kelly ran to the stairs to see Mum punching and screaming at Dad.

A glass flew across the hallway, luckily Dad being a martial artist his reflexes were quick and he moved enough to escape a blow. I just remember staring from upstairs, frozen to the spot and shaking, so terrified of what was happening. Without a thought Kelly bolted downstairs and put herself in front of the door, pushing Mum back onto the stairs and restraining her to physically stop her from leaving the house with the car keys (this wasn’t long after the DVLA letter). Dad was nursing his bleeding head and hand from where a glass tumbler had been launched at him and trying to compose himself as he couldn’t go near Mum without her totally losing it.

In the end Mum managed to get out without the keys and went for a walk in the dark. After a long and worrying wait she came home. Kelly was in her room and didn’t want to talk about it, she was dealing with it in her own way. Dad needed some space and to tidy up the broken glass and pans that had been thrown around the kitchen. And my poor Mum, so clearly terrified by what was happening to her, was curled up in bed clutching a photo of her Mum, sobbing and apologising.

I remember sitting next to her and just hugging her, and it’s probably from that moment that I told myself I’d always look after her. And guess what I had to do in the morning? I had to put my big girl pants on and go to school and carry on like nothing had happened as none of my friends knew at this point.

To go from teenage life to suddenly having to be a carer for a disease that was so unpredictable and so complex, I definitely grew up quicker than my friends. The grief was continuous, every day I would think about how my future would be different without Mum being Mum. When would she change? How long did we have? Will these mood swings ever be in public? On top of that I grieved for my sister, I would have amputated my leg there and then if it meant she didn’t have to have Huntington’s Disease.


Grief can’t be fixed. It’s not something to be cured. It may seem less dominant in your life over time, but it’s still there. Time is a healer for sure but it will wake up occasionally and remind you of that pain. If you have a friend going through this, LISTEN and be there. Don’t wait for them to ask you, they won’t. Offer a coffee, cook a meal, go for a walk. Don’t tell them that it will get better, because it won’t, they’ll just learn to put it in a box. Tell them that no matter how sh** they’re feeling, you’ll be there.


I think it’s also important to say that everyone will deal with grief in their own way. Don’t be fooled my someone who looks happy and coping on the surface, it doesn’t mean they aren’t grieving, they are just better at concealing it. Be patient, be kind, and be available if your friends need you, let them know they have a safe place to talk to you.

Emma x

Copyright © Campaign for My Brain 2020
Registered in England & Wales: Company number: 12372906
chevron-down linkedin facebook pinterest youtube rss twitter instagram facebook-blank rss-blank linkedin-blank pinterest youtube twitter instagram