Living with Cerebral Palsy 🍋🍋

Friday, 13 September 2019

Hello Goodbye

Happy Autumn! The "season of mists and mellow fruitfulness" is definitely my favourite time of year. I adore the beautiful leaves, the first coal fire, the roasted chestnuts, the shining conkers outside our door, the apples, the pumpkin picking, the fading sunlight, the chunky knits, the cosiness of it all. I love it. I think Autumn is also feels special to me because after years in the education system, my brain processes the year as September to September. So the start of this month almost feels like New Year when it rolls around. It feels like a time for fresh starts. Sometimes, it also feels like a time for goodbyes.
This month we have experienced one huge fresh start and one sad goodbye.
Yesterday we attended the funeral of Paul's Aunty Brenda. Depending on how long you have been reading this blog you may remember pictures and mentions of her. She was one of Paul's Mums sisters. The three Golden Girls. She was a second Mum to Paul as he grew up and left a lasting impression on him and in later years me, too. As Paul's mum had sadly passed away when I was pregnant, Brenda and younger sister Sylvia came to mean a lot to us as the matriarchs of the Woods/Drake family line. Brenda was unendingly kind, gentle, selfless and possessed that great vintage "scouse humour". Everyone who met her adored her. She in turn cared for everybody and in particular had a huge soft spot for children of any age and description. She loved Elin as she did all her great nieces and nephews and I believe Elin most certainly inherited her strength of character and resilient nature. At her funeral I was in awe of, though unsurprised by, the outpouring of love for her and the continuous tales of her good humour and huge heart. It was inspiring. As we were told in her Eulogy, perhaps when leaving that sad day behind us, the greatest debt we could pay to her memory was to try, where possible, to just be a little more 'Brenda'. It would certainly make the world a better, brighter, place.
May 2019 
Brenda (right) and Paul's other amazing Aunty, Sylvia (left)
As Brenda made the world a brighter place, so Elin continues to shine her light on those who surround her! I am SO PROUD of my sunshine girl this past fortnight. She has experienced a giant change, an enormous new start- that of beginning her new school. She has definitely been very 'Brenda' through this transition- serene, happy and taking absolutely everything in her stride without fuss. I'd like to say I'd been the same but instead I've been typically emotional about the whole thing. I just can't believe my baby is in Year 7!! Seeing Elin settle so happily at her new school thus far has provided the necessary antidote to my acute sentimentality though. Elin's New Year consists of meeting and creating a whole new school family and support network to enjoy over the next few years. She is so lucky. My New Year consists of quelling waves of grief and strange feelings of loss with the wonderful positives of the past fortnight and the knowledge that Elin is entering an amazing new chapter of her life which she is going to love.
As a final thought as we enter this open book of the 'next stage' in Elin's incredible life, it struck me last week just how many messages of support we had and wishes of good luck from friends before she started school. I have always known this love for Elin exists but big milestones in her life make it so much more apparent. She is one lucky girl. We are one lucky family. It brings it home to me that Elin is not the only one with an incredible support network surrounding her and I am eternally grateful for that. So going forward, my New Year's resolutions are that I am going to channel my inner bravery more often, take my lead from my girl, always focus on the positives and as much as I possibly can, just generally "be more Brenda".
Happy "New Year" folks
xxxxxx



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Friday, 1 March 2019

Angel of Anglesey

Well February half term brought two surprises, one extremely wonderful and unexpected break and one bone achingly sad piece of news. These two surprises provided a contrast of emotion so complete this week that I found it quite overwhelming. Deep sorrow flanked by deep joy, or was the joy so potent because it was so infused by a sense of gratitude, a feeling that once again we find ourselves in the amazing position of being able to enjoy such quality time with Elin in the face of the devastation of another family we know?!? Someone once said to me you can’t feel total happiness until you have faced total despair. I would say that is a true statement. Certainly our emotions this week were all the more heightened for knowing, always, just how blessed we were to be able to experience such a lovely half term with our girl. We will never stop taking this position for granted.
So we went to an utterly gorgeous holiday home in Anglesey (thanks to lovely friends of my Mums!!) where we were already lucky enough to stay last October. Crazily I hadn't been there since I was way too small to remember prior to this! Never in a million years did we dream when we booked to stay in the stunning, accessible beach front home that the weather would be more typical of Miami than Wales in February. I might tweet my photos to Donald Trump. If global warming  doesn’t exist perhaps he can offer me an alternative explanation for the unnervingly incredible weather!  Feeling horrendous about our poor dying planet doesn’t have to stop you enjoying the sun though, right? The two are not mutually exclusive (are they!?!!!) So we enjoyed it! I think it’s fair to say it was just what we needed. 
There is little in this world so calming and able to give perspective so brilliantly as gazing out at the sun- soaked sea. It just makes you think everything is going to be alright. 
Even better than the weather was Elin’s mood. Neither of us can remember such a successful break from start to finish including all sitting and all car journeys. She has been outstanding. We thought last time we visited that she loved Anglesey, now we know for sure. The beautiful open plan beach house which is full of light, the salty air, the sound of the sea, the sunshine- the combination- who knows? Something about this place agrees with Elin. Can’t say I blame her. We are already booked to return twice this year and hopefully in the future too. I think we found our home-away-from-home happy place. When Elin is happy, we are overjoyed.
So as you can see from the photos, Elin really did have the best time. We didn't do too much! We walked (rolled), we talked, we found some lovely little cafe's, we sat on the beach (even though we weren't dressed for it!), we gave her lots of cuddles. We even ate good tapas. In Anglesey! Who knew. Everything and anything delighted Elin this week. She was smiling and laughing from the moment she opened her eyes to the moment she closed them at bedtime. It was joyful, but as I've said, never not tinged with a certain sadness. I thank god that Elin knows nothing of this sadness, nor of any sadness and never will. It is the one part of her condition that I can honestly say I am glad of. Elin has the "Eternal sunshine of the spotless mind" and boy, does she deserve to.
When trying to process impossibly sad news all we can do once again is take our lead from Elin and face negatives with positives, keep strong in the face of adversity, remember all the good things and acknowledge that we will never forget a beautiful angel with a truly beautiful soul and what we have all learned from being touched by that soul, as beautifully as the sunrise touches the sea-stunningly, wholly, breathtakingly- but far, far too briefly.

Take care everyone
Ruth  x

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Saturday, 26 January 2019

Smile

Today, there was a rainbow outside Elin's window. It was really beautiful. It made me cry. I cried because I wanted to share it's beauty with Elin and I couldn't.  She can't see that far away and she can't understand my descriptions. For Christmas she had a rainbow projector light which creates a lovely arc of a prism of colours across her bed. I was thrilled with it because I thought finally, she can see a rainbow. But today it doesn't feel like enough. Today everything feels a little dark, a little heavy.  I want her to see the real thing, in nature,  not something powered by batteries, as she sits as patient, serene and as good-humoured as ever in the relative prison of her bedroom. It made my heart ache.
Today is not just about the rainbow. Today is the end of a long, miserable mid-January week. It has also been a week of unhappy anniversaries. 8 years ago this week, Elin lost her gorgeous friend, Harvey, whose photo sits in Elin's room and who we still miss and always will. Also this week, Elin's cosmic twin, Ellie, should have been celebrating her 8th birthday, but she is forever six years old. In addition, on Wednesday, the world said goodbye to another old school friend of Elin's. An inspiringly strong, cheeky, joyful, clever young lady. Today, I think, is about all of that.
When you have a child who is severely disabled and/or described as life limited, there is a lot to process. I think the entirety of this blog is testament to this. None of it is easy to digest, it takes years. You never get over it, you learn to negotiate your new normal. Part of the new normal is that you suddenly realise somewhere along the way that children you get to know and love will pass away. Families you share each joy and sadness with on this journey will go through the worst grief imaginable in front of your eyes. You have to come to terms with the fact that one day, this could be your child and your family.
Since Elin was born the children we have lost from our lives has reached double figures. Nothing and nobody prepares you for this. In truth, it's probably something you just can't 'prepare' for. The strength of the families utterly humbles you, the legacy of love the children leave behind floors you. The outpouring of kindness and support to these families inspires you, the reality of the hole that is left devastates you. Sometimes, it all feels too much to bear. There is just too much sadness, it starts to get impossible to process, to make any sense of. It never gets easier (and why should it?) in a way, it gets harder. With the passing of each of the eleven children that have left our lives so far, the world just seems more cruel, more unfair and more terrifying.
So how do you deal with it?
I suppose you navigate the sadness by thinking of all the wonderful memories you have of these amazing kids. The memories you know will stay with you forever, the ones that will, when the initial shock and grief has worn off a little, make you smile. Isn't that the only way anyone can make grief bearable at all? Also by looking to Elin. She, as ever, teaches us so much. As I tried to pull myself together after the rainbow set me off today, she laughed. She laughed A LOT. It was as though she was trying to tell me she didn't care about seeing the rainbow. In the end I started laughing too. As ever, we take our lead from her, our sunshine girl, because she shows us the way. Sometimes, there is nothing else left to do but smile, even if you have to have a really good cry first. Smile, remember the good things, pick yourself up and just try to get on with it. Today, I'm smiling for you, Paige. There were so many good things in your life and you gave so much joy to everyone who knew you. We will never forget you.  If I know you at all then I know that somewhere you are smiling too.
Have a good weekend, folks.
Ruth x


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Wednesday, 28 November 2018

One love

I've had a bit of a blogging hiatus lately. I've been chewing a few things over I suppose. Elin, you'll be pleased to know, is fine. Since my last post we've had a wonderful holiday in Anglesey and Elin's dystonia has, if anything, calmed down again. In reading over my last piece I realise again how everything can shift in an instant in our world, how mole hills can suddenly turn into mountains with the passing of a few days, or, perhaps more crucially , vice-versa. It is becoming a strangely common pattern for me that following a period of wallowing or self-pity (see aforementioned previous post) something will happen to make me realise how misguided my upset was. Not invalid, but misguided. Four days after I wrote that post bemoaning the fact that Elin was growing up, she lost another one of her friends. He was 15, a warrior and taken far too soon. His family are all warriors too and always have been. There is nothing on this planet that makes you freeze and take stock of your blessings like the loss of a child like Elin from a family like ours. It feels personal, it hurts beyond words, you feel desperate. The special needs family is a small one and in being so is close, supportive and endlessly understanding. We don't even need to communicate with words, often a hug says a thousand things, a smile betrays a thousand conversations never had. How can you look into the eyes of someone you see much less than your own family, yet recognise their soul?  
We are bonded together as parents of children with similar conditions, in dealing with the initial horror of a life changed and then gradually coming to terms with our 'new normals'. We have all been through the same patterns. The obliteration of any kind of post-natal joy, the constant stress from the word go, the fights for help, the hospital stays, the helplessly watching your child suffer, the worry, the equipment, the medication, the home adaptions you never believed you'd have to have, the blessing of every birthday, the sorrow of what could have been. We know one another because we are each other.  In the realms of our exclusive little world, in the family of parents we have become, bound by sorrow and despair and great joy that no ordinary parent could ever understand, we are all one person, one child, one family. So when one is lost, then we are all at sea.
Two weeks ago, amazing, fierce, beautiful, funny, strong, miracle-warrior Josh was lost. But never, ever forgotten. 
Two weeks ago my perspective was found. 
Goodbye Josh, thank you for all you taught us and will continue to teach us. Thank you for your smile, for your spirit, for your attitude to life, for your cheekiness, for your love. 
Nobody who met you will ever forget you, squashy. The impact you had on those around you was extraordinary, as the huge numbers of people queueing to say goodbye to you (and beautiful words written by family, friends and teachers) at your funeral paid testament to. You achieved in your short life much more than most people could ever dream of, just by being you. Love is your legacy. What an amazing legacy to leave behind. 
Rest in peace, little man.
xxx

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Tuesday, 24 October 2017

Saying goodbye..


It's taken me a while to write this and I didn't know if I would write it at all actually, because I couldn't seem to formulate the words.
You might have picked up from my previous post that a month ago one of Elin's little friends passed away. Her name was Eleanor Rose Wheeler, but everyone called her Ellie (or Ellie-Moo or Moo, or Moo-ster), and she was beautiful.  In 2011 Ellie's parents, Richard and Annie, got in touch with us not long after Ellie was born, through a mutual acquaintance. Like us before them,  they had been catapulted into an upside-down world that made no sense after their little girl was born with profound brain damage. Like Elin, Ellie has Cerebral Palsy in it's most devastating and severe form. The similarities between newborn Ellie and our two year old Elin were such that Annie and myself christened them the 'cosmic twins'. They even looked quite alike, especially when they were both little, though as she grew there was no mistaking Ellie's amazing trademark wild curls.
Ellie's death hit us hard, though she had been bravely battling against all the odds for some time. It was a testament to her strength and incredibly courageous character (echoed by the strength and bravery of Richard and Annie throughout her life) that she continued to defy the predictions of the medical staff for so long before she passed away. As we said goodbye to Ellie eleven days ago it struck me that most people will never have to attend the funeral of a child in their lifetime, a good thing obviously and a position I envy acutely. When you have to say goodbye to a child you have known it changes you. It makes the world seem an (even more) unfair and sinister place. Nothing makes much sense. It makes you question everything you know. You never forget the details of the day, the sheer magnitude of the situation. It's devastating in the truest sense of the word.
 I thought of that poem I hate as I stood in Ellie's beautiful funeral service "Welcome to Holland"(http://www.our-kids.org/Archives/Holland.html) If you don't know it, it is basically a massive extended metaphor for the life of a Special Needs Parent. I hate it because even though I applaud the sentiment, it simplifies the depth of feeling and complexity of emotions that this life brings with it way too much. I do agree that the only thing to do in life is to make the best of a bad situation, that yes our path has deviated from the 'norm' but that it can be just as wonderful. Except that quite a lot of the time, it isn't. It just isn't that easy. As I watched Ellie's family saying an unthinkable goodbye to their daughter, sister, granddaughter, niece and cousin I thought it's not like being in Holland, parenting a child with severe disabilities. Sometimes, it's like being in hell. A hell which no other parent can begin to truly imagine, unless they have been in the exact position themselves.
This is where we are bonded together as parents of children with similar conditions, in dealing with the initial horror of a life changed and then gradually coming to terms with our 'new normals'. We have all been through the same patterns. The obliteration of any kind of post-natal joy, the constant stress from the word go, the fights for help, the hospital stays (and Ellie's Mummy and Daddy had more of these than you could imagine), the helplessly watching your child suffer, the worry, the equipment, the medication, the home adaptions you never believed you'd have to have, the blessing of every birthday, the sorrow of what could have been. We know one another because we are each other.  In the realms of our exclusive little world, in the family of parents we have become, bound by sorrow and despair and great joy that no ordinary parent could ever understand, we are all one person, one child, one family. So when one is lost, then we are all at sea.
Despite this exclusivity of fully understanding the deepest depths of parenting a child with complex needs, I think most people instinctively understand the bravery and courage of kids like beautiful Ellie and their impact on the world around them. Something that will stay with me always from Ellie's funeral were the descriptions of how happy she made everyone around her. How she bound people together with her smile and how she was able to provide a new perspective on the world for all who cared for her. Just how special her place on this Earth was, how important. Six years is not long enough for any child to live, but how Ellie packed such a lot of love into those six years! There are plenty who could only dream of having such an impact after a whole lifetime.
We will miss and remember you always, Ellie, you gave the world so much more than you could ever know. You changed us all for the better and you did it all in six years. Elin's little cosmic twin, you were a shooting star in the universe of all who knew you- shining too briefly but so magical, brilliant, luminous and unforgettable.
Everyone was proud to know you and we are all richer people for it. This is your legacy.
Rest in peace, little Moo.
xxxxxxxx


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Wednesday, 4 October 2017

A Manual For Heartache


                                                    

Years ago I read an article about a condition which is prevalent in parents of severely disabled children, 'Chronic Sorrow Syndrome' , which really resonated with me.
Chronic Sorrow is the presence of recurring intense feelings of grief in the lives of parents or caregivers with children who have chronic health conditions. It runs alongside your everyday life, you may not be fully aware it's there a lot of the time. It’s like a virus running alongside a programme on your computer. It’s each time you have to attend yet another medical appointment, its each time you watch your child struggle or worse lie in a hospital bed for days, each time a friends child reaches a milestone your child never will. Its seeing children the same age as yours in the street and feeling the massive chest blow of comparison. Its filling in endless forms, its finding more space in the house for more specialist equipment, its ordering the nutritional liquid feed which is the only thing keeping your child from starvation, ordering repeat medication at a rate of knots, homing specialist syringes and feeding equipment in the kitchen. It's selling your beloved car and getting a mobility car. It's having tracking hoists running along your ceilings. It’s looking for a new house when you never want to leave the place you call home. It's seeing nothing but a black hole of uncertainty past education where University and adult life would have been. It’s a calendar so full of appointments you can no longer read the dates. It's watching Elin suffer when her dystonia takes hold. It's saying goodbye, as we have had to do again this week, to another beautiful little friend of Elin's and watching amazing parents you have befriended in your joint despair having to cope with the very worst possible case scenario imaginable. It’s having to face the thought of your own child’s death. It's a never-ending oppressive thoughts that can sometimes get the better of you.
My friend Anna bought a book for me recently that has helped me to see this kind of 'chronic sorrow' grieving for what it is and which provides advice on how to deal with bereavement of any kind, as well as touching on different kinds of  anxiety disorders and depression. 'A Manual For Heartache' by Cathy Rentzenbrink focuses on dealing with loss and grief and the ensuing feelings of anxiety and depression that sometimes never go away after experiencing a life changing incident. The author's 19 year old brother was involved in a car accident when she was 17, but lived on life support for the next eight years before he died.  Her first book 'The last Act of Love' which I haven't yet read, charts this part of the story and then this book  describes how the author has subsequently dealt with what happened and forged a life in the wake of her devastation.
I would recommend this book for anyone dealing with any kind of grief or loss, or tragic incident, however long ago in your life it occurred. Mostly what she writes is common sense but there is something very comforting in reading what you know to be true written down in a simplistic, logical way by someone else who has been through something unspeakable. The writing comes from a place of bleakness, but turns into a tender appreciation of life’s beauty.
At one point she thinks of Nancy Mitford saying that though life is often dull and sometimes sad, there are currants in the cake. “Look for the currants.” Ultimately, we might never fix our broken hearts, but we can still live, and our hearts can grow and appreciate life’s wonder. That is the feeling the reader is left with. 
I found this book comforting for many reasons. I'm not sure how useful it would be in the immediate aftermath of something horrendous, where even the suggestion that a book could help you get through it would probably seem laughable. But for me, I think I really would have benefitted from reading it in the early years following Elin's birth, during my grieving process for the daughter that was never born and whilst I was trying to negotiate what I now understand to have been pretty severe but undiagnosed (largely because I wouldn't talk to anyone about it) Post Traumatic Stress Disorder whilst trying to care for a very sick baby.
Grief is such a strange beast isn't it. It is almost entirely universal but affects everyone so differently. No one-way of dealing with grief is correct, but I was glad to discover that the classic 'five stages of grief' are no longer really being referred to in psychological circles, since the more modern realisation that grief is a fluid, chaotic crazy mixed bag of emotions that sometimes never actually ends.  Thats good, it means anyone suffering does not have to feel like it is time they 'moved on' or 'were over it'. Sometimes we just have to learn to live with what has happened to us and accept we will never quite be the same. 
Obviously I am a "look for the currents" kind of person.  Or at least I am now, perhaps less so in the immediate wake of what happened to Elin. It takes a long time to come to the conclusion that you can't change your loss and so the only way forward is to accept it. But very occasionally, even after all this time, the loss will resurface and can be almost as ferocious as it was initially. Apparently this is common and known as a 'second drowning'. I think I have experienced this once or twice in the past nine years. The times when you are struck dumb by the magnitude of what happened and it's a struggle to get out of bed. The way your heart aches for the child you almost had and then aches with guilt for the betrayal of Elin as she is now by feeling that way. 
Both the article on Chronic Sorrow and the book have helped to re-focus my attention on managing my thought processes lately. They make you realise it's not just you, it never was and it never will be.  The phrase "Do not ask 'why me?' but rather 'why not me?' " is a simplistic but effective way of thinking during black moments I think. As I grow older, so many of my friends confess suffering from anxiety or depression or, PTSD or Post Natal Depression or even just ongoing worry about things which they can't control. I am glad we are able to openly talk about this stuff, as we may not have been years ago. So I share this information in the hope that we can all, whether navigating tragedy or not, somehow take back a little bit of control for ourselves by not being ashamed of looking after our mental health the way we would our physical health. We all know it's just as important. 
As the author of 'A Manual For Heartache' writes 'Something that always consoles me, that never fails to throw a chink of light into a dark day, is remembering that others have walked this path before me. Even as your heart breaks and aches and you can't imagine how you will ever feel better, you can know one thing for certain. You are not alone"
Such a simple yet powerful and important message.
Xxxx




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