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Wednesday, 23 January 2013

How did we get here?


I’ve been meaning to get my blog up and running for a while, I created it a few weeks ago and haven’t written a post yet. I apologise for that. I’ve struggled to write anything legible and remotely interesting due to pain, fatigue, brain fog and good old writer’s block. I hope this post is worth the wait.
My health is very poor at the moment, and I’m deteriorating all the time. I don’t notice it so much on a day-to-day basis but when I look back it becomes very apparent. All I can think is “what happens if I continue to deteriorate like this?”, “how bad will things get?” and “how will we cope?” I have no quality of life now, so what happens if I keep getting worse? It’s scary. I know not much can be done for me anymore, and I’m a very complex patient to treat, but I feel like my doctors aren’t even trying. We ask them not for a miracle cure but simply to try and improve the quality of my life. I am hoping we will get somewhere over the next few months, and that 2013 will be a better year than the last 5 have; it’s been 5 years that I have been “ill” now. I want to say it can’t get any worse, but I know it can. I often say “it can’t get any worse than this” but life seems to take that as a challenge, so I don’t say it anymore. What about if I said things can’t get any better? Maybe then my life will take that as a challenge and my quality of life will improve? Oh I don’t know.
How did we get here? I feel like I’ve stepped into someone else’s life. My quality of life is so poor and I suffer so much. I’m alive, but I exist rather than live. I want to be able to live a little, but my body keeps letting me down. It’s like mum and I live in a bubble. This bubble is our own little world, and it’s different from the outside world. People come and visit, they come into our bubble and they do their bit or we chat and enjoy their company, but then they leave our bubble and go back to their “normal” lives and so we’re just left, mum and me, in our little bubble on our own. And that’s how we feel; we have plenty of people around us, yet we still feel very alone. 
 
 
We do however have each other, and we have a wonderful relationship. And we’ve never lost the ability to laugh. Sometimes we begin laughing and end up crying, but we laugh all the same. We have had some hilarious moments over the past 5 years and I will share some these with you in the future. We often say the same things at the same time; too often really, it’s scary how alike we think. This is a source of much of our laughter on a day-to-day basis; we have the same sense of humour and quite regularly say the same funny things in unison. It’s like we’re merging into one person. I bet I’m probably the only person to say that I’m glad I’m turning into my mother!


I started a Facebook page recently called Lucy's Light, to raise awareness of Ehlers Danlos Syndrome and Chronic Intestinal Pseudo Obstruction, which is what I suffer from. I also hope to raise awareness of the issues chronically ill individuals and the disabled face to access the community and to get the help they need; it's a constant battle. I am desperate to make a difference and to help others. I struggle with feeling useless and I hope this will help me to feel like I can contribute in some way. It's hard to feel useful when you're stuck in bed, have limited energy, poor concentration and you're reliant on others.

The name of this blog reflects my attempt to have a life and make a difference by overcoming all the obstacles I face.



I hope to update my blog regularly from now on, and I hope people will think it’s worth reading.
 Lucy x

About Lucy Watts MBE


Lucy is a disabled 22 year old young lady with life-limiting complications of Ehlers-Danlos Syndrome. She writes and speaks for a number of charities and runs this blog. She is an Ambassador for Together for Short Lives and Dreams Come True, Trustee for the Pseudo Obstruction Research Trust and is the first Youth Ambassador for the International Children's Palliative Care Network, also working with charities such as Scope and the Council for Disabled Children as well as Association for Young People's Health via the Young People's Health Partnership, the Children's Health and Wellbeing Forum and the Children and Young People's Health Outcomes Forum. Lucy was appointed MBE in the Queen's New Year Honours 2016 for her Services to Young People with Disabilities.
View all posts by Lucy →

7 comments:

  1. Well done Lucy! You are right about blogging...it gives you a sense of purpose and something to focus on. I found it really helps me make sense of my feelings. I hope it helps you honey and im more than sure it will help others out there so keep going sweetie im behind you all the way! If you like i will add a link to you blog on my page for you, just let me know xxxx

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  2. I think you're wonderful, and you're an even better writer. Feel free to check out my bog as well. I understand the feeling about sharing and feeling useful through your pen...I would love to invite you to join my Facebook page too! It's www.facebook.com/cushingsawareness...u don't just have to have cushings to be our friend!

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  3. Hi Again Lucy, hopefully you'll have seen my last comment elsewhere on your blog. Would like to give support to your Mum as well. I've been on her side of helplessness and it hurts so much. Saying that, I'm not at all detracting from your braveness and suffering. Stay strong treacle. Thinking of you all. kiss kiss. Wayne.

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    Replies
    1. Thanks again Wayne. I will let mum know what you've said, that's very kind of you. People don't realise how much illness impacts on everything. We're learning all the time x

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