
image from http://www.josephinewallart.co.uk
“I did the only thing I knew how to do: I built my own walls of silence to disguise my desperation and what later came to be recognized and diagnosed as depression.”
― Sharon E. Rainey, Making a Pearl from the Grit of Life
A strange thing happens when I sit or recline to write. Either I’m eager as a beaver because I feel I have a stunner of an idea, I sit and look at a blank screen and finally something surfaces like a safety line thrown to a drowning person, or I languish forlornly staring at the accusing emptiness and suddenly words will flow and something is on the page. Ideas like bubbles blowing in the breeze wash over me in a magical haze and words appear in front of me.
Amazingly, the latter are the best of all, so I need to tap into my well spring of creativity or, do more prep work because I love writing and love seeing the finished item as I hit that publish button. I was told many months ago that writing for the acclaim of others was a waste of time. If I didn’t like writing for myself it was a lost cause and I should simply stop right then. Incredible as it sounds, that advice was true then and is still true now.
Having said that, it certainly is wonderful having people enjoy what I write and comments are always appreciated because they give me a chance to learn more, about myself and this craft of writing. Yet this is not what I wanted to talk about.
I am a terrible ‘patient’. Terrible doesn’t cover it. Abysmal is closer to it really. I hate the whole illness, can’t do things, must take pills by schedule, do this, do that, everything ordered by someone other than myself. This is not independence. I am, or rather was a fiercely independent person. No – I still am. I haven’t changed, I simply have had to accommodate some changes that irritate but I have to accept as a necessary evil! Temporarily!
For three days I’ve been incredibly emotional after a unpleasant , horrific dream. Even though it turns out the dream is not as bad as it felt, it left me emotional. I hate emotional. It is a loss of control, it is an undermining of the little independence I have left and it leaves me tired, in pain, unimaginably so, and with a burning desire to do something, anything to make me feel, even for a short time that I am ‘normal’ once more.
Normal, what a stupid word to use. What is normal? Well, for me it is being able to do what I want, when I want without needing any assistance, even that given freely and with love. Independence. It is a heady draught and having it taken away is dis-empowering. Yes, everything revolves around empowering ourselves. Illness removes that empowerment in the cruelest way.
So, after another sleepless night and emotional day before it, I lashed out. I secreted my clothes and sand shoes in the laundry before ‘officially’ going to bed. At 4am I decided my husband was deeply enough asleep I could afford to get up. He is used to me getting up and down during the night now anyway. Quick trip to the bathroom and a little makeup, just in case someone should see me and I crept out to the laundry where a light wouldn’t disturb anyone.
Yes, I sneaked out of the house like a teenager breaking curfew! I even had the forethought to grab a water bottle and my phone. I haven’t walked to the beach where I live and I’ve been here a year. I haven’t sat on the beach and seen the sunrise (at the beach) for a year either. I used to do both regularly when I was alone, independent, before I was engaged or married. I was like a drunken sailor, or a drugged up lunatic, weaving and staggering down this hill. I thought the beach was at the bottom of the road. A kilometre later I reached the sandy access to the beach.
All I could hear was the pounding of the waves. I wished I’d brought my camera but I don’t think I would have made it to the beach if I had. My whole body trembled from the exertion and I staggered down onto the hard sand to sit down. Thankfully seeing someone staggering in the soft sand doesn’t raise eyebrows. I was there and I wasn’t going to be able to move. But I was THERE!
I watched the sun rise above the horizon and the clouds.
It was beautiful. It wasn’t hot – I can’t take the heat and the meds had made me burn easily. I could feel the calm wash over me with every wave breaking along the shore line and the rays of the sun peeking over the horizon. I hadn’t known it was a dog beach. A dog. OMG – how much I want a puppy, a miniature fox terrier and all my own. It’s like an ache, never ending. The dogs began appearing with their owners and I was truly happy when they came over to say hello. To pat them, scratch behind their ears and look into those kindly brown eyes, was blissful. Strange how little it can take.
My photos are grainy – even the lauded iPhone can only do so much. But I will be returning with my camera,and soon. By 7am I was beginning to feel more than a little uncomfortable. Couldn’t move my legs properly and turning around brought a sharp twinge. A few more canine cuddles and I knew I couldn’t wait, it was time to start the trek UP the hill to get home. The sun was now a blazing ball in the sky but it was still cool.
I hit my first hurdle. I couldn’t stand up, couldn’t twist around and couldn’t bend my legs enough to kneel up. Just a little problem. Soft sand….. I finally managed to flop around like a beached whale until I I got one knee pulled under me enough to lever myself onto hands and knees. Humpf! This is what emotional independence gets you. Somehow I made it upright only to fall flat on my face – almost, hands and knees again. After my third staggering attempt and fall someone noticed it wasn’t quite normal and offered to help.
Help! I had to acknowledge I needed help to get up that soft sandy dune and she was a nice and concerned lady. So we managed to get to the seat at the edge of the dune so she could stretch after her walk and I could regroup after hiking up the sand dune! I was determined to walk up that darned hill. I stood up and walked to the footpath with my new found friend. My body, not one part of it, wanted any part of moving in a co-ordinated fashion. I staggered like a drunken sailor with palsy until I finally reneged on my independence and accepted a lift to the top of the hill. So much for being independent. After showering and changing I’ve been sequestered in bed, complaining body reminding me of my foolhardy outing at every turn. Yet desperate circumstances require desperate measures to be taken.
I may have paid for my intemperate haste to be independent, but I have my doggie pics and a few hours of remembering what it felt like to be able to go where I wanted, when I wanted to with impunity. For a while I forgot I was this person with an illness. I was Susan all over again and it felt wonderful. One day, one day soon, I will be that person again… come hell or high water I will be.
Blessings, Susan x
© Susan Jamieson 2014
Well, well, well! AND probably expects to not get into trouble. And NOT a spur of the moment thing…a predetermined act of utter rebellion.
(Pssst, was it worth it? Did it feel good? Will you do it again? Susan, your a bad ass! 🙂 )
Ahem…and if you ever do it again….your grounded for a week, you hear!
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Rebellion is good for the soul once in a while. I never said it was good for the body 😦 It felt absolutely marvelous. The beach underfoot and butt, the clean fresh air, the sound of the ocean and the sunrise. Dogs (doggy beach) coming to visit – for a short time it was a little piece of heaven. …Until I moved OUCH! I let the stubborn streak go reluctantly, and accepted help. I was given a lift up the hill, (I swear I had no idea it was so far). By th time I got inside (and Ray was awake and looking for me) I was feeling stiff and sore, A cup of tea, tablets (Yuck!) and shower and I had to go to bed. Perhaps not the best laid plan but it sure felt good at the time. And it seems I haven’t lost any of my old skills 🙂 Grounded ? I’m sorry – that does not compute!
Blessings, Susan x
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Mark, WHEN she does it again, next time I’ll be a little closer… A bit more available… And I think it was important, and worth it… I do understand..
Ray
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I have to admit it must be a very frustrating thing to lose that independence. Even a simple thing that we take for granted i.e. a walk on the beach, becomes a Grade A pain in the nether region of grand proportions. Time for compromise, and this isn’t just for Susan, as it would put your mind at rest also, but does a mobility scooter give more independence, safety AND she may even have the energy left next time to ACTUALLY go for a walk 🙂 It’s only in how we look at something. Try to look at that type of change positively, not to turn it into a pig’s mud wallow, which is in fact a place to pack mud on gloriously for the skin and the complexion, millions pay mega bucks for the luxury 🙂 And it gives Susan back some of her independence. Have a great day! Namaste
(Psst, Ray…handcuff’s at the reject shop are on special! 🙂 )
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Fluffy ones? 😉
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lol, yes, pink too if she insists! 🙂
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I have nothing to say…. although you may regret the fluffy pink comment… the things they have for guys are ..hmmmm interesting (evil chuckle).
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Susan, you’ve got another cheerleader over here. I remember being more independent, too…and I relish the day that I can get that back, and then some 🙂 Keep believing in it.
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Belief is all we have… with a groundswell of belief from all of us we will make a huge impact… all these fabulously fit and excited people doing everything with a smile, because we will know what it’s like to have lost it.
Blessings, Susan x
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Showing some true grit there Susan. You’re on your way to some physical independence.
Cheers
Laurie.
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It will come back – I cannot and will not let it steal myself away. Like a vampiric energy drain this thing need a good spell – willpower and patience (heaven help me there) but it’s a happening thing. Just a tad slower I guess 🙂
Love, Susan x
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That’s the spirit.
xoxo
Laurie
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It sounds like it was a very healing (although exhausting) outing. I hope you get to do it again soon.
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When I recover 🙂
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