Saturday, June 02, 2012

Day 2 - Sleepy sleeps

At around lunchtime today, Ash came and told me that Cedar was asleep on the lounge. "That's ok", I said to him. Only a little later did Ben tell me that Cedar had actually fallen asleep standing up and leaning on the couch, which is rather more unusual!

He doesn't typically sleep in the day at all, unless unwell, but he had come in to our bed in the early hours of the morning with a temperature. Obviously whatever his immune system is fighting had him extra tired today.



I was thinking, I know that I often don't get enough sleep. It isn't intentional, but comes about because of the way I work and the way the kids do things. Sienna suffers insomnia and usually takes a long time to get to sleep. Ben leaves for work early in the morning - 5:30 normally, 4:30 on Fridays and occasionally other days - so tries to get to bed with enough time to have a decent sleep. Most days, Sienna isn't yet asleep when Ben goes to sleep. I stay up until she falls asleep, as well as using the time to do work on the computer, or for scrapping deadlines, while watching tv.

Then in the morning, Ash tends to come in to my bed for a hug around 6. I might have had 6 to 7 hours of sleep at this point, which isn't really enough for my liking. But I get to rest from 6 until 7:30 on weekdays, and tend to catch up in snippets on weekend mornings. I don't mind so much how things turn out, though it would be nice (mostly for her) if Sienna could switch off more easily. It made me realise, though, how much of a haven it is to sleep in a warm, cosy bed. Even when it gets squished full of more people than actually fit, especially on some weekend mornings, it is a soft, pillow-laden sleeping place for which I am truly grateful.

A detail of our Orla Kiely quilt cover
Especially my electric blanket. I really love that.

  
I am blogging grateful posts for the 21 challenge, raising awareness and funds for Australia's homeless youth.

If you would like to sponsor me or donate to the challenge, please click here.

Friday, June 01, 2012

Day 1 - crafty kids

Today I am grateful for crafty kids - crafty, that is, in the scissors and paper and glue way. Not the manipulative, sneaky way so much. This morning Ash woke up before 6 and hopped in my bed for a quick cuddle. Then he hopped back out again and said that he wanted to do pirate crafts before school. He spent two hours making a sword and hook out of cardboard (which he had started the night before) and having breakfast before I got him to get ready for school.




After school, Sienna hid away in her room making a 'spy suitcase' out of a cardboard box, with sticky tape and using only scissors.

We had a slight altercation at dinner time between Ash and Cedar over this paper pirate hat (pictured). Ash had made it for doggie, Cedar had put it on his own head and then crumpled it up during their tussle. I got Ash another bit of paper so he could make a second one and everyone settled down!

There are days when the kids seem like they can only be entertained or absorbed in electronic devices - the ipad, ds, watching movies, playing pc games. While these tools are limited as necessary, I so much prefer it when the kids use their own initiative to be crafty instead. And they are usually a lot happier for it.

I am blogging grateful posts for the 21 challenge, raising awareness and funds for Australia's homeless youth.


If you would like to sponsor me or donate to the challenge, please click here.

Thursday, May 31, 2012

The 21 Challenge - restart and love

A couple of hours ago I signed up for the 21 Challenge.

In Australia more than 32,000 young Australians will sleep on our streets every night.

Challenge yourself, your friends and your workmates to do, or not do, something from June 1st to 21st.  June 21st is the longest night of the year and a particularly difficult time on the streets for our homeless youth.


The 21 Challenge is your chance to help homeless youth by doing something you love, perhaps something you don’t love, or even something you’ve never done before for 21 days and asking friends and family to sponsor you.  Be as creative or ridiculous as you like and the money you raise will go to Open Family Australia’s Outreach programs, supporting youth at-risk.

You will be supporting a great cause with all the benefits of your efforts going towards Open Family Australia’s Outreach programs to benefit at-risk and homeless young people. 


(Description from the official website)

I'm not sure how I stumbled across the link on Facebook, but I read a couple of the stories on there about the challenges some young people have to cope with on a daily basis, and the efforts of the outreach officers to bring some stability into their lives. And I just clicked on register. I'm not sure what difference it would make but a small amount of awareness makes it worthwhile... with awareness comes greater empathy, not to mention the fundraising itself that will actually help individuals get assistance.


So my challenge is in two parts. At first I saw that some had declared that they would quit sugar for 21 days, which is something I've been meaning to do anyway. So that is one part. But then, I was meaning to do it anyway and it isn't really related. And being fussy about what food to eat seems so first-world compared to the challenges of homelessness and disadvantage. I still want to do it but I wanted to add a second part that would be more confronting for me.


The other part of my challenge is 21 days of being mindfully grateful and blogging that gratitude every day.


If you read my blog regularly, you will probably have noticed that I've been updating less and less lately. It's a combination of a lot of things - time, energy, lack of taking personal photos to share, and a lot of self-censorship, as well as distractions and deadlines. Partly, also, that I sometimes find it emotionally crippling to be the recipient of attention. A sort of antithesis to craving it (which also comes and goes). So, blogging every day would have been a big challenge anyway, but given the topic of homelessness, and my general tiredness at the moment, I wanted to make it a more affirmative, constructive challenge. Therapeutic, even.


This is something I try and think about anyway (positivity), but only inside my own head. And it's certainly not always natural. So I'm going to bring it on out. Instead of thinking how things might be challenging, or the difficulties of a day, or negative feelings, I'm going to find one thing to celebrate about each day, and do my best to share it. Because, in truth, I am not homeless, the subject of abuse of any kind, addicted to drugs or uncertain of where my meals might come from. And that is something to be grateful for to begin with. 


If you would like to sponsor me or donate to the challenge, please click here.

Monday, May 21, 2012

Port Lincoln it is!

Does that sound odd? LOL. I've never been to Port Lincoln. But, as I have said before, I love new places. Big or small. Far or near. Blah blah blah. And I jump at the opportunity to explore a new location.

So, did you know I keep waiting lists for all sort of locations? It depends on the spot itself how many bookings are needed to make a trip possible, but once I have two people interested from one place I look more seriously into making it happen, putting out feelers, spreading the word. And if it looks like enough people would love to have me photograph their family, kids, themselves, etc, in that location, then it's a go ahead!



This is how I happen to be visiting Port Lincoln in South Australia in September, offering photo sessions for the 3 days that I will be there. A couple of spots are booked so far, and I know a couple of more are in the works, so here is current availability:

Friday 28th September: 2:30pm, 4:30pm
Saturday 29th September: 7am, 2:30pm
Sunday 30th September: 7am, 9am, 2:30pm

And if anyone has any tips or recommendations for spots to see, shops to look at, places to eat while I am there, please let me know!

Sunday, May 06, 2012

Away with friends

This weekend I have flown with my cousin Bec to Byron for a few days. We are staying with my friends in Bangalow who live in a little house with farmland around and it's a beautiful view, with chooks running around and goats in the field next door.

We flew in yesterday afternoon and are about to head to Byron to check out the markets, look around a bit. Tonight it's back to Bangalow for Bic Runga's show here. We fly home on Tuesday :)


Monday, April 30, 2012

danielleQ to ‘I Wish I Didn’t Have Aspergers: #AutismPositivity2012

I stumbled upon this blog project that's happening today called "Autism Positivity Day". It came about, as the website says "A couple of weeks ago, someone somewhere googled “I Wish I Didn’t Have Aspergers”.  The phrase popped up in a blogging dashboard and struck the blogger as being particularly sad.  She wished she could have answered.

We don’t know who it was.  We don’t know where he/she lives.  We have no idea if he/she found what he/she was looking for in that search."

As a result, "We are asking every blogger in the autism community to write a message of positivity to #IWishIDidntHaveAspergers.  So that next time that individual (or another) types that sad statement into Google, he or she will find what they need – support, wisdom, and messages of hope from those who understand."


Well, hi. I am a blogger. And I am part of the autism community I suppose, though I don't know if I think of it like that. I am just me, we are just we. Let's start with an introduction.

My name is Danielle. My blog is about all sorts of things, creative things mostly, photography and scrapbooking, food sometimes, family sometimes. Of my three kids, my daughter Sienna, the eldest child at 8 1/2 years old, has Aspergers. Ash, my 6 year old son, has high-functioning autism (the main difference in diagnosis is that Ash has had receptive and expressive language issues from an early age as well as the pragmatics and other elements). My husband, who is 35, also has Aspergers, diagnosed after the kids as a result of reading about Aspergers and recognising himself in the descriptions. Our 2 year old, Cedar, has a developmental paediatrician keeping an eye on him. We are an interesting family, for sure, we have a lot of love, and we have a lot of things to be grateful for.



I don't know who you are, and I don't know why you wish you didn't have Aspergers. It's such a sad thought, and though it may seem to be so logical to you, please don't wish yourself away. While not the sum of your parts, Aspergers is a part of who you are and comes with a beautiful flip side to the challenges you are feeling. I don't personally have Aspergers, I can not claim to share your experience, but I can tell you what I know to be true.



My daughter is so adorable. She is quirky, passionate, creative and fascinating. She looks at things in such interesting ways and is intrigued by details that others don't even notice, or possibilities that never occur to the people around her. I sometimes watch her and see, behind those beautiful eyes is a brain working overtime, seeing so much, absorbing so many nuances of light and sound and colour. She is a work of art. Every day she experiences fear and anxiety, and every day she feels love, excitement and joy. There is at least a moment of everything, and I admire her every day for the way she just keeps on being her amazing self, she is just so much of herself regardless of the perspectives of others or the words of those who don't understand. I feel her pain and sorrow, I experience her warmth and I embrace her enthusiasm. She loves me so much, and I am blessed to know her deeply every single day. She is an incredible girl and she has Aspergers.


When I was a super-emotional and sporadically depressed teenager, I often thought about the depth and intensity with which I experienced things. The black is so black, emotional pain echoes with physical force. When it hurts, instinct tells us to wish the pain away. But knowing that the flip side of that deep experience of life is infinitely valuable, and a kind of balancing force to the difficult side - to see beauty in unique ways, to experience positive emotions with equal intensity, has always been worth it. I would not sacrifice that which makes me who I am, with all the beauty and pain, to be less of myself, for the sake of less intensity of being, because I wouldn't know how to be that person. I don't know how to want that. No one who loves you would want that of you either.

Sometimes it feels natural to wish it away, the core of who you are, to want it to go, and that is the pain speaking, I know. But you have the power to remember, to recall and re-focus. Remind yourself. You are amazing. You have gifts and spirit and a unique view that is irreplaceable. Aspergers gives you strengths and individuality which are awesome possessions. You possess them. Your strengths and interests, they are yours. And they are part of how fabulous you are. Even when you don't feel it to be true, reach out to those who love you and be reminded.



Ash, my middle child, is so fantastic. Along with his bewilderment at much of what goes on in the world comes infectious enthusiasm and eagerness to embrace the people he comes across, in all their variety. He shares his love of pirates with all he meets, and was saying to me just today "I don't know why I like pirates but I just love them so much" while we discussed the relative merits of treasure maps, ships and swords. He has a smile to light up the day, and experiences the ups and downs of his emotions with dramatic intensity. So many days are the "best day ever" for some small detail he has such appreciation for, even if it disappears minutes later. He embraces things that other people would barely notice, or just shrug off. Where other boys are embarrassed to display themselves so honestly, Ash is abundant in personality and quirky uniqueness, jumping out of his skin to just be himself, regardless of what anyone else might think. To worry about that just never occurs to him. The negatives of his autism are vastly outweighed by the power of what a fantastic person he is. He works so hard, and feels so much, everyday. I am blessed to receive his adoration and beautiful warmth in each day that I know him. He is amazing. And he has autism.

While a positive message, this is not a rose-coloured glasses post. Life is full-on for these kids. They spend their days trying to decode the world around them, and sometimes this doesn't work so well. Things get broken, others don't understand, they don't understand and their hearts are damaged piece by tiny piece when people say hurtful things. They take people at face value, they take words spoken very literally, and are not always rewarded for their open trust. They worry, they fear, they cry. But they always win. They remain passionately, intensely themselves and they remain incredibly loved and supported by their dad and I. We wouldn't want anybody to change who they are inside. Because they are brilliant human beings.



I don't exactly remember meeting my husband, as we were on the fringes of one another's radar growing up. I remember getting to know him on the Wednesday bus home from school, when he would also be on the bus on his day off from work. He would be returning home from Adelaide, where he would have bought at least one new drum and bass cd. He spoke passionately about his music, and shared his love of beats with me. He would comment on the Shakespeare plays I'd be reading for my English studies. We would talk a little and then a little bit more, and then we wouldn't stop talking. At other times, too, and so it grew. I always found him interesting, and loved that he was different from other people, just as I felt I was, though in different ways. Now we've been married for 13 years.

Ben is incredibly intelligent, and technology is his area of expertise and passion. Just as he counted the beats per minute of every song while making mixtapes when we were young, he pays attention to each technological detail around us. We laugh at some of his quirks, his 'Sheldon chair' and microwave rotation calculation, just as we laugh at the paint in my hair and, well, pretty much whatever. He has travelled, learned new things, adapted to new jobs and gotten to know new people again and again. In parenting, he observes and embraces and considers how best to support these amazing people we are caring for. And he loves me so much, so much that even after all these years I feel self-conscious about inspiring his devotion. But I don't doubt it.

Aspergers? Yes, it's there. It's here. It's part of our home. Regardless of autism, or because of it, I don't know. But I do know three things: I am never bored. We have love. And I am grateful.