Saturday, January 03, 2015

It's a New Year.

I am loving our summer holidays. 6 weeks really gives you time to party and to wallow and to get some jobs done too. This morning Dad and my nephew snuck out in the wee small hours to drive back to QLD - about a 12 hour car trip. My plan is to reclaim the house following all the Christmas and New Year cheer and clutter and dust that has accumulated. THe annual clean out.

The aquisition of a desk has been great for Kit so I am hoping to turn the spare room into more of an 'office' for Hannah to share with me. She's had 2 weeks of no 'work' so it's time to clock back on. The learning support may have been on vacation but the health focus has been well and truly present. I don't know how long I can keep up the regime but it is really helping little brat at the moment. She has a 'colonised staph' infection that has been playing havoc with her skin and also expressed itself in some nasty boils last year - the regime is 3 months of antibiotics, twice daily face and nasal creams (one of which cost just over $100!!!!! - although I'm more worried about the 5 repeat scripts it came with - I hope we don't need those!!!). All washing has a disinfectant rinse in it and Hannah's wardrobe gets the hot water treatment.

Avisit to her paed provided some concern about her hips as her gait is quite stiff legged but hip xray was fine so we just have to keep at it - bike riding and walking her as much as we can to help her build up some stamina. She has a vitamin D deficiency and I am giving her a supplement each night for that. A visit to the dentist is priority for this month as her teeth have been affected a bit by that. The 'inevitable' thyroid issues have arisen so we have started her on meds for that which entails regular blood tests and really regular blood tests while the levels of medications are getting sorted. sigh. I'm hopeless at routines like that - lucky the holidays are making it all a bit more manageable.

Festivities in the Dock have included the following:
A home talent show that ended in some free dancing to Girls Just Wanna Have Fun.
 Some spanish dinners inspired by one of my Christmas gifts.
 Chorizo bread from My Barcelona Kitchen - delicious.
 Some backyard games including cricket and boules
 Just heading out and about.
 Fireworks from a suburban backyard where P and I were lucky to see the new year in with a wonderful group of families from the twins school.
 A late afternoon swim for Hannah and I

 A happy ole poodle with her pack never far away.
 Some holiday reading for me.
 A visit or two to the local park.
 I have lost count of the number of photos of Hannah like this I have - from since she was just a little bub to just this week..... love them all .... cos her face is just a picture.
 A sampler of Hannah's Christmas gifts from Santa:



Friday, December 05, 2014

Round up from the Dock

Well, well.... I have been in 'special ed' for a year now.... and I love it. It's not easy. The view from the back of the room is often quite tainted. I wish inclusiveness came more naturally to some staff and teenage boys. But the days that are good - wow. It's good. The people I work with  - they're great. All the changes in the disability dialogue - what happens in the wider society - is happening in schools. In just 15 years we are making such progress. We still fail quite abysmally too though.

Hannah's primary school fail too, sometimes. But boy oh boy - they keep at it - and they get it so much more regularly than they don't. They are a wonderful pinup poster for inclusion. It pervades the community.

Just today was another small example, a small example that reveals so much. It was the day of the school swimming carnival. My MIL was at the carnival for a couple of hours (she and my FIL often go). Both Phil and I got calls from her - did we think Hannah could swim in a 50 metre race? Well I didn't know - but I figured it was worth a shot so long as she had a noodle or kickboard and was in the lane near the edge - I figured she be ok. In the end sheswam it with a kickboard and a student from Year 5 in the pool with her. A friend texted me this afternoon to tell me about it. My MIL rang both of us to tell us about it.... Her teachers were at the side of the pool encouraging her to make it to hte end. When she got out and went to the stand for her ribbon (a first!) one of the teachers who had the microphone asked everyone to give 3 cheers for Hannah - my friend tells me they all raored their cheers. Ah, my eyes are misty just thinking of it. That is inclusion. At the same carnival Hannah's brother who is not necessarily a great swimmer went in 5 different races. He had a go. He got some place ribbons too - I've strung them up across our fridge with magnets - a banner of pride. I am so proud of my children and so blessed by the community we belong to.

I want to translate that experience to the HS that I work at. It's worth it. Wish me luck....

In other news:
Hannah still loves swimming - and is working on her 'big bubbles'
 Building Hannah's birthday gift together
 The boys went camping - looks like a beautiful spot.

 The husband's birthday had a recycled vinyl theme - appropriate given that he has obsessively been playing all our vinyl records from Z-A for the past 6 months or so - and logging each album played on fb and twitter. We are somewhere around 240 at the moment - maybe half way there.
 Hannah has been having fortnightly Occupational Therapy and daily obsession with Scooby Doo - this is her most recent drawing of her as Shaggy and me as Scooby.
 Kit and I went to see the Nutcracker ballet at the Opera House
 We had a wonderful weekend away with friends and the girls prepared a dance item for us
 One of Hannah's readers involved Teasing Mum - where a hose was turned on the hapless Motherby her dreadful child as a joke. Hannah loved the idea so much she mad her won version (and actually followed through on it too) - Teasing Dad. So while she and her father were washing the car ... yep. Lucky he's a good sport and a total sucker for his children.
 Tangled has also had a bit of an airing on the tv - and the lego set has been constructed and the scarf Hannah knit has become a staple in the dressing up like Rapunzel game.
 More swimming - and getting better at it all the time.
 The joy of a pre Christmas spring clean. Their room is looking so much better and we bought a desk for Kit which has turned out to be a very good idea.
 There have also been a number of parties to go to...
 Including Kit's minecraft with 'water' (jelly) shots
 and Hannah's sushi and kokeshi doll do.
 Kit has finally made it into squads and is very happy.
 Some composing, just because she can. She is recording herself on the ipod in this pic.
 Formal piano lessons have come to an end... that's a separate post but suffice to say that she has enjoyed the opportunity immensely.

Concert season began with a Dancing Heart soiree - it's her dance class for children and adults with disailities. It was a blast of a concert.


 And then her mainstream dance class had their concert. She LOVES that one - especially her Musical Theatre teacher. She danced to Little Shop of Horrors.
 Finally, Tis the season....
 my favourite season...
Happy Advent indeed.

Sunday, November 30, 2014

Advent

The countdown to Christmas has begun. I love this time of year. Work is on the downhill run and so is the treadmill of the kids activities. Hannah has finished her regular dance concert and the one for people with disabilities. She was fab and we all enjoyed cheering her on. She's also been enjoying her swimming - she is swimming every day at school at the moment and while packing fresh swimmers and towel each day is a pain - she loves it.


10 proved to be a bit of a milestone birthday. Double digits and growing independence suits my monsters. Kit had a mnecraft party and Hannah a sushi party. Both were lovely.

Kit is still dancing. His ballet concert is coming up soon. Last night he and I went to see The Nutcracker Ballet at the Opera House - a wonderful night - to quote Kit - "it was awesome!"


Wednesday, August 06, 2014

Democracy, adults and children.

Years ago a colleague and I who taught Legal Studies had a cartoon we both liked. We'd use it to generate discussion in our classes. Essentially it was about democracy - and how great it was - and the drawback that every person gets to vote - whether you agree with them or not. The punchline was along the lines of  'beware the morons bark'. In times when every troll and fool gets to have a say on social media it still has resonance.

Last Friday driving home from work, I heard about Gammy for the first time. Since then he has been getting lots of  social media time. Reports of the matter are a bit blurry - so this is my summary of what I understand to be reasonably accurate about the matter. An Australian couple paid a surrogate Thai woman through an agency to carry 2 embryos for them. At some stage during the pregnancy it was realised by ??? that one of the twins had Down Syndrome. The Thai woman was asked to have a selective termination, anywhere between the 4-7 months stage according to what I've read, but she refused. Two babies were born. A 'typical' girl and a boy with Down Syndrome who also had a congenital heart defect. The commissioning parents took the girl baby home with them. Gammy, the boy, is being raised by the surrogate who does not have the $$ to ensure that he gets the major heart surgery and after care he requires. She claims to have entered into the agreement to help pay of her family's debts and says that she has not received all the $ agreed in the surrogacy arrangement. She is raising Gammy. Without surgery Gammy will die. The biological 'donors' technically seem to have abandoned him in Thailand.

As I listened to Richard Glover retell the tale on abc radio 702 Drive program, I cried. There are things happening in the world that disturb me greatly. The children killed in the Gaza conflict. The children seeking refuge in Australia. These are 'big picture' happenings where I can see how children's lives are disrupted, disturbed and sometimes destroyed by the conflict between adults. Gammy provides a peephole on to some of the same issues as they play out in the life of just a few individuals. His story resonates with me for many reasons. Firstly, like his biological parents, I am Australian. I have twins via ivf. One of my twins is male, the other female. One of my twins has Down Syndrome, the other is 'typical'. My twin with Down Syndrome was born with a congenital heart defect that required major heart surgery when she was just two months old. There the resemblence ends. I never dreamed of separating my twins.

Gammy's story may have turned out so differently with just a few different twists and turns in the course of events. If a surrogate hadn't been required, his biological mother could have sought a selective termination here.  The biological donors could have accepted both babies from the surrogate. The surrogate may have gone ahead with the selective termination... and no story may have eventuated. You see, not only is the role of power, privilege, human trafficking, parenting and the dignity of the child significant in this case, so is chance. I believe that just like democracy, people need to be able to make choices. Those choices are not necessarily ones I agree with but we each need to be able to come to our own conclusions, and in collaboration where the decision affects other adults, as it often does in complex situations.

If there is a dispute between conflicting adults the family court applies the principle that the interests of the child are paramount. I wish that was the case in the wider world. Gammy's story makes me sad. It also gives me hope. I was touched by the compassion with which Richard Glover related the news the first time I heard it. He commented that it was one of the saddest stories he'd heard. There is a rapidly growing 'help fund' for Gammy's care. Discussions are occurring in many different places. Democracy only works if people are informed, if a range of views get listened to, if everyone has a say.

I have been part of the growing movement of people with disabilities, carers, families and friends who have been raising awareness about issues of fairness and justice for people with disabilities in our society. As the media attention fades away on this and hopefully Gammy gets his surgery and settles down with his loving family... what have I learned from this story? Advocacy never ends. We need to stand strong for the dignity of children, for the value of adults whose lives are too often undervalued in society. The ultimate goal is self advocacy. I want to raise a daughter who can speak for herself. And I want a world that will value and listen to her.

We have seen some significant reforms in Australia through the piloting of the National Disability Insurance Scheme (NDIS). My daughter attends mainstream primary school where she is resepcted and liked by her peers and teachers, where the other families of the school inlcude her in the community. I work in special education in a mainstream high school - and I can see real changes continuing to happen - to make life fairer and better for all. I have crucial networks with other advocates each with their own way of fighting the good fight. The Mum whose handsome boy is featured in fashion ads, another who focuses on ways to help women who receive a prenatal diagnosis have up to date and 'real' information when making life altering decisions, the countless public fb pages raising awareness of people with Down Syndrome, the love and support and understading we show each other when things get tough, as they do sometimes on this journey.

When I walk down the busy city streets, laughing and chatting with Hannah, my precious daughter who has Down Syndrome, I am showing you a peephole into our world and I hope that that glimpse will allay the fears and misconceptions that are held about difference and disability in particular.  She is part of the happiest story that I have ever experienced. So like the tattered beast that is democracy, we are not always going to agree. My shoes are not yours but That doesn't mean we can't learn from each other.  Almost 10 years into this journey I have found a steel core of openess and support in the people I meet and in some noteworthy institutions too. I can see a future where the dignity and rights of children will be seen universally as being of paramount importance, if we continue to work for it. That knowledge and the article I read recently about Gen Z.... these kids, yours and mine, growing up now with all their privileges and access to information, are going to be awesome! And so the story of Gammy is not 'happy' or 'sad' but a bit of both and all the bits inbetween too....

Here are some gratuitous 'twin shots' because the hardest part of the whole story for me, the reason I cried when I first heard it, was the apparent disregard for the bond of the twins themselves. Twins are magical however they are conceived. They have grown together from the very beginning and it is not the place of adults to experiment with or destroy it.








Tuesday, August 05, 2014

August begins

Well hello!
It has been a very busy 6 months in the Dock. Kids are both doing well. In different classes this year - both working and learning. I am settling into the new job - I have almost been there for a year. I am also studying again - this time it is a Certificate in Gifted Education.

Winter has been mild. The vege patch has been restocked. Here are some random pics:
Both kids are still swimming....


And dancing....



And learning piano


And just goofing off as twins and siblings do