On the last 4 months

Wow, I didn't realise I hadn't been on here since September! Before the big move to the middle of nowhere! Life has been so busy, that I simply never seemed to have the time to come over here.
And, now, when I finally sit down to write, I have a certain 11 year old standing over me wanting me to spell every single word of a letter to her friend out to her. Well, not quite EVERY word, but it sure seems like it!! No rest for the wicked eh?!
Our move to Roma was a bit of a disaster. One of the wheels fell off the caravan, before Michael and Christiana had even left the outer city limits of Brisbane. The RACQ towed them to safety, and they had to drive out here without it, arriving at 4am the next morning! The following week, they drove down to get the now fixed caravan, and got as far as Toowoomba before another wheel fell off the same side! This time, they managed to tow it to a repair place by just going really slowly! (it's a twin axle caravan). They left it with the mechanics, and this time asked them to check EVERYTHING!! Went back down the following weekend and finally got it home. All in all, it cost us $2000 we hadn't planned on!
We have found Roma to be a very friendly town for the most part. Having a child with a disability is actually a real advantage when you are somewhere new! Through Samara we have met a lot of people, and people I have no idea of having met, stop to talk to us in the street, because at some stage they have crossed our paths, and they remember Samara!!
The only pediatrician out here visits the town once a month. We have only met him once, but he seems really good. He put an action plan in place so that if we take Samara to the ER with a cold, she is automatically admitted and monitored, which is great. Not that I like being in hospital, but she can go from perfect sats to crashing in a matter of minutes.
She has only had to be admitted once since we came out here, and I have to say, she was pretty popular, being the only child in the hospital! LOL
The early education unit at the state school is not as good as the one in Woody Point. I guess I expected that anyway, but I do miss Woody Point. Next year, things are going to change a bit, and Samara will be in a smaller class meeting once a week, rather than the current once a fortnight, with a lot of bigger boys on the autistic spectrum - a bit hard for her to take. I am hoping to get the teacher to impliment some more music and art once this happens.
We have had 2 floods out here since we moved. In one of them, our house ended up on the channel 9 news! We had to move the stuff in storage under the house up onto the porch. Good thing this place is up on stilts!!
Samara has had several trips to Brisbane and Toowoomba for various appointment since we moved out here. She had another sleep study, which has shown no improvement since she had her adnoids removed. I have asked them to do another one in the winter time, as her sleeping is a lot worse then. She has also been fitted with hearing aids, but it is such a pain to use them, cos she takes them out and hides them! Sneaky little child! LOL. But her speech is certainly more clear and she is more talkative when she has them in.
Also, her overall demeanor has changed a bit lately. I took her in for blood tests, and they are showing high levels of Renin and Tri-glycerides. The first test showed high potassium levels too, but this has settled. She is going for a scan today of her kidneys to try and figure out what the problem is. She may need further testing on her liver as well, but that will be determined after her next blood test in a months time.
A month ago, Renata came back home from her year in New Zealand. At first she was unsure if it was for a holiday or to stay, but she is now working at Woolworths, and intends staying for a while at least. It has been good having her here, and she has grown up and matured so much during her time overseas.
Christiana is also working at Woolies, which has been great for her confidence. She is coming along really well, and getting over some of her shyness issues (but not all! LOL).
Sara is still in New Zealand, and has moved in with Alicia in Christchurch. I am really missing them both at the moment, and wish we could be closer.
Bryanna is becoming a real teenager now. Making a lot of her own friends, and even overcoming her intense dislike of boys! She still vows and declares she is never getting married or having a boyfriend cos that's gross, but at least she isn't automatically dismissing half the population as potential friends any more! At this point in time, we are thinking her learning difficulties are more likely to be related to an acquired brain injury she had at 5 years of age, rather than Aspergers Syndrome. But we can't investigate it further until we have our Permanent Residency sorted out!
Mahalia is coming along a lot with her reading difficulties. She is even reading chapter books now. She is still a bit behind maturity-wise, but I can see some changes that will hopefully be enough to see her through.
For Christmas, we made a Christmas Tree for the town's Christmas Tree Festival, that was all decorated in blue and yellow (DS colours), and had photos of many of the DS children I have 'met' through the internet. I think it was pretty successful, and the local Disability Support Services took pictures to include in their newsletters.
This week, along with the floods, we are in the process of moving. The owners of this house are moving back in in a couple of weeks, so we have to move on. We thought we were going to have to live in the caravan, as we can't find a place to rent, but we have been offered a 'crisis' house in the meantime. Pretty disgusting though. The last tenants were obvious druggies, and very messy! But at least we will have a house to live in! Speaking of which, I should probably be doing something to help with the move.......

A Party and a Shake-Up

Well yesterday's earthquake is still top in most Kiwi's minds. There were a few of us at the party yesterday, including to Ch-Ch families. Alicia is working today which seems a bit soon. They are expecting a quake measuring 6.0 by the end of the day, and they have gale force wind warnings in place for today as well. Hopefully there are no more injuries. Just really thankful that there were no deaths! Even in Timaru there were breakages, like the top of the spire of St Mary's church. There was also a pub in Temuka demolished (Temuka is a small town about 20km north of Timaru.

Last night Bryanna prayed that Alicia would sleep under the table. But not because she was scared. Because it was cool! That child comes up with some interesting logic sometimes LOL. I do still worry about her. Having a child in the midst of it all kinda changes how you view these things. They are feeling aftershocks every half hour or so, some over 5 magnitude.

Here's a picture I swiped from the internet. Tried to get some better ones, but I kept getting this one as it was part of a slideshow.

On a happier note, Samara had a great birthday party. Apart from a major choking session after eating a Dorito that is!

I haven't uploaded the camera yet, but last night I took this picture of one very exhausted little dinosaur.

She fell asleep in her highchair without touching her dinner at about 6.30 and slept through until 9am this morning!

Christchurch Earthquake

Well, I was woken at 5.30 this morning by Sara ringing me from New Zealand to tell me that there was a massive earthquake in Christchurch this morning. She knows me well enough to wake me up and let me know they are all okay, rather than let me read about it on Facebook and freak out!! LOL.
Alicia lives in Christchurch, and said while it was freaky, they are all okay. Power is out in most of Ch-Ch, but not her place, so she is pretty lucky there!
It seems kinda hard to believe really. I mean, there are quite a few small earthquakes there, but I don't ever remember there being one that caused damage. Seeing the photos online doesn't really equate with Christchurch in my mind!
Personally I hate earthquakes. They really scare me. So I have to say, I am so glad I wasn't still in New Zealand right at this moment.
Apart from Samara's birthday party later today, it is also her cousin Hannah's 10th birthday party today. I am thinking that maybe the attention will be more on the earthquake than her. I hope not though. And I hope she has a great pool party! Good thing it's in Timaru, not Christchurch. Otherwise it may have had to be postponed.
Well, it is 7am now, and the family will start to wake soon. But I am exhausted, so going to try and catch a few more zzzz's.
Please keep the people of Christchurch in your prayers, as damage becomes more apparent, and as they deal with the cleanup, sewage problems, and looting.

Nearly 2 years

Well, in 13 hours time, we are going to be celebrating Samara's 2nd birthday. Her actual birthday isn't until the 23rd, but because we are about to move away from Brisbane, we thought we'd have an early party where Samara can have her friends over.

Today has been spent making and decorating her cake. Actually, the last 2 days have been spent making and decorating her cake.

And now, I am so exhausted. It was a bit of a work of art, complete with the mess that accompanies such endeavours. And the whole nutty artist who really loses the plot. But the results are worth it. Don't you think?

Reflections on Disablility

Ever since Samara was born something has been plaguing me. Should something be done to 'fix' our kids, or does accepting and loving them mean accepting the way they are and not trying to change it?

Is Samara's whole personality, or even her human-ness tied up in her disability? I know she would seem like a different person if the DS were taken away suddenly, but is that a good or a bad thing?

When we were first given the diagnosis, the only hope I held was that we could give her a 'normal' life if we found out about the alternative treatments. So I jumped online and began my search. You would think it would be fairly easy, considering these treatments have been around a while now. But it took weeks of searching, until I found a few that looked promising. Basically Nutrivene (a Targeted Nutritional Intervention) and The Changing Minds Foundation, which uses a combination of natural therapies with prozac.

Well, I don't know about in the States, but in Australia, it is not so easy to get a script for Prozac for a baby! So we decided to go with TNI. We ordered the stuff (which turns out to taste terrible), and started on our way.

After 6 months, we ran out of supplies, and simply haven't had the money to renew. Now, there is no major research been done into how effective these miracle cures are, and particuarly with TNI, there is the obvious implication of the hundreds of dollars they make out of you for every order you place. Changing Minds is a bit different, as they pretty much give you the information, but don't sell the products.

But in trying to decide whether or not to continue persuing these or any other 'treatments', I am left asking myself a difficult question. One that doesn't seem to have a real answer.

I love Samara just the way she is. There are aspects of the Down Syndrome I don't like. There are other aspects that are totally awesome and I wouldn't want to lose.

But this isn't about me. It's about her. It doesn't matter what I want, like, need etc. It's not about whether or not I am happy with her diagnosis. The real question is 'What is best for Samara'?

Is she better off if we can raise her intellectual ability to within 'normal'? Is she better off if she doesn't 'look' like she has DS? Would she have a better life if we could make her appear as 'normal'?

Or is her disability actually a blessing for her? Is it really so bad that she doesn't ever have to worry about the world ending tomorrow? Is it a problem that she won't be a doctor, lawyer (or worse) a politician? Does it matter if people make assumptions about her because of how she looks (which is incredibly adorable IMHO)?

I struggle to find the answers to these questions. Questions she is too young to understand. But questions that beg answers now, while she is young, and there is a chance to change things.

Questions that are clouded by my own wants and needs. I personally have gained a lot through having a Special Needs child. But why should she 'suffer' (if indeed she does) just so I and others can learn from her?

Every human is born with potential. But is life really all about doing all we can do to reach the limits of that potential? Is it such a bad thing is Christiana becomes a stay at home mother of 12 (her current ambition), rather than using her brain (she is pretty intelligent) and becoming a paediatrician? (as our neighbour is trying to push her towards).

Is it okay for Samara to stay intellectually disabled, or should we try and extend her capabilities to their limits? Which is better for HER?

Tutu's and Superheros

As I mentioned the other day, I am going to start collecting dress up costumes for children who are in hospital at Royal Brisbane Childrens and The Mater Childrens hospitals with life-threatening conditions.

I have been doing a bit of thinking about how I could go about this. We are moving next week out into the middle of nowhere, so I will be doing this to co-incide with Samara's appointments at the two hospitals.

I am going to approach the Starlight Foundation (once I know I have enough support to keep this up as I can't do it on my own) and see if they would mind passing on the gifts to the children, as they meet children on every ward, and I didn't want to limit it to oncology. This would also remove any burden from the hospital staff in trying to keep track of it all. I think they already have enough to contend with! LOL

If I get enough support and it becomes popular, I would love to find people in other areas to do the same thing for their local childrens hospitals. But for now, it's just Brisbane (although feel free to send stuff from anywhere!!)

Also, if you would like to help, but don't have the time etc, I will accept donations of tulle, non-roll elastic, crochet-style headbands (available at Terry White and some of the discount type stores), ribbons, and fabrics suitable for making hero capes for the boys. Alternately gift cards for Spotlight or Lincraft stores could be used for buying fabric. If I get enough support, I will also approach some stores to see if they will donate or discount some fabrics for us, so maybe we could all meet somewhere and go do a bulk buy.

There are several free patterns out there on the internet for tutus and for hero capes. I would advise doing a google search, as it would be nice to get some variety going. Also, some styles may suit some people's budgets, sewing abilities, likes and dislikes, etc better.

If you want my no-sew directions, let me know. These are the ones I make to sell, so please only use these directions for this charity.

At this point, I will not be doing anything to register as an official charity. The paper work isn't really worth it for something so small scale that might not even take off. If we got to the point of doing this country wide on a regular basis, I would reconsider this option.

And, I think that's about it for now. If you would like to help out in some way, please contact me. When Samara was born, we spent 4 months at Ronald MacDonald House. We saw a lot of very sick kids. My heart would break for them, and I really wanted to do something for them. If this can put a smile on a childs face, it would mean the world to me, and more importantly their families.

And those of you with children blessed with an extra chromosome, I am sure you know about the statistics for our kids with the likes of leukemia. I think it sits in the back of all of our minds as something we never want to face. Well, these families are facing it and living with it every day. If you are at all able, please help me to bring a little bit of cheer into their lives.

Sorry for all the grovelling. It is just I am feeling very passionate about this right now, and getting it off the ground is the first hurdle. If I don't get support at this stage, the whole idea is likely to fizzle out. But if we can get it up and running, then we are more likely to be able to expand and share the love around!

The Last 5 Months

Ooops. I didn't realise it had been so long since I checked in here. I keep meaning to do it, but there's always something else happening and I don't get around to it.

Thanks to all who sent their condolences when Jes died. Even now, 6 months later I have my times when it all hits me like a flood and I cry yet another river. I don't know if it will ever be entirely real. Michael's other brother had a little girl who at 19 months was burned with boiling water. 4 days later she died of septicemia. I thought I'd never recover from that one. It was 8 years ago, and sometimes it still feels raw. But not in the same way. We didn't know her (they lived in the North Island and we were in the South Island) except through pictures etc. And also what happened to her was a horrible accident. There's a whole separate layer of things to come to terms with in Jes's case.

Anyway, I don't want to bog myself down with all that again right now, so I am going to switch gears and do a bit of a fill-in.

In June, Michael started a new job doing IT for a shire council in Roma (which is 7 hours inland from Brisbane, and only has 7,000 people). The girls and I are still in Brissy, but will be moving up there at the end of next week. Michael loves it, but we really don't want to go. I like having all the access to services, shopping etc that the city holds. But, on the good news front, we should be able to get Permanent Residency through the governments rural jobs scheme, so that would make it worthwhile. The current plan is to move back to Brissy by the time Samara is school age so she can go to a special school. I'm not a big fan of mainstreaming (having worked in that situation during teacher training) and I don't know that homeschooling Samara when the others have grown up and moved on would be fair on such a social child. But that's a few years away yet, we'll wait and see.

At Samara's regular paed checkup in May Dr Slaughter (yes, that's his real name!) decided based on Samara's sleep study that she needed her adenoids out. She was also failing her hearing tests, and had glue ear, so they put in grommets as well. They were going to take out her tonsils, but when they got in there they decided it was too risky. Her airways were so narrow they couldn't even get a ventilation tube down without giving her steroids. This meant that to get at her tonsils, they would have to tip her neck back a long way, and with the neck instability thing our kids can have (and there's a higher chance with her, as all my family has Ehlers Danlos Syndrome - a joint instability problem) it just wasn't worth the risk. Anyway, the upshot of it all was that she almost never snores now!! Her hearing went from being moderate to severely affected to being moderately affected. Not as good as we hoped. So she is waiting for hearing aids now. She hates anyone touching her face or ears. She won't wear her earplugs when she has a bath (to keep water out of the grommets). So I know that getting her to wear hearing aids is going to be real fun. NOT!!

Speaking of Samara, we are going to be having an early 2nd birthday party for her on the 4th (the day before we leave) so that will hopefully be fun. We're going to go with a Wiggles theme (this will be the 3rd Wiggles party I have done over the years!)

Last month, Renata surprised us with a visit home for a bit over a week. Michael knew she was coming, and I had a vague suspicion but didn't really know. It was nice to see her again.

Samara's new tricks include learning a lot of songs. Her favourites include 'rock-a-bye your bear' (Wiggles), D_O_R_O_T_H_Y the Dinosaur (wiggles again!), Twinkle Twinkle Little Star, and the welcome song they do at school. She is good at picking up the actions, and attempts the words too. She isn't walking yet, but can stand herself up without using anything to climb against. In the morning she asks to 'det up', then yells at the girls to 'det up' too!

As for me, I have started a new hobby business making kids clothes. Here's a few samples....

Samara modelling a Tutu Dress which converts to a skirt to fit up to 6 years.

My lovely niece Jayde in the dress I sent back with Renata (despite it being a New Zealand winter, and the poor child freezing!!)

My other gorgeous niece (who I missed meeting when we were in NZ), Autumn who is wearing a smaller version.

Amy modelling the dress as a skirt, and her little sister Emma in the dress. (These two are my adorable neighbours who we will miss terribly)

I have also been refashioning clothing by taking good quality used clothes and making them into something worth having! This cute little dress used to be a hideous mens shirt! In fact, Bryanna suggested we call it the 'ewwww, ahhhh' dress. Because it used to be 'ewwww', and now it's 'ahhhh'.

Another refashion (a bit small on Samara, but she was the closest model I had!). This one is made from new stripey fabric and button, new singlet with the bottom removed and given a 'lettuce' edging, a preloved shirt (for the shoulder frills and the skirt frill), and a pair of pumpkin patch jeans.

This one is technically refashioned (I am keeping this one for Samara) but I will be making them from new materials for sale. It is a corset top and a 3 layer skirt. The picture was taken at night with flash, so it isn't the best, but just believe me when I say it is adorable!

If anyone wants to have a look, become my fan on Facebook. Just do a search for Just Juniors. I am actually running a competition til the end of August (not much time left), where you go in the draw to win a Tutu Dress. One entry for each friend you refer who becomes a fan. (just make sure they let me know who sent them)

Well, it's 2.20am, and we have therapy in the morning, followed by a visit to some ex-Kiwi's we used to vaguely know (but didn't know were here until Mahalia ran into them at a homeschool sports day last week!). So I'd better go get some sleep. Tomorrow I will try and get here a post about the Tutu Drive I am doing to get little skirts for young girls who are seriously ill. I will be asking for donations of any dressups (boy or girl - seems a bit mean to just do the tutus...) but they must be new. Keep watchin for further information.........