Showing posts with label Courage. Show all posts
Showing posts with label Courage. Show all posts

Friday, 19 October 2012

Update on goings on

I feel  like I haven't written in a while even though  things have been happening. 

First off let me start by saying the lice went and much easier than I thought Peanut looks amazing with short hair. 

 We have been on school holidays and having catch ups with friends and just relaxing. 

This wednesday backpacker stayed with the kids all day while I did day 1 of a 2 day positive partnerships workshop. 

This is a free program about how to better communicate with schools  how to tackle those tricky teachers and IEP's and how to know your rights and stand up for yourself with out getting emotional. For me its been so valuable Im a pretty proactive mum but sometimes you just get stuck or confused by the system and with Peanut next year attending two schools, Mainstream 3 days with an Aid some of the time and Early intervention the other two days this is going to come in handy. 

Im not super pleased with the mainstreams schools responses so far they have been a bit hit and miss my initial reaction to the school was good ( its big but pretty and well established nice trees and the kids seems okay) but then I found some flaws and I had people chirping in my ear " oh they are not a good school the students are messed up  blah blah the teachers can't control them"  and various other bits of wisdom (I didn't ask for) we live in a low socioeconomic area and there are children with all sorts of needs behavioral and emotional which is why I was actually told in the first place they perhaps would be better able to deal with a child with autism compared to the higher end schools with middle class students ( mainly people from working class pasts immigrating and pretending to be above their stations).  
Surely that makes sense that the funding allocation and understanding of special needs would be better at a school thats seen all sorts of children from all walks of life. yes / no?  
Meh who knows (not me).  Private is too expensive for us I don't want to send my son to catholic school due to the fact I might burn alive when I walk in. Id like to walk him to school and I've not heard great things about the other school in walking distance and its on a main road. There are a few others public schools  not to far away 5 - 10 minutes drive that have good reputations with special needs but I want to give his local school a chance. 

Any way I have started rambling back to the facts  

I now feel empowered and like I have the right tools to approach the schools and ask for an IEP or CAP meeting before next year and I will be ringing about it next week I want to know how much aide time and If we can meet the aide and teacher for next year and see the class room, I can bring my LAC along and therapy focus if I feel I need it. 

The  program also made me sad that so many parents and carers felt alone.  I have Skips and they have been a wealth of knowledge, support and understanding and because of this I feel positive and prepared. Some of these mothers and fathers were lost, never pushing for things they are able to receive no knowledge about programs and funding options they are entitled to. 

Part of me got angry at them. "where have  you been  why have you just been sitting back excepting this you have no right to complain if you never went out and scratched the surface and pushed for more information" some people had excuse after excuse and were so negative but then I was angry that the information can be so hard to find. By the end of the second day most people had made friends and started to become more positive and were ready to take the next steps but there were still a few that still had not grown like they were upset they didn't get that special and all mighty magic pill that was going to "fix their child"  any suggestion  people come up with was knocked down even though they had not tried it and that made me mad!  

I think its the lack of knowledge people have about what they can and cant apply for and the fact people aren't working together for each child individually because they don't know where to start. We are only at the beginning of my journey and Im ready  to roll Im nervous and excited and Im sure we will have good years and bad years but I feel better prepared. I also feel like Id love to be a part of the disability sector helping those familys and children get what they rightly deserve. 

In Other news Peanut started Early intervention ESC Thursday and did well the teacher mentioned "he has a few scuffles over compliance but things he will get there soon". 
He has a little boy in his class whom is the same age and will be attending with Peanut until the end of 2013 his mother seemed lovely. The others kids will be heading off to mainstream or esc year 1 at the end of this year as they had been there nearly two years and were close to or already 6.

On Thursday after school Peanut started speech therapy with his federal funded service provider. Peanut did really well considering he was tired. His therapist (now named Irish) used the words visual genius she said he has very good with nonverbal language (eyes gaze pointing etc - that surprised us) and also his vocab and pronunciation was good (this we already knew). 
There was one bit that nearly brought me to tears. The speechy started to play simon says and Peanut was doing really well then she wanted to stop and get him to go get something but Peanut wanted to continue and he said Simon says close your eyes, so she copied and then he said close mouth and close chin (lol) and finally close ears she helped him along with the simon says bit but I was so proud of him Ive never seen that side of him before he wanted to take control in the correct way and that to me was the first spark of proper joint play with anyone else outside the family and certainly the only joint play Ive seen that require verbal skills ... so cheers to that!







Friday, 27 July 2012

Flash, Raven, Boop and Bee xxxx


We recently had to say goodbye to Peanut and Shrimples cousins and Aunt and Uncle (my brother).

They are moving to the other side of Australia and I wish them the best we don’t get to see them much any way being a 5 hour drive from each other but when the cuz’z get together it’s a blast. My brother Flash, is a hands on dad with his girls Boop (5) and Bee ( 3).  He runs after the kids lets them climb all over him and is genuinely hilarious to all children they love him always have. He is the dad at the park making all the kids laugh by playing the fool. Peanut usually takes a while to warm to people but Flash and Raven( my sister in law) have a way of cracking through Peanuts shell pretty darn fast.

So all the kids run around having a ball being eaten by monsters and dinosaurs and using up all their energy and imagination, we all get involved. We had a really great day but it was an emotional good bye (we are the sort of family they don’t need to live anywhere near each other to still be close) recently Flash and Raven have been having a not so great time. Flash damaged his ankle on the job over 4 years ago and its been pretty stressful on them all he has been the stay at home dad with the girls and doing some odd jobs here and there and Raven has been the main earner. Raven was offered a job over in Canberra and it was too good to miss out on. 

On friday the 13th (yep I know bad luck and all) two weeks before moving they found out Raven had Cancer yep the dreaded C word, Crappy crappy crapy ole Cancer. Raven had surgery on friday (for the second time in a few weeks) and will start on radiation therapy once they move to Canberra.

 It all looks like its going to turn out okay but its been a rough ride for them.

I guess this post of my way of acknowledging them and letting them know how proud of them I am. They just keep fighting and striving for the future with their amazing girls. 

Both Boop and Bee have hearts of gold, are really smart and incredibly beautiful and I know they will grown into amazing strong women. Xxxx