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ADVICE RATING
 (Worth a try) (Worth a try) (Worth a try) (Worth a try) (Worth a try) 4.43 (Worth a try) from 12 votes (728 Visits)

children and families living with autism its not your fault

silly-mummy by silly-mummy Walking(August 2006) (rank 500+)

hello, i have a 5 year old son who is in the final stages of his assesment for the autism spectrum disorder and its been a long hard road to go down.

i first noticed my son lived in his own world when he was about 12 months old,

he woulnt look me in the face he seemed to look through me, he hated loud noises and would often scream at the washing machine, hoover, tv etc.. by the time he was 18 months old his behaviour was very difficult he couldnt seem to communicate with me at all the only thing he could do was get really upset scream and bang his face on the floor or walls when he wanted something, i faced alot of very opinionated people who would often say he was just naughty and i needed to be strict with him, the looks and comments i got when i was in town with him could be unbearable to the point where i often thought it was my fault and i was failing him.

it slowly got worse by the time he was 2 1/2 he was very violent towards me as he still couldnt talk his only way of telling me how he felt was either to be very loving or the total opposite and be violent.

it took him to start nursery for anyone to pick up on there being a problem even though i had been asking for help for a long time, at first i got the questions of how did i treat him as a baby, what did i feed him, did i do this or that and again i felt it was my fault, but then my son was refered to speach and language therapy which was fantastic for the first time he could tell me what he wanted, he still found emotions hard to deal with but at least he could ask me for a drink of milk or tell me if he wanted something to eat, the feeling of communication between us felt amazing, after then he was refered to a pediatrition who is fantastic, he has done all of the assesments with my son and built up a good relationship with him, he was the first person in 5 years to say  "it isn't your fault"  i could have cried with relief, my son now has help at school which has made a big improvement to his self esteem and also gets some home help.

he is nearly 6 now and has changed so much in the last year with all the assesments and there are lots of them and a change of school i thought it might make him worse but he has took it in his stride with the right help and support you can have a fantastic life with an autistic child, one thing nobody told me about untill recently was the picture exchange communication system ( pecs ) where you use pictures to help your child to understand better, it was my sons school carer that told me and iv made some up and he is amazing with them, iv got a 2 year old daughter who thankfully is very understanding to my son and is developing normally but my son can now play with her and talk to her, its great having as near to a normal family life as this but my point to all this is your not alone and its not your fault, but please keep pushing for the help you are intitled to.

i hope this helps someone in the same situation as i was in, i felt very low alot of the time but now life with my children is great. thank you.

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eilishsmummy
5.00 (Excellent) | December 2006 | eilishsmummy
grrrrr

i understand where your coming from. we are still in the process of the diagnosis at the moment feb 6th 2007 is the next specialist appointment. we get comments from the family and just random ppl. ppl really can be hurtful it really p****s me off to no extent. i dont feel i should need to explain why my child does not listen, or is difficult.. what business is it of everyone elses. i am just sick of all the stares and the whispers.. yes i hear them. i am looking at getting my child some tshirts.. just to help them see what the issue is and get over it and move on instead of stare and make judgements. i am so sick of this. does anyone else get made to feel so small. i love my child. i am here to try to protect her and sometimes its hard for me to deal with that i cant always protect her i am just happy she doesnt care or really understand. we love her and thats all that matters.

we have had a nasty dr appointment where a paediatrician told us that our daughter was stupid and an oddball.. so we are getting used to bastards being assholes. some ppl just cant understand my hostility when they begin to lecture me or whatever.

i am getting angry while i write this. she is not naughty. she is autistic. its time for ppl to be able to see a difference. YES she makes noises... deal with it ppl.. what is classed as normal anyways!!

my 2c worth.



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exquisite-flower
5.00 (Excellent) | November 2006 | exquisite-flower
Glad that things
... are on the way to being sorted.  It is good to have a diagnosis, because even though it does not take away the hardship it does explain and proide a support network.  I wish you every success inthe future and i am glad that it has strengthened your bond. 
Peace
EF.x 


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MumKim
5.00 (Excellent) | October 2006 | MumKim
It is not your fault, but what you do makes a big difference.
As a Speech Pathologist I can only marvel at the way some parents handle the situation. While it is certainly  not the parents fault that a child has autism, how the parents parent a child with autism or other spectrum disorders has a big impact on the childs development. I take my hat off to these parents, they are true heros.


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momoftwo
4.46 (Good) | October 2006 | momoftwo
Keep up the good work

I know exactly what you are going through your children and my children are the same age.  I have a 5 1/2 boy and a 2 1/2 boy.  My oldest son is PDD (Pervasive Delayed Disorder) he was diagnosed with this lable of Autism when he was 2 1/2.  He has since then been in all the right therapies with all the right people.  He communicates on the level of a 3 year old. Also functions on this level as well.  Not long after his 5th birthday he has received another diagosis, This one called him Mild Developmental Disablity just another way to tell me that he is not at the level he is suppose to be at.  After all the doctors and therapist I have come to realized their help is needed to aid me with the proper care that must be given to him.  I am the one who knows my son best.  My advise to you would be do what you feel is best for your son and family but also what is best for you.  You need to keep yourself together and don't listent to the people that make comments in public and stare because if they had to walk a mile in our shoes they would be reacting totally different.  I say this to you because I am now waiting on the assements to start with my 2 1/2 year old son who is showing most of the signs.

Give yourself a pat on the back you can only do what is humanly possible even though as moms we think we should be able to do everything for them in reality we just can't.  We can only do our best.



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silly-mummy
5.00 (Excellent) | August 2006 | silly-mummy
i now have the assesment results
if you have read my advice above and are going through the same situation you will know how hard it is waiting for the final results, iv had my son's results today and got a complete shock to the system, i understood he was autistic but didnt know to what degree iv been told he is boarderline aspergers, he has conduct disorder, adhd and forgive me for forgetting the tecnical name for it but a disorder that gives him the inability to feel safe and secure, so all in all there is still a long way to go but one thing is for sure it will never change how much i love my son in fact its given me a much stronger bond with him.


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      JadieLady
5.00 (Excellent) | August 2006 | JadieLady
i now have the assesment results

HI, I really admire you courage! this information isnt easy to recive, but i beleive you are doing the best thing you can- love your son :)

THere is help out there!!! And you are never alone with these things!

Medication can go a long way in helping children with aspergers lead a normal childhood with noone knowing the difference :)

Hang in there!



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JadieLady
5.00 (Excellent) | August 2006 | JadieLady
good!
autism is not uncommon in my family, and i really feel for you! and it is NOT your fault! :)


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Susan
5.00 (Excellent) | August 2006 | Susan
good first steps

I also have a six year old son who has been diagnosed with an ASD, and my heart goes out to you. It's so hard to shake that feeling that if ONLY I had done something different, this wouldn't be happening; it's also difficult to explain to people who don't have an autistic child what life in your house--or mine--is like. I'm so glad you're here, at Minti, and I hope you will join the Autism group.



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lindterbean
5.00 (Excellent) | August 2006 | lindterbean
when things happen
I think it is only natural to ask why when we are faced with something like this, and I'm so glad you pointed out that sometimes we do just need to hear someone else tell us it isn't our fault, because as mothers we are always trying to shoulder the blame, even if it is only inside.

I'm glad things are looking up for you, you've been though quite a lot. It sounds like you also have a lot to share with others in a similar situation.
Have you had a chance to visit the Minti autism group?


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      silly-mummy
5.00 (Excellent) | August 2006 | silly-mummy
when things happen
hi i havent visited the autism group yet i definatly will though it is a long hard road with an autistic child but things do get so much better, thank you for your comment, keep in touch.


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