So how is it going? Slowly...
There seems to be a lot on in October, what with Statement Reviews, Transition Plans, DLA Interrogations, all to do with our younger son who has ASD turning 16. Apparently when you turn 16 you should be able to fill in your own DLA application renewal form....Um...what is it about Autism that you bureaucrats don't understand? Why is it that everyone makes things so difficult? Goodness, most adults struggle with filling in these forms let along teenagers, especially those with an ASD. Perhaps a few of you should try living with and helping a child with Autism? Whilst there is much joy, it is also very, very hard work, and something that we don't necessarily see an end in sight as much as we would like to think he will eventually be able to live independently, there is no way he is going to be able to cope without significant help. Of course by the sheer nature of his Autism and one of the ways in manifests itself, he doesn't see himself as 'disabled' and why should he to a certain extent, and yet there does come a point where some acknowledgement and awareness of the difficulties ahead has to become a reality. Can he travel independently in unfamiliar areas? NO. Could he cook 'properly prepared' meals? NO Does he needed to be reminded frequently of various needs that need to be met? Yes. Well the list could go on. So yet more pressure is being heaped upon our shoulders as we try and justify why we feel our son's Disability Living Allowance should continue, after all, just because he is turning 16, doesn't mean the Autism is magically going to disappear! I'm sure we would all wish that! Whilst he is going to have to try to come to terms with things we have written about his needs, which he is going to take offence to and disagree with as he doesn't see things from anyone else's point of view. Why is everything a battle to get his needs met?
So now I also have to get the place sorted, tided and spotless for this INTERROGATION by the beginning of the second week in October. Nothing like a bit of pressure eh?
So not only that but I also have my hospital visit to see the Neurologist to see if he can do further tests to see if the Chiari Malformation has progressed/changed in any way and also to see if he has any more suggestions of ways to get rid of the chronic pain.


































































