Left Brain Right Brain

Naomi (my better half who in an amusing but unrelated event took an online test to find out what sort of leader she was recently and came out as Hitler 😀 ) used to work at a Health Clinic as a receptionist. It was a bit ‘new agey’ this place and offered chiropracters, massage-therapists, hypno-therapists and homeopathists.

As is my wont I sneered at most of these treatments without actually trying them or even reading up about them. Yay me.

Anyway, when Megan was diagnosed with ASD, Naomi kept in touch with the homeopathist who she used to work with and this homeopathist, Karyl, began to treat Megan.

I was totally unprepared for how succesful it was. I mean I was really shocked at the difference. All I could see was Naomi giving Megan various combos of these little sugar pills but gradually, over time, Karyl got the balance right. It still needs tweaking as Megan grows but the Homeopathic regime Megan is on has cleared her body of a lot of the toxins introduced by the immunisations she had and-best of all- has helped her settle back down into a much more stable sleeping pattern. Megan has her Homeopathic stuff twice daily with Eye-Q and a multi-vitamin and the combination really has worked wonders on her patience, temper, perception, concentration, cognition and general happiness.

I’d strongly recommend Homeopathy as a treatment. If anyone wants to speak to our Homeopathist in particular, let me know by posting here and I’ll send her details to you- she really has changed our lives with Megan.

As well as the LEA meeting on Thursday, we also had Megs scheduled for a buggy test.

We need a buggy for two reasons. Firstly, she won’t walk anywhere and as neither of us drive yet that tends to limit us. Secondly, she’s wearing clothers for an 8 year old (she’s only 4) so as you can tell, she’s a big girl (very tall for her age) and so an ordinary buggy just doesn’t cut it.

So we go along to Cannock Hospital, have her ‘sized’ and hey presto, we now have a nice buggy on order- another positive tale this week 😀

And so on Thursday just gone it came to pass that I finally got to sit down in front of someone from the LEA and explain our position.

There was one main topic of conversation- the Statement Proposal that the LEA sent through. Basically, this proposal is a ‘draft’ of a childs statement of needs.

It was a very simple thing completley lacking in any sort of detail. In fact I made a post about it on AADFriendly which also contains our response. You might want to read the thread and the response to get a feel of where we’re coming from.

Anyway, so the meeting starts and it becomes clear nothing’s going to get sorted today- this meeting is more about staring your enemy in the whites of their eyes for both of us. Basically, our positions can be laid out thusly:

The Proposal: They feel they’ve performed adequately. I point out neither the law, nor Naomi and I feel they have. Things get a bit frosty. The LEA invite me to write what we feel is acceptable- I quickly agree.

The provision: They outline their position that they don’t think that one-to-one provision for ASD kids is a viable solution as they feel its detremental to a childs education as it shields them from too much (translation: its too expensive and they don’t want to cough up). I explain that whilst I have sympathy with that position, its not suitable for Megan. I explain our options:

1. Megan goes to a specialist ASD unit- except none exist in Staffordshire so there goes option one.
2. Megan goes to a ‘special school’- except the nearest one is the one she attended last year for half a day and wasn’t good enough for us. The other 2 in Staffordshire are over 20 miles away and neither of us drive. They (the LEA) also explained that they only funded transport to the nearest suitable school.
3. They pay for her to be privately educated. This will never happen but I’m cheeky and rude enough to have a go for it.
4. One to one provision at a mainstream school. This is what we’ll be concentrating on from this point on. Even if it takes courts and lawyers.

All in all, a good meeting as I knew exactly where they stood at the end but they had no idea where I was coming from yet. Element of surprise and all that.

So I’ll be writing a draft proposal myself and I’ll also be contacting the local Parent Partnership to get some feedback from them.

Onwards…

Life’s been a bit of a challenge of late- and in my last blog entry I noted how much I seemed to be moaning about stuff lately so its nice to write a really positive entry for a change-

My employers (feel free to comment on how excellent the website looks by the way 😉 ) called me in for a metting last week and said they were aware of how much Naomi and I were struggling with things like keeping appts, attending hospital visits etc so they wanted to offer me the opportunity to work from home 2 days a week.

This is excellent news and I was totally bowled over and couldn’t thank them enough. So, proof that the corporate sector do care about their staff sometimes!

I’ve just had a read through of this blog and decided I’m a right moaner.

There are good times- this week, Anthony (my son who lives with his Mum and I see at weekends) rang me to tell me he’d got a new bike and was offered a free one to go with it so he got a little one for Meggy.

I’m so so proud of him. He’s one of the most thoughtful people I know and this is so typical of him to think of his sister. I can’t let myself get stuck in a pit of cynical despondancy, both my kids are worth more than that. Its just very difficult sometimes to see an end in sight as it were- a time when we won’t be fighting tooth and nail for Megan and have to put health, career, sleep and family aside whilst we do. Poor Meggy, its not her fault, but neither is it Anthony’s or Naomi’s. I have to work harder to get us some ‘autism-free’ time. If anyone would like to donate me a couple of million pounds in order for me to do that, that’d be great 😀

Its bugging me that I havn’t got around to making this blog totally standards compliant just yet. 😦

Unfortunately, I’m a bit swamped with web projects at the moment so it’ll have to wait- the front page validates but the rest doesn’t so apologies to anyone who might have come across broken bits.

You may remember how the LEA denied Megan a place at Nursery. Well, a couple of days ago, I spoke to Megans case worker at he LEA. This contact was prompted by a visit from Megan’s Health Visitor. She was rifling through some papers from a totally unconnected point (nappies if I remember rightly) when Naomi noticed she’d had a letter from the LEA– Naomi asked what it was and Lucy- our excellent Health Visitor- says “Oh, its a copy of the Statementing letter from the LEA.”

Alarm bells ring- we’ve never recieved this letter dated from October 2003. Lucy lets us take a photocopy. It basically says that our opportunity to say anything about Megans Statementing will expire on 11th December 2003. Great. We’re dumbstruck- how could they not have sent us this letter? It closes by saying they will write to us by 18th March 2004 to let us know the outcome of the assessment. Its now way past the 18th March.

To say we’re angry would be something of an understatement. I phone the LEA then and there to see what the hell’s going on. Speaking to Megans caseworker, she says there’s no cause to panic as Social Services haven’t responded to the request for information which they’re legally obliged to provide. No surprise there- we still haven’t even met Megans Social Worker coming up for a year after she was diagnosed.

I explain how angry and let down we feel and demand a meeting with the head of the department. I also insist that I will attending the Statementing hearing- Megans case worker says that is not allowed. I insist. She refuses. I ask why. She says parents are never invited. I explain the meaning of the word ‘reason’ and why what she’d just said wasn’t one. She said it was because many cases were discussed at one hearing. I said I’d wait outside until Megans case was discussed. She went very quiet. I said I wasn’t going to let this go. She then said her superior was on holiday and would get back to me with an initial meeting. I said that was fine but the subject of me attending the Statementing hearing would be point one on the agenda.

I now have an appointment to se her superior on the 16th April where I intend to be as bolshy and high handed as they’ve been so far. I will get the best for Megan and they will supply it.

Life with ASD kids, whilst never the easiest of lifestyles is blghted mostly by that most evil of conditions: lack of sleep. When we got Megan diagnosed last year Naomi was exhausted as I was working which meant she had to look after Megan on her own all day and get up with her in the night as she (Megan) didn’t really sleep much at all for the first 3 years of her life.

Diagnosis brought the primary relief of being given Valleragn for Megan which we could give to her and which would help her sleep- she goes to bed about 8.30pm and gets up about 7am usually.

Naomi and I cherish the post-8.30pm time period as its the only time we can watch somethinbg adult on the TV, talk to each other without running around after Megan or just read a book with a glass of wine.

Unfortunately, over the last 4 days it seems Megan has adjusted to something (as she doesn’t talk its very hard to say what) and now screams whenever we try to take her to bed. Bedtime is getting slowly but inexorably pushed backwards. We’re now waiting for her to fall asleep then carry her up to bed- this usually happens by about 9.30-10.00pm by which time we’re both exhausted and don’t have the time or energy for each other. On two occassions (including last night) she’s also woken up early. 4.30am approximately. And, yet again unfortunately, she’s very attached to Naomi right now and screams if she’s not around.

I love my wife very much and am really worried about what this is doing to her. Apart from the sheer physical exhaustion of looking after Megan for approx 16 hours out of every 24, the mental strain is enormous- I’m constantly in awe of her ability to cope but I know it gets her down. I do what I can to alleviate the strain but as I’m at work, poor Naomi’s still right in the middle of it all day, every day.

We’re also finding it increasingly difficult to keep things together financially, last week for example, Naomi concussed herself and I had to take 4 days off unpaid to look after her and Megan- this creates a bad atmosphere at work and directly affects our finances. The end of this month is going to be difficult to say the least, we claim all the benefits we’re entitled to so can’t expect any more. Life’s a bit of a challenge at the moment.

In the last of this guilt-ridden mass update, I thought I’d let you know how Meg is herself.

Basically, she’s great. Her speech is gradually improving- she’s using words more and more often although we’re not convinced she see’s the need to talk much!

We’re trying to put together a plan for her to learn through play a la Son Rise and our Play Therapist. Could take years but it’ll be well worth it.

You may, or may not, have heard of Son Rise.

Its basically revolves around the concept of unconditional acceptance and bringing the child out of isolation. Looks quite interesting. Unfortunately its American and costs $lots$. They do run courses over here though and some people have had some joy getting their LEA to fund or part fund their course. Have a look on their UK forum for examples.

We’re going to have a go at getting some funding for it as we’re now seriously considering home educating Megan, at least part of the time. This is due to our bad experiences with the LEA mainly. We’re a bit concerned about the social aspect of it but at the end of the day we’ve got to do whats best for Megans education as it seems the LEA aren’t going to take responsibility.

Other options include leaving our LEA area and moving somewhere with a better attitude.