I bought a new phone some months ago. I have never taken the plastic off the screen because it needed a case. I have been known to drop my phone! But everytime I looked at it, the little piece of plastic mocked me.
No more will it taunt me! I got my finger out, and here is the fruit of my labour.

Acrylic felt, embellished with roving, lace, net, angelina and yarn (cos it's not wool!). We're just waiting for the big girls to get home so they can tell me where they tidied the heat gun to, and then I can finish off those ends.
The back

A detail shot

And another!

I like this as much as I've liked anything for ages, which I guess is a good sign.
Some people hit the ground running after the Christmas holidays, but I just hit the ground this time. I think my low point came at Sixth Form Open Evening on Tuesday, but, to be fair, Phil went for a job interview at 2pm and I hadn't heard from him by gone 6. (He left at 1, the interview started at 2.) Who interviews at 6pm? I figured he'd either had an accident or left me (frame of mind might need a bit of a boost!), like you do. I dragged everyone back to school for the fun, and he called just as we got there at 6.30. After upsetting one of Penny's friend's mothers, inadvertantly (she caught me on the hop, phone in hand, confusion in brain, stress levels through the roof) because she's American and it was Tuesday and I wasn't bothered (face? look? you know the drill), we had a speech ordeal, which Penny wasn't allowed in the hall to hear. What was the point of that, I wonder. I'm not going into Sixth Form! V boring man, forgotten most of it. On the way out I was cornered by another of Penny's friend's mothers, whom I know because she has a lovely son with Down's. He's a cracker. She wanted to tell me all about this meeting she'd had about Speech and Language Therapy (SaLT), but she made the mistake of assuming I knew all about it, which I didn't. So I said I was sorry, but I didn't understand. 'Why not?' she raged. 'We need more SaLT!!' 'Do we?' I blundered, 'We have all that we need'. 'Well good for you!' she yelled as she started to storm off. Anyway, I calmed her down a bit and tried to get her to explain and it turns out she'd had a meeting with the education department (I guess) and someone had agreed to more SaLT because, as she said '
some of us parents don't want to have to put our children in special school in order to get it!'
Well, I have smarted about this ever since. Mostly because I don't think I deserved it. But I have realised a few things. Firstly, she was incredibly angry with me because I chose special school for my child, and for some reason that seems to spin her out, like we have been disloyal or something. We agonised for
years about where to send Lexie, and I do mean agonised. And in a way, we still do. Did we do the right thing? I wonder on a regular basis. Particularly after my MiL was going on about how she is 'too clever' for special school on Saturday. So far, I have only met children I don't know who go to mainstream school, and they have consistently been shy and withdrawn (which isn't a given for Down's, Lexie certainly isn't backwards in coming forwards). I would be so interested to come across the ones I used to know who moved from special to mainstream school, just to see if they've changed at all. I think that would help me a lot (not that I have any intention of moving her, regardless of the outcome).
Then I thought about all the things that made us choose special school in the first place. Battledown, where she went for 3 years, was started as a specialist centre for...wait for it......SaLT! One of my last duties as a governor was to agree funding for a third therapist. This woman's child is 2, just the right age for there, but she would rather send him to a nursery attached to a mainstream primary school and then bitch about there not being a SaL therapist! At Bettridge they have a SaL therapist, and, as they do in Battledown, they
communicate with the classrooms so each day is filled with SaLT without the children even noticing. At Bettridge, we can see our community consultant so we don't have to take our child out of school for most of the day. Hearing and vision people come into the school. There are at least 2 physiotherapists who come in every week, and if I had any doubts about what they do they were dispelled when Lexie's phoned me up to tell me that her new boots meant her orthotic inserts were wrong and needed replacing, she got me an appointment, and was even there when we turned up to explain to the orthotist. There are also 2 dedicated music therapists. None of this would happen in mainstream school.
I have given this subject a lot of thought and at the end I decided that Lexie has Down syndrome. It isn't going to go away, or get better. Yes, she is coming on and really is quite clever, but, and it's a massive but, she's clever
for her. We can see how far she's come. Drop her in a top infants class and she would drown. Put her in Reception, and she'd drown. Very quickly. We chose special school for her because it's where she needs to be. Her friends have SEN too. Her friends will always have SEN. However lovely and charming she is, no 'normal' teenager will want to be best mates. So it's better to face that now and give her what she needs not what will make me feel better about myself. Yes, she will have to live in the 'real world' when she leaves school, but that won't be the same 'real world' that 'normal' school-leavers live in, no matter how much we love her. Her friends will always have learning disabilities.
And it's the same for this woman's little boy. He's a lovely lad, but he isn't going to be Professor of Difficult Sums at Sheffield University. He might be a trolley boy at Tescos. I don't mean to be nasty, it's realistic. Lexie'll probably be inside stacking the fruit.
In a way, she's helped me realise that we have chosen the right place for Lexie and I shouldn't worry about it anymore. I'm still annoyed with her for her attitude - that in some way Phil and I have let the side down by not making all our lives almost intolerably difficult (most of all Lexie's!). We fought for Battledown to stay open so that children like her's could have SaLT - as much of it as they need. It's a bit like having a lovely cake shop in town. It's been there for 20 years and makes the most delicious cakes. This woman wants a cake, but she wants to buy it from the greengrocer, and he doesn't sell cakes. So, instead of going to the cake shop, she decides to get angry and shout until someone gets her a cake. I'd prefer to go to the cake shop myself.