I am dealing with a really frustrating scenario. My teenage son (16) has dyspraxia so the fine motor skills, memory and timekeeping are affected. He is still in school full time. He knows of many other peers (similar to him) who are receiving Adult Disability Payment. I’ve explained to him that while he has the condition he lives at home with us, has everything he needs and doesn’t have ‘extra costs’ associated with his condition. He thinks we are being blockers. He went ahead and made an application behind our backs. We received three follow up letters requesting further evidence and I put them all in the bin as I morally disagree (of which he is aware). I grew up with a severely disabled single parent who could not work and had two children so I have a very clear view of what I think the purposes of these payments are. My son, I think, sees this as pocket money. I asked him to name one extra cost he incurs because of his dyspraxia and he can’t. He simply thinks he’s entitled to it and no explaining is helping. So frustrated. I don’t think I am being harsh but surely he can’t just claim money because he has a life long disability?!