And I feel that it is no coincidence that my seizures have got worse and worse over the two years since I have lost my disability benefits, because my disability is a Neurological condition made worse by stress.
What could be more stressful than losing your opportunity to be able to have a shower because your DLA was taken away, or having to eat less meals each day because you still HAVE to find the £230 you need to pay for transport costs each month out of nowhere, because you lost your free bus pass because, oh yes, you lost your DLA.
What could be more stressful than having to try to cook a meal for your children (two if whom also have disabilities btw, though different to mine, and have also not yet got DLA, though the charity is also going to work on that one) when you are falling asleep and burning your arm or face on the job because you have just had a seizure and are post-ictal, yet can't afford to phone the Care Agency to send someone out, because you can't pay them as you no longer get Direct Payments because, oh yes, your DLA has been stopped.
I am on double the amount of anti-seizure meds that I was on two years ago, I am frightened to go to sleep in case I have a nocturnal seizure because I can't afford to replace my anti-suffocation pillows, and they are unlikely to be effective after two years of continuous use. And that's not stressful? And that stress has been DIRECTLY caused by losing my disability benefits. ALL of it.
The stress of losing my DLA, ESA and Direct Payments HAS had a negative effect on my health, that is even noted in my medical file by my Neurologist.
So I am sorry to disagree with you Novack, but in respect of my case at least, you're talking bollocks.