The hottest day of the year so far was a fitting backdrop to a debate that had the potential to be one of the most heated of the election campaign...
The best time to read is late at night when you ought to be going to sleep. Don't let that stop you though, illicit reading when your parents have told you to turn your light out is the best kind of reading.
Like many disabled people, I just want access to the same places and products as everyone else, and I hope disabled people feel as encouraged as I do that this report may be the best way in which we can start to access them. So if you are reading this as a disabled person, the next time you feel discriminated against, my advice is to do a Julia Roberts...
What does sadden me is how many young disabled people still feel that a happy love life is out of reach. I started using my wheelchair at the age of fifteen and at the time I was sure I would never find love.
Politicians who want to protect and support that which is best about our country need to help people reconnect with our sense of fairness and our desire to live in a decent community that welcomes all human beings, in all their diversity.
Hear my voice is about making sure people with a learning disability's voices are being heard by politicians in the run up to the General Election on 7 May this year. We want to make sure people are not excluded and have the opportunity to have their say about the issues that impact them.
Often I hear "They're just words!" "I didn't mean anything by them!" "I wasn't talking about an actual person!", I understand that. The word has been absorbed into popular culture, but that doesn't make it acceptable.
It is a daily experience that anyone who is disabled will know all too well. I have been a wheelchair user for 35 years, and while there is now a law stating that businesses should make every "reasonable adjustment" to ensure that they are accessible the real experience is that many places are still closed to disabled people.
I don't want a fancy life, just enough of one so I do not go stark raving mad with boredom and loneliness... If more of the public were aware of what being on Job Seeker's is like long-term, they might be less negative towards us.
Not satisfied with canning the lowest rate of Disability Living Allowance (DLA) care, or reducing the distance one can walk from 50m to 20m in order to be able to qualify for its successor benefit Personal Independence Payment (PIP)...
So, while the UK was talking about Scotland, someone has died: David Clapson's awful death was the result of grotesque government policies (9 Septemb...
I don't want any child with a learning disability to go through what I went through - to be told you're worthless, no good, stupid. Around 200 children are born every single week who will have a learning disability. This is our chance to make a difference to their futures. The public is demanding the next government to make this change happen - candidates must listen.
As a charity representing thousands of people with multiple sclerosis (MS) it's concerning when we see sensationalised stories in the media about 'benefit cheats' and 'disability scroungers'. These unappealing headlines, along with the much publicised Government benefit crackdown, do little to help members of the public understand what it's really like to live with a disability.
Whoever forms the next Government must acknowledge and tackle the many barriers people with mental health problems face in finding and retaining a job. The benefits system is very complex and we often hear how people struggle to navigate it, so we also need to ensure such individuals can access advice and support to help them.
I think able bodied people are in denial about their thoughts and feelings towards us - they don't want to deal with the thought process, so they shut it out. Well, we are here! And with medical advances and people living longer, there are only going to be more of us! So maybe it's time for people to start coming to terms with their feelings about disability.
Vilification of benefit claimants and disabled people is endemic, perhaps the government should just stitch on the black triangles and be done with it or bring in the Welfare Games to keep us at a more manageable number and remind us how grateful we are for all the 'pitty money' (in Simon Stevens words) that we get.