DISABLED ENTREPRENEUR – DISABILITY UK
Disability UK Online Health Journal – All In One Business In A Box – Forum – Business Directory – Useful Resources – Health – Human Rights – Politics
DISABLED ENTREPRENEUR – DISABILITY UK
Disability UK Online Health Journal – All In One Business In A Box – Forum – Business Directory – Useful Resources – Health – Human Rights – Politics
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How one woman’s journey through grief and hardship led to the creation of two powerful charities – and why her story continues to inspire global change. When we think of JK Rowling, most picture the global Harry Potter phenomenon. But behind the fame is a woman who once lived on state benefits, writing in cafes while caring for a young child as a single mother battling grief after losing her mother to Multiple Sclerosis.
Claimants are not inferior. They are individuals navigating hardship through no fault of their own. The people who work within the DWP and Universal Credit should be trained and reminded that respect is non-negotiable. Every human being deserves to be treated with dignity, especially when they’re asking for help, not handouts.
For millions of people in the UK living with chronic pain, applying for Personal Independence Payment (PIP) can feel like a battle against an invisible enemy. Pain, especially when it’s invisible or fluctuating, is difficult to measure, explain, and prove. The PIP assessment system, designed to support people with additional care or mobility needs, often falls short in recognising the daily impact of pain, leaving many to feel dismissed, doubted, or denied.
Living with an invisible disability is a silent struggle, one that is often met with doubt, judgment, and unsolicited advice. The absence of visible symptoms often leads others, sometimes even friends or family, to minimise or dismiss the very real impact such conditions have on daily life. This ableist mindset can be harmful, especially when it’s cloaked in “concern” or feigned expertise.
Raynaud’s disease (also known as Raynaud’s phenomenon or syndrome) is a circulatory condition that affects blood flow to certain parts of the body, usually the fingers and toes. When exposed to cold temperatures or stress, the small blood vessels in the extremities constrict excessively, leading to pain, numbness, tingling, colour changes, and functional limitations.
An urgent letter from the United Nations Committee on the Rights of Persons with Disabilities (UNCRPD) to the UK government has sparked outrage and concern within the disability community. The correspondence, sent Monday evening (07/07/25), follows a coordinated campaign by disabled people’s organisations (DPOs) who presented damning evidence of how the proposed cuts to out-of-work disability benefits could worsen the lives of thousands of disabled people.
“Vouchers Are Not A Lifeline, They Are A Limitation. This move is discriminatory, removes choice, and reinforces stigma”.
Furthermore, vouchers could severely isolate individuals with non-visible or fluctuating disabilities who may already struggle to go outside, use public transport, or interact with others due to pain, fatigue, or anxiety. For example, someone with severe OCD, PTSD, or Crohn’s disease may rely on online retailers or niche services for survival, many of which may not accept government-issued vouchers.
The Independent Parliamentary Standards Authority (Ipsa) has announced plans to invite members of the public to deliberate on the salaries of Members of Parliament. In an attempt to increase transparency and trust following the 2010 expenses scandal, IPSA will be sending out 10,000 letters through a lottery system in the coming weeks.
In a significant pivot, the UK government has introduced major concessions to its welfare reform bill, aiming to balance fiscal caution with social justice. The move follows mounting pressure from disability rights advocates, backbench MPs, and public concern about the sweeping changes initially proposed.
When a simple request for care turns into a battle against bureaucracy, poor communication, and ableism. Accessing GP care should be straightforward, especially for disabled individuals who already navigate life with added barriers.