“What It Takes To Be Me!”: A Journey Of Independence And Resilience With Spina Bifida

Disability blogger and advocate Daniella Jade Lowe, who lives with spina bifida and hydrocephalus, shares her determination and resilience to be independent.

How Aphasia Affects Speech And Communication

Wolfgang Wolf, a disabled blogger and counsellor living in New Zealand, shares his experience of living with the neurological conditions aphasia and apraxia that affect speech and communication.

Time To Talk Day: The Challenges And Benefits Of Having Care Support From Parents As A Disabled Adult | Guest Post On Spokz People

With today being Time to Talk Day, Emma – who is a loyal member of the Spokz People community – shares her personal experience of continuing to rely on her parent’s support and how it impacts her both positively and negatively.

Disabled People Also Need To Talk About Mental Health

Today on Time to Talk Day, Spokz People – an organisation that provides online mental health support for disabled people and their families – wants to encourage the disabled community to talk more about mental health and wellbeing. 

GP Appointment Crisis: A Chronically Ill Person’s Perspective

Trying to get a GP appointment can be very difficult, and, in many cases, impossible. Zec Richardson, who lives with ME, shares his personal experience of trying to get to see a doctor and how it affects his health and wellbeing.

How Will AI Help Disabled People? | Guest Post On Disability Horizons Shop

In this guest post on Disability Horizons Shop, Emma Purcell gives an AI overview, discusses some of the concerns people have about AI and looks at the many ways artificial intelligence can benefit disabled people.

A Coalition Group Has Initiated The First-Ever European Myasthenia Gravis Day

Today marks the first-ever European Myasthenia Gravis Day, a symbolic date that will shine the light on this neuromuscular autoimmune disease that affects between 56,000 to almost 100.000 people in Europe.

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