Welcome to The Ability Alliance, a platform dedicated to raising awareness of both visible and invisible disabilities. Our mission is to empower individuals by providing accurate information, valuable resources, and a supportive community.

A colourful digital illustration featuring diverse individuals with disabilities, including people using wheelchairs, prosthetic limbs, mobility aids, guide dogs, and other adaptive tools. The text "THE ABILITY ALLIANCE" is displayed across the centre in bold, pastel lettering on a pink banner. The background consists of alternating pastel blue and green panels, creating a vibrant and inclusive representation of disability empowerment

Introduction and Mission Statement

We believe that every person deserves to live a life without barriers, and we’re here to help make that a reality.

Why This is Important to Me

Living with Myalgic Encephalomyelitis (ME), Endometriosis, Steatohepatitis, and De Quervain’s Syndrome, I have faced countless challenges that many people don’t see. I know first-hand how isolating and difficult life can be with an invisible disability. This journey has been my biggest fight, but it’s also been my greatest teacher. It has taught me resilience, empathy, and the importance of community. The Ability Alliance was born from my desire to make a difference, to give others the support and information I wish I had when my life changed so drastically.

What We Aim to Do

The Ability Alliance is here to:

  • Raise awareness about visible and invisible disabilities.

  • Provide information about disability legislation and rights.

  • Offer guidance on financial benefits and eligibility.

  • Highlight schemes like the Access Card and Purpl, designed to improve accessibility.

  • Share resources about services that cater to disabled people, including companies that offer home visits for those who can’t get to stores.

  • Visit places and review their accessibility.

  • Test products designed to help people with disabilities and provide honest feedback.

Legislation and Financial Support

We aim to simplify complex legislation and provide clear information on the financial benefits available to disabled individuals. This includes eligibility criteria and how to apply for support.

Accessibility Reviews and Product Testing

We will visit places to give honest opinions as disabled users, highlighting accessibility features and areas for improvement. Additionally, we will try out products designed to help people with disabilities, ensuring they do what they promise and sharing unbiased reviews.

Community and Empowerment

The Ability Alliance is more than just a resource hub—it’s a community. We want to build a space where people feel supported, understood, and empowered. We encourage everyone to share their experiences and ideas, fostering a community that advocates for change and mutual support.

Join us on this journey to break down barriers and create a more inclusive world.

My Story is not unique

Life with Myalgic Encephalomyelitis is hard, before I was diagnosed with Myalgic Encephalomyelitis symptoms I worked full time as well as also being a Wife & Mother. 

My life is really tough but that is why I have to share my story with the world. Living every day with this debilitating illness makes me even more determined to raise awareness of how life-changing life with Myalgic Encephalomyelitis symptoms is. People and medical professionals need to see the real side of life with a chronic illness so that we can begin to change whatever prehistoric preconceived ideas that exist in today’s society.

A digital illustration titled 'Things That Help Me Feel Better on a Bad ME Day.' It features six comforting activities represented by cute illustrations: taking a bath (a woman in a tub), wearing clean pyjamas (a person in blue PJs), warming up with cozy socks, getting lots of rest (a comfy bed), getting comfortable (pillows), and cuddling a black Labrador (Alfie). The background has soft clouds, and the design has a warm and calming aesthetic

Recent Blog posts

The Rise of Robotic Wheelchairs: Revolutionizing Accessibility and Affordability

Robotic wheelchairs represent hope and possibility for those of us living with mobility challenges. But for these devices to truly revolutionize accessibility, we need to address the affordability gap.

The Mathew Street Festival

Liverpool, a city synonymous with music, culture, and history, is home to one of the most iconic events that celebrates its rich musical heritage – the Mathew Street Festival. This annual (fingers crossed )event, deeply rooted in the city’s identity, has grown over the years to become a symbol of Liverpool’s enduring love for music and its vibrant cultural scene.

Cable Management System

Don't let cable chaos take over your space! Discover the ultimate guide to cable management and transform your home or workplace into a clutter-free oasis. Learn how to organise, protect, and optimise your cables with a comprehensive cable management kit. From cable sleeves that provide protection and aesthetic appeal, to cable clips and holders that keep cables in place, and cable ties for easy adjustments, this guide covers it all. With cable raceways to hide and protect cables, and cable labels for easy identification, you'll have everything you need to create a safer, more organised, and visually appealing space.

I had to have my Engagement and Wedding rings cut off by the fire service

These aren’t just any rings—they hold so much sentimental value. My engagement ring for obvious reasons but my wedding ring was my Nan’s wedding ring, a cherished gift she gave us on the day we got engaged.  I had never took my rings off since the day of our wedding so having them cut off left me in tears 😭 

A Tragic Loss: The Urgent Need for Change in the Care of ME Patients

It is with a heavy heart that I write this blog post today, reflecting on the tragic and untimely death of Maeve Boothby-O’Neill, a young woman from the Myalgic Encephalomyelitis (ME) community. Maeve’s life was cut short at just 27 years old, not by the disease alone, but by the failings of a healthcare system that was ill-equipped to manage the complexities of her severe condition

Travelling Abroad with a Wheelchair: A Comprehensive Guide for Smooth and Safe Journeys

As a wheelchair user, I understand the anxiety that comes with entrusting your mobility device to an airline, knowing that if something goes wrong, your entire trip could be jeopardised.

ME Pyjama Party for Severe ME Awareness Day 8th August 2024

Join the ME Pyjama Party and Raise Awareness for Myalgic Encephalomyelitis! Each year for ME Awareness Week in May and for Severe ME Day in August we wear PJs with the aim to make a significant impact in the lives of those living with Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS)

Anfield from a Wheelchair: An Inclusive Experience

Anfield's Accessibility Features Anfield Stadium is designed with accessibility in mind, boasting over 200 wheelchair bays on match days. This ensures that disabled fans can enjoy the game with the best possible view and comfort. Additionally, the stadium provides various other accessibility features to accommodate different needs:

Amazon Prime Day

In our house, every day is like Amazon Prime Day. This year I wanted to share some of my favourite items so you don't spend money on something that isn't worth it. So here are some of my favourite Amazon products -

making a difference

An illustrated poster promoting the ME Pyjama Party, featuring diverse characters in fun animal onesies and pyjamas. The text encourages people to wear PJs for ME Awareness Week and Severe ME Day, sharing photos on social media using #MEPJPARTY

The ME Pyjama Party

Get comfy for a cause! The ME Pyjama Party is a powerful yet simple way to raise awareness for Myalgic Encephalomyelitis (ME). During ME Awareness Week and Severe ME Day, we’re inviting you to wear your pyjamas in solidarity with those who are bed-bound due to this debilitating illness. How to Join: ✔ Take a picture in your PJs ✔ Post it on social media using #MEPJPARTY ✔ Tag friends & spread the message!

An illustrated image of a diverse group of family members and caregivers sitting together, representing the Myalgic Encephalomyelitis Carer Community. The text above them highlights the supportive network for those caring for ME sufferers.

Myalgic Encephalomyelitis Carer Community

Caring for someone with Myalgic Encephalomyelitis (ME) can be challenging, but you are not alone. 💙 Join the ME Carer Community—a safe space for support, advice, and connection. Let's uplift one another. 🤝 #MECarers #ChronicIllnessSupport #YouAreNotAlone

A digital illustration of Alisha Whittam lying on a bed, smiling alongside her two black Labradors, Alfie and Archie. One dog is sitting happily while the other is sleeping. The image features the Alisha Whittam YouTube branding in the corner

My Youtube Channel

Welcome to my world! 💙 Join me, Alfie & Archie, as we navigate life with Myalgic Encephalomyelitis, share our favourite moments, and spread positivity. Subscribe for real-life stories, disability awareness, and lots of dog love! 🐶✨ #AlishaWhittam #LifeWithME #BlackLabs

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