Blog
Hi, I’m Alisha Whittam, and I live with Myalgic Encephalomyelitis, a chronic illness that has profoundly shaped my journey. Here, I want to share a little more about who I am beyond the challenges I face every day.
💔 Maeve Boothby-O’Neill’s tragic passing at just 27 highlights the urgent need for change in the care of ME patients. Despite multiple hospital admissions, Maeve was failed by a system that lacked the specialised care she desperately needed. Her story is not an isolated incident—it’s a wake-up call. This post explores the failures of our healthcare system, the stigma surrounding ME, and the urgent reforms needed to prevent more lives from being lost. Maeve’s death must not be in vain.
Struggling with messy cables? Learn how to organise your wires and prevent pets from chewing them with these simple and effective cable management solutions!
Robotic wheelchairs are transforming mobility for people with disabilities, offering smart technology, AI navigation, and new levels of independence. But the high cost keeps many from accessing these life-changing devices. This post explores both the promise and the barriers — and why we need to make this tech more accessible.
Could ketamine therapy offer new hope for people living with Myalgic Encephalomyelitis and other chronic illnesses? We explore Dr Bryan Henry’s powerful personal story, the latest clinical research, and whether treatments like ketamine, stem cell therapy, and microdosing could shape the future of chronic illness care.
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.
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 😭
Join the ME Pyjama Party! 💙 Each year, during ME Awareness Week (May) and Severe ME Day (August), we wear pyjamas to raise awareness for Myalgic Encephalomyelitis (ME/CFS). How to join: 🛏️ Wear your PJs 📸 Take a picture 📲 Post on social media with #MEPJParty Help shine a light on this often misunderstood illness. Every post makes a difference! #SevereMEDay #MECFS #InvisibleIllness #ChronicIllnessAwareness
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 -
As Liverpool gears up for another joyful Pride celebration, it’s time to ask—who’s really included? For many disabled people, Pride remains physically and emotionally inaccessible, despite its message of love and acceptance. From parade routes with no wheelchair access to ableist attitudes at afterparties, this article explores the barriers disabled LGBTQ+ individuals face—and how we can do better. If Pride is for everyone, then it’s time to prove it.
Facebook
X
LinkedIn
Reddit
WhatsApp
Pinterest
Threads
Follow me on Instagram
