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Alisha
Proud Wife, Mother and Nanna . We married 19 years ago in Rome, Italy surrounded by our friends and family. We have the most beautiful, caring, considerate daughter, she makes us proud every single day.
I am nan to Alfie, our Black Labrador and he is my best friend in all the world, I love how he understands that just laying next to me is all I need on a bad day and on a good day well it is cuddles and kisses galore.
Liverpool born & bred, I never had enough guts to ever move away. Maybe it’s on my cards in the future.
I have an illness that has destroyed my life, that illness has led me to blog my life with no filter. I put everything into raising awareness of Myalgic Encephalomyelitis and I would do anything to make sure no one else has to feel the way that I do.
We have fun in our little home and I do anything to make my family happy.
Love meeting new people over the web and hearing their stories.
I Love making new friends and just trying to make a difference in this world.
More Blog Posts
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.