Say hello to Alfie, a beautiful Black Labrador from Liverpool who’s not just a pet—he’s family, a best friend, and a true companion in every sense of the word.

At 8 years old (turning 9 in 2025), Alfie has become a lifeline for his Nanna, Alisha, who lives with Myalgic Encephalomyelitis (M.E.), a complex chronic illness that has left her completely bedridden. Through the toughest days, Alfie is right by her side—offering love, laughter, and an unspoken understanding.

🖤 “He just knows,” says Alisha. “He’s calm and gentle with me, but cheeky and full of energy with my husband. He walks slowly by my side, waits on the stairs, and checks on me through the night. It’s like he’s my guardian in dog form.”

Despite the challenges of life with M.E., Alisha is learning everything from scratch to share their story online. 💻 “Back in my school days, computers were black screens with green text,” she laughs. “Now I’m teaching myself how to edit, upload, and connect—bit by bit.”

✨ This year, Alisha is determined to share more of their journey—highlighting the bond between a woman living with chronic illness and her extraordinary dog. She’s launched a YouTube channel filled with sweet, funny, and heartfelt moments from their life together.

🐶 If you love Labradors, dog content, or stories of resilience and love, you’re going to fall in love with Alfie too.
Support us by following Alfie’s adventures and subscribing to our channels—it means the world to us. 💕

📍 Follow Alfie here:
📸 Instagram: @alfiewtheblacklab
📘 Facebook: Life With A Black Lab
🎵 TikTok: @alfietheblacklabrador
▶️ YouTube: Alisha & Alfie

🎥 Check out our latest video – it’s adorable and guaranteed to make you smile:
👉 Watch Now on YouTube

Let’s celebrate the magic of dogs who change lives, one wag at a time. 🐾


#BlackLabrador #DogLoversUK #LifeWithME #ChronicIllnessWarrior #SupportDogs #EmotionalSupportAnimal #LabLife #LabradorLove #DogsofInstagram #LiverpoolDogs #MyChronicLife #DisabledAndProud #LifeWithAChronicIllness #AlfieTheBlackLab

More Blog Posts

A recent Dragons’ Den episode pitched ear seeds as a cure for Myalgic Encephalomyelitis—an illness I live with every day. Here’s why that claim is not only wrong, but dangerous. Let’s raise awareness, push for better education, and demand accurate health information in the media.
t’s not just tiredness. It’s the kind of exhaustion that steals your ability to move, speak, or even think clearly. Myalgic Encephalomyelitis has taken so much from me — but I’m still here, sharing my truth in the hope that someone else feels a little less alone. This is what life with Severe ME really looks like
Are you living with Myalgic Encephalomyelitis (ME/CFS) in Liverpool, Southport, Wirral, or Chester? I’m collecting personal stories to highlight the gaps in care across Merseyside and push for better support. This is a confidential, community-led project — your voice could help drive real change.
Myalgic Encephalomyelitis (ME/CFS) is a life-changing chronic illness that affects millions worldwide. In this post, I share my own experience of living with severe ME, explain the symptoms and challenges, and offer support to anyone facing this condition. You are not alone.
Living with a chronic health condition like Myalgic Encephalomyelitis (ME) can be an isolating experience, often leaving individuals feeling unseen and unheard. The invisible nature of ME compounds the already challenging journey, leading to profound feelings of loneliness and isolation
Disabled people make up over 16 million in the UK, yet only a handful are represented in Parliament. This post explores the barriers disabled candidates face—like inaccessible campaigning, ableism, and lack of funding—and why increasing disabled representation is urgent for real political change.