Category: Disabled blogger

A woman in a wheelchair with the Eiffel Tower in the distant foreground with text over which reads Happy International Wheelchair Day
Happy International Wheelchair Day

Happy International Wheelchair Day!
Today, we celebrate the incredible resilience, strength, and freedom that wheelchairs bring to millions around the world.

Vlogmas
Christmas with Myalgic Encephalomyelitis is Hard

Christmas with Myalgic Encephalomyelitis is hard so if you are suffering this Christmas I send you all my love.

You are not alone, I just wanted to let you know that if you have Myalgic Encephalomyelitis and need a friend or just someone to talk to over the Christmas holidays, please feel free to message me. I’m not claiming to have all the answers or to be able to solve your problems, but I am a sufferer too.

Vlogmas
A Cuddly Labrador, A Sneezy Labrador and a Funny Labrador

A Cuddly Labrador, A Sneezy Labrador and a Funny Labrador it must be Vlogmas Days 14 & 15.

📆 This video was published on or around 17th December 2023

Welcome to my enchanting world, where the holiday spirit dances in each frame, somedays🎅✨

Labrador hits the jackpot on Vlogmas Day 13
Vlogmas Day 8

Vlogmas Day 8 : Unboxing Pooch & Mutt Treats & Advent Calendar Time

Alfie has his favourite treat box delivered The Pooch & Mutt Treat box 🐾

Watch Alfie Our Black Labrador open Day 8 of his Lilys Kitchen Advent Calendar🐾

Vlogmas Day 2 - A Cartoon Black Labrador, A Snowman and A Reindeer
Vlogmas Day 2

Vlogmas Day 2: The Blush & Gold Planner Unboxing & Alfie opens up his Lilys Kitchen Advent Calendar door number 2 🐾

Watching Alfie opening day 2 of his advent makes me so happy, he deserves the world🐾

Skelton with his feet up and hands behind his head. The text reads “Not a Lazy Bones” “I have Myalgic Encephalomyelitis”
Book Recommendations for Chronic Illness/Myalgic Encephalomyelitis Sufferers

I think it is only right for me to share with you my must-read book recommendations for Myalgic Encephalomyelitis sufferers. I have turned to these books many times since my diagnosis as it is incredibly scary to start feeling worse with an illness like Myalgic Encephalomyelitis. So any time that I started getting more pain or I felt worse than normal I have used these books to see if it could be additional Myalgic Encephalomyelitis symptoms.

Sick and tired of feeling sick and tired
The Government has a plan

The Government has written a plan to improve the lives of people living with Myalgic Encephalomyelitis but is it too little too late? When I was first diagnosed with Myalgic Encephalomyelitis in 2012 I was relatively lucky, now ok The appointment to see the ME Team in Liverpool was lost and then budget cuts happened so I didn’t see someone as soon as I needed to

ABOUT Alisha
Alisha a woman with long dark hair sits on her bed with her hair falling to one side. Alisha wears a white top
Alisha Whittam

As a passionate advocate for Myalgic Encephalomyelitis (ME) a complex and debilitating condition, I am deeply committed to raising awareness about the complexities and overwhelming impact of this condition. 

White background with black text which reads Alisha Whittam
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