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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.

Feeling "sick and tired of being sick and tired"? Discover the real symptoms of life with ME/CFS and why awareness and support matter more than ever.
Being bedridden, I spend almost all day in Pyjamas, so when I needed a little retail therapy, I thought it would be silly not to film the unboxing and put the Pyjama Haul up on Youtube.
Help make a real difference to my life by donating to my Gofundme page, your donation will help me purchase a larger car, Progeo wheelchair and Mototronik
From my toilet I share how life with Myalgic Encephalomyelitis really makes me feel and why it is so hard to win against ME
Today, I’m remembering Katarina Pavelek — a fellow woman living with Myalgic Encephalomyelitis, whose light left this world far too soon. Katarina made the incredibly difficult decision to end her life through assisted suicide after experiencing overwhelming illness and suffering. I’m not here to judge that choice — only to honour her, her life, and the love her friends shared for her. Her story is heartbreaking, and it’s not the first time we’ve lost someone to this illness. ME is
I was diagnosed with Non-Alcoholic Steatohepatitis (NASH), a silent liver disease. Here’s my journey, family history, and why I’m finally taking it seriously
Alfie never fails to make me smile — and today, he’s choosing his favourite treat from his beloved Whimzees stash! Watch this short and sweet video for a dose of Labrador joy and see why he fills my days with love, laughter, and plenty of crunching sounds.
I aim to create a community that embraces diversity, fosters understanding, and supports one another on our good and bad days on this beautiful journey we call life.
Yesterday I had an appointment with my doctor to discuss the pain and loss of movement in my hands
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