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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.
Millions of people around the world don’t get an end to lockdown
My home feels like my prison.
Should you exercise with ME ?
Independence
Getting a motorised wheelchair delivered filled me with hope, I didn't realise I needed a wheelchair accessible vehicle to make my dreams a reality.
Anxious
Tier 3
Feeling Forgotten
Over this Quarantine, lots of us have been feeling forgotten but what when this is your life. I was officially diagnosed with ME in December 2012 but a long time before that I felt that I had to withdraw from my life.
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