Blog

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 ?

Coronavirus

Lockdown of the country should mean lockdown.

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.

It’s all about ME

Getting to know more about ME sufferers than just that they have ME

Anxious

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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