I am incredibly honoured and blown away that someone took the time to nominate me for a National Diversity Award. Category: positive role model – Disability. The National Diversity Awards – is a swish black tie event, which celebrates the exceptional achievements of grass-root communities that tackle the issues in today’s society, giving them recognitionContinueContinue reading “I have been nominated for the National Diversity awards”
Tag Archives: Miltonkeynes
Life isn’t fair, but I can make the best of it
If we lived in a fair world, Muscular Dystrophy would not exist. But that also goes for all diseases, yes? Unfortunately, life isn’t fair. Life has a way of dealing you cards you wouldn’t of picked for yourself, I was diagnosed with the muscle-wasting disease 18 years ago. Even with an uncertain future, there’s noContinueContinue reading “Life isn’t fair, but I can make the best of it”
Our accessible home anniversary
Wow I can’t actually believe we are in May where has the time gone!? The first weekend in may ‘bank holiday weekend’ is a special memory for hubby and i, but more for me it was the weekend we finally moved into our accessible home provided by Habinteg – I have spoken a few timesContinueContinue reading “Our accessible home anniversary”
Why I am in the activist
Let’s face it this last year has been a number of emotions for all of us. In the midst of it all, I have been thinking a lot about activism. I’ve been thinking about why and how I became an activist in the first place, plus about how activism is even more essential now thanContinueContinue reading “Why I am in the activist”
I am ready to move forward after my second jab
I am officially vaccinated up! Twelve weeks ago i had my first dose, i can finally say that on April 21st, I received my second dose of the AstraZeneca COVID-19 vaccine. According to AstraZeneca who confirms 100% protection against severe disease, hospitalisation and death in the primary analysis of phase III trials. Like most vaccinationsContinueContinue reading “I am ready to move forward after my second jab”
An open letter to muscular dystrophy parents
It’s easy for me to sit here writing about my experiences when it comes to living with muscular dystrophy but what about the parents that live though every fall, slip, hospital appointment. Muscular dystrophy can affect all ages at any point in life. Whether your child has been living with muscular dystrophy for years orContinueContinue reading “An open letter to muscular dystrophy parents”
Overcoming being self- conscious about using a power chair
If you already follow my journey though this crazy imperfect life, you will already know the exciting new i announced a week ago about receiving my new wheels, and if your new to my page welcome it nice to have you here. I think it’s easier for society to automatically think that if you’re aContinueContinue reading “Overcoming being self- conscious about using a power chair”
I have my legs back!
Ten months ago i wrote an article called ‘you stole my legs’. After being so sick and tired of being lied to and treated like i was ‘less than’ by a company that has contact with the disabled community every single day. There is a huge misconception that most people believe that when you haveContinueContinue reading “I have my legs back!”
Kerry Thompson - My Life, Kerry's Way. 