<div>my name is Sophie, I am 23 years old, and last year was diagnosed with a life changing rare disease CRPS. I was modelling, and cat walked in shows a part of London and Paris fashion weeks, and featured in international magazines. I was also very into fitness. I was also doing sales for a company that allowed me to travel not only around the uk, but internationally too. However following my diagnosis, being unable to walk, and with constant chronic debilitating pain, and the affects of the medications I have to take to try and ease this, I was unable to work, and lost my job.
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<div>March 2023, after many doctors and hospital visits, and a stay in hospital, I was finally diagnosed with CRPS, and told that there was no cure, and I may never walk again.
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<div>this year, I have found a treatment clinic in Italy, offering a treatment with a high remission rate. It is however €35000, I was reluctant at first to ask for much help, but I feel I can’t not give this treatment a go.
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Anonymous

Alan Dixon

The fashion event Nottingham 

The Fashion Event Nottingham

Ilona Jagielska

Justin Neill

Kimberley Edwards

Paul Green

Chris Melling

Sarah Roberts

Alfie Martin

Gloria Chambers

Ashten Kissoon

Susan Rounsley

Ryan Dumayne

Help with medical costs for treatment for rare disease CRPS

Help with medical costs for treatment for rare disease CRPS

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