Help with medical costs for treatment for rare disease CRPS

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.

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.

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.