Get Tarcs to London and Back!

In the last 12months Ryan Tarca has had some bad news in regards to his long term health. Until very recently, only his closest friends knew that he has tested positive to a type of Familial Amyloidotic Polyneuropathy, specific to his genes. FAP is a hereditary, neurodegenerative disease that can appear between the ages of 20-50years and within Ryan's family has come on strong after the age of 30 and progressed rapidly with degeneration of cells. Ryan has shown very small signs already in part of his hands. There is no cure, however, there is a specialist in London, who he is going over to see in June/July, 2017 to have multiple tests, scans and research done, in the hope that some sort of remedy or treatment delaying the onset of symptoms can be identified.

After receiving this information, Ryan has been working away trying to save to book flights to London, along with paying for the expensive hospital fees, tests and scans in London and locally. The trip to London is likely to be just the start of on-going medical cost that Ryan will be paying for the remainder of his life, therefore, his closest friend have now come together in the hope of raising some money to fund the trip and what ever else we can.