I'm no-one special , but i know many people that are .
This time last year i heard about PMP for the first time in my life, my mam was diagnosed with Pseudomyxoma at Christies hospital in England . I am 22 , my mam is 47 . Through being with her every step of the way in her battle of this confusing + rare 'condition' , i have met some of the bravest , brightest + most inspirational people of my life . i know how lost + dark the days can seem sometimes , for both the diagnosed + their family + friends . so this is for everyone affected in someway from PMP or any other cancer, to make them smile , offer comfort + to let you know your really not alone .