One In A Million: Tuesday

26/05/2009

Tuesday

[ click to enlarge - passiveaggressivenotes ]

[ postsecret ]

[ le love ]

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[ Steve Boland ]

Please see Kay from Australia's blog which documents her day to day life with PMP . It's great for those of you who have recently been diagnosed & wish to know more from a 'real' person rather than a doctor . She notes her daily challenges & how to overcome them. Congratulations Kay on being an 8 Year survivor , i think your blogs an amazing thing for you to have started .

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please all know

it is not brave to fight when one knows one can win, it takes true courage to fight when the outcome is unknown

to the world you may be one person , but to one person you are the world.

I'm no-one special , but i know many people that are .

In 2008 i heard about PMP for the first time in my life, my mam was diagnosed with Pseudomyxoma at Christies hospital in England . PMP affects one in a million people and is one of the rarest forms of Cancer. 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 .