Hard to believe where the time has gone, but on the 22nd June 2015 we received my diagnosis. That is definitely one day I will never forget, the feelings of shock and disbelief, but also the relief that there was a valid reason for the way I have felt for years. It wasn’t all in my … More The First Anniversary of my Diagnosis
It’s been a busy and interesting month, starting with us finally getting the decorator booked to do the hall, stairs, landing and downstairs loo. Had to change our ideas about a few things, and I still can’t find a wallpaper that we both agree on!! There is so much on offer out there, but boy … More Everyday Life and making new friends
You don't have to leave your job to travel the world
expressing our experiences through the power of art
A blog about life with Hannah who has a rare genetic syndrome, autism and other stuff...
This is the story of building a cottage , the people and the place. Its a reminder of hope and love.
Our roller coaster ride with neuroendocrine cancer, parenting, and life.
Death through the eyes of science, history, and anthropology
Elli's Journey: A glance at a life of tumors, triumph, and treasures
The Road to Personal Advocacy
Local news and weather reports for the people of Hammerwich and surrounding areas.
Or, when lightning strikes...twice
Ramblings of a mature student, husband, father & visitor at Christie Hospital for carcinoid cancer
Encouraging you, because being positive helps everyone.
Oncology Institute Director at Christus Trinity Mother Frances
Living Positively, living with Neuro-endocrine Cancer
