Although I'm officially diagnosed with UC (at one point they called me TYpe unspecified as have a fistula), I am part of a gene testing trial (drs love you when you let them experiment on you or take blood - gets you faster medical attention). THey haven't yet given me feedback but take blood out of me periodically and have me fill out questionnaires, eg, what did you eat as a child that you don't eat now, what allergies do you and members of your family have.
Cheers and thanks for the link.
Officially diagnosed Jan 2005 with UC & anthropathy arthritis, RV Fistula April 2005
Misdiagnosed for over 20 years re the above!
4 DVTs and 1 PE (blood clots) Nov 2007 (caused by flare ups)
Oesteopenia in right hip and spine (caused by pred)
Present meds: 6 x 750mg Colazide, 50mg 6MP, off warfarin but on stage 3 clinical drug trial Rivaroxaban
Take 1000IU Vit D, calcium, magnesium, vit C, vit B, Evening Primrose Oil