Story
I was diagnose with genetic haemochromatosis in 2013 following some tests for unexplained tiredness, lethargy and other symptoms. Before the diagnosis I had never even heard to term.
My ferratin level was just under 2000 with the normal range around 100, and I was started on weekly venesections. After about 4 months, my ferratin was down to 100, or there abouts.
Without this treatment, my ferratin levels would have continued to rise, leading to organ problems.
I now have 6.monthly checkups and venesections, but all is now under control. My medical team.of haemotology and gastroenterology specialists do a great job in ensuring I remain healthy.
I am running the Great North Run this year to raise sponsorship for the Haemochromatosis Society, (haemochromatosis UK) to help raise awareness for this condition which effects 1 in 200 uk citizens, although many are undiagnosed.
Please spend 5 minutes looking at my page, their Facebook page, or internet site, and donate through my just giving page
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