Valerie
"I can’t get a venesection or give blood. It’s a death sentence."

After managing genetic haemochromatosis for 15 years, Valerie moved to another healthcare board, which has now prevented her from being able to give blood or get a venesection. Valerie reflects on the pain of having her treatment options removed from her, worried that her diagnosis that was once manageable, is now a death sentence.

Watch Valerie's story


Please let us have venesections.

When I first discovered that I had it, I had to tell my daughter. We were in the car, I couldn’t look at her, because I didn't want to say to her that I could die.

But through donating blood regularly, I got my levels down.  

Then I moved house and was put on a waiting list of 5 years and 5 months to be seen by a consultant to be able to restart treatment.

For 15 years I’ve managed this; I’m at over a hundred and fifty donations. I want to help people, I can help people, but I’m not being allowed to.

Please let us have venesections. I worry about dying from iron overload because I can’t get a venesection or give blood any more. It's a death sentence. 

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