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StomaGirl
Hello and welcome to my blog! My name is Hannah and at some point this year I will be having my large intestine removed and a stoma fitted! To say this is a shock would be an understatement!
I have a rare condition, which is hereditary called FAP, HMPS, Gardeners syndrome (all of the above). I will go into more detail of what this is to hopefully raise awareness later.
My main aim is to show people that it’s ok, I stay upbeat by talking to people and not bottling up my feelings, after all I will need every bit of support I can get! I will be blogging my journey from life before a stoma and life during and after surgery.
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