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Educating GP's on Ctoma

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It really is amazing that GP's don't know about this. When I went to

my GP to have a physical before my surgery, I had to explain to her

what ctoma was. Thankfully, she was curious enough to say she wanted

to do some research. Hopefully she has.

> I must say a big thank you to , Ilona, Barbara, June and Tom.

> I have printed off all your messages and will be giving them to my

> Mum just after Christmas, along with a few case studies I have found

> on the net, and a box of tissues (a good recommendation from June).

>

> I got off quite lightly with my cholesteatoma, but I don't think my

> Mum realizes this. I know it must have been a lot harder for my Mum

> to watch me go through the illness than it was for me, as a child I

> took everything in my stride.

>

> Just out of interest, my husband is in the British forces and we

> move around a lot, as a result I register with a new GP every few

> years. It's interesting that only about 1 in 4 have even heard of

> cholesteatoma, when I go to request an ENT referral. One doctor

> even argued with me when I explained to her what it was, she

> insisted it was a term for progressive deafness. Needless to say I

> found a different doctor.

>

> I wish everyone a good Christmas and hope the New Year brings

> happiness and love to you all.

>

> Dawn

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