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Old 03-27-2008, 05:17 AM   #1 (permalink)
flowerpower27
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I am really annoyed that nobody told me about PCOS. I think the UK is seriously lacking in information, why are we so ignorant to this problem? Is there anything we can do to inform people of PCOS?
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Old 03-27-2008, 05:38 AM   #2 (permalink)
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I know what you mean, i hadn't even heard of PCOS until i was diagnosed with it back in 2006!
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Old 03-27-2008, 09:09 AM   #3 (permalink)
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The UK PCOS Oganization is Verity. You might want to get involved with them. Next month, they're having a big conference. PCOS Conference in London - 26 April 08 (Verity thing...)
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Old 03-27-2008, 09:50 AM   #4 (permalink)
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i know what you mean! Ive never heard of pcos, either until i got dx.
eva
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Old 03-27-2008, 10:27 AM   #5 (permalink)
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Or me - and to be honest, the first time it was mentioned the woman doing my scan just said 'oh, you've got PCOS - no more puddings for you'

And that was it!!

Since I went back to my GP and got a really good consultant, I felt so much happier, informed and in control.
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Old 03-27-2008, 11:01 AM   #6 (permalink)
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What a very unsympathetic woman doing your scan!!
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Old 03-28-2008, 10:20 AM   #7 (permalink)
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Thanks for the replys girls. I think I will get involved with Verity, raise some money perhaps. Not only did I not know what PCOS was but neither did my doctor, I asked him a bunch of questions and he just couldn't answer! Its mad that all I was told was go on the pill when I was 15, never told that it could be masking anything. I would never of know I had PCOS if I hadn't come off the pill. I do have a gyne now and he is great, only problem now is it takes months to get an appointment. A very slow process.
So are you all having to educate your families and friends about PCOS?
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Old 03-28-2008, 12:58 PM   #8 (permalink)
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Well for me i am trying to give as much info to my family as possible, i think they are finally understanding it!
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Old 03-28-2008, 01:39 PM   #9 (permalink)
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this website is great for explaining things. Ive also got a lot of pcos book - probably about 8 by now

eva
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Me - 41, hubby 36 son 11. Married 14 years

She is buffeted by the wind, but she does not sink.



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Old 03-28-2008, 01:42 PM   #10 (permalink)
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I showed my dh, mum, dad and my sisters this website and they find it very helpful as it helps them understand about PCOS.
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Old 04-01-2008, 06:02 AM   #11 (permalink)
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PCOS is such a growing problem at the moment you would think that there would be specialised clinics to help women like ourselves ??
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Old 05-03-2008, 11:05 AM   #12 (permalink)
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id actually knew wat PCOS ws wen i was DX!! I feel like the only person!! Id seen it in magazines alot and always thought i had it but then thought 'nah that wouldnt happen to me'... well it did!! It explains alot though!! And it didnt really stop me being shocked at the whole idea of it!! Im on a mission to get it out there though... Iv made a FB group about it... I hope i can help people get diagnosed younger... I was 18 but had the symptoms since i was 12!! [well about 10 if you count hair loss] id love to set up a charity or something...
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Old 05-04-2008, 05:16 PM   #13 (permalink)
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Well i think there should be more media and stuff on PCOS , i mean i was 10 when i got DX so that was great but did not get no help because pedis did not know what to do for me!
I would not mind doing a pcos talk , i am going to think of that maybe at a community center do a big talk on it so people understand it and are aware of it!
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Old 05-05-2008, 03:58 PM   #14 (permalink)
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