Hello and welcome to this new and hopefully soon to be very exciting site. This is a none medical, voluntary site which offers help and support to women who suffer from PMS/PMDD, from other people who have the same condition, so they understand what they are going through!
My name is Julie and I'm 37 from Swinton, Manchester, I have suffered with PMS(Premenstrual Syndrome) for years. When I started to feel that I really didn't want to do things that I'd always enjoyed or just couldn't be bothered with normal everyday things and I was moody and angry, I just put it down to PMS, but then I decided to do some research on this condition and I found out that there was also a similar, but more severe condition called PMDD(Premenstrual Dysphoric Disorder) This can totally impair a womans life.
THE CONTENTS OF THIS WEBSITE ARE MEANT FOR INFORMATION AND SUPPORT PURPOSES ONLY. THE MATERIAL IS NOT INTENDED TO REPLACE PROFESSIONAL MEDICAL CARE.
Site Designed by Julie Hull
(c) 2003
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Do you suffer from Premenstrual Syndrome or Premenstrual Dysphoric Disorder?
Did you know reports show that 1 in 3 women suffer from PMS!
Do you sometimes feel your on an Emotional Rollercoaster?
Would you like to talk to other people who understand what you are going through?
Do you feel like you would like to have somwhere that you can just let off steam?
Can you help and support other members of the group who have the same condition?
There is a story page, could your story be helpful to other members?
Are you a man who's partner suffers from PMS/PMDD? Do you understand? Would you like to understand more??
People don't understand how a normally loving, caring, helpful person can suddenly become an angry, aggressive, unpleasant person. Maybe we could educate them between us by providing information.
PLANS FOR THE FUTURE!! with the help of some funding!!
*To find a suitable meeting room/office.
*Coffee mornings and a good chat.
*Set up Internet acces for members who don't have the use of a pc, to enable them to access useful websites.
*Information Centre, with leaflets, books, and maybe videos explaining this condition and where to get help.
*Access to a photocopier/scanner to enable members to copy relevant information which would be useful to them and their families.
*Good help and support from others who understand.
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