Endometriosis UK
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**Can everyone PLEASE sign & share PETITION to David Cameron, Endometriosis needs faster diagnosis & greater education amongst medics**

**Can everyone PLEASE sign & share PETITION to David Cameron, Endometriosis needs faster diagnosis & greater education amongst medics**

Hello ladies, it doesn't looks as though endometriosis UK have done a post about this on here? They have revived their petition to David Cameron:

"PETITION to David Cameron: Endometriosis needs faster diagnosis & greater education amongst the medical profession. Please sign and share. We already have over 12,000 supporters - lets get it to 100,000 so it has the chance to be discussed in Parliament!"

change.org/p/endometriosis-...

Can you all PLEASE take the time to sign it and share it as much as possible on social media, and also hassle all your friends and family to sign and share it too. If everyone keeps on doing it we CAN reach 100,000! Thank You so much!

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Done

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Thank You! :-)

Can everyone please sign and share!

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Great idea! It would also be worth petitioning Welsh Government (and Scottish/NI) or via petitions committees as I think health service decisions are generally taken here. Might be biased as I'm in Wales. Can't do any harm to try all avenues though! Thank you 😊

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Hello Tilly79. If you haven't heard of us, or are not currently a member of FTWW please have a look at my profile - you are most welcome to join our FB group. We are currently campaigning for better care for endometriosis in Wales.

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We need a CZAR for this awful disease. If they can transplant wombs why in god's name cant they help the 1 in 10 women who struggle with this. I am 68 now and things sound no better.

HOW DO WE HEARD???

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Done 👍👏🏻

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Thanks!

Can everyone PLEASE sign and share!

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Done and shared....

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Done and shared.

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Signed

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Just bumping this post, loads more signatures needed, please sign and keep sharing!

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Signed x

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Signed and shared on FB.

It's about time women were taken seriously when approaching doctors with severe period pains and not just treated like wimps or headcases who imagine the pain to be worse than it is. Taken 25 years and a partial hysterectomy for me to get a diagnosis. Unfortunately I'm now stage 4 severe with this disease after struggling my whole young life to put up with this pain because I was dismissed so many times.

Please, young ladies, don't keep suffering like I did. Keep at the docs to find out why you are in so much pain. Just hope that the specialists in your area are well educated to endo and its symptoms.

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Done

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