I have suffered with Endometriosis my whole life and it's a year today since I had my last operation but I'm still in chronic pain everyday and on painkillers.
I would like to form an Endometriosis group where we all meet up face to face every month and have a coffee and a chat.
I would stand up for this as I can't sit down due to the pressure which gives more pain but that's fine I'm use to standing by now.
I want this to be an uplifting experience for everyone because as you all well know Endometriosis really gets you down!
Other people without Endometriosis, with due respect, don't really understand what we completely go through.
So let's all fight this B.... together.
So if anyone is interested please send me a message on here or to my personal email which is sarah.archangel@live.co.uk
Look forward to hearing from you all.
Sending Well Wishes
Many Thanks
Sarah π xxx
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sp123452017
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Hey I live in Leeds and I would be interested in this! I wrote a similar post not too long ago about a group in Leeds as I know there isnβt one yet x
Hello, just to let you know there is a Facebook group northern endometriosis sisters support who do meet ups (they are meeting in hull today but have done leeds and Wakefield) not to stop you doing something similar but you may want to check it out, not managed to get to one myself yet but hope to in the future x
Thats exactly what ive been searching for. Just for some answers as drs cant give any. Im being treated for endo but they dont know for certain it is?? Now im getting more n more problems im terrified n i just want ppl who have suffered the same. So count me in!xx
Thank you so much for your reply that's brilliant!
It's so lovely to hear that this group is what you have been searching for.
It will be great to talk to each other about our different experiences with Endometriosis and be able to just support each other.
Hope this group can help you with some of your questions although we can't diagnose as we're not medical professionals but we can have a really good chat about your symptoms and try and help you as a group.
I'm going to leave it a little bit longer to see if anymore people would like to join the group and then ill be in touch with the details.
I'll speak to you really soon and thank you again.
Hope you can join I'm just waiting a little bit longer to see if anymore people would like to join and then ill be in touch and we can sort out where is best for people to meet.
Hi Chelsea, I am New too and also from Cheshire. I am keen to meet others who are going through the same thing as at the moment donβt feel like anyone else understands. Hopefully see you at a meeting soon
Thank you for the reply Hannah, hope to see you there! This is quite out of my comfort zone to be honest but chatting can only be a good thing, take care x
Donβt worry I feel completely the same way, itβs daunting speaking to strangers but I think itβs the only way I will get the emotional support I need. Speak soon π
It's great that you want to form your own group to support others with endometriosis!
I don't know if you (and the others who have replied) are aware that Endometriosis UK do run a number of face-to-face support groups where people meet up on a regular basis. Sometimes they have guest speakers and some groups have Endo Nurses who attend.
You can find the locations of the support groups here:
If you are unable to find a group in your area, please do let us know. Whether you are able to run a group or would just like to attend one, we would love to know where you would like to see one. Fill out our Local Endometriosis UK Support Group enquiry form with your address and select on 'No group in my area' to let us know.
Just to let you know we will be training some new volunteers for a new support group in Wakefield in June. Will put more information out as and when it is up and running!
I haven't officially been diagnosed yet I'm waiting for my first lap. I've been on a 8-12 week waiting list for 3 weeks so not long hopefully. but I know its endometriosis. You know when you just know haha.
I'm glad you wrote this post as I have just joined this site after suffering with this for years, I was diagnosed a few months ago and have some days where I really struggle to do jobs because the pain gets so bad, noticed your Comment about sitting down makes it worse with the pressure and that's exactly what I'm having at the moment I haven't been able to sleep for a few nights as everytime I lie/sit down it's awful! I would be interested in joining the group thanks, Jo x
Thank you for your kind reply about my post and its so brilliant to hear you would like to join the group! π
Sorry to hear you are in pain and haven't been able to sleep. It really can get you down and make everything difficult to do. What I do all the time is take painkillers, rub my whole belly and back where pain is with 10% Ibuprofen gel, use heat pads and my life saver little soft cushions which I tuck under each hip while I'm layed down ready to try sleep they help take some pressure off too. I also use a flat cushion under each foot to relieve more pressure. Some nights a flat cushion under knees too.
Just check with pharmacy before you use anything though hun incase you have any other medical conditions especially with mixing ibuprofen gel and painkillers you cannot use ibuprofen tablets at same time as ibuprofen gel the pharmacist told me.
Hope you manage to get some sleep tonight and some pain relief too.
Just waiting a little longer to see if anymore people would like to join the group and then we can all plan a place time etc.
Ill be in touch really soon.
Sending you Well Wishes for a peaceful nights sleep.
Thank you for your reply, and tips will definitely come in handy wouldn't of thought to use the gel and I actually have that here so that is great had a bit of a better sleep and isn't too bad today still will have to push mysef into work, it's strange how some days you literally struggle to even move around with it, x
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