hi everyone for the last 3 months I've been passing very large fist sized clots during my period never had them this big before. I have been back and forth to my gp as in a lot of pain. Been told this is normal. But something is telling me that passing clots this big is not normal. I'm not due to see my gynaecologist until September/October.
The pain I'm having aswell is the worst I've ever had with my Endometriosis.
Never had clots that size poor you Have you had any fibroids treatment?
That sounds really scary, all I can say is there is no way that can be normal. I understand large clots but fist size is huge. It sounds like fibroids or cysts coming out. I would maybe see if you can reach your gynae as to me that doesn’t seem right. I would insist on seeing your specialist. Please let us know how you get on xxx
Will keep trying to get through to my specialist.
Yeah I would just to be 100% sure
Thank you xx
Hi, I have had the same for years I had one the size of a small watermelon before and ended up In hospital. My gynaecologist says it’s normal 😩 I haven’t been diagnosed with endometriosis yet as ongoing tests and they keep brushing me off. I hope you feel better soon, try a tens machine that works xx
I had a endo operation in january and plus last week.Beetween I had a two large blood clothes to remove naturaly.The size was incredible and came with lot’s of blood and water.
It’s was a horror movie.And the smell I couldn’t take it.
When I went to see them the only things just make a scan and book a MRI.
They told me it’s not natural to move liki this but possible.They wanted to drained.
So my suggests try to speak to your gp.She have can get you a scan just to make sure everything ok and make you relax.But to be honest I am not getting surprise anymore.Because they just keep saying sorry and giving a painkiller.
It’s not a life to live like this.But the only way we have now.Up and down.
Darling we have to be very strong for all this situation and don’t be scare.If you feel something not right try to get a second opinion or change gp.My support me so much and this is mean for me a lot’s.
A week ago I am living with stoma as well,my endo spread out and my first gp wasn’t care enough.So all this time and wait and mistakes cost for me now a lot’s.
Life too short just for suffer.
Go for it.You know your body than any other doctor and someone out there will be generous enough to listen to you.
I have....i used to get clots that i had to pull out literally (sorry for graphic image there) but i truly suggest, as nasty as it is, taking a photo for evidence and speaking to gynae and GP..... Since my coil fitted i get huge pain, and they cant actually leave as simply as they were before 
so they break down extremely slowly.... my private gynae consultant is monitoring me quite closely to work out what is happening....but yes i suggest contacting the GP as a bare minimum.... if you wanna chat just message me.
Tow year a go I had same situation and they did mri ,and find out that I had polyp.
And that’s why I had Havy blood clots
Yes...
I had large clots and backache and was diagnosed with Adenomyosis.
I have similar getting a camera to look this week
Don't normally post but feeling abit sorry for myself today and in so much pain and like I am the only one who goes through this.
Hi everyone I'm new to the group 😊 has anyone had their work contract terminated due to time off with endometriosis?
Advice pleassee :D x
Really low and unbearable pain.. 
Prostrap 
