I got scan on 24th MRI pelvic , does it ever show any thing like endometriosis? Thanks
Scan MRI: I got scan on 24th MRI pelvic... - Endometriosis UK
Scan MRI
Hi Vasiliki99,My endo diagnosis was made via CT scan/MRI, I know it is often missed on images but I was quite fortunate that it showed up.
Best of luck for the 24th 🤞🏻
It can show endo possible more severe endo as it can be seen easier. If you do have endo hopefully it shows because it can be so hard to get a diagnosis I hope you get the care you need. Annabel x
It is missed sometimes but for the majority (thousands od women who post here too) an MRI picks it up and shows it quite clearly. My diagnosis was via MRI as are most women but for some reason (sometimes having a poorly trained sonographer doing the scanning) there are occassions when it doesn't show.But thechances are it will, if it doesn't and you have what you know are endo symptoms keep pushing for help.
Mine was diagnosed via MRI - tends to show deep infiltrating endo only though, but still a useful tool
I wa diagnosed with stage 4 endo in July, large ovarian cysts and fused bowel all from an mri. I was immediately put on prostep which has been a god send and referred to the specialist endo team. I met with my gynaecologist last week and I am now on the waiting list for a full hysterectomy and endo removal. I am very grateful that mine showed up and I will have the correct and very experienced surgical team in place without having to have multiple surgeries beforehand. The mri itself took about half am hour and I almost fell asleep during it.
That's good I hope it all goes well the hysterectomy and endo removal go well and the gynae supports , the medication sounds good du need any natural or bio identical or medical HRT? I was on 2 years bioidentical HRT but now at 42 my periods look like they r menopausal which I was told by endocrinologist and this is the way it is..... hopefully be relaxing I presume pants bit no trousers should be then the MRI of head that revealed pituitary adenoma....god knows what the tumour is doing nothing hopefully xxxx
Hun it only shows up deep infiltrated endo and cysts and things like that. If you only have mild endo it may not show like the pockets of it xx
Pockets of it maybe and yet the laparoscopy is also difficult if you have ME potentially.. ....thanks Cocoacupid.
Aww sorry 😢 I had sepsis after lap but am having more surgery soon had my notification from nhs as to where I want to have it. Xx after this bowel operation will have to potentially have another operation for a hysterectomy xx I do hope they find it for you . Xx
Yes, it does but only to an expert radiologist. Many may still miss it. Make sure you get the cd with the results and ask for a second opinion if you don't feel confident about the results.
I had stage 4 endometriosis didn't show on CT scan ,then they opened via laproscopy and found it everywhere, in my pouch of Duglas,ovaries, tube,bladder and bowel. All removed with excision. As I still have same symptoms now 4 months after the operation the surgeon send me for MRI again nothing But the doctor told me it may no show. Now treating an infection Streptococcus B,Ureplasma and Sibo, He said come back after the treatment for those and if still have the symptoms, will do laproscopy again to diagnose and have a look....I'm still daily in pain. ALL the best on 24th xxx
Thanks 👍 it's so complicated pelvic pain it's terrible to be in pain though the doctors have removed it and then you feel the pain goes on and on , I really the infections get better and the laparoscopy goes well. I think the MRI won't prob reveal and it is so sad and hellish xxxxxx
That is not a suprise as from what I've read CT is not the right scan for endo. Don't know why they would send you for that. Sounds like you've been to hell and back with infections and it coming right back after your op. That does happen but after 4 months is unusual, I hope you get over all these hassles and things improve without the need for another lap. Fingers crossed for you.xx
It's very difficult when things are painful or there are infections it's so unfair on us who suffer and I don't really what we can do but we will get through it.....
Xx
I had my endo and adenomyosis diagnosed by MRI so it’s definitely worth it xx
i had it it was tiring the noise and claustrophobia if my head had been any more enclosed with ME it wud been even more difficult