Hi ladies, not sure if this thread is still active but it’s been lovely reading all of this knowing I’m not alone! 
I have recently been diagnosed APSN, I’m only 28 and absolutely heartbroken with the thought of needing a hysterectomy. They have said I can be monitored for the next 10 years or have a hysterectomy and I’m really torn. But I’m not sure I could live with this anxiety for the next 10 years! My daughter is 3 and a half, I had a manual removal of placenta in theatres after her birth so I believe that may have caused this issue. And I’m worried that it’s been in there for almost 4 years already! My symptoms are like a constant “dull/toothache” kind of pain and I’ve had non stop heavy bleeding since my daughter was born, as well as painful/bleeding after intercourse. My GP kept fobbing me off until I was finally seen in June (3 years after symptoms started) and that’s when they found this abnormal area after a laparoscopy had hysteroscopy and it’s taken until now, almost 7 months since the procedure to give me the diagnosis of APSN (there was a delay from my local hospital sending it to the trophoblastic disease centre) 

Those of you that had a hysterectomy young, how was that? How are you doing now? I’m so worried about future health issues from having a hysterectomy young. 

I have just received the news that I also have aspn too. I’m awaiting my referral letter for my first appointment at charring cross. The thought of being monitored for 10 years is crippling to my anxiety. When all my issues started I begged my doctor for a hysterectomy which was refused due to my age (32). I have my two miracle boys, one of which has ASD so I have my hands full and do not wish to have any more children. Do charring cross give you an option for a hysterectomy? I just want my nightmare to be over. So glad I found this forum to know it has been one of the most settling pieces I have found because as we all know it is extremely rare and there doesn’t seem to be much out there! 

I’m with the Sheffield trophoblastic team, I was first seen just before Christmas and my operation date is March 15th, so it’s come really quick! I think as soon as you know that’s the route you want to go, they book you straight in x

I see you guys have had an MRI, I’ve only had X-rays so far and my hysterectomy is next week? I wonder why I haven’t had one! I am also absolutely dreading the recovery. Other half isn’t great when it comes to sorting the kids out, so pack lunches and school uniforms is going to be hard to stop myself from doing them! 
i am also in the Facebook group :) 

Yeah I have been grateful to come across real life stories rather than the research papers online! I honestly thought the worst with being 5 years since my last pregnancy and having access to my biopsy reports as I got it done at the private hospital I worked at and googled all of my markers and it just didn’t look good ! But the doctor spoke me through everything with me and answered all my questions so I honestly left feeling much better! You sound like you are very prepared ! I have a huge family holiday coming up so I’m hoping for it all to take place after that so in the mean while I just send of my blood and urine tests for them to monitor ! But come 19th April I should hopefully have a date in place and prep can start then ! Sending you positive vibes ! 

What is the group called ? 

Atypical placental site nodule, there’s only around 10 members in it, I think it’s the only group on there x 

Oh I’m on that one ! I posted on the 16th feb ! If you ladies are comfortable we can do a little messenger group ️

Yes let’s do WhatsApp group that would be really helpful. Can we put numbers in here or not? Or I can find you on Facebook? 

It’s crazy there’s so few of us. Mine had grown from leftover placenta because it ruptured in labour. 

Or messenger group 

Hysterectomy sisters UK

Hysterectomy sisters UK