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33 and my 1st ever papsmear

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teganw83
33 and my 1st ever papsmear

hi i am new to this forum I have just had my 1st papsmear ever yes I know stupid me :( just found it really invasive ha ha seems funny now anyways. it came back with glandular andecarcinoma in situ so I was like ok I have no idea what this is anyways was booked straight in to get a coloposcopy done and they took 3 biopsies there he also said you don't have cancer so you don't need to worry he also said mine is rare and he only sees 2 percent of people with it anyways didn't get the results of that test as I was booked in to get a cone biopsy done in a week when I was going into the operating theatre I asked what I was doing there as I didn't have cancer so why did they need to take another biopsy she looked at me strangley and said darling I don't know who told you that you don't have cancer but you do :( she said the last biopsy they took it was further up in the canal so that is why they had to do the cone biopsy has anyone else had this happen to them please she said she would ring me up this week sometime with the results

HarleeKwin

Hi Tegan 

I'm fairly new to this Neenon here for 2 weeks now I think and these women are amazing! As for your situation.....don't feel silly I'm 36 and never had a smear. Had an emergency colposcopy last week an after taking the biopsies she sat me in her office shut her door ad brought out the tissues. Depends told me to my face and my mother's that I have advanced cervical cancer and due to the size iwould need chemo and radiotherapy....I was told someone would ring me for screening scans but not happened,I was told someone called Nathan would contact me and that as my biopsies were rushed through as urgent I will have them back by today after something called an mdt talked through my case. My results weren't back the meeting went ahead for others and I'm stuck in limbo.. No contact no support nothing. I have chased up colposcopy the gynae oncologist who took the biopsies her secretary even found a number for support. And no-one is calling back let alone answering.  I have brn pushed through the system via urgent rapid access that should take two weeks. TWO MONTHS later I kniw I have it but no plan no-one to contact and no help or anything in writing. I feel your pain as I'm a high risk I have no immune system due to Iran transplants an m medication for other health issues make things worse. I spend my days chasing I end up more fears and worries than I do answers and keep getting told nextcweeknect week.

I know how this feels lost alone scared and bring completely out of contact of those who promise to help u begin losing faith wondered if you're lost in the system. I'm here if you need to talk. Sorry for long message a rant helps a little. And you're not alone xxx hugs and love H xxxx

Didn't get colp til 2nd Nov told was cc stage 2 @least&inoperable as 4cm tumour

18th Nov staging op with biopsies told stage 2b now 6-8cm and spreading to lining

17th December 2017

Am in remission! 

Thank you everyone xxx

Scans needed as Dr believes I have bone cancer fingers crossed hope he's wrong! 

HarleeKwin

Oops organ transplants not Iran transplants sorry. Texting not my forte

Didn't get colp til 2nd Nov told was cc stage 2 @least&inoperable as 4cm tumour

18th Nov staging op with biopsies told stage 2b now 6-8cm and spreading to lining

17th December 2017

Am in remission! 

Thank you everyone xxx

Scans needed as Dr believes I have bone cancer fingers crossed hope he's wrong! 

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