Hi All, I am new to this forum, so please let me know if I have posted this in the wrong forum. I have 2 questions:
Is there a connection between rectal neuroendocrine carcinoid tumours and increased risk of cervical cancer?
Is there anyone else out there with a diagnosis of rectal NET?
Here is my background if interested:
Mother x3 children (normal birth - full term - healthy children). Non-smoker, rarely drink, exercise regularly, very active,
Gynae - Abnormal smears since 2008. Lletz x4 Various results from CIN I -CIN III (P6)
- Awaiting latest (last year) Colposcopy result - PCOS - Endometriosis
Gastro - 2014 NET (Grade 1) discovery and removal - Colon Adenoma
- Awaiting results of recent OGD & Colonoscopy
Neuro - Chronic insomnia since childhood. Diagnosis: Severe restless leg syndrome, due to dopamine deficiency. - Raynauds Syndrome
I have read through a few of the posts here on the forum but I can't find anyone with NET but I hope there will be a few out there. Thank you for your time :)