I have been going through this experience for so long now! I am going through a clinic, so appts. are scheduled weeks in advance, and only done 1 or maybe twice a month. I origanlly went to the Dr. because I had non stop bleeding.. I mean non stop months at a time. I had recently been diagnosed with Multiple Sclerosis. I was given progesterin 3 rounds of it. Nothing worked. So off to the gyno. I went... Had a pelvic exam, the dr. diagnosed an enlarged uterus, said she felt a mass in the muscle, and scheduled an internal saline ultrsound and biospy. The soonest they could do it was six weeks from then. Three weeks later, a nurse called to tell me I had high grade severe dysplasia, and that the dr. wanted to schedule an immediate colpos. and leep. Well both of these tests are fine and dandy except I had to keep cancelling due to the bleeding. So I took my records to a new dr. hoping for an easier time scheduling the tests. This was the first time I actually sat face to face with my records and had the results explained to me. I was told they cells are high grade invasive squamous cells. Basically explained that this is cancer, I forgot to ask but there has never been a mention of HPV. She feels that due to the fact that there is something going on with the uterus, tumors fibroids endometrosis, etc. something... That I due the ultrasound biopsy because what ever is causing me all the pain and bleeding most likely stems from there and a hysterectomy will solve both problems. This is actually fine with me since I want no more children. So now the ultrasound is scheduled for the end of the month, and they will do it regardlous of bleeding. Then 10 days later Dec. 3 I will meet with dr. to discuss results and come up with a plan.
I am very confused, my first dr. is upset because I went to a second dr. with my results. The second doctor is concerned that they have been dragging there feet on this for 4 months or so now. So what do I do should I try for a 3rd opinion. In the meantime I have become anemic, and have to do daily injections for this condition, pain is so bad and costant most of the time I feel as though I been repeatedly beaten in the stomach and back and left severly bruised. The pain runs down my legs and causes numbness. I still have a hard time descerning what is the MS symptoms and what is this.
So please give me input do I do seek a 3rd opinion or try to trust these people.
I also should mention I have been in thyroid cancer remission for almost 2 years.





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