posted
I had cervical cancer (carcinoma in situ~~~contained)5 years ago. This was before being dx'd with Lyme and Co's. I posted a couple of weeks ago about an ER trip with an ovarian cyst that ruptured.
I just got a call from Dr's office that I have squamos cells (pre-cancerous). Has anyone else had recurrent problems? They did mention that since my immune system is compromised that it certainly isn't helping.
Anyone else have recurrent issues like this?
Thanks in advance.........
[ 05-19-2009, 12:20 PM: Message edited by: Tif ]
-------------------- TL Posts: 365 | From OK | Registered: Jul 2007
| IP: Logged |
bettyg
Unregistered
posted
tiffany, i'm sorry to read this; buried on page 2 so up we go!! hopefully others will chim in.
tiffany, i'd edit subject line to draw more attention to using your own words:
squamos cells (pre-cancerous). Has anyone else had recurrent problem?
just click on pencil, 3rd box to right of your name that opens up subject line and body text....good luck! xox
IP: Logged |
posted
Ever since I got Lyme this has happened time and time again. I'm scheduling another pap before it's time citing pelvic pain because my insurance won't cover it. Plus, it's true. My ovaries hurt and my left one feels hard as a rock. But I've had CT scans, 3 abdominal and transvaginal u/s and the CA-125 blood test and everything came back fine.
I think I'm going to ask for a laperoscopy (sp) because I'm sick of worrying why my left ovary is so hard. They say it's probably endo but I need to make sure, but dang, I'm terrified of being put under. Good luck.
Posts: 63 | From Hell - Or at least it feels like it, Oh, I mean Tampa, FL. OOOps! :D | Registered: May 2009
| IP: Logged |
klutzo
Frequent Contributor (1K+ posts)
Member # 5701
posted
I was just diagnosed with squamous cellular precancerous changes in my esophagus.
klutzo
Posts: 1269 | From Clearwater, Florida, USA | Registered: May 2004
| IP: Logged |
posted
nessa, anesthesia is my biggest fear also because I have tachycardia.......I just had a cyst rupture on my left ovary (that is what started these apt's that found the cells). PROBABLY endo? That is not very definitive IMO.
klutzo, do they do anything for that besides monitor it?
-------------------- TL Posts: 365 | From OK | Registered: Jul 2007
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic