Hello have not checked in here for a long time

azgrandma
azgrandma Member Posts: 609 Member

I have not been here for a long time how is everyone doing here??

I am still doing great and feel good most of the time

Hugs Azgrandma

Comments

  • kikz
    kikz Member Posts: 1,345 Member
    Still here

    Good to hear from you Azgrandma, glad you are doing well.  My count is up and my onc wanted to do pet scan.  I didn't get to remission the last two times so chemo is an inevitability.  I asked her if I could take Tamoxifen again because it has helped lower my count before.  It only delays chemo for a few months.  I have fatigue and a lot of aches and pains but my spirits are pretty good.

    Karen

  • azgrandma
    azgrandma Member Posts: 609 Member
    Kikz so glad to hear from you

    Are there any of the ones that was here 7 years ago still with us or is it just you and I. I need to make time to come here

    good to hear from you hon. I am sorry your still h aving to do the chemo that sucks

  • kikz
    kikz Member Posts: 1,345 Member
    There are several but of

    There are several but of course we have lost many.  I don't come here very often either.

  • Tethys41
    Tethys41 Member Posts: 1,382 Member
    Still here

    I'm still here. 

    Been visiting this page occassionally as of late, but it's pretty quiet these days. 

    I am still NED after first line chemo, finished 3/2010. 

    Wishing you well.

  • JoanC
    JoanC Member Posts: 231 Member
    Just Checking In

    Hi, I am also still Ned after first line chemo...finished 10/06/2008

     

  • kikz
    kikz Member Posts: 1,345 Member
    Tethys41 said:

    Still here

    I'm still here. 

    Been visiting this page occassionally as of late, but it's pretty quiet these days. 

    I am still NED after first line chemo, finished 3/2010. 

    Wishing you well.

    Good to hear from you ladies

    Good to hear from you ladies Tethys41 and JoanC.  You're the miracle ladies, still NED after first-line chemo.  I wish we would hear from more of the ladies who have been members for a while.  This board has gotten quite inactive compared to how it was a few years ago.  That's too bad because it was a a Godsend to me when I started this journey.  God bless all the wonderful women we came to know who are no longer with us.  My heart has been broken many times by their loss but my life is richer for having known them.

    Karen 

  • lovesanimals
    lovesanimals Member Posts: 1,366 Member
    Hi All!

    It is good to hear from you "veteran" teal sisters!  I'm still here too and still dancing with NED (no evidence of disease) since I finished front-line chemo in March 2011.

    Warmly,

    Kelly

  • csoyyo
    csoyyo Member Posts: 1
    Scared

    I am 68, no children, no history of cancer.  Had partial hysterectomy in 2002, kept my ovaries. I went to ER for kidney stone two weeks ago. The ct showed left ovary cyst 3x5 cm. called my gyno but she is in vac so I called another gyno and saw him last week. i took results of pap and mammogram I had 8 months ago. He sent me for a Ca 125 test. I Will be getting a tranvaginal ultrasound Tuesday. I have no pain, but today I have felt some discomfort on my upper rt side, but no pain.  I have had discomfort on my rt side for years and all they see is a fatty liver. The CT showed everything looked normal accept for where the stone was and the cyst.  I am scared to find out the results.

  • LorettaMarshall
    LorettaMarshall Member Posts: 662 Member
    Good morning CSOYYO~We R often scared too~Keep us informed

      Hello “Scared” …And Who isn’t?

     Just want you to know that I’ve read your letter.  Since my own cancer was found quite by accident, and not due to any intense pain either, you are right to get yourself checked out right away.  A Transvaginal Ultrasound is necessary and it is good that you are having it tomorrow.  I’ll refrain from diagnosing you before the doctors do, so I’ll just put a link here to let you know what to expect when you go in for your Transvaginal Ultrasound.  And as always, I recommend a SECOND OPINION whenever preliminary testing seems to indicate cancer PERIOD!  And when you do, choose an oncologist whose specialty is female organs.  (Gynecologic Oncologist)

     So let us know more when you find out more.  We all can identify with the “scared” feeling, but I just read an article recently that indicated all cysts are not necessarily cancerous.  And let us know what the CA-125 tumor marker test number is. 

     There are plenty of ladies here who have different diagnoses all related to the female anatomy.  Depending on what you find out, there’ll be others here who will most certainly be knowledgeable about your particular case.  And the best news would be that it is something that can be taken care of and falls in a category LESS than cancer.

     Prayers for you,

     Loretta Marshall (Peritoneal Carcinomatosis/Ovarian Cancer Stage IV) diagnosed November of 2012

     _________________________________________________________

     1.      http://www.inches-to-cm.com/cm-to-inches.php

     CM to Inches converter

     

    On a conversion chart a “3 centimeter is equal to

    1.181102362 inches

    5 centimeters is equal to

    1.968503937 inches

     2.   https://medlineplus.gov/ency/article/003779.htm

     Transvaginal ultrasound

     Transvaginal ultrasound is a test used to look at a woman's reproductive organs, including the uterus, ovaries, and cervix.

     _____________________________________________________

     3.  http://www.mayoclinic.org/diseases-conditions/ovarian-cysts/basics/treatment/con-20019937

     Ovarian cysts – treatments and drugs

     “…Surgery. Your doctor may suggest removal of a cyst if it is large, doesn't look like a functional cyst, is growing, or persists through two or three menstrual cycles. Cysts that cause pain or other symptoms may be removed.

     Some cysts can be removed without removing the ovary in a procedure known as an ovarian cystectomy. In some circumstances, your doctor may suggest removing the affected ovary and leaving the other intact in a procedure known as oophorectomy.

     If a cystic mass is cancerous, however, your doctor will likely advise a total hysterectomy plus removing both ovaries and the fallopian tubes, as well as your uterus. Your doctor is also likely to recommend surgery when a cystic mass develops on the ovaries after menopause…”

     ______________________________________________________

     4.  http://www.baymoon.com/~gyncancer/library/weekly/aa032201a.htm

     “…What is a Gynecologic Oncologist?

     Gynecologic oncologists are specialists in the area of female reproductive cancers.  By training, they are ob-gyns with an extra specialty added on.  This means they complete 4 years of ob/gyn training after medical school, and then 2-4 years of more specialty training beyond that.  They are trained in all the treatments used for gyn cancers - surgery, radiation, chemotherapy, and experimental treatments.

     What can a gyn-onc do that other doctors can't?

     Not only do gyn-oncs learn to do surgery on the female reproductive system, but on all the organs of the pelvic and abdominal tissues and organs which may be involved if cancer has spread.  Perhaps most importantly, they are extensively trained in the vital techniques ofsurgical staging and cytoreductive surgery (also called "debulking").  These procedures can ultimately be a matter of life and death.  In Susan's case, for example, accurate surgical staging did not take place.  Even when other specialists perform surgical staging procedures, they are less likely to do it accurately than gyn-oncs. Finding the exact stage of the cancer is vital to planning the best treatment.  In the case of cytoreductive surgery, gyn-oncs simply do a better job of finding and removing tumors that have spread in the pelvic and abdominal areas.

     Another advantage to seeing a gyn-onc is that one doctor can manage all the treatment for a patient, since they are trained both as a surgeon and a specialty oncologist.  They can prescribe and oversee all aspects of a woman's treatment, and are the most likely professional to be well-versed in the latest treatments in the area, including experimental ones…”

     _____________________________________________

     5.  http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650202/

     Multimodality imaging of ovarian cystic lesions: Review with an imaging based algorithmic approach

     "Abstract

     Ovarian cystic masses include a spectrum of benign, borderline and high grade malignant neoplasms. Imaging plays a crucial role in characterization and pretreatment planning of incidentally detected or suspected adnexal masses, as diagnosis of ovarian malignancy at an early stage is correlated with a better prognosis. Knowledge of differential diagnosis, imaging features, management trends and an algorithmic approach of such lesions is important for optimal clinical management. This article illustrates a multi-modality approach in the diagnosis of a spectrum of ovarian cystic masses and also proposes an algorithmic approach for the diagnosis of these lesions…”

     ________________________End of references_______________________

     

     

     

  • azgrandma
    azgrandma Member Posts: 609 Member
    always good to hear from you ladies

    good to hear from you all

  • lgraha
    lgraha Member Posts: 2
    Just joined today Hi

    First diagnosed with clear cell ovarian cancer August 2012. Surgical removal of 10 cm. cyst along with all my lady parts, several lymph nodes, omentum. No follow-up treatment and passed all the hurdles including a clear PET at 1 1/2 years and no elevated CA125 test (ever).  March of 2016 presented at the emergency room with a partially obstructed small bowel.  Had my oby-gyn oncologist do the surgery.  They can do bowel resections too.  Ovarian cancer is back.  No immediate treatments. Opted for a watch and wait as it seems to be very slow growing since it probably took almost 4 years to cause trouble again. PET 4 months post surgery showed no other evidence of disease but the residual of the tumor still there and slightly larger.  Considering radiation now, but the tumor is in a pretty tricky place, increasing risk to bladder and bowel.  This particular type of Ovarian cancer is apparently resistant to the standad chemo for ovarian cancer or may even cause unseen, immature cells to be more aggressive.  Just researching every day, especially the area of immunotherapy.  check out Bristol-Myers Opdivo along with a second immunotherapy drug.  Recently read a book about this kind of treatment, initially approved for Melanoma.  Book is called "A Series of Catastrophies and Miracles"  by Mary Elizabeth Williams.  Very interesting.

  • childofthestars
    childofthestars Member Posts: 251 Member
    Hellooooooo

    Hi ladies

    I'm still here - NED from ovarian since diagnosis in 2010 (having had a blip in 2013 with recurrence of breast ca - bilateral mastectomy & DIEP reconstruction) but life is gooooood ....... Like most of you I only check this board rarely these days  happy to hear from some of the 'old timers'! 

     

  • LoveButterflies
    LoveButterflies Member Posts: 74
    edited September 2016 #14
    I'm back on...

    Hi AZgrandma! I'm back after almost a year of not being on, but something prompted me to get back on.  I'm also in AZ!

    I started here back in July 2011 I was diagnosed with Stage 3C Ovarian Cancer and was on a clinical trial for 15 months.  I've been blessed with a remission since then and I'm sneaking up on 5 years!  Definitely beating the odds that were presented to me at diagnosis.

    I'm visiting my oncologist for my 6 month followup on the 26th and looking forward to a low ca125 and a clean exam.

    Good to see Kikz on here also!

    Blessings,

    Carmen

  • Trubrit
    Trubrit Member Posts: 5,804 Member
    kikz said:

    Good to hear from you ladies

    Good to hear from you ladies Tethys41 and JoanC.  You're the miracle ladies, still NED after first-line chemo.  I wish we would hear from more of the ladies who have been members for a while.  This board has gotten quite inactive compared to how it was a few years ago.  That's too bad because it was a a Godsend to me when I started this journey.  God bless all the wonderful women we came to know who are no longer with us.  My heart has been broken many times by their loss but my life is richer for having known them.

    Karen 

    Board hopping

    Sorry for butting in - I'm a colorectal Cancer patient, butting in is what we do :) - but I was interested in your remark about your forum slowing down. 

    We have noticed a slow down on our forum as well (Colorectal). When I joined in 2013, there were several posts every day, if not every few hours; it was a fast moving, friendly community. But it has definitely slowed down this past year or so. 

    Makes me wonder if its a general thing, and now I see that your forum is expereincing the same, I'm guessing yes. 

    So, just thought I'd have my say on the matter. 

    I'm searcing out the troll who is posting on all the cancer specific forums. I'll go back to my flagging now. 

    Good luck to you all. Cancer is the pits! 

    Trubrit

  • Jodisgoing180
    Jodisgoing180 Member Posts: 97
    Waiting on PET Scan Results...

    I am still here.  Finished up chemo in mid-June 2016.  My CA-125 was abnormal (90, it has not fallen below 90).  So the doctor ordered a PET scan, and I get the results tomorrow.  MAJOR scan-itis.