Just diagnosed with Endometrioid Adenocarcinoma: What to expect?
I was just diagnosed with this uterine cancer. I am 68 and I'm so freightened. Waiting to see doctor for hysteroctomy. This is all I know. I had a biopsy done and this is the result. Anyone please let me know what ro expect and do before hand and any suggestions are embraced. ❤
Interested in more discussions like this? Go to the Gynecologic Cancers Support Group.
Hi Rose, Wishing you an easy surgery and recovery. Feel all the emotions and know that you are supported in all of this. The unknown is so scary and hopefully after surgery it will really clear what is need to do. Sending you lots of love, Eileen
Eileen,
It is so encouraging to know that even though we don't know each other, you are wishing me well. I feel close to you already as if we have known each other. I needed this. Thank you and best wishes for you as well.🥰
Hello @rose53. Yes, the roller coaster ride of cancer is all too familiar for those of us who have dealt with it. While I've not had gynecological cancer, I have had three surgeries for carcinoid cancer of the digestive tract. It is not something you "get used to."
You are doing good things for yourself now in terms of getting support from others who have been down this road as well as getting a sound medical opinion. I'm glad to find that you have also found some spiritual support through prayer. I will be glad to join you in praying for your surgery on Nov. 17.
Keep posting on Connect as you feel you need support and some shoulders to lean on. That is why we are here!
Will your surgery be at a Mayo facility?
Hello everyone. Its finally approaching for that day to have my surgery at Mayo Jacksonville on the 17th of this month. I feel I have made the right decisions to go with Mayo. After visiting for the first time for my consult, I could not be more pleased at how nice and uncomplicated my visit was. The staffs, nurses were very pleasant and so helpful. I'm still anxious of the unknown but sharing thoughts with those who have reached out, thank you for your encouraging words. I thank you: Teresa, Nature girl, Ellen, Eileen, ejohn, and Colleen. Bless you all.
Hello, @rose53 I'm so happy to hear back from you and to know that you feel good about your decision. Your experience at Mayo is much like my own. The physicians, nurses, and all staff I encounter are helpful and listen to me. Yes, the uncertainties you face are anxiety-provoking. Your faith and your prayers will sustain you.
I will keep you in my thoughts and prayers on November 17.
Blessings to you,
Helen
🙏❤
@rose53 I believe you wrote that your surgery (hysterectomy) was scheduled at Mayo Jacksonville on November 17. You were in my thoughts on that day and you still are. How are you doing? Did you surgeon give you information about the surgery afterward? Please remember that you are supported here.
Hi @andrea69 I've been thinking about you and wondering if you heard back from the GYN/ONC. Do you have some new information to share? How can I help?
I was diagnosed with endometrial adenocarcinoma in 2007. My gyn called to tell me that he wanted to refer me to the local gyn/onc team. He told me that when cancer is present he always refers to gyn/onc for surgery because that surgery involves tissue that only a gyn/onc has the ability to remove: uterus, tubes, ovaries, 29 lymph glands, omentum. All of these were removed by my gyn/onc in a 4 hour surgery. The lab reported cancer in uterus and in 11 of the lymph glands. I had 3 rounds of high dose chemo, 25 days of radiation, 3 internal radiation, and 3 more rounds of chemo. I saw my doctor every three months for a couple of years, then every 6 months for three more years and once a year until my 10 years were completed. It is now 14 years and no more evidence of cancer.
Hello @ejrdevries Thank you for sharing your journey through endometrial cancer. I'm happy to know that your gynecologist referred you to GYN/ONC. My gynecologist did the same right away. Your journey provides hope for all of us, including myself (recently diagnosed with recurrent endometrial cancer). Like you I was presented with a cancer survivorship plan. My plan included recommended visits every 6 months (my cancer was Stage 1a with no evidence in lymph nodes) and I went back for visits as I was supposed to. It was at a recent visit when the recurrent cancer was discovered. I'm starting radiation on December 6 (25 days) followed by 3 brachytherapy visits (internal radiation). After that I will go back every 3 months in my new and then longer periods of time if no other cancer is diagnosed. You are 14 years out from your original diagnosis with no evidence of cancer. This is wonderful news. This gives me and I hope others who visit Mayo Connect hope that treatment does work.
If I may ask how old were you when you first diagnosed in 2007 and how is your life now?
Blessings to you and yours as we approach Thanksgiving.