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My daughter was diagnosed with stage III-C, rare fallopian tube cancer.

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November 5, 2008 was the day our life’s changed forever. I know, not original, but it really did. My 34 year old daughter, mother of two little ones (6 year old boy and 4 year old girl ) went into the hospital for what was supposed to be a small in/out procedure to remove two cysts from the right ovary. Five days later she walked out a cancer fighter. Who New!!! She was diagnosed with stage III-C, rare fallopian tube cancer. That was 8 months ago and she continues to fight this awful disease. She is so sick and seems to feel defeated. She is normally such a fighter. .. So to make a long story short, when they put a small camera inside her belly, they saw a whole lot going on that should not have been. She ended up with a hysterectomy, her spleen, appendix and a few lymph nodes removed, the tail of her pancreas and some kind of fatty tissue that I guess covers your stomach. After recovering at home from major surgery for 4 weeks, she started her first of six rounds of chemo on Thursday, December 4. 2008 She spent over 7 hours hooked-up to an IV. She was on Taxol Carboplatin and Avastin. She lost her hair; it started 2 weeks after the first chemo treatment….In and out of the hospital many times …But all was tolerable until …she could not eat anything …3 weeks she was complaining about it to the doctors and answer was it is possible side effect from chemo or maybe some score tissue from first surgery or something was twisted in there.
May 20, 2009 she went in for a surgery to fix a problem with a “kink or scar tissue” as doctors have told us, that turned out to be over on 6 hours surgery and it was not just a “kink or scar tissue” it turned out to be metastatic cancer that attacked her small intestine…they have removed all of her small intestine…but there is still more cancer left on her large intestine. She is on ostomy and tubes in her arm for the IV nutrient and most of her medication… On Friday, May 29, 2009 she was admitted again to the Hospital with a low back and pelvic pain, slightly higher fever and elevated WBC. After CT-scan she was told that fluid was found in her abdominal and that could be from on infection. She was treated with IV-antibiotics and her pain medications were increased. I know she is still recovering from lest surgery and she needed more rest…
Thursday, June 11, 2009 her doctor recommended she try a chemo drug called Doxil. It's usually the next line of defense when the carboplatin and taxol don't work. My daughter feels like she can't sit, wait and not do anything. So she agreed to the Doxil. They immediately set her up for the first round same day. Contrary to what most would believe given this is a second line of defense, this was going to be much milder chemo drug with almost no side effects. (That was not fact with my daughter, she is so sick and all possible side effect are there) Treatments are shorter, running about 2 hours in length, and are only given once every 4 weeks. She has her next treatment on July 9. After 3 rounds of chemo treatment, she will have a PET scan to see if any progress is being made and we'll go from there….
I hope she will be getting the right treatment and get her strength back, and she will once again, enjoy a healthy, happy life…. emotionally … She needs to get ready and determined to kick cancer’s ass. I trust she will succeed... she has cancer but cancer doesn't have her. It’s the power of positive healing

Wish YOU ALL the ladies on this site with this horrible disease only the best outcome, my prayers are with you!!!

Thank you, worried mom, Rada

Explore topics in this journal entry and replies:

Cancer Taxol Surgery Hysterectomy Avastin Fever Ostomy Pain Carboplatin

7 replies

I am so sorry your daughter is going through all of this.
I am also stage IIIc. I pray that your daughter finds the right chemo that will stop her cancer.

Blessings to you both.

Teresa

its me again here is advice i do on myself everyday,,,,,KEEP A POSITIVE ATTITUDE AT ALL TIMES. ,,,yes i do break down sometimes.its hard to go thru what we do. keep the faith .i too have a ostomy and YES i hate it but i'm alive.jay

unbelievable!what a roller coaster.yes, your correct 'we all' have experienced that moment that ""changed our lives."""i know and or it's my perspective of what i've written on this site seems to be more positive then negative.well, i'm here to tell you that Yes it's been a struggle But a struggle that's been worth it.up until just recently i've actually been improving. don't get me wrong--i've been cancer free since August of last year verbally and October of last year from a very successful 9 hour surgery.it seems that's when the ''real fight'' started. even though i posted how well i was doing i ended up ""which i later wrote"" with infections.an infection that i acquired from the hospital (no fault of mine) and subsequent infections that were defined to me acquired from the transmission of poor hygiene from the nurses that were coming to my home to clean the wounds and change the dressings.the infections caused by poor hygiene mutated into my bloodstream and lungs.in retrospect i didn't write more about this because i really didn't know what was going on and my energy was very low. well, there so much more to this and this really is the first time i'm sharing this in more detail.my reason for sharing this with you----and if there's one thing for Certain=NEVER GIVE UP!your daughter and you sound so strong so i Pray you never loose that strength.

ed

I was also diagnosed with stage IIIc ovc. Think possitively. I honestly think that miracles do happen.
My prayers are with you and your daughter. Good Luck!

Note to tqm1ed: You also have alot going on, my prayers are also with you. Good Luck!

Big Hugs to all of you,

Love,
Esther

God Bless you, your family, the grandchildren and most of all, your daughter. Just keep encouraging her to fight and do what you can to keep her spirits high and outlook on life wonderful. Like you said...SHE has cancer, the cancer does NOT have her.
Your daughter is very fortunate to have such a supportive mother, believe me, not all mother understand exactly what a daughter goes through in times like this. Keep the faith!!
Dawn~~

I just want to say God bless you for getting so involved and being so supportive and hopeful. I too have fallopian tube cancer.... very rare cell type of small cell. I am being "experimented on" since small cell only occurs in about 300 cases of ovarian or fallopian tube.
My mother has become cold and distant. She bought me a cemetary plot the day after my surgery in April of 08 and seems more concerned about my will more than anything else.

I am so sorry and I cannot believe that mothers can be so cold, She is possible very afraid too, but is not able to show her trough feelings,
I wish you all the best in this world and let's pray together for a cure!!
Each and everyone one of us are going through tough times right now, but God is getting ready
to bless you in a way that only He can!

Keep the faith. Seka’s mom, R

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