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KayBB
Posts: 15
Joined: Nov 2014

I have stage 3A Carcinosarcoma of the endomtrium.  Had a hysterectomy and found that the fallopian tubes, right and left positive for tumor bilaterally.  Had three lymph node removed.  One positive for metastatic carcinosarooma.  Ovaries, right and left negative for tumor.  Getting ready to take three rounds of chemo, then 6 weeks of radiation.  Will have three weeks to rest then three more week of radation.  Need support and need to hear stories that has had this type of cancer.  I have fear of the Chemo and radiation.  I am a very spiriual person and medically trying to be positive.  Good days and some Bad days.  I am 62 years of age.  If it hadn't been for the bleeding, I would not have known.

 

 

Ro10's picture
Ro10
Posts: 1579
Joined: Jan 2009

sorry you have to join us.  I do not have MMMT, but UPSC  Stage 3-C  which is also an aggressive Cancer.  I did have the sandwich treatment of 3 chemo treatments, then 28 radiation treatments and 3 more chemo treatments.   i can understand your fear of chemo and radiation.  I think we all had that fear before we had it.  Chemo was not as bad as I had anticipated.  The drugs they give you make it tolerable. It is normal to have good days and bad days.  Take it one day at a time.  Keep that positive attitude as much as you can.  I was 60 when I was  diagnosed, and this October I celebrated my 66 th birthday.  There is always hope.  Come back with any questions you might have.

Good luck with your first treatment.  Are you going to get a port.  I highly recommend getting one.  I did not get one at first and the chemo destroyed my veins.  In peace and caring.

KayBB
Posts: 15
Joined: Nov 2014

Sorry also having to meet you under these circumstances but also grateful that you women are here to know what to expect and your support.  I went through my first chemo and so far I feel good but a little tired but will rest today.  Can you tell me a little about the radiation and what to expect.  Yesterday it was a 5 hour chemo and I go back every three weeks (two more chemo) and rest for two week and then radiation.  What to expect and any suggests what to do after treatment.  I will have five weeks Monday though Friday.  Little fear but it is the unknown of what to expect.  Happy Birthday and thank all you women for the encouragement and hope.  I haven't discussed about the port yet but will talk it over with my doctor.  Thank you again

NoTimeForCancer's picture
NoTimeForCancer
Posts: 2599
Joined: Mar 2013

KayBB you are so sweet to stop to answer each of us, really, this is a fluid conversation and everyone understands if you reply to one of us, we know you are talking to all of us :)

I saw you write something about a port.  Everyone does that differently.  Some people get them and some don't.  I didn't and I remember after my first chemo I thought, "That wasn't so bad!" and I said to the nurse, "we will have to remember that spot for next time!"  (the spot being where they stuck me)  She said chemo hardens your veins so without a port they have to find a new place to poke you every time.  Having small veins didn't help, so I really only had a problem finding a vein once.  It was the third one and then my onc hoped that the break with the radiation would give them a rest.  (a lot of women have 3 chemos after the radiation - it is called a "sandwich treatment" - chemo, radiation, chemo)

No one talked about chemo brain as far as I see. It is just complete blanking out.  It hit me after my chemo, kind of like a fog, but it gets better.  I think a lot of women still have remnants of it, and there are times I have my moments, but again, it does get better.

Radiation freaked me out, but it really was ok.  You don't feel anything.  There is external radiation and they make a body mold with a bag of beads vaccumed around you and you lat there.  I don't know about the other women, but I had IMRT (super digital type radiation) and had to insert what looked like a glow in the dark dialator for every treatment.  No one had told me in advance so when the two male techs showed it to me and asked if they wanted me to do it I told them I would but this should have been explained to me in advance (to this day I don't really care for the radiologist I had).  Ha!  I did take them with me half way through and joke with my friends about making Christmas "icicles" for my friends front porch!

I did talk with a dietician who works with cancer patients and that was worth the money to me since it wasn't all covered by my insurance.  I would recommend, if you don't already, taking probiotics especially during radiation.  She gave me a study of 400 cervical cancer patients, 1/2 that took probiotics and 1/2 that did not.  The results were DRAMATIC.  I can't even imagine a barbaric study like that to see how women who did not take probiotics had such severe diarhea that they were hospitalized from dehydration.  I have been taking it for years, and when I showed the dietician the type I take "Accuflora" she said it has both types of good 'guys' in the pills.  I don't tell you that to scare you,  you can do this, and you can help yourself. 

I think most women here would tell you radiation is exhausting.  I have never been so exhausted in my life.  Other than two weeks off after surgery and the 6 chemo days, I worked through it all.  I remember sitting at my desk and just thinking, "wow, I just can't move".

A lot of us have internal radiation too.   (I should have kept count of how many people looked at my private parts!!!) I remember not being told about this until I sat down with my radiologist and I was not happy.  Internal radiation depends on what type of cancer you have, you may not have it.  I know I asked my radiologist why did I need it if I don't have the EQUIPMENT.  Again, it was because of the type of cancer I had.

Ok, I have been writing too long!  LOL!!  I am sure the other women will chime in.  You can do this.  One step at a time.  It seems like such a mountain to climb but you will amaze yourself.  We are here to help.

NoTimeForCancer's picture
NoTimeForCancer
Posts: 2599
Joined: Mar 2013

KayBB, first off, thank you for starting a new thread so we could reply to you appropriately.   I am sorry you have found us but you have a safe place to ask any question, vent, cry, etc...said by one of the the dearest women we have all know, "you are a statistic of one".  Do not read the statistics out there, the information is old and there are many here who have proved them wrong.  

Cancer is a journey, but it is doable.  You may not think you will ever see the end, but one step at a time, you will get there and the people on this board are always willing to help.

Take a breathe and if anyone starts to say anything negative, tell them to STOP, I AM ONLY THINKING POSITIVE THINGS! 

KayBB
Posts: 15
Joined: Nov 2014

I started reading the statislics but had to put it down.  The statistics was in the year of 2007, I believe.  I then realized that all I need to know is whats now.  My daughter encouraged me to come to this web site and grateful because I am not alone.  Thank all of you for sharing.  I know there are going to be days that are going to be bad but I am a fighter.  Enjoy my life today!  I have a great support of women in my life, family and now I have you ladies.  I am taking one step at a time.  SometimesI need someone to say stop and stay in the moment.  Thank you so much and I am thinking positive today and today is good.  

It happened to Me's picture
It happened to Me
Posts: 206
Joined: Apr 2014

This is a great group of women who have a vast knowledge of alot of things.  I don't have MMMT either but was diagnosed with UPSC (like Roberta) Stage IIIA in July, 2013.  I had a hysterctomy (took uterus, tubes, ovaries, cervix).  It had already spread to the paracolic gutter, left ovary and a pea sized tumor on the back of my pelvis.  I had 6 rounds of carbo/taxel.  1 round every three weeks.  The doctor didn't believe that radiation would benefit me.  I was 51 when diagnosed.  I am currently 10 months past chemo. and am NED (No Evidence of Disease).

Cancer is a scary thing.  However, it doesn't define us.  We are stonger than that.  I was told early on, only focus on what you know is fact and only look to the next event or the next appointment.  Don't look at the end because it's a very long journey.  We take things day by day.  It changes your perspective on life. 

Humor is very important and your attitude is equally important.  I tried to make a bad thing fun if that makes any sense.  If you can journal or blog, that tends to help too.  I agree with the other ladies. 

These ladies will answer all your questions to the best of their knowledge.  You can laugh, cry, vent etc..  You have a group of ladies who understand because we have been there. 

Jeanette

cleo
Posts: 145
Joined: Sep 2009

August 2007. Aged 66  Excellent health! Bleeding first sign.   Stage 3/4 carcinosarcoma of endometrium with pelvic and para-aortic lymph nodes and bladder metatstases.

Today.  No recurrance.  My advice...do not research [many would disagree] and stay positive.   I wish you well.

Linda1234
Posts: 11
Joined: Jan 2013

Great to hear someone doing so well with this awful disease 7 years later! I hope to see a lot more "success stories" and thank you women for sharing your wisdom to navigate through this journey.

KayBB
Posts: 15
Joined: Nov 2014

Good mornign Jeanette,  I had my first Chemo and a lot of fear.  I know with Gods help he will give me strength and courage to fight.  I have to much to live for.  I am grateful my daughter found this web site cause it is given me hope and know I can love, live, and be happy.  I know there will be hard times but this to will pass.  So far I am feling good but a little tired but I do what I can and then when my body tells me, I rest.  Sometimes my mind is a little foggy and then this morning my daughter told me it was from Chemo treatment and she said it is called chemo brain fog.  I realized at the beginning of this journey not to research,  I started and felt as if there was not hope because all the information was in 2007.  Then when I came on this site, I started taking suggestions beacause all of you have given me hope and strength.  Thank you for sharing Jeanette.  I am grateful for the team of doctors I have at Duke Hopital in NC.  When I walk in smiles and love is with each one and make the fear go away and I fill safe.  I am not afraid of the chemo today but the unknown of radiation a little fear.  Thank again!  Love all you women and pray for each of you.

Teamkelly's picture
Teamkelly
Posts: 63
Joined: Sep 2012

Hi Kay, my name is Nicki I post for my sister in law Kelly. Kelly was diagnosed in August 2012 stage 3C. Kelly had ignored bleeding for almost a year when diagnosed. It was through the wall of the uterus, and one ovary, several lymph nodes, there were cells in her abdomen when they did a wash. I don't remember all the details but if you go and look for my name and look for past post you may be able to find all the details. She had carbo taxol  then radiation. She has had recurrence and is currently doing experimental treatment at a sarcoma treatment center in Southern California where she lives. Kelly was 65 when diagnosed, she is a very young 67 and remains active. Kelly is a very strong Christian and her faith is the mainstay of her life.

Kelly did go to Sloan Kettering for a second opinion when diagnosed, basically they confirmed her diagnosis and treatment plan in SC, her doctor would not do an assay of her cancer, even though she asked multiple times, when he ran out of treatments for her then he suggested an assay (basically this takes your cancer cells and matches it to treatments to see which work best), why he refused to do it in the beginning when asked I will never know.

if you are in a state that has medical marijuna I highly recommend it, it has helped Kelly to sleep and eat.  MMMT is now called uterine carcinomasarcoma, if your doctor is not using this lingo, I would question his knowledge, in 2012 the doctors that study this cancer agreed that this is what it is to be called.

Kelly had no problem with chemo, she had six rounds, she continued to workout and walked most days, she was never sick, just tired, radiation was different she took lots of supplements to protect from neurothrophy (sp), had more fatigue and a little loss of appetite.

i do not check this board that often, you could contact me at riknick29@gmail.com and I will try to answer questions. The ladies on here are a good source of support and information, you might try posting with the subject of uterine carcinomasarcoma which may attract more people with your cancer.   Nicki

 

Abbycat2's picture
Abbycat2
Posts: 644
Joined: Feb 2014

Welcome, KayBB, but I would much prefer meeting you under more favorable circumstances. I am sorry you are facing this cancer diagnosis, but I can assure you that the chemo is not so bad, thanks to the drugs that are delivered along with the chemo drugs. I can't tell you about the radiation treatment, but others here can address that part of the treatment. You can do this Kay even when your heart just simply isn't into it. Believe me, you will grieve the loss of your health and the self-image that you once had; but this too will pass. That's not to say that I embrace cancer, but I've made room for it. It's like sitting in a crowded bus and making room for a stranger to sit next to you. It's never comfortable but it's not a stabbing pain, either. You can search here by keywords such as carcinosarcoma or MMMT. I did, and there is a wealth of information about this rare uterine cancer. Try to be gentle with yourself whenever possible. Treat yourself with the same gentle kindness and unconditional love you would bestoy on your very closest friend facing a similar circumstance. 

Please keep us posted with your progress.

Warm Wishes,

Cathy

KayBB
Posts: 15
Joined: Nov 2014

Good morning Cathy,  got home feeling good after my first Chemo.  I won't lie I was filled with fear about the chemo but as soon as I walked into Duke Hospital and asked God to help me the fear went away and remembering what you ladies shared.  The treatment was 5 hours and thank God I have not or felt sick YET.  I am grateful that my daughter encourage me to go to the website becaust of it being  a rare cancer.  They believe that got it all but I know it can return. I am living one day at a time.  I am a fighter and have a good support group.  I really don't have any problems about my hair,  My friend are coming over and we are going to shave my head to let them know, it is ok.  I still have my make up though.  I promise to take care of me cause I have to much to live for.  My youngest grand daughter is graduating in 2015 and my oldest is in college.  I have to wonderful daughters that I am very proud of and a big support and there when I need them.  God blessed me with my husband that is by my side and encourages me daily.  I am still a little afraid about radiation but will read and take advise on the website.  I know this is part of my journey but today I am at peace and going to enjoy my day with some rest.  Thank you Cathy.  I to am sorry also meeting under these circumstances but grateful at the same time.  Thank again for sharing.

KayBB
Posts: 15
Joined: Nov 2014

Good morning Kelly,  I thank you for sharing.  My doctors do use the term uterine carcinomasarcoma when discussing the cancer.  I found it easier to post MMMt but you are right that I need to use the correct term for others to find what they are looking for.  I have a great team of doctors at Duke Hospital in Durham, NC.  They have research to determine what treatment they thought I should take.  They called it the sandwick treatment which is three round of chemo, then 5 to 6 weeks of radiation and then another three rounds of chemo.  I had the hsterectomy they are pretty sure they got all the cancer but had to remove three lymph nodes.  Two had the carcinomasarcoma cells with another type of cancer cells. The third had a growth.  I know what the futher can bring but with the help and God, friends and family I find strength and courage to fight.  Thank you Kelly for sharing.  I am grateful for this website and the hope that all of the women share.  Hope your sister in law is doing well and prayer are with you and your family.

Maggie_mac
Posts: 32
Joined: Mar 2012

Dear Kay,

I'm so sorry to have to meet this way.  Like many of the others, my cancer is 90% upsc and 10% clear cell.  Mine is IVb.  My surgery was three years ago this week and I started chemo mid-December 2011.  I had the often recommended taxol carboplatin combo for six sessions every three weeks.  I'm now considered platnum resistant. My first recommendation is to have your head shaved at the first sign of real hair loss.  There are so many things you can't control, but losing my hair on my terms helped me.  It was going to go anyway and I didn't want to see it in the shower or have to vacuum it up off the floor.

Even though the chemo hasn't been very effective for me, I'm trying to live as though cancer is just a word I know, but hasn't really touched me.  My CA125 held for about 10 months after the first round of chemo so round 2 started in February 2013.  That ended in June 2013 and I was good until January 2014.  In May of this year I finished round 3.  With that aside, in August of this year I was feeling pretty good so my husband and I went on vacation.  Whether it is a weekend at a local park or a grand vacation, having something fun to plan is important.  My next test is December 3rd and right now I'm planning our next vacation.

For me, my spiritual belief has been key.  I really want to see my grandkids grow-up, but it is more important to me that they remember me as someone who was fun and who loved them.  I'm 67 and have lived a wonderful life.  I hope you have or will find peace as you fight this battle.

Maggie 

 

 

KayBB
Posts: 15
Joined: Nov 2014

Thank you Maggie for sharing.  I took my first chemo yesterday (5hours).  It went well yesterday and this morning feeling good but tired.  I have no expections of this is the way it will be though all of my treatments.  I live into the day that is all I can do at this moment.  I have a great support group of women in my life and a loving family as you said I want to enjoy my family.  Have beautiful grand daughters and two daughter, want to live.  God only know what my path is.  I dont have to know.  I hope everything goes well with you.  I found a book that I read everyday call Jesus Calling by Sarah Young.  Very spiritual book.  It is about peace.  Love Thanksgiving and have many gifts that I have received that money can't buy.  I am grateful even during this time of difficultity and that is the love I am receiving from my friends and family.  Today life is good and very grateful that I have today.  I am thankful that My daughter found this website for me.  It gives me hope to fight this cancer.  I do relieve the spirituality is the key and my loving God will be with me through this to the end.  I go back December 11th for my next treatment and don't think I will have the fear as I did yesterday but as soon as I walked into Duke Hospital peace came over me.  All I could say was Help me God.  He answered my prayer. I also thank you Maggie for sharing and know it is a long journey but we can do it.  I have reason to fight as you do, to watch and enjoy those grand children family and friends.  Thank again for sharing

survivingsu's picture
survivingsu
Posts: 134
Joined: Apr 2013

Hi there,

I had a very aggressive and rare form of undifferentiated small cell uterine carcinoma 5 years ago when I was 50.  I had chemo and radiation treatments simultaneously, then internal radiation, surgery, then follow-up chemo.  Seems like a very long time ago now, I am doing great.  Here's my advice, in case it's helpful:

1. Forget the internet research studies until you are well through treatment.  Most of the stuff is out of date.  Especially the survival statistics.  I'm glad I didn't know how abysmal the survival rates were for my cancer until I was past the big treatment stuff.  I paid attention to what my doctors and nurses said, and that was the most information I could handle at the time. 

2. Don't worry if you need a port.  I had one for about a year, it saves your veins since one has so many chemos, transfusions, etc.  I didn't like having it and was glad to have it removed later, but it was an important tool to have for treatment.

3.  Don't worry if you need transfusions throughout treatment, I learned that's kind of par for course as white, red blood cells tank due to the treatment.

4.  I felt crummy during treatment, but looking back it is hard to know what contributed to that - weakness from the cancer, affects of radiation, affects of chemo, menopause, aging, etc.  But it certainly improved after treatment!  But it was a gradual thing, do give yourself time.  I felt very run down when I returned to work - but my doctor found that my thyroid tanked, not sure if the chemo-radiation caused this, or it just happened.  So keep going to your doctors and doing labs and scans and such after treatment, that will help you in the long run.

5.  No one in my whole family had this.  Initially I felt I failed somehow, and that my body let me down horribly.  But one grows from experiences.  I now feel very, very lucky to be here.  I learned I am stronger than I thought, never having been tested before like this.  I also learned from others I've met, co-workers, friends, etc. that cancer touches a lot of people.  You are never truly alone.  This website shows this as well.  Give yourself time to grow, and know that you can help others if the opportunity arises.

6.  It's do-able.  :0)

Susan

txtrisha55's picture
txtrisha55
Posts: 684
Joined: Apr 2011

I am a 3 year survivor of mmmt. I did not have any radiation as my dr was savinf that for if it came back. They did remove everything plus ten lymph nodes back in 2011. So far so good. I did have six chemo treatments. It is doable. Keep a positive attitude and take one day at a time. Trish

KayBB
Posts: 15
Joined: Nov 2014

In the beginning I was so afraid and I have to be truthful there are times I still am.  I know that God is giving me strength and courage to fight this.  I have to much to live for.  When the fear comes, I come to this web site and it helps a lot knowing that I am not alone.  I have faith that I can fight this and I thank each of you ladies for sharing.  I have a great support group here in North Carolina that are here for me and I for them.  I feel blessed and try to have a positive attitude.   Yesterday was a beautiful day with my family that I haven't seen for sometime.  Tired today but going to rest.  Thank you again Trish

flyerette65
Posts: 65
Joined: Oct 2014

Hello everyone!

After I finished my 6 rounds of chemo (and I had pneumonia 3 times during treatment so it took a bit longer to finish up the chemo because you can't receive chemo while ill with pneumonia) I was told I had a lymphocele by my oncologist and that it wasn't cancer.  However, when I went to see the radiologist he told me "we have to ASSUME this is PROBABLY cancer and had me talked into 35 external and 3 internal treatments.  He did not volunteer information about using a dilator I knew to ask because of the research I had done, also I was frightened of vaginal atrophy and bladder, bowel and kidney issues.  When I talked to my son who, at the time was 29 years old he said "Mom! Assume and Probably don't belong in a doctor's vocabulary.  Get a second opinion, another test, a biopsy anything dut don't take all that radiation if you don't need to".  I called my gyn/oncologist and told him what the radiologist had said and between the two of them decided I should have a PET scan.  When I did the PET scan was normal and I elected not to take any of the radiation treatments as it would have only offered a 7% reduction in the possibility of recurrence. If I had listened to that radiologist I would have gone through all that treatment for nothing.  Question, question, question, anything that doesn't seem right to you! Cancer is so scary, you need God, friends, family and a sense of humor.  I was not married at the time and did not have the support that I needed from a man I had been dating for 6 years but I did have support from many of my female friends and relatives.  I am now 3 1/2 years NED! Had USPC 3A,grade 4.  The radiologist told me we're trying to save your life, I think he was more interested in padding his wallet, sorry but I'm cynical!

 

txtrisha55's picture
txtrisha55
Posts: 684
Joined: Apr 2011

I was afraid too but the chemo was not as bad as I thought it would be.  I worked through it except for bad days when the the legs hurt more than going to work.  The biggest thing I had was the taste buds going away about day 3.  Nothing tasted good.  But it come back around day 7.  I lost weight but now I have gained it all back but I am eating better not great but better. Rest when you have to because your body is telling you to and do not force yourself to keep going.  I still have fear but I do not let it control my life.  Keep your faith and postive attitude as it will keep you going. trisha

KayBB
Posts: 15
Joined: Nov 2014

Just realize I typed trash instead of Trish.  

Ziva
Posts: 16
Joined: Nov 2013

Hi Ladis. I am new. I was diagnosed with Ovarian MMMT last Oct, 2014. Stage 3c. I don't here many people having the Ovarian type very often. It is treated slighly different than the uterine mmmt. I was told that Ovarian is even more rare than the Uterine. I am 57 years old and had always been in good shape and good health. I never had even a cold before this. It's very hard to understand why people get this.My onocoligist even told me I was not the typical cancer patient. Everything you read about this I had already did all the precautionaries. Like having at least one child, hysterectomy, not over weight, active and so on. My Dr. couldn't give me any answers. I have gone through the 6 chemo treatments rather easily. The only negative outcome was neuropathy in my feet. And I gained weight. I go every 3 months for a CT, bloodwork, and physical examination. I do have two spots on my lungs that are being watched. I did have a spot on my spleen being watched and it had gotten larger so last time instead of a CT I had an ultrasound. It was gone! I was told more than likely it was a cyst. I feel pretty good. In Dec. my body has started aching for no reason. Just areas at diferent times. I will be asking about that at my next visit. Bu if I have to live with that discomfort I don't care. As long as it's not this cancer. So this is me and my life. I hate hearing of other people having this but it is also nice to have somebody to talk to who understands. I hope everybody is doing well.

Ro10's picture
Ro10
Posts: 1579
Joined: Jan 2009

if you put MMMT in the keyword box on the first page you will find many other posts regarding MMMT.   Welcome to the site, but so sorry you have to be here.  May you continue to feel better.  In peace and caring.

NoTimeForCancer's picture
NoTimeForCancer
Posts: 2599
Joined: Mar 2013

Ziva, I am sorry you have had to find us an hear there is yet another form of this horrible disease.  May your aches ease and you have good results.

Kaleena's picture
Kaleena
Posts: 1978
Joined: Nov 2009

So sorry you ladies had to meet us here!   As you will soon find out, although we are labeled under one roof, there are so many different types of cancers just in this one catagory.   As many others have already mentioned, question your doctor until you understand.    It is right to question and no doctor should get mad or irritated if you do.   Also, don't let your physician just push you through the process.    They deal with so many woman that sometimes it just happens.   You have to stop and slow them down.   It is so scary the first time being diagnosed that we just take for granted that you can't ask questions and such.   So take a deep breath and get all your questions down.

When I was first diagnosed, it was found after a hysterectomy and so a total surprise.   Had to go back in for staging surgery.   Final diagnosis was Endometrial Adenocarcinoma Grade 2 Stage 3a found in my uterus and ovary however it did indicate that it could possibly have been mesonephric duct carcinoma but said is was most likely from the pelvic endometriosis.  Final ruling was mullerian/enodmetroid origin of the tumor - which I just now saw!  They never did find the primary site.

I did have a port - in fact I had it in for over 6 years - probably because they were never sure where the primary site was from.   Did the chemo as a precaution.   Then had 3 brachytherapies.  I was 45 at the time and now 54.  

As the others have said, don't research on the internet.  The stuff there is outdated.   treatments have come a long way.   There are reputable sites as others have said.

This is a good place to vent and to ask questions before your appointments.    This site has helped me so much.

Just let you know you both are very welcomed here and we will be here for any support you need.

My best to both of you.

Kathy

KayBB
Posts: 15
Joined: Nov 2014

I have just finished three rounds of chemo.  I was surprise that I did not feel or get sick.  I only side effects were joint pains and constipation.  Oh don't let me forget the chemo fog.   It would take me around  9 to 10 days before I started feeling stronger.  Tomorrow I am meeting with the doctor about radiation and  having a CAT scan.  I have fear about the c-scan but know this will happen each time.  The unknown and fear go together.  I thank everyone for sharing and it helps me and gives me hope that I can fight this.  It is a part of my journey in life.  I am thankful for the day.  It has been wonderful and  I get to spend some time with my nephew and his wife.  I am thankful I have the support of my family, friends and thankful for the experience, strength and hope that each of you share.   I will be taking 6 weeks of radiation and then three more rounds of chemo.  Thank you everyone and peace be with you and your families. 

Ziva
Posts: 16
Joined: Nov 2013

Thank you for the welcoming. This cancer is very frustrating to me. I had also had a hysterectomy prior to this cancer, I had my hysterectomy over 10 years before this cancer attacked me. I had no bleeding. The only symptom I had in the beginning was my bladder was starting to fall and I had to urinate constantly. I went to my Dr. twice and she sent me home with premarin cream. I then started to get cramps, went to the Dr. again and was told I probably pulled a muscle. Cramp went away but later came back a month later. I figured I pulled a muscle again and never went back to Dr. At the time I had my hysterectomy the Dr. I had do this had said my bladder was drooping and he tacked it back up at that time. So when my bladder seemed to be getting worse I went back to him and told him my symptoms and he said it wasn't my bladder and did an ultrasound. That is when the mass was found. It was the mass that was causing my bladder to fall. If I hadn't gone back to this Gyn. I would have never known. After my surgery the Dr. came into my room and told me it went very well and the prognosis was good.  This is before the pathology report came back as MMMT.  I knew Ovarian cancer was bad but when he came back and told me about MMMT my stomach turned. The right ovary was 14.9 cm and the left was 7.8 cm. I would also like to inform anybody who reads this that I was told because I am a small person I will be able to feel my ovaries if they were to enlarge. WRONG. The Gyn. and my onocolist could not feel the masses. I pray every night to be cured but I know it will be this cancer that will end my life. But I am hoping it will be later and not sooner.

KayBB
Posts: 15
Joined: Nov 2014

Dr Appointment went well today.  I met with my radiation doctor and I had a cat-scan.  I woke really nervous and afraid what the results were going to be from the cat-scan.  Didn't find anything and getting ready to start radiation January 26 for six weeks.  Hope I do as well with radiation as I did with the chemo.  Still have more chemo after radiation.  I got to say that I really have a lot of trust with my team of doctors.  Grateful for today.

NoTimeForCancer's picture
NoTimeForCancer
Posts: 2599
Joined: Mar 2013

KayBB, I would say the one thing we ALL have noticed as a side effect of radiation is FATIQUE.  My recommendation is not to fight it and SLEEP.  Radiation can continue to work for up to six weeks, so be gentle on yourself. 

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