CA-125 levels

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Comments

  • Kvdyson
    Kvdyson Member Posts: 790 Member
    Withdrawal after frontline

    Becca, it seems that withdrawal after frontline is something most of us experience. I did, for sure. It's been almost six months now and life is finally back to "normal" (for me, that means cancer is not my main thought/concern). Keeping busy with family, work, my dogs, garden, etc. has certainly helped with that so I agree with your friends about getting a new hobby. The more you can re-focus your mind away from the cancer, the faster you'll start feeling like yourself again. Congrats on making it through treatment and may you be NED from here on out! 

  • ConnieSW
    ConnieSW Member Posts: 1,688 Member
    I pushed the imaginary like button

    i like the " withdrawal after frontline".  Well put and we should add it to our terminology because it's very real. I thought I was weird when it happened to me and didn't dare mention it because of what you might think about me. Seems like our chemo nurses should educate us that we might experience this and reassure us it's normal and will pass.  Think of all the poor people who go through it without us (I'm including all the other boards here) to tell them it'll be ok.

  • TeddyandBears_Mom
    TeddyandBears_Mom Member Posts: 1,814 Member
    I think I am the anomoly in

    I think I am the anomoly in this cancer war.... I couldn't wait to finish everything and not have any doctor appointments.

    When I went for my "next" 3 month check up last Monday, I asked when they start the two year clock. I was hoping it was right after surgery. But, she said it starts at the end of final treatments. Bummer. She laughed and said that most women panic when they shift from 3 month to 6 month check ups.  So, you ladies are right that the withdrawal for most is very real and very normal.

    I have white coat hypertension and will look at any excuse not to go to the doctor. At least I did prior to cancer. Now, I am diligent about going to all appointments but I have to fight myself not to go back into that 'old me' routine of skipping checkups.

    Love and Hugs,

    Cindi

  • bluehyacinth
    bluehyacinth Member Posts: 54 Member
    Immediate side effects not

    Immediate side effects not really, but I have not been on it long enough to form an opinion, but will report back when I know for sure whether it is working or not.

  • bluehyacinth
    bluehyacinth Member Posts: 54 Member
    Lou Ann M said:

    Keytruda

    You are the first person that I have heard of the is also on Keytruda.  Good to hear that the CA 125 may still be accurat.  It always has been for me. I kind of figured that the rise in numbers after the first infusion was from inflamation from my immune system attacking the cancer cells.  It was coming down until last time when it rose again..  I have a lot of inflamation caused by my SI joint and possible some diverticulitis going on. The tumor cells hat I have in my neck has increased in size.  I am thinking that is a good thing,  hopefully my I,unexpected system is attacking it some more.

    Are you having any side effects?  I feel so much better than I did on chemo and have so much more energy that I don't know if some of the things going on are side effects or just old age.  I sure hope this works for both of us.  It is certainly a more humane way to treat this disease.

    Hugs and prayers, Lou Ann

    Sry reply ended up at the

    Sry reply ended up at the bottom, no side effects as of yet, perhaps some fatigue the first couple of days after the shot, but I have a lot of other things going on. 

  • EZLiving66
    EZLiving66 Member Posts: 1,483 Member
    edited December 2016 #27

    I think I am the anomoly in

    I think I am the anomoly in this cancer war.... I couldn't wait to finish everything and not have any doctor appointments.

    When I went for my "next" 3 month check up last Monday, I asked when they start the two year clock. I was hoping it was right after surgery. But, she said it starts at the end of final treatments. Bummer. She laughed and said that most women panic when they shift from 3 month to 6 month check ups.  So, you ladies are right that the withdrawal for most is very real and very normal.

    I have white coat hypertension and will look at any excuse not to go to the doctor. At least I did prior to cancer. Now, I am diligent about going to all appointments but I have to fight myself not to go back into that 'old me' routine of skipping checkups.

    Love and Hugs,

    Cindi

    You and me, Cindi!!  I was

    You and me, Cindi!!  I was never so happy to be done with that place!  I hate going back even though I love my oncologist's PA who does my exams.  Just walking in there makes my heartbeat go from 78 to over 100.

    I have my own home blood pressure cuff because my BP also goes sky-high when I walk into that office.  I did not like the chemo nurses and it was probably because of them not being able to use the port.  They had to find a vein and that took a lot of pokes - they wouldn't listen to me when I told them they were trying the wrong places.  Finally when they did listen, they got a vein right away, just not in the place they wanted it.  They also didn't take my infected port seriously and didn't want to refer me to the Wound Care Clinic.  

    Love,

    Eldri

  • MAbound
    MAbound Member Posts: 1,168 Member
    No Comparison

    I'm another one who didn't have a Ca-125 level before surgery. It was in the 70's post op, but that could be from all of the inflammation resulting from the surgery. It was in the normal range through chemo. I don't know yet if my oncologist measures it after treatment.

  • Nellasing
    Nellasing Member Posts: 528 Member

    You and me, Cindi!!  I was

    You and me, Cindi!!  I was never so happy to be done with that place!  I hate going back even though I love my oncologist's PA who does my exams.  Just walking in there makes my heartbeat go from 78 to over 100.

    I have my own home blood pressure cuff because my BP also goes sky-high when I walk into that office.  I did not like the chemo nurses and it was probably because of them not being able to use the port.  They had to find a vein and that took a lot of pokes - they wouldn't listen to me when I told them they were trying the wrong places.  Finally when they did listen, they got a vein right away, just not in the place they wanted it.  They also didn't take my infected port seriously and didn't want to refer me to the Wound Care Clinic.  

    Love,

    Eldri

    oh Eldri- I'm so sorry!!!

    That was such a BAD set of nurses and making things even more tense during such a stressful time is NOT OK!  Did you happen to report them?  The only reason I ask is that perhaps you can save a sister later if that happens again.  I HATED BEING POKED MORE THAN ONCE- it got so very painful I started to panic and that made it worse- SO glad when I got my port!!! 

    I just had it flushed and I had a bad experience- the chemo nurses do it- I went to a different office because it was closer and this gal must not have been familiar with my type of port (smart port) because she grabbed my skin and pushed down hard- which still hurts me as my port area is tender- I think she was thinking there were tabs on the sides to hold down????  She ended up pulling my skin over so now when released the poke mark is below the port?!  It hurt and I had the lido cream on there but she pulled the skin up and over so it probably wasn't covered- it's been sore all week :'(  I will NOT go back there- I'll drive the extra miles.

    (((HUGS)))

  • janaes
    janaes Member Posts: 799 Member
    Becca I am so glad you will

    Becca I am so glad you will be done with treatment for christmas.  My first cancer I had I had to do two cycles of radiation with a month break in between.  I finished my first cycle on my birthday.  I still remember how important that was to me 20 plus years later.  I did not feel like doing any thing it was just good to have that mildstone on my birthday.  Withdral symtoms are real and its okay to have them.  I sure did. It takes time and thats okay.

  • beccabtown
    beccabtown Member Posts: 234
    edited February 2017 #31
    First post-treatment test is good

    The latest in my CA-125 saga: the first post-treatment test result was 7.6! I'm completely flabbergasted that it's possible for it to go so low after starting out so high. I have plenty of other symptoms that worry me on a daily basis, but this is one indication that something had an effect. 

    The truth is that I think I'm more depressed than I've been since being diagnosed, but that is a topic for another thread. 

  • Kvdyson
    Kvdyson Member Posts: 790 Member
    edited February 2017 #32
    Becca, I'm sorry to hear that

    Becca, I'm sorry to hear that your depression isn't subsiding. Are you seeking professional assistance? This is not something you should be trying to fix alone.

  • CheeseQueen57
    CheeseQueen57 Member Posts: 933 Member
    edited February 2017 #33

    First post-treatment test is good

    The latest in my CA-125 saga: the first post-treatment test result was 7.6! I'm completely flabbergasted that it's possible for it to go so low after starting out so high. I have plenty of other symptoms that worry me on a daily basis, but this is one indication that something had an effect. 

    The truth is that I think I'm more depressed than I've been since being diagnosed, but that is a topic for another thread. 

    Please seek help

    Becca,

    I felt the same way and I found seeing a counselor really helped me. 

  • Nellasing
    Nellasing Member Posts: 528 Member
    edited February 2017 #34
    YAY Becca!!!!

    So glad your CA125 came down- hang on to that as a WIN today! 

    Sorry about the depression- I agree- get some help with it- our bodies have been through SO MUCH and those chemicals have really done a number on them- how could they not affect the brain?  Plus, we've gotten through a life and death experience but it still hovers over us and is tramatic in ways that we can't begin to understand.  Please go talk with someone- if you don't know where to go get with your primary care and ask for a referral.  You are not alone in this.   (((HUGS)))  Keep us posted- your journey could help others

  • MAbound
    MAbound Member Posts: 1,168 Member
    edited February 2017 #35

    First post-treatment test is good

    The latest in my CA-125 saga: the first post-treatment test result was 7.6! I'm completely flabbergasted that it's possible for it to go so low after starting out so high. I have plenty of other symptoms that worry me on a daily basis, but this is one indication that something had an effect. 

    The truth is that I think I'm more depressed than I've been since being diagnosed, but that is a topic for another thread. 

    Chemical Imbalance

    Dear Becca.... the thing about depression is that a lot of people don't realize that it is often caused by a neurological chemical imbalance and that there is no shame in that or seeking treatment for it. It is treatable. A psychiatrist rather than a psychologist or therapist would be the Dr. to see first to get this possibility checked out because he is a M.D. specialist that can diagnosis or rule out depression from underlying physiologic causes. Our bodies have been put through the wringer by all of the anxiety, surgery, and treatments we've undergone and it wouldn't surprise anyone if you've been under assault from high cortisol levels or hormones being out of wack leading to this. Even this time of year can be an issue if you are affected by Seasonal Affect Disorder and could benefit from light therapy. Don't think or put up with anyone poo-poohing how you are feeling. You don't need to tough out or endure feelings of depression. After all you've been through, you deserve the ability to savor coming out on the other side of treatment.

  • beccabtown
    beccabtown Member Posts: 234
    Thank you

    Thank you for all the suggestions and support. I think I will feel better once I can sort out the problems with my legs. Gabapentin has been helping with the pain but now I'm having weakness and unsteadiness. Talking to my doctor about it soon.

  • Lou Ann M
    Lou Ann M Member Posts: 996 Member
    So glad

    That the Gabepentin is helping.  I hope you get answers for the other problems.  I always felt week and unsteady when I was dehydrated. I always have a problem with drinking enough. Low red blood cells can also cause anemia that makes you feel that way.  I love your new hair!!!

    Hugs and prayers, Lou Ann

  • beccabtown
    beccabtown Member Posts: 234
    Thank you, Lou Ann!

    Thank you, Lou Ann! Dehydration is a real possibility and one that I need to start dealing with today. I hadn't even thought about anemia. My potassium was very low when I had labs done last week. Still trying to sort that out. Leg weakness could be a side effect of gabapentin or a symptom of neuropathy or low potassium--so it's very confusing.

  • Lou Ann M
    Lou Ann M Member Posts: 996 Member
    Bananas and apricots work

    Bananas and apricots work wonders for low potassium 

    Lou Ann

  • Kamushka
    Kamushka Member Posts: 22 Member
    Leg pain

    Following you down the rabbit hole....i am not a complainer but was advised to tell of all my symptoms which, in itself, was hard for me...but.when I was in my sessions and I would tell the uncaring chemo nurses I had once every three weeks they brushed me off....... but one suggested I take magnesium....didn't help me and after I told oncologist she lowered taxol and said put my feet and hands on ice during the great m ent, which helped.....ask you doctor about magnesium or B12.....and good luck....I notice I am unstable especially after chemo treatments...Didn't think of dehydration.....had last chemo thank goodness and will be going thru radiation at a different hospital....after radiation I am determined to live my life. Our daughter is expecting her second baby and this will make five grandchildren. ages 12...9...7..2 and a newborn...between her and our two sons....so..grandma's got other things to be busy with. This Christmas the kids decorated Styrofoam wig heads for grandma...i loved it! I am also a Federal investigator with the Bureau of Alcohol, Tobacco, Firearms and Explosives (but I only deal in boom and bang) and want to get back out in the field....Hoping the radiation side effects won't stop me! 

  • Soup52
    Soup52 Member Posts: 908 Member
    edited February 2017 #41
    Gaboplatin didn't really help

    Gaboplatin didn't really help my neuropathy,so I quit using it. I am on a slow magnesium which also contains calcium. I don't know that is anything that helps my neuropathy, but it hasn't gotten worse. I think it has helped a bit with my constpation though.