blurred vision & sometimes seeing double

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blurred vision & sometimes seeing double

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  • red5902
    red5902 Member Posts: 72
    edited November 2007

    I am half way through CEF chemo and my eyesight is getting blurry.  I have also had a few episodes where I am seeeing double.  It does not last long but it is a little frightening.  I have reported this to Oncology but am on my "two weeks off" so probably will not get any answers until I go back.  Has anyone else had this problem.  Does it get better after chemo is done? 

  • shrink
    shrink Member Posts: 936
    edited November 2007

    I've had blurry vision since chemo started and just finished a week ago.  So, I can't tell you yet if it will return to what it was.

  • TenderIsOurMight
    TenderIsOurMight Member Posts: 4,493
    edited March 2008

    Hi Red, I think many of us have noticed a degree of blurring or fuzziness to our vision during chemotherapy, yet double vision is distinct. You say it lasts only briefly, and has occured intermittantly, which is good in the sense it is not persistent or always there. But best to call back to your oncologist for guidance; perhaps they'll have you seen sooner, or get in to see an opthomologist during your two weeks off. 

    It's good you keep on top as you do. Funny things can happen while on chemotherapy, so a call back to your oncologist seems appropriate.

    I'll be thinking of you, and post back should you wish to.

    Tender 

  • red5902
    red5902 Member Posts: 72
    edited November 2007

    Thanks to both who responded so far.  I sometimes feel like I just can't get through this.  I have lots of support but each chemo seems to bring on a new side effect and I feel weaker with each session.  Blood transfusion, neupogen injections, extremely painful hemhorroids, mouth sores and now blurred vision.  I feel like I'm a bit of a whiner as I know that some go through worse than this.  I am thankful for this website and the support here!

  • chemo072
    chemo072 Member Posts: 682
    edited November 2007

    My onc. office has a nurse who will call back the same day; if not, it's ok to bother the on-call doc at night too.  Blurred or double vision seems like a qol issue that you shouldn't have to put up with.  Just my two cents.

    I used to feel bad about bothering the docs but then I figured out that my onc. office has gotten paid $60K to treat me.  That puts me in the "important customer" category in my book, so I stopped feeling guilty about bothering them with my questions.  (Not saying that you are at all, just saying that that's how I felt about it.)

    Hope the vision issues get resolved and that you feel lots better soon!

    My mouth sores got better with sucking on ice chips during the chemo infusions, and with the magic mouthwash.  But they hurt like heck during chemo.   

  • BrendaK
    BrendaK Member Posts: 55
    edited November 2007

    Hi Red,

    When I had AC, I didn't experience anything like that, but when I started Taxol about 4 days after I noticed that on and off I would have blurry vision, I didn't know what to think, nor did I say anything to my doc, seems to be ok now. I didn't have many mouth sores, I wonder if it is because I rinsed with baking soda and water after every meal.  Finished all chemo on Nov 8th - moving on to radiation.

    Hugs and prayers!

    Brenda

  • kimmie39
    kimmie39 Member Posts: 319
    edited November 2007

    Hi,

    Im just finishing my chemo and I have episodes of blurred vision as well. I dont think it is uncommon.

    Just so you know I feel EXACTLY the same way with all the changes  we have to get used to its OVERWHELMING!!!!!!!!

    Im actually glad you vented because I didnt dream anyone else was dealing with the painful hemorrhoids..

    Ive said this many times I WANT MY OLD LIFE BACK

    hugs in va

    kim 

  • Angel359340
    Angel359340 Member Posts: 4
    edited November 2007

    Hello all,

    When I was on AC, I had dizziness and lightheadedness on days 4,5,6,7.  I literally stayed under the covers with my eyes closed.  I couldn't look at the TV, because all of the moving caused me lightheadedness and nausea.  It's because of the Neulasta working its course...it's the time that you start to become anemic because your counts are going low...this is the lightheadedness,dizziness that you're feeling.  I''ve even gone as far as taking an iron supplement along with my daily multivitamins...it helps.

    Good luck. Keep fighting and hang in there during the rough days.

    Helga

  • rosebud1962
    rosebud1962 Member Posts: 196
    edited November 2007

    Some chemo meds can cause your eyes to dry.  Always check with your Onc first but simple eye drops may help this problem..rosebud

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Hi Red  xxx

     I hope you are feeling better. I had my first treatment of epirubicin 12 days ago...and for the first week my eyes were blurred and I couldn't read anything at a distance...it has worn off now... it scared me at the time .... I am going to mention it to my onc next time xxx

  • judyr
    judyr Member Posts: 61
    edited November 2007

    Hi Red,

    Hang in there it does get better!

    I had occular migranes when I was going through chemo (was done in Feb.) as well as blurred vision. It was very freaky and scary, ?i called oncologist and they said that it was not a side effect of chemo, but I think that is rediculous now. I know it was. My ob (I was pregnant at the time as well) saw me right away with the problem and said to keep track of the episodes and if they occur more and more frequently to call again. They did bloodworrk ect. to make sure it wasn't something else causing the problem.

    My vision did take a while to get back to normal. I din't have any occular migraines after I had been done with chemo for a month or so.

    I think the whole thing just puts so much stress on your body that it reacts in different ways.

    I will keep you in my prayers,

    Judy

  • booklady
    booklady Member Posts: 70
    edited November 2007

    Hi RED, I did TAC and vision definitely got worse.  Per my onc, it is a known SE.  They told me to wait until after treatment finished  to see if vision improved before getting eyes checked.  I've been thru treatment for a couple of months and need to schedule eye exam.  Also, a co-worker on different treatment had vision problems as well -- so it seems fairly common SE.

    Hope it gets better for you soon.

  • jdg1
    jdg1 Member Posts: 608
    edited November 2007

    Red and Kimmie,

    For your hemorroids try Tucks medicated pads with Witch Hazel.  They helped for me and OMG mine hurt and bleed so bad.  It has been about two wks now and they don't hurt as bad and they don't bleed.  I also am almost finished with chemo but I to have had problems with my vision.  My Drs. office actually told me that this would be a side affect of the chemo and that when I am done should probably have my eyes checked.  I mean just think about it they are poisoning the whole body with the chemo and it has to affect the other organs as well. 

    I am looking forward to my last tx that is the only thing at this point that is keeping me holding on. 

  • Maarifa
    Maarifa Member Posts: 1
    edited May 2009

    Hello, it' comforting to know that the headaches, the hemmoroids and the blurry vison are all the side effects from the poison they put in us. You'd think that someone would have told us ahead of time.

    Having a hard time going along with this kind of treatment (2 chemos, 3rd coming up and then perhaps surgery, according to the docs). It's amazing to me that they don't take time to catch their breath by saying that they would check the status of my tumor before deciding suregery is absolutely necessary. I am looking into alternative cures, not just settling for Western medicine treatments. You can email me at maarifa@sbcglobal.net to see how.

    Thanks - Marilyn 

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