Cataracts, memory and concentration

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Hello Sisters

Did anyone develop cataracts in both eyes while taking chemo or after treatment?  The reason  I asked is because I developed cataracts. I wonder if one the side effects is from one particular chemo medicines.  Secondly, my memory and concentration status are weaken or should I say not like they were before.  

Myra

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  • ahmelvin
    ahmelvin Member Posts: 1
    edited March 2010

    Myra,

    Yes on all three.  Cataract surgery was completed in 2003 - three years prior to bc diagnosis.  Following chemo (6 rounds of TAC) my eyes clouded again.  It was corrected in-office procedure by my eye doctor who originally performed cataract surgery.  My eye doctor let me know in advance that it may happen and not to worry that he could correct it.  So it is fixable!  It's been almost three years to the day of my completion of chemo and I still have "chemo brain" and concentration is quite limited.  My doctors have assured me that I have not forgotten anything ... I just have a faulty retrieval system!  ;)  

    Anna

  • katsie
    katsie Member Posts: 19
    edited March 2010

    Myra,

    I finished chemo in February, 2009, and April, 2009, my eye doctor told me that I was beginning to develop cataracts in both eyes.  I have always worn glasses, and my vision was fairly good.  20/40 corrected.  I noticed, in April, 2009, that my vision was blurring a lot.  I never seemed to have that problem before, and I was also having trouble focusing on the television, as well as reading.

    I had new glasses made in 2009, and just made another appointment, two weeks ago, for a check up.  My vision is so much worse than last year.  I am really concerned.  My eye doctor told me, last year, that she would not do anything about the cataracts yet.  They were small, and not 'ripe'.

    I am 57 years old, and before the chemo, like I said,  I never had these vision problems, not like this.  Also, I have been telling my doctor that my memory is not what it was.  I have other health problems, but it was not until the chemo was over, that I noticed this change as well.  As a matter of fact, I probably would not have noticed it much, until my son said something to me about it.  He is worried.

    I told my doctor, and he said I needed time to recover.  Well, it has been a year, and my memory is still not what it was before the chemo.  I really depended upon almost exact memory, since I worked as a paralegal for more than twenty years.  However, today, I can hardly type up a document without using a form, which is NOT me, believe me.  I used to have all of these documents memorized!

    Then, I saw an old acquaintance, while shopping.  She knew me, and we talked for fifteen minutes.  After I walked away, I told my son that I did not know what her name was!  I knew her face, but could not remember her name!  This was not the first time that this happened to me (after chemo).  

    I never thought there was any relationship between chemo and these new developments, so I never discussed it with my oncologist, but I have an appointment for April 1, 2010, and I am going to talk to him about it.  Thank you for the heads up.  I realize we tend to down play things because we, naturally, do not want to worry, but maybe there is some connection between these symptoms.  Stranger things have happened.

    I will post when I talk to him.

  • GointoCarolina
    GointoCarolina Member Posts: 753
    edited March 2010

    Glad I found this! My eyesight has worsened and I have been seeing light flashes,have an appointment with opthamologist next week.Quite often I have a hard time thinking of the right word.I finished chemo January 2009 and herceptin October 2009,56 years old.

  • katsie
    katsie Member Posts: 19
    edited March 2010

    I almost forgot about the flashing lights, pandazankar.  I guess I thought it was because the cataracts were developing, so I didn't give them any serious thought. 

    I am going to make a list to take with me to the eye doctor and oncologist, so I don't forget anything.

    That 'word thing' used to happen, occasionally, when I was going through menopause.  My sister started to have it too, during menopause.  I think what concerns me the most is that it is not just words now,..it's names of people I used to know, and things I did everyday,..forms, etc..   Menopause started early for me, (a year or so after the lumpectomy 15 years ago), when I was 42, and finished up a few years ago.  

    I don't know what herceptin is, but I wonder if the chemo is the common denominator, and maybe our ages???  Lets update when we talk to our doctors.  Then we will have more information. 

    This is a great site.  I am so thankful I found all of you!!! 

  • GointoCarolina
    GointoCarolina Member Posts: 753
    edited March 2010

    I saw the opthamologist and have to go back in 6 weeks to be sure I do not have a retina detaching.He said it is doubtful.I do have the beginnings of cataracts.The tech who did most of the work told me she had just seen another woman who had chemo who also felt it had affected her eyes.This doctor was not a very warm person, made me feel like he wanted to hurry up and get done, so I am seeing a different one for my followup and I will question him about the chemo affecting our eyes.Herceptin is a targeted drug as my cancer was  HER positive.I do know the herceptin caused blurred vision almost every time I had it,which was weekly during chemo, then every three weeks after for a year.Another thing is chemo puts us in menopause,that may be a factor too.

  • Diane-SC
    Diane-SC Member Posts: 1
    edited September 2010

    I was diagnosed with breast cancer about a year ago.  Went through chemo and radiation and completed treatmen in May.  Have had vision problems for over a year and thought it was due to giving up hard contacts, I went to optometrist this spring and could not get vision corrected so went to someone yesterday for a second option and found I have cataracts in both eyes.  I don't know if this is somehting new or previous Dr. had missed them but new Dr. did say he has seen this before, a link between cancer treatment and cataracts and that treatment can exacerbate cataracts.  At 62, this could also be due to age - hope to learn more when I see an opthamologist in a couple of weeks.  One of those things I wasn't told to expect though. 

    As far as memory and concentration, I have noticed a slight change in both and work with two breast cancer survivors who have expereienced this also.  What hit me the hardest was low energy which seems to be returning to normal at last.

  • ljocef
    ljocef Member Posts: 7
    edited February 2011

    I haven't had my eyes checked yet, but did notice rapid decline in eyesight during chemo and for about 6 mos after.  It still is not what it used to be, but it did get a little better in recent months.  I finished chemo in Jan. 2010.  Was on 4 cycles of Adremycin and Cytoxin. And as far as "chemo brain", sadly it does exist, and I haven't had any improvement in a year.  This really bothers me as I have always considered myself to be very intelligent, and sometimes when I talk now, I sound like a stammering idiot.  I can't remember words, I lose my train of thought.  It's very embarrassing.  I didn't realize that I would end up with long lasting side effects.  I was 47 at time of chemo.  When I went back to work, I had a hard time with my concentration and memory.  I am a Civil Drafter, and work on a computer drafting program.  There were numerous commands I couldn't remember.  I just hope it gets better. 

  • Mouser
    Mouser Member Posts: 245
    edited February 2011

    I didn't have chemo, but i did have 3 major surgeries (overnight in the hospital) plus 2 "procedures" with full anaethesia in 14 months -- and my eyes have been blurry ever since. My optometrist was sure he'd find cataracts, but he didn't, so he sent me to a retinal specialist. I have something called "retinal scarring" or "cellophane retinopathy" -- it's like a membrane over the retina. Unless it gets very bad, there's nothing to be done. Luckily it doesn't get really bad in most people, and mine seems to have stabilized. Everyone says it's age -- but i wonder if all the anaesthesia didn't help it along ....

    And i got chemo brain from Femara. Badly enough that i went off it. I could take the rotator cuff and wrist problems that i also got -- but i need my brain. I *think*  i've recovered, but of course i'm getting older (67 now), and those word blocks are not going to go away, ever again.  But at least i know when i'm forgetting something! At the worst of the blur, i didn't remember a major project that i'd started a month earlier. Not that i didn't remember the details -- i didn't remember setting it up. Or that it existed. Or what it was, when i did remember that there'd been a project That was scary!

  • angeljoy
    angeljoy Member Posts: 128
    edited February 2011

    Hi ladies,

    At age 52 and about a year and a half after my treatment ended(BM, chemo - AC+T, and rads) my eye doc mentioned that I had the beginnings of cataracts in both eyes, but was many years away from needing to do anything about them.  Then over that year they rapidly worsened to the point where I already needed surgery.  I have since learned that the steroids I took during chemo, and tamoxifen and arimidex have all been linked to cataracts/excerbation of cataracts.  Breast cancer - the gift that keeps on giving, right?  I had both cataract surgeries over the past month,and the good news is that it is pretty simple surgery with quick recovery. And of course my vision is great now.

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