Skip to content
Forum IndexForum: Depression, Anxiety and Post Traumatic Stress Disorder → Topic: Does chemo destroy Brain cells?
« Forum: Depression, Anxiety and Post Traumatic Stress Disorder: Meet and support others who are affected by these issues.

Topic: Does chemo destroy Brain cells?

Log in to post a reply
  • Posted on: Sep 28, 2009 04:49 pm
Joined: Sep 2009
Posts: 36
spar wrote:

The dr's say alcohol destroys brain cells and drug abuse destroys brain cells.  My husband says I have not been the same since chemo and that was nearly 5 years ago since the last treatment, but my memory, spelling, and handwriting are not nearly as good as they use to be.  For example he can say lets watch so & so movie, half way through I will ask again what the name of the movie is and he will tell me again but by the end of the movie I will have forgotten the name again.  And peoples names, I use to never have a problem with names and I am having a terrible time remembering peoples names.  I can't even read my own writing sometimes and my daughter will call and tell me my grandson has a ballgame at such & such time and I will call her a few days later and ask if he can spend the weekend and she will say remember I told you he a a game and I would have forgotten.  I am tired of being so forgetful and is there anything we can do about it.  I read a lot and study the bible to keep my brain active and my hands are always busy doing something.  If anyone has any suggestions or has this same problem I would love to hear about it and what you think about chemo causing it.  thanks.  Sherry  I will be back later have to go for now.

Page 1 of 2 (31 results)

1 2
Posts 1 - 30 (31 total)
Bayyyy
NJ
Joined: May 2006
Posts: 1,311
Sep 28, 2009 05:17 pm Bayyyy wrote:

Hi Sherry,

I would swear it does. My doctors, however, have told me that lack of estrogen and menopause in general can cause similar symptoms. I am tempted to blame it on chemo. It's funny you mentioned handwriting. At back to school night, my son's teacher asked parents to write something they should know about our child but maybe the child would be too embarrassed to let her know himself. So I was writing about my son's handwriting issues--he used to have an occupational therapist, he has a hand tremor that makes writing tiresome--anyhow, as I'm writing and seeing my horrible scribble and actually having trouble forming letters, I thought when did MY handwriting get so bad. It was ironic and embarrassing for me.

I don't know what the solution is but wanted you to know, you're in good (but frustrated) company!

The grand essentials of happiness are: something to do, something to love, and something to hope for~Allan K. Chalmers
cherneski
Belvidere, NJ
Joined: Mar 2009
Posts: 517
Sep 28, 2009 06:21 pm cherneski wrote:

Sherry, It is frustrating to know that I will continue to have this problem.  I am sorry for you for us.  I hate it!  I cant spell, one day I forgot my mothers phone number, I grew up in that house and it has been the same number since I was 3!  I used to pride myself on how good my memory is (was).  Before chemo I could still remember phone numbers of friends from 6th grade! 

I have lymphedema in my right hand also.  I am right handed so I thought it was because I cant grasp the pencil correctly anymore.  But I guess it is a combination.

I sure hope someone comes along and tells us something that will help.

Hugs

Deborah age 38 DCIS, IDC, ILC, BRCA- Started chemo TCx6 on 06.22.09
Diagnosis: 4/9/2009, IDC, 2cm, Stage IIIa, Grade 3, 7/13 nodes, ER+/PR+, HER2-
cherneski
Belvidere, NJ
Joined: Mar 2009
Posts: 517
Sep 28, 2009 06:43 pm cherneski wrote:

Does anyone have hearing problems since chemo?  I am now almost deaf, something that was never a problem before.  I am wondering if this is temporary like vision?

Deborah age 38 DCIS, IDC, ILC, BRCA- Started chemo TCx6 on 06.22.09
Diagnosis: 4/9/2009, IDC, 2cm, Stage IIIa, Grade 3, 7/13 nodes, ER+/PR+, HER2-
erika-canad…
Joined: Dec 2006
Posts: 121
Sep 28, 2009 07:14 pm erika-canada wrote:

Hi Spar:

I believe it does. I don't care what the Doctor's say....didn't you all notice how they seem to dodge questions on chemo, AI's, all things related to cancer?

Taxotere can only be dissolved in Ethanol'\; give that to the brain, I'm sure it's worse than sniffing glue?

I was a medical transcriber....making a living spelling. Ask how I spell now...and the doctor says "could be from chemo, but will only be temporary". I feel like saying he should take a reality check it's been 2 1/2 years.....how long is temporary?  Sorry, for venting but why can't they be honest so you know exactly what you are facing.

Big Hugs...so grateful for this site.

Erika

flash
ct
Joined: Oct 2007
Posts: 655
Sep 28, 2009 07:30 pm flash wrote:

the latest research  using MRI and fMRI does confirm that the brain changes from chemo.  In particular they noted changes in the size of the frontal lobe and some other areas.  It changes memory and  processing speed.  the good news is that the brain is slightly more "plastic" than we thought and the neurons do learn to use adjoining cell areas of the brain in compensation.  So, for some, there will be no long lasting effect and for others there will be some. 

 CHEMOBRAIN IS REAL!

dcis, idc, pagets er+,pr+ her2+++
Diagnosis: 10/10/2007, Paget's, Grade 3, ER+/PR+, HER2+
idaho
Joined: Feb 2009
Posts: 953
Sep 28, 2009 07:31 pm idaho wrote:

Of course it causes brain cells to die-- they have filled your body with potent chemicals!  Some of them are found in agent orange and we all know what that did to our soldiers.... I remember hearing about a study they are doing now on "chemo brain"-  so evidentally they are finally listening to patients and trying to figure out if it is ligitimate-- of course it is....  Tami

There's no place like home......There's no place like home
Diagnosis: 2/1/2009, IDC, 1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2-
Mandy1313
the North East
Joined: Aug 2008
Posts: 522
Sep 28, 2009 07:42 pm, edited Sep 28, 2009 07:43 PM by Mandy1313 Mandy1313 wrote:

The latest theory is that chemo brain is real and that for some it is permanent. http://www.nytimes.com/2009/08/04/health/04brod.html?_r=1&ref=health  (that is an attempt to post a link to an August 4, 2009 article in the New York Times by Jane Brody).  

 I fear that I may be one of those----a few months into chemo i would feel as if there was a space in my head and I just could not process the information that I needed to speak or think.  I finished chemo in May and I still have this feeling from time to time---my mind is not exactly the same as before.  However it has improved from when I was actually on chemo.  Hopefully,  it will continue to improve.


Diagnosis: 7/2008, IDC, 1cm, Grade 1, 1/2 nodes, ER+/PR+, HER2-
spar
Joined: Sep 2009
Posts: 36
Sep 28, 2009 09:26 pm spar wrote:

Well, I am sorry for us but glad to know I am not alone and that some research is being done.  It makes me angry that dr's don't tell all or they don't know all.  I hate being in a conversation and then my mind just goes blank and I'll say jokenly it must not have been important but I know for me to say it, it was important to me but what can ya do.  I have done this in church and it is so embarrasing.

cherneski, i already had a hearing loss before chemo but not it is worse and not only that I have a ringing in my ears and also a noise that sounds like crickets chirping that just drives me nuts.  I can't sleep unless I can get my mind off the noise I hear in my head.  Everynight I read until I can't keep my eyes open.

Hopefully something will help us in the future.

cherneski
Belvidere, NJ
Joined: Mar 2009
Posts: 517
Sep 29, 2009 12:10 am cherneski wrote:

Chemo is so bad.  I know I should be thankful it is saving my life.  But the SEs are so bad.  I pray to God that all of my SEs are not perm.  I hope none of them stay with me but the chances of that I think are slim.

How about stuttering.  Not all the time.  I now stutter, has anyone had that?  Does that stay?  That was truly the most embarrassing at my 6 y/o daughters soccer game on Sat while I was cheering her on from the stands stuttering as I was yelling.

Sherry hope you dont mind me asking questions on your thread, but it seems like the right place. 

Hugs

Deborah age 38 DCIS, IDC, ILC, BRCA- Started chemo TCx6 on 06.22.09
Diagnosis: 4/9/2009, IDC, 2cm, Stage IIIa, Grade 3, 7/13 nodes, ER+/PR+, HER2-
leaf
Joined: Dec 2005
Posts: 5,944
Sep 29, 2009 10:34 am leaf wrote:

I've not had chemo, but sometimes I stutter.  For me, if I say out loud that 'I'm stuttering again' (or something like that), then that usually stops my stuttering.  I don't know if it would work for you, but it would be simple to try.

If you're going through hell, keep going-Winston Churchill
lexislove
Joined: Sep 2007
Posts: 1,942
Sep 29, 2009 10:59 am lexislove wrote:

Im definatly not the same up top since having chemo. My concentration is zero. My vocabulary is getting back though...it will be 2 years since finishing chemo in February for me and I still have side effects here and there.

+++++++++++

Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
spar2
OK
Joined: Jan 2004
Posts: 6,036
Sep 29, 2009 01:43 pm spar2 wrote:

Cherneski,  I haven't had stuttering but try what leaf said and see if that works.  I love for you to ask any questions here, that is what it is for.  That is how we learn and don't feel so alone.  No matter what don't let stuttering keep you from yelling from the stands.  I bet it will get better.  Yea Cherneski, keep on yelling.  I get frustrated because I can't keep up in the chat room, it just goes so fast that by the time I think of an anwer the topic has changed and the humor games.  I can't even do the word games any more, just not sharp enough and this is from a 4.0 average in college. No one understands us like each other.  I love all of you.  I know I am feeling kind of mushy today but just wanted everyone to know how much they are appreciated.

www.spar2.multiply.com Lets help make each other's life better
cheryl58
OH
Joined: May 2006
Posts: 564
Oct 1, 2009 12:58 am cheryl58 wrote:

Well, my last chemo was 10/4/2006, and I still have major problems.  I would say that my memory issues and lack of ability to focus are my biggest concern at this time.  I also do medical transcription.  It takes me almost twice as long as it used to just to get through my work.  I am constantly looking things up that I "used" to know.  I have the same problems with the movies, except I don't remember watching them when my husband tells me we did.  I cannot remember what books I have read.  I lose track of time daily, weekly, monthly, yearly.  I am shocked that it is September (well, really October). 

My doctor does not think it was chemo (or so she says), my husband blames it on "our age"..51, my kids think it is because I don't pay attention, but I truly believe it was the chemo.  I was very organized, etc. before BC and now, I do not resemble that person at all.  I really feel good if I get something accomplished on any given day no matter how small it is because it meant that I had to focus and follow through on something.  I was put into menopause from chemo so maybe there is some truth to that, but wow, it was a dramatic and fast decline.

I wish someone had the answers.  It is very frustrating that my family/friends sometimes must think I am making excuses for my forgetfulness when I know that "something" just is not right.  My husband and doctor have both at one time implied that I gave myself amnesia somehow because I do not remember any day at all that I was given chemo once the needle went in.  I think it is because my doctor over-drugged me.  Doesn't Ativan (which I know was in that huge bag of pre-drugs) cause memory loss?  That is my answer as to why I cannot remember chemo days, but as to the rest of it, I just don't know. :(

cherneski
Belvidere, NJ
Joined: Mar 2009
Posts: 517
Oct 1, 2009 01:50 am cherneski wrote:

Cheryl, I was told they give us medication in/ the chemo purposely to cause amnesia.  During one of my TX I asked now what am I getting, the nurse replied "do you really want to know?"  At that moment I really didnt care, but yes I really want to know.  My nurse practiconer told me about them giving us that, I told another nurse in the same office that and she looked at me as though I had 3 heads and said no they dont (but she didnt sound real sure on her answer).  Well I believe the first one.  I have been told this also by a friend of mine that was told this when she went through chemo with her mother.  The apparently give you more of whatever that drug is when they up you dose (and of course dont tell us).  After TX #4 I lost 5 full days of memory.  I realize you ladies are talking about after, but I think it starts during and stays. 

Deborah age 38 DCIS, IDC, ILC, BRCA- Started chemo TCx6 on 06.22.09
Diagnosis: 4/9/2009, IDC, 2cm, Stage IIIa, Grade 3, 7/13 nodes, ER+/PR+, HER2-
cherneski
Belvidere, NJ
Joined: Mar 2009
Posts: 517
Oct 1, 2009 02:00 am cherneski wrote:

Eighteen patients with advanced epithelial ovarian cancer were given 36 courses of cis-platinum-containing chemotherapy at Cedars-Sinai Medical Center. Patients were given lorazepam (Ativan) prior to chemotherapy. Amnesia for the day of chemotherapy was reported in 29 courses. Lack of recall for the chemotherapy infusion and the subsequent 8 hr or greater was reported in 33 of the 36 courses. In two courses, no amnesia effects were noted. No serious side effects of lorazepam therapy occurred and all patients believed that the amnesic effect was beneficial during chemotherapy. Lorazepam (Ativan) appears to be a safe medication to induce amnesia for cis-platinum chemotherapy and deserves further study to determine its effect on anticipatory vomiting, nausea and vomiting, and patient compliance with continued chemotherapy.

from http://www.ncbi.nlm.nih.gov/pubmed/6538534

PMID: 6538534 [PubMed - indexed for MEDLINE]

Deborah age 38 DCIS, IDC, ILC, BRCA- Started chemo TCx6 on 06.22.09
Diagnosis: 4/9/2009, IDC, 2cm, Stage IIIa, Grade 3, 7/13 nodes, ER+/PR+, HER2-
cherneski
Belvidere, NJ
Joined: Mar 2009
Posts: 517
Oct 1, 2009 03:08 am cherneski wrote: I Have Chemo Brain t-shirts
Deborah age 38 DCIS, IDC, ILC, BRCA- Started chemo TCx6 on 06.22.09
Diagnosis: 4/9/2009, IDC, 2cm, Stage IIIa, Grade 3, 7/13 nodes, ER+/PR+, HER2-
leaf
Joined: Dec 2005
Posts: 5,944
Oct 1, 2009 05:40 am, edited Oct 1, 2009 05:40 AM by leaf leaf wrote:

I'm a hospital pharmacist, and at our hospital, they routinely give Ativan (or other benzodiazepines) before/during chemotherapy, not only to relieve anxiety but to help prevent nausea/vomiting.

They often also give corticosteroids, which can help with nausea, which can also affect memory.  This paper says that corticosteroids can have different effects on different individuals, and over time, but it sounds like they CAN affect memory. http://www.ncbi.nlm.nih.gov/pubmed/18824040

There is an ongoing study via Army of Women about chemobrain.  I'm sure there are others also.  I do not doubt chemobrain is real.

If you're going through hell, keep going-Winston Churchill
lbrewer
Joined: Dec 2008
Posts: 148
Oct 1, 2009 08:06 am lbrewer wrote:

new study on chemo brain:

http://www.medicalnewstoday.com/articles/164463.php

Pill
Joined: Sep 2009
Posts: 190
Oct 13, 2009 11:34 am, edited Oct 20, 2009 12:00 PM by Pill Pill wrote:
This Post was deleted by Pill.
WowCool
Joined: Nov 2009
Posts: 1
Nov 3, 2009 09:04 am WowCool wrote:

My general practitioner put me on Focalin for my cognitive issues.  It has changed my life, and I am actually feeling like ME again.  We have had to tweak the dose, but it has worked wonders.  Ask your doc about what is available.  It sure made a world of difference for me.


Diagnosis: 9/14/2008, IDC, 4cm, Stage IIb, Grade 3, 2/2 nodes, ER+/PR+, HER2+
msdmckee
Joined: Jan 2004
Posts: 83
Nov 3, 2009 09:36 pm msdmckee wrote:

I first "noticed" loss of hearing when my son said "Mom! The crickets are singing" ( It was the first part of spring)  I could not hear the crickets.  I had had a hearing test about a year before chemo and all was normal.  I went for another hearing test and, yep, there was significant loss.  I am 5  years out from chemo now, and can again hear crickets, but there are somethings that haven't come back.  If you think about chemo and the loss of hair, all your hair, it includes those tiny little ones in our ears that we never think about.  Until you lose hearing of course.

Sierra
Joined: Feb 2004
Posts: 4,894
Nov 4, 2009 02:28 pm, edited Nov 4, 2009 02:29 PM by Sierra Sierra wrote:

Hi Ladies:

I definitely notice my brain affected

and did go to my TX centre for some tips

my concentration can be just dreadful at times

Now I am today at the library

and have just ordered this new book

called:

OUR BRAIN AFTER CHEMO

by D. Silverman

it looks good

I hate to admit this, but I have of recent found

phone # in my purse, and gosh, I dont know whose it is

for the life of me.. mind you I meet a lot of people

but I dont like this.. at all

so, I shall try more puzzles

I listen to radio now, dont have a TV and try to absorb more

Hugs to all

Sierra

You really have to use the old brain

use it or lose it as they say :)

(near 10 yrs out)Laughing

Friends are more important than money!
cmharris59
GA
Joined: Nov 2007
Posts: 408
Nov 4, 2009 02:52 pm cmharris59 wrote:

Hi All,

I was just told yesterday by a friend that is a breast cancer survivor being treated at the Mayo Clinic in Fl, that there is a new study being conducted there to address the issues of chemo brain. She said that she didn't qualify to be in the study, so she didn't know the details.

It is irritating. My oncologist said that he had never heaard of chemotherapy causing chemo-brain and dismissed me completely.  i hate cancer docs and I hate cancer and most of all I hate chemo brain. I can no longer focus, concentrate, process math problems, remember important dates, balance my checkbook, etc. Prior to chemo, I had an excelllent memory, excellent math, calculuis, and physics skills, and beautiful handwriting. Forget all of that now. 

C

"The first thing I do in the morning is brush my teeth and sharpen my tongue." ~ Dorothy Parker
Diagnosis: 6/8/2007, IDC, 5cm, Stage IIb, Grade 3, 0/1 nodes, ER-/PR-, HER2+
Mandy1313
the North East
Joined: Aug 2008
Posts: 522
Nov 4, 2009 05:42 pm Mandy1313 wrote:

Hi cmharris!

Isn't it aggrivating when your oncologist denies a side effect?  Mine told me that chemo brain happened rarely but it was temporary.  Well mine hit badly last April...I became unable to produce words.  My chemo ended in May and I still have remaining issues:  like you it has affected my memory, math, and concentration.  I can't solve simple tasks; I can't remember names; and I still have times when I can't remember a word.  While it is not as bad as it was in April, I am far from back to normal.  

Mandy


Diagnosis: 7/2008, IDC, 1cm, Grade 1, 1/2 nodes, ER+/PR+, HER2-
cmharris59
GA
Joined: Nov 2007
Posts: 408
Nov 4, 2009 08:22 pm cmharris59 wrote:

Hi Mandy!

It seems that my oncologists live in a world of denial. It took months for them to admit that I had neuropathy - "because it was supposed to "go away"".  I do hate them! At least after I confronted my surgeons, they became more attentive and stopped treating me as though I was the most ignorant person in the county. 

C

"The first thing I do in the morning is brush my teeth and sharpen my tongue." ~ Dorothy Parker
Diagnosis: 6/8/2007, IDC, 5cm, Stage IIb, Grade 3, 0/1 nodes, ER-/PR-, HER2+
Mandy1313
the North East
Joined: Aug 2008
Posts: 522
Nov 4, 2009 08:32 pm Mandy1313 wrote:

Hi again C:  It drives me crazy that my onc was not supportive and did not say something like, I know it is tough because of the side effects but hang in there, we are fighting your cancer. Instead I was told that it could not be from the chemo.  I had edema and was told that since it was on day 9 it could not be from the chemo....I am talking about serious fluid retention. The next treatment on day 9 guess what came back---edema. I would bring articles in to show that the side effects were from the drugs because I got sick of being treated like a crazy person.    Here I am going through chemo and doing research to prove that I am having side effects rather than being supported and helped by my oncologist.    Finally my neuropathy was so bad that I could not sleep---I went in and asked for a bone scan because I thought it must be mets.....only then did they say that it looked like it was severe neuropathy. And I am still waiting for my pre chemo cognition to return.

Mandy

PS I hope some doctors read these threads....it would be good if someone somewhere supported their chemo patients. 


Diagnosis: 7/2008, IDC, 1cm, Grade 1, 1/2 nodes, ER+/PR+, HER2-
kareylou
Joined: Mar 2008
Posts: 16
Nov 5, 2009 12:38 am kareylou wrote:

I am having problems, still, five years out from diagnosis. A couple recent examples--I found a note I had written to myself. I have been writing a lot more notes and lists as a way to cope with my memory problems. It said, "Return special keys". I have no idea what that means. Now that's just not normal. Also a couple days ago I put a frozen meal in the microwave. I went to change laundry downstairs while it cooked. I came back up, cooked myself a nice pasta dinner, did dishes, went to bed. The next morning I opened my microwave and there was the frozen meal. I used to have the proverbial steel trap of a mind and it is very disappointing to me that I do these things. I feel in my bones that it is chemobrain.

A friend gave me a book called "Your Brain After Chemo" by Silverman and Davidson. It was very readable, informative, and hopeful. I recommend it.  

Maire67
NJ
Joined: Sep 2007
Posts: 406
Nov 5, 2009 02:03 pm Maire67 wrote:

YES....I miss my brain...it's embarrassing ( Did I spell that correctly?)  I can't write anymore. My thoughts are all scrambled.  Thank you all for your comments.  It's 4 years for me and I'm not about to tell anyone  it's chemo brain anymore.  Sometimes I see people I work with give me the strange look my dh gives me when I ramble on trying to get something out.  BUT I'm still here so they will have to put up with me.  I'm looking forward to finding the book.  


Diagnosis: 6/2005, ILC, 5cm, ER+/PR+, HER2+
Mandy1313
the North East
Joined: Aug 2008
Posts: 522
Nov 5, 2009 06:32 pm Mandy1313 wrote:

Thanks for the booik suggestion kareylou. I just ordered it.


Diagnosis: 7/2008, IDC, 1cm, Grade 1, 1/2 nodes, ER+/PR+, HER2-
lbrewer
Joined: Dec 2008
Posts: 148
Nov 5, 2009 07:12 pm lbrewer wrote:

I found out today chemo brain is acknowledged by the Americans with Disabilities Act (ADA).  SOme doctors have found ADHD medicines like Ritalin or Altzheimer drugs help their patients. There was also another name for chemo brain but I forgot it!

Page 1 of 2 (31 results)

1 2

© 2009 Breastcancer.org. All rights reserved.