EYE SIGHT ISSUES!!!
I am currently having some weird eye issues going on post chemo. I was wondering if anyone else has experienced sight issues after chemo. My last chemo was Oct 13. I do have an eye appt. today as well. Just a little freaked out.
Symptoms
Dry and irritated
Blurry vision
Pressure
Really hard time driving at night as the head lights and brake lights seem to be double for me or kinda of like a cloud below the light. ( if that makes any sense)
Comments
-
Hi Tanya,
Vision and eye problems can sometimes be a side effect of treatment. See the main Breastcancer.org site and the Vision and Eye Problems side effect page.
Hope this helps!
--The Mods
-
tanya, it's probably a residual SE from the chemo. I had some problem immediately following TCx4, but it seemed to clear up within a couple of months. My problem could best be described as just a vague lack of clarity -- to the point that I wasn't comfortable driving at night for a month or two because I felt I wasn't seeing everything, especially along the really dark edges of the road. And there have been other threads here talking about temporary eye problems after chemo.
When it comes to chemo SEs, it seems we're all a bit different, so maybe yours just came on later/slower than mine did, but will hopefully clear up soon. But I'm glad you're getting it checked out. Deanna
-
I also had eye problems from chemo. Bright lights would give me an instant headache. I also experienced blurry vision.
My eyes got better about 1 year after I completed my treatment. My vision used to be 20/15 (better than normal) and now I have to wear glasses whenever I read or get on the computer. I know some of this is due to old age but my eyesight progressively got worse from chemo for the first year.
The good news is that this may not be permanent - just a problem to get through for the time being. The bright lights don't bother me much anymore.
-
When I started rads, I had eye problems. The RO seemed unconcerned. His nurse advised eye drops. So also did ALL the previously raded women in my support group. It's on the list of those things they don't tell you about, so you don't develop it by anticipating it. (Soooo unhelpful not to have information, isn't it!?)
Anyway, from rads, the eyes, skin, throat, hair all become very dry. You need to keep up your water intake and use drops a lot and often in your eyes.
I was so worried when it first happened. It was scary! I wish they had told me.
The eye drops took care of it though. Just dry eyes.
-
Thanks everyone for your help! I really thought I was going crazy! It was just all of a sudden there and i could not figurer out what was going on. I really hope its just dry eyes.
-
I had my 15 rad tx today and afterwards my eyes were sore and dry. Thanks for the tip about eye drops.
-
Thank you all so much for responding and making me feel better. .it's always good to know that you are not crazy! I went to the eye doc yesterday ( 2hrs it took ) and he said I have very dry eyes and sever eye strain in both eyes. He gave me some drops I have to put in 4 times a day. Thanks again for all the support. This wed site has been so great!
-
I totally had weird eyesight issues. I thought it was the tamoxifen, but it could have been post chemo because I was probably 5-6 weeks PFC when it started. I'm not a headachey person but it was like a light migraine. My eyes felt like they weren't shaped right anymore. Headache in the light, etc. it went away in about 2 weeks I think. You're not crazy!
-
Glad I found this thread. I've also had issues with my eyesight since treatment. Started about 6 weeks after chemo ended....blurred vision and halos around bright lights. My eye doctor said I had extreme dry eye & prescribed drops, which helped a lot. Then during rads, I developed a really bad headache that lasted for about 2 weeks. My onc was about to send me for a cat scan, but fortunately it went away. I'm 9 months out from treatment and it's much better, but I still have some residual issues. I don't think I see as well as I used to, especially at night. And I have to wear glasses instead of contacts to my job, where I work at a computer all day. Of course, this could also just be the aging process, but I really think it's treatment related.
-
I think this is a very important thread. I know with radiation, they just don't tell you about the eyes unless you start freaking out.
I am an artist and, even if I were not, I would still value my eyesight and I was VERY worried I was damaging -or had already damaged- it! My eyes were sore, scratchy, red, and I had blurred vision they were so dry. Now THAT IS SCARY! A heads-up from the doc or team about this would have been helpful.
And, even after I started the eye drops, my right eye (I was radiaited on the right side) stayed more blurry and needed more drops than the other. I am about three weeks out now and still using drops but my eyesight has seemed to resolve for which I am quite grateful.
If I had had to seriously risk my eyesight though, I would have been piping mad about not being told.
-
It seems to me that most of us aren't told about all the side effects our treatments can cause. Reading through these boards, there are a lot of ladies with vision problems, hearing problems, and other physical stuff that started after treatment. And most of the time, their oncs aren't concerned, or they claim it's not from the treatment. I for one don't believe it. Don't get me wrong....I would have had my treatment no matter what....but I agree with truebff -- a heads up would be helpful.
-
I had, and am still having, strange blurry spots that come and go several times a day. My onc says chemo does not cause that. I never had any problems prior to chemo and the night of chemo I had vision problems so bad I could not see and had to feel my way to the bathroom. It was very dark and blotchy. Same thing with my next chemo then none. I reported it to my Onc and nurse. Huh they said, strange, maybe I had a clot or something. Then brushed it off. My eye dr says it is an Ocular Aura/Ocular Migraine without the Migraine. MRI of brain was neg for any pathology. It is just so strange that this has happened since the chemo (Taxotere and Cytoxan) and not before. Like I said, I still have those blurry spots. Anyone else have this? Ijust cant help but think it is related to chemo some how.
-
Hey Ladies!! I thought I would share these great photos that my BF took. I think everyone that has gone through what we have should have a great photo session.
http://www.rj3photography.com/Portraits/Tanya-S-Portraits/19214251_GfhrxD#!i=1498539970&k=FRfL46F
-
Could my current blurred vision (looking through a dark gray fog) be related to my chemotherapy treatments? On Aug. 31, 2011, I completed six cycles of Herceptin, Taxotere, and Carboplatin (cisplatin) for Breast Cancer-HER2/Stage 3 and Lung Cancer. I am now receiving a maintenance dose of Herceptin every three weeks and finished my 12th dose of Herceptin on January 18, 2012.
The gray fog first occurred in October 2011 in the right eye only. It came and went away in two weeks. However, this recent occurrence in January 2012 is more severe and came on slowly. Again only in the right eye. I've been looking through the dark gray fog for two weeks now. I just visited the ophthalmologist and he has referred me to a neuro-ophthalmologist because there may be a problem with my optic nerve. I hope this problem is only temporary. Has anyone else had vision problems with the chemo drugs, Herceptin, Taxotere or Carboplatin. I have no vision problems in the left eye.
-
I have been having those eye symptoms for about a year. I went and got my eyes checked and everything is fine. I tihnk the chemo and all the meds I was on messed up my sight. I am still taking effexor and xanax so those both make my eyesite a little fuzzy. But yes, I think your symptoms are residual from checmo and I would not worry too much. I would tell your onc about these symptoms just to be safe.
-
Now, I have all these "spots" on my eyes.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team