Facial Numbness / Neuropathy on Taxol
Has anyone experienced facial numbness around the mouth during Taxol treatments? I've only had 2 of 12 weekly doses and the entire area around my face is numb. Under my lip, my chin, and my cheeks up to my cheek bones. It's like when you leave the dentist after getting numbing shots in your mouth, only just the skin part. I'm freaking out because I understand this is a form of neuropathy and it's so early in treatment that if I continue it will only get worse and be permanent. I can't find much on facial neuropathy. Anyone else experience this
Comments
-
Yes, I had this happen on Taxotere, starting from the first infusion. I took L-glutamine and B-6 to keep it from getting worse. It resolved completely once chemo was done, as did the tingling/numbness in my hands and bottoms of my fee. I believe there is at least one on the weekly taxol thread who also experienced this. You might talk to your MO about adding the supplements - I used 30g of the L-glutamine, broken into 3 10g servings mixed with non-acidic old drinks. I took one regular capsule of B-6 daily. I also took one capsule of acetyl l-carnitine, but studies using megadoses had some contraindications so it has fallen out favor during chemo.
-
Really?! SpecialK, that's such a relief!! My nurse said something about maybe reducing amount and I'm worried about that because I want to hit this with everything I have. So yours didn't get worse with each treatment? Did you get the finger/toe neuropathy at the same time? No signs of tat yet for me.
I'm on the Glutamine powder but haven't taken any B6 yet. Will definitely start that.
Did your doc say anything about changing your course of treatment from it
-
Yes, this happened to me too. It started after 9th round of Taxol. It is around the left side if my mouth and chin. I also developed numbness in my feet ant fingers that would come and go but then stayed. I also developed the darkening of the skin on the backs of my hands an a red rash that spread across the backs of my hands and fingers. The skin was rough and sore. Due to all these side effects they stopped the Taxol therapy after round 10. I've had to pause my AC treatments halfway too because of a nail infection that will not clear. My doctor prescribed Gabapentin for the neuropathy and my feet are a bit better but I still feel the slight numbness near my mouth. I'm anxious to get my last 2 AC treatments done to see if the face numbness goes away. I will say that I do not notice it too much but I am aware of to off and on. Good luck to us!
-
I had facial numbness from Taxol for the first 3 infusions. It didn't get worse and I didn't get it with subsequent infusions. For hands and feet I did icing. Finished Taxol a month ago and have no numbness at all.
-
Thank you so much for your responses. My oncologist and her nurse, very experienced, have never had a patient experience this form of neuropathy! Unfortunately she asked me to sit this week's Taxol out. Pretty devastating for me. If it doesn't get worse, we'll resume next week at a reduced dose (85%) for the remaining 10 infusions.
Lonestar: sorry about all your symptoms! It's great you got 10 treatments under your belt - I'm hoping for that myself. Did your doctor ever try reducing your dose to see if the SE's were lessened?
Maya: did your face numbness go away between those first three treatments? It's so weird but mine isn't getting any better and it's the area all the way around my mouth - my chin, the skin between my nose and upper lip, and my cheeks all the way up to my cheek bones. Today is day 8 with it. If it even lessened a bit I'd feel better about it. Was your doctor worried about it? Did they suggest that it could get worse or be permanent? It's so encouraging that you experienced it early on too, and that it went away!!
Thanks again for all the responses. It helps to know I'm not alone with such a rare SE
-
I just thought I'd provide an update to this in case anyone in the future is experiencing this symptom and looking for information (aka hope). I did resume treatment at 85%, after postponing the third dose by one week. The numbness hadn't gotten better, but it hadn't gotten any worse either. I have now completed my 9th treatment, and the facial numbness is nearly completely resolved. I would say there is some residual numbness, residual in that I would probably never have noticed it if I wasn't paying so much attention to my face. However, at this point it's all a head game and it could be completely resolved and I just THINK it's still a little numb. Who knows. Either way, I can now feel my sons face when he rubs it against my cheek! Yay!!
That's all. Just good news.
-
Hello! Just wanted to revive this thread since I am experiencing numbness in my chin this week. I had dose dense Taxol on Thursday, Neulasta on Friday, and then Tuesday noticed numbness in my chin. Feels like I just came from a dental procedure where they numbed up my mouth! I went to the ER because my doctor wanted to rule out something more serious, like a stroke. So that's good it isn't a stroke, but I still have the numbness. Does anyone else have some input about this? Thanks so much!
-
My MO offered to cut back on the dose of Taxotere. He made it my choice as we were treating an aggressive high risk cancer. I choose to go forward. I have numbness & tingling in my fingers a couple of times a week - but it is so much better that I'm willing to settle. Unfortunately my feet are still lumps of dead ice. Luckily no pain, but no feeling either - which throws off my balance and makes it extremely hard to wear most socks & shoes. The conventional wisdom says you may continue to see improvement for 2+ years after treatment ends. My treatment ended 3-1/2 years ago so I guess it's permanent.
BTW - I did ice both my hands & my feet. Guess I was just lucky.
-
MinusTwo, thanks for the input. I'm sure at my next appointment I can discuss the option of decreasing the dose. My doctor was not even sure that the Taxol is causing the numbness in my chin. Did you have numbness in your chin/ facial area? I really hope this isn't permanent! It's good to be able to get input from other people out there! I appreciate it! On another note, I see that you did Neuasta. How did that go for you? I had one injection so far and had a lot of bone pain, even with the Claritin/ naproxen combo that was suggested. But definitely don't want low WBC to become a problem (again). Thanks!
-
I don't remember facial numbness. That said there are lots of things I don't remember. Chemo brain is magical. I do remember some highlights (or rather lowlights) but have put most of the other memories of pain, etc. on an external hard drive & deleted from my every day brain.
Yes I took a neulasta shot 24 hours after every chemo. My WBCs were still low so I was glad for the boost. Make sure you (or the nurse) holds & warms up the liquid before injecting. I had mine in my belly. The Claritin worked for the most part, but I started it the day before chemo and continued for 5 days to a week afterwards. Some people just stay on Claritin the entire treatment period, but I wasn't comfortable with any more meds than necessary. BTW - be sure it's regular Claritin and not the "D".
-
I had some numbness in my nose and upper lip during Taxol and, to a lesser extent, the entire left side of my face. The left side is where I had Bell's palsy many years ago and it's also the surgical side. It mostly resolved without a problem, but not so with the neuropathy in NY fingers, toes and, at times, left shin. I hope you regain feeling soon.
Lyn
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